[Title 21 CFR ]
[Code of Federal Regulations (annual edition) - April 1, 1996 Edition]
[From the U.S. Government Publishing Office]


          21



          Food and Drugs



[[Page i]]

PART 1300 TO END

          Revised as of April 1, 1996
          CONTAINING
          A CODIFICATION OF DOCUMENTS
          OF GENERAL APPLICABILITY
          AND FUTURE EFFECT

          AS OF APRIL 1, 1996
          With Ancillaries
          Published by
          the Office of the Federal Register
          National Archives and Records
          Administration

          as a Special Edition of
          the Federal Register



[[Page ii]]


                                      




                     U.S. GOVERNMENT PRINTING OFFICE
                            WASHINGTON : 1996



               For sale by U.S. Government Printing Office
 Superintendent of Documents, Mail Stop: SSOP, Washington, DC 20402-9328



[[Page iii]]




                            Table of Contents


                                                                    Page
  Explanation.................................................       v
  Title 21:
    Chapter II--Drug Enforcement Administration, Department of 
        Justice...............................................       3
    Chapter III--Office of National Drug Control Policy.......     247
  Finding Aids:
    Table of CFR Titles and Chapters..........................     309
    Alphabetical List of Agencies Appearing in the CFR........     325
    List of CFR Sections Affected.............................     325

[[Page iv]]



      




----------------------------------------------------------
    Cite this Code:  CFR
    
    To cite the regulations in this volume use title, part
      and section number. Thus, 21 CFR 1301.01 refers to
      title 21, part 1301, section 01.
                                                                                                                
----------------------------------------------------------
                                                                                                                


[[Page v]]



                               EXPLANATION

    The Code of Federal Regulations is a codification of the general and 
permanent rules published in the Federal Register by the Executive 
departments and agencies of the Federal Government. The Code is divided 
into 50 titles which represent broad areas subject to Federal 
regulation. Each title is divided into chapters which usually bear the 
name of the issuing agency. Each chapter is further subdivided into 
parts covering specific regulatory areas.
    Each volume of the Code is revised at least once each calendar year 
and issued on a quarterly basis approximately as follows:

Title 1 through Title 16.................................as of January 1
Title 17 through Title 27..................................as of April 1
Title 28 through Title 41...................................as of July 1
Title 42 through Title 50................................as of October 1
    The appropriate revision date is printed on the cover of each 
volume.

LEGAL STATUS

    The contents of the Federal Register are required to be judicially 
noticed (44 U.S.C. 1507). The Code of Federal Regulations is prima facie 
evidence of the text of the original documents (44 U.S.C. 1510).

HOW TO USE THE CODE OF FEDERAL REGULATIONS

    The Code of Federal Regulations is kept up to date by the individual 
issues of the Federal Register. These two publications must be used 
together to determine the latest version of any given rule.
    To determine whether a Code volume has been amended since its 
revision date (in this case, April 1, 1996), consult the ``List of CFR 
Sections Affected (LSA),'' which is issued monthly, and the ``Cumulative 
List of Parts Affected,'' which appears in the Reader Aids section of 
the daily Federal Register. These two lists will identify the Federal 
Register page number of the latest amendment of any given rule.

EFFECTIVE AND EXPIRATION DATES

    Each volume of the Code contains amendments published in the Federal 
Register since the last revision of that volume of the Code. Source 
citations for the regulations are referred to by volume number and page 
number of the Federal Register and date of publication. Publication 
dates and effective dates are usually not the same and care must be 
exercised by the user in determining the actual effective date. In 
instances where the effective date is beyond the cut-off date for the 
Code a note has been inserted to reflect the future effective date. In 
those instances where a regulation published in the Federal Register 
states a date certain for expiration, an appropriate note will be 
inserted following the text.

OMB CONTROL NUMBERS

    The Paperwork Reduction Act of 1980 (Pub. L. 96-511) requires 
Federal agencies to display an OMB control number with their information 
collection request. Many agencies have begun publishing numerous OMB 
control numbers as

[[Page vi]]

amendments to existing regulations in the CFR. These OMB numbers are 
placed as close as possible to the applicable recordkeeping or reporting 
requirements.

OBSOLETE PROVISIONS

    Provisions that become obsolete before the revision date stated on 
the cover of each volume are not carried. Code users may find the text 
of provisions in effect on a given date in the past by using the 
appropriate numerical list of sections affected. For the period before 
January 1, 1986, consult either the List of CFR Sections Affected, 1949-
1963, 1964-1972, or 1973-1985, published in seven separate volumes. For 
the period beginning January 1, 1986, a ``List of CFR Sections 
Affected'' is published at the end of each CFR volume.

CFR INDEXES AND TABULAR GUIDES

    A subject index to the Code of Federal Regulations is contained in a 
separate volume, revised annually as of January 1, entitled CFR Index 
and Finding Aids. This volume contains the Parallel Table of Statutory 
Authorities and Agency Rules (Table I), and Acts Requiring Publication 
in the Federal Register (Table II). A list of CFR titles, chapters, and 
parts and an alphabetical list of agencies publishing in the CFR are 
also included in this volume.
    An index to the text of ``Title 3--The President'' is carried within 
that volume.
    The Federal Register Index is issued monthly in cumulative form. 
This index is based on a consolidation of the ``Contents'' entries in 
the daily Federal Register.
    A List of CFR Sections Affected (LSA) is published monthly, keyed to 
the revision dates of the 50 CFR titles.

REPUBLICATION OF MATERIAL

    There are no restrictions on the republication of material appearing 
in the Code of Federal Regulations.

INQUIRIES

    For a legal interpretation or explanation of any regulation in this 
volume, contact the issuing agency. The issuing agency's name appears at 
the top of odd-numbered pages.
    For inquiries concerning CFR reference assistance, call 202-523-5227 
or write to the Director, Office of the Federal Register, National 
Archives and Records Administration, Washington, DC 20408.
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                              Richard L. Claypoole,
                                    Director,
                          Office of the Federal Register.

April 1, 1996.



[[Page vii]]



                               THIS TITLE

    Title 21--Food and Drugs is composed of nine volumes. The parts in 
these volumes are arranged in the following order: Parts 1-99, 100-169, 
170-199, 200-299, 300-499, 500-599, 600-799, 800-1299 and 1300-end. The 
first eight volumes, containing parts 1-1299, comprise Chapter I--Food 
and Drug Administration, Department of Health and Human Services. The 
ninth volume, containing part 1300 to End, includes Chapter II--Drug 
Enforcement Administration, Department of Justice and Chapter III--
Office of National Drug Control Policy. The contents of these volumes 
represent all current regulations codified under this title of the CFR 
as of April 1, 1996.

    The Table of Exempt Prescription Products to part 1308 appears in 
the volume containing part 1300-End.

    Redesignation tables for Chapter I--Food and Drug Administration 
appear in the Finding Aids section for the volumes containing parts 170-
199 and 500-599.

    For this volume, Christopher R. Choate was Chief Editor. The Code of 
Federal Regulations publication program is under the direction of 
Frances D. McDonald, assisted by Alomha S. Morris.

[[Page viii]]

[GRAPHIC] [TIFF OMITTED] TFRORDR.FRM

[[Page 1]]

                                                                     HN




                         TITLE 21-FOOD AND DRUGS




                  (This book contains part 1300 to End)

  --------------------------------------------------------------------
                                                                    Part
chapter ii--Drug Enforcement Administration, Department of 
  Justice...................................................        1301
chapter iii--Office of National Drug Control Policy.........        1401



Cross References: U.S. Customs Service, Department of the Treasury: See 
  Customs Duties, 19 CFR chapter I.

Regulations of the Public Health Service, Department of Health and Human 
  Services, applying to narcotic addicts: See Public Health, 42 CFR part 
  2.



  Editorial Note: Other regulations issued by the Department of Justice 
appear in title 4, title 8, title 28.

[[Page 3]]





CHAPTER II--DRUG ENFORCEMENT






ADMINISTRATION, DEPARTMENT OF JUSTICE




  --------------------------------------------------------------------

Part                                                                Page
1300      [Reserved]
1301            Registration of manufacturers, distributors, 
                    and dispensers of controlled substances.
1302            Labeling and packaging requirements for 
                    controlled substances...................
1303            Quotas......................................
1304            Records and reports of registrants..........
1305            Order forms.................................
1306            Prescriptions...............................
1307            Miscellaneous...............................
1308            Schedules of controlled substances..........
1309            Registration of manufacturers, distributors, 
                    importers and exporters of list I 
                    chemicals...............................
1310            Records and reports of listed chemicals and 
                    certain machines........................
1311            Registration of importers and exporters of 
                    controlled substances...................
1312            Importation and exportation of controlled 
                    substances..............................
1313            Importation and exportation of precursors 
                    and essential chemicals.................
1314-1315  
[Reserved]
1316            Administrative functions, practices, and 
                    procedures..............................

[[Page 5]]





PART 1300--[RESERVED]--Table of Contents






PART 1301--REGISTRATION OF MANUFACTURERS, DISTRIBUTORS, AND DISPENSERS OF CONTROLLED SUBSTANCES--Table of Contents




                           General Information

Sec.
1301.01  Scope of Part 1301.
1301.02  Definitions.
1301.03  Information; special instructions.

                Fees for Registration and Reregistration

1301.11  Fee amounts.
1301.12  Time and method of payment; refund.
1301.13  Persons exempt from fee.

                      Requirements for Registration

1301.21  Persons required to register.
1301.22  Separate registration for independent activities.
1301.23  Separate registrations for separate locations.
1301.24  Exemption of agents and employees; affiliated practitioners.
1301.25  Exemption of certain military and other personnel.
1301.26  Exemption of law enforcement officials.
1301.27  Exemption of civil defense officials.
1301.28  Registration regarding ocean vessels.
1301.29  Provisional registration of narcotic treatment programs; 
          compounders.

                      Applications for Registration

1301.31  Time for application for registration; expiration date.
1301.32  Application forms; contents; signature.
1301.33  Research protocols.
1301.34  Filing of application; joint filings.
1301.35  Acceptance for filing; defective applications.
1301.36  Additional information.
1301.37  Amendments to and withdrawal of applications.
1301.38  Special procedures for certain applications.

  Action on Applications for Registration: Revocation or Suspension of 
                              Registration

1301.41  Administrative review generally.
1301.42  Action on applications for research in Schedule I substances.
1301.43  Application for bulk manufacture of Sschedule I and II 
          substances.
1301.44  Certificate of registration; denial of registration.
1301.45  Suspension or revocation of registration.
1301.46  Suspension of registration pending final order.
1301.47  Extension of registration pending final order.
1301.48  Order to show cause.

                                Hearings

1301.51  Hearings generally.
1301.52  Purpose of hearing.
1301.53  Waiver or modification of rules.
1301.54  Request for hearing or appearance; waiver.
1301.55  Burden of proof.
1301.56  Time and place of hearing.
1301.57  Final order.

         Modification, Transfer and Termination of Registration

1301.61  Modification in registration.
1301.62  Termination of registration.
1301.63  Transfer of registration.

                          Security Requirements

1301.71  Security requirements generally.
1301.72  Physical security controls for nonpractitioners; narcotic 
          treatment programs and compounders for narcotic treatment 
          programs; storage areas.
1301.73  Physical security controls for nonpractitioners; compounders 
          for narcotic treatment programs; manufacturing and compounding 
          areas.
1301.74  Other security controls for nonpractitioners; narcotic 
          treatment programs and compounders for narcotic treatment 
          programs.
1301.75  Physical security controls for practitioners.
1301.76  Other security controls for practitioners.

                  Employee Screening--Non-Practitioners

1301.90  Employee screening procedures.
1301.91  Employee responsibility to report drug diversion.
1301.92  Illicit activities by employees.
1301.93  Sources of information for employee checks.

    Authority: 21 U.S.C. 821, 822, 823, 824, 871(b), 875, 877.

    Source: 36 FR 7778, Apr. 24, 1971, unless otherwise noted. 
Redesignated at 38 FR 26609, Sept. 24, 1973.

                           General Information



Sec. 1301.01   Scope of Part 1301.

    Procedures governing the registration of manufacturers, 
distributors, and dispensers of controlled substances pursuant to 
sections 1301 through 1304 of the Act (21 U.S.C. 821-824) are set forth 
generally by those sections and specifically by the sections of this 
part.

[[Page 5]]



Sec. 1301.02   Definitions.

    As used in this part, the following terms shall have the meanings 
specified:
    (a) The term Act means the Controlled Substances Act (84 Stat. 1242; 
21 U.S.C. 801) and/or the Controlled Substances Import and Export Act 
(84 Stat. 1285; 21 U.S.C. 951).
    (b) The term basic class means, as to controlled substances listed 
in Schedules I and II:
    (1) Each of the opiates, including its isomers, esters, ethers, 
salts, and salts of isomers, esters, and ethers whenever the existence 
of such isomers, esters, ethers, and salts is possible within the 
specific chemical designation, listed in Sec. 1308.11 (b) of this 
chapter;
    (2) Each of the opium derivatives, including its salts, isomers, and 
salts of isomers whenever the existence of such salts, isomers, and 
salts of isomers is possible within the specific chemical designation, 
listed in Sec. 1308.11(c) of this chapter;
    (3) Each of the hallucinogenic substances, including its salts, 
isomers, and salts of isomers whenever the existence of such salts, 
isomers, and salts of isomers is possible within the specific chemical 
designation, listed in Sec. 1308.11(d) of this chapter;
    (4) Each of the following substances, whether produced directly or 
indirectly by extraction from substances of vegetable origin, or 
independently by means of chemical synthesis, or by a combination of 
extraction and chemical synthesis:
    (i) Opium, including raw opium, opium extracts, opium fluid 
extracts, powdered opium, granulated opium, deodorized opium and 
tincture of opium;
    (ii) Apomorphine;
    (iii) Codeine;
    (iv) Etorphine hydrochloride;
    (v) Ethylmorphine;
    (vi) Hydrocodone;
    (vii) Hydromorphone;
    (viii) Metopon;
    (ix) Morphine;
    (x) Oxycodone;
    (xi) Oxymorphone;
    (xii) Thebaine;
    (xiii) Mixed alkaloids of opium listed in Sec. 1308.12(b) (2) of 
this chapter;
    (xiv) Cocaine; and
    (xv) Ecgonine;
    (5) Each of the opiates, including its isomers, esters, ethers, 
salts, and salts of isomers, esters, and ethers whenever the existence 
of such isomers, esters, ethers, and salts is possible within the 
specific chemical designation, listed in Sec. 1308.12 (c) of this 
chapter; and
    (6) Methamphetamine, its salts, isomers, and salts of its isomers;
    (7) Amphetamine, its salts, optical isomers, and salts of its 
optical isomers;
    (8) Phenmetrazine and its salts;
    (9) Methylphenidate;
    (10) Each of the substances having a depressant effect on the 
central nervous system, including its salts, isomers, and salts of 
isomers whenever the existence of such salts, isomers, and salts of 
isomers is possible within the specific chemical designation, listed in 
Sec. 1308.12 (e) of this chapter.
    (c) The term Administration means the Drug Enforcement 
Administration.
    (d) The term compounder means any person engaging in maintenance or 
detoxification treatment who also mixes, prepares, packages or changes 
the dosage form of a narcotic drug listed in Schedules II, III, IV or V 
for use in maintenance or detoxification treatment by another narcotic 
treatment program.
    (e) The term detoxification treatment means the dispensing, for a 
period of time as specified below, of a narcotic drug or narcotic drugs 
in decreasing doses to an individual to alleviate adverse physiological 
or psychological effects incident to withdrawal from the continuous or 
sustained use of a narcotic drug and as a method of bringing the 
individual to a narcotic drug-free state within such period of time. 
There are two types of detoxification treatment: Short-term 
detoxification treatment and long-term detoxification treatment.
    (1) Short-term detoxification treatment is for a period not in 
excess of 30 days.
    (2) Long-term detoxification treatment is for a period more than 30 
days but not in excess of 180 days.
    (f) The term Administrator means the Administrator of the Drug 
Enforcement Administration. The Administrator has been delegated 
authority under the Act by the Attorney General (28 CFR 0.100).

[[Page 6]]

    (g) The term hearing means any hearing held pursuant to this part 
for the granting, denial, revocation, or suspension of a registration 
pursuant to sections 303 and 304 of the Act (21 U.S.C. 823-824).
    (h) The term maintenance treatment means the dispensing for a period 
in excess of twenty-one days, of a narcotic drug or narcotic drugs in 
the treatment of an individual for dependence upon heroin or other 
morphine-like drug.
    (i) The term narcotic treatment program means a program engaged in 
maintenance and/or detoxification treatment with narcotic drugs.
    (j) The term person includes any individual, corporation, government 
or governmental subdivision or agency, business trust, partnership, 
association, or other legal entity.
    (k) The terms register and registration refer only to registration 
required and permitted by section 303 of the Act (21 U.S.C. 823).
    (l) The term registrant means any person who is registered pursuant 
to either section 303 or section 1008 of the Act (21 U.S.C. 823 or 958).
    (m) Any term not defined in this section shall have the definition 
set forth in section 102 of the Act (21 U.S.C. 802).

[36 FR 7778, Apr. 24, 1971, as amended at 36 FR 12735, July 7, 1971; 36 
FR 20687, Oct. 28, 1971. Redesignated at 38 FR 26609, Sept. 24, l973]

    Editorial Note: For FR citations affecting Sec. 1301.02, see the 
List of CFR Sections Affected in the Finding Aids section of this 
volume.



Sec. 1301.03   Information; special instructions.

    Information regarding procedures under these rules and instructions 
supplementing these rules will be furnished upon request by writing to 
the Registration Unit, Drug Enforcement Administration, Department of 
Justice, Post Office Box 28083, Central Station, Washington, DC 20005.

[36 FR 7778, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 23, 1973, 
and amended at 51 FR 5319, Feb. 13, 1986]

                Fees for Registration and Reregistration



Sec. 1301.11  Fee amounts.

    (a) For each registration or reregistration to manufacture 
controlled substances, the registrant shall pay an application fee of 
$875 for an annual registration.
    (b) For each registration or reregistration to distribute controlled 
substances, the registrant shall pay an application fee of $438 for an 
annual registration.
    (c) For each registration or reregistration to dispense, or to 
conduct instructional activities with, controlled substances listed in 
Schedules II through V, the registrant shall pay an application fee of 
$210 for a three-year registration equating to an annualized fee of $70 
per annum.
    (d) For each registration or reregistration to conduct research or 
instructional activities with a controlled substance listed in Schedule 
I, or to conduct research with a controlled substance in Schedules II 
through V, the registrant shall pay an application fee of $70 for an 
annual registration.
    (e) For each registration or reregistration to conduct chemical 
analysis with controlled substances listed in any schedule, the 
registrant shall pay an application fee of $70 for an annual 
registration.
    (f) For each registration or reregistration to engage in a narcotic 
treatment program, including a compounder, the registrant shall pay an 
application fee of $70 for an annual registration.

[58 FR 15274, Mar. 22, 1993]



Sec. 1301.12   Time and method of payment; refund.

    Application fees shall be paid at the time when the application for 
registration or reregistration is submitted for filing. Payments should 
be made in the form of a personal, certified, or cashier's check or 
money order made payable to ``Drug Enforcement Administration.'' 
Payments made in the form of stamps, foreign currency, or third party 
endorsed checks will not be

[[Page 7]]

accepted. These application fees are not refundable.

[52 FR 20599, June 2, 1987, as amended at 53 FR 4963, Feb. 19, 1988]



Sec. 1301.13  Persons exempt from fee.

    (a) The Administrator shall exempt from payment of an application 
fee for registration or reregistration any hospital or other institution 
which is operated by an agency of the United States (including the U.S. 
Army, Navy, Marine Corps, Air Force, and Coast Guard), of any State, or 
any political subdivision or agency thereof.
    (b) In order to claim exemption from payment of a registration or 
reregistration application fee, the registrant shall have completed the 
certification on the appropriate application form, wherein the 
registrant's officer certifies to the status and address of the 
registrant.
    (c) Exemption from payment of a registration or reregistration 
application fee does not relieve the registrant of any other 
requirements or duties prescribed by law.

[36 FR 7778, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971; 36 
FR 18728, Sept. 21, 1971; 38 FR 756, Jan. 4, 1973. Redesignated at 38 FR 
26609, Sept. 24, l973 and amended at 53 FR 4963, Feb. 19, 1988; 59 FR 
8859, Feb. 24, 1994]

                      Requirements for Registration



Sec. 1301.21   Persons required to register.

    Every person who manufactures, distributes, or dispenses any 
controlled substance or who proposes to engage in the manufacture, 
distribution, or dispensing of any controlled substance shall obtain 
annually a registration unless exempted by law or pursuant to 
Secs. 1301.24-1301.29. Only persons actually engaged in such activities 
are required to obtain a registration; related or affiliated persons who 
are not engaged in such activities are not required to be registered. 
(For example, a stockholder or parent corporation of a corporation 
manufacturing controlled substances is not required to obtain a 
registration.)

[36 FR 7778, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, l973]



Sec. 1301.22   Separate registration for independent activities.

    (a) The following groups of activities are deemed to be independent 
of each other:
    (1) Manufacturing controlled substances;
    (2) Distributing controlled substances;
    (3) Dispensing controlled substances listed in Schedules II through 
V;
    (4) Conducting research with controlled substances listed in 
Schedules II through V;
    (5) Conducting instructional activities with controlled substances 
listed in schedules II through V;
    (6) Conducting a narcotic treatment program using any narcotic drug 
listed in Schedules II, III, IV or V, however, pursuant to Sec. 1301.24, 
employees, agents, or affiliated practitioners, in programs, need not 
register separately. Each program site located away from the principal 
location and at which place narcotic drugs are stored or dispensed must 
be separately registered and obtain narcotic drugs by use of order forms 
pursuant to Sec. 1305.03;
    (7) Conducting research and instructional activities with controlled 
substances listed in Schedule I;
    (8) Conducting chemical analysis with controlled substances listed 
in any schedule;
    (9) Importing controlled substances;
    (10) Exporting controlled substances; and
    (11) A compounder as defined by Sec. 1301.02(d).
    (b) Every person who engages in more than one group of independent 
activities shall obtain a separate registration for each group of 
activities, except as provided in this paragraph. Any person, when 
registered to engage in the group of activities described in each 
subparagraph in this paragraph, shall be authorized to engage in the 
coincident activities described in that subparagraph without obtaining a 
registration to engage in such coincident activities, provided that, 
unless specifically exempted, he complies with all requirements and 
duties prescribed by law for persons registered to engage in such 
coincident activities:
    (1) A person registered to manufacture or import any controlled

[[Page 8]]

substance or basic class of controlled substance shall be authorized to 
distribute that substance or class, but no other substance or class 
which he is not registered to manufacture or import;
    (2) A person registered to manufacture any controlled substance 
listed in Schedules II through V shall be authorized to conduct chemical 
analysis and preclinical research (including quality control analysis) 
with narcotic and non-narcotic controlled substances listed in those 
schedules in which he is authorized to manufacture;
    (3) A person registered to conduct research with a basic class of 
controlled substance listed in Schedule I shall be authorized to 
manufacture or import such class if and to the extent that such 
manufacture or importation is set forth in the research protocol 
described in Sec. 1301.33 and to distribute such class to other persons 
registered or authorized to conduct research with such class or 
registered or authorized to conduct chemical analysis with controlled 
substances;
    (4) A person registered or authorized to conduct chemical analysis 
with controlled substances shall be authorized to manufacture and import 
such substances for analytical or instructional purposes, to distribute 
such substances to other persons registered or authorized to conduct 
chemical analysis or instructional activities or research with such 
substances and to persons exempted from registration pursuant to 
Sec. 1301.26, to export such substances to persons in other countries 
performing chemical analysis or enforcing laws relating to controlled 
substances or drugs in those countries, and to conduct instructional 
activities with controlled substances; and
    (5) A person registered or authorized to conduct research with 
controlled substances listed in Schedules II through V shall be 
authorized to conduct chemical analysis with controlled substances 
listed in those schedules in which he is authorized to conduct research, 
to manufacture such substances if and to the extent that such 
manufacture is set forth in a statement filed with the application for 
registration, to import such substances for research purposes, to 
distribute such substances to other persons registered or authorized to 
conduct chemical analysis, instructional activities, or research with 
such substances and to persons exempted from registration pursuant to 
Sec. 1301.26, and to conduct instructional activities with controlled 
substances;
    (6) A person registered to dispense controlled substances in 
Schedules II through V shall be authorized to conduct research and to 
conduct instructional activities with those substances, except that a 
mid-level practitioner, as defined in Sec. 1304.02(f), may conduct 
research coincident to his/her practitioner registration only to the 
extent expressly authorized by state statute.
    (c) A single registration to engage in any group of independent 
activities may include one or more controlled substances listed in the 
schedules authorized in that group of independent activities. A person 
registered to conduct research with controlled substances listed in 
Schedule I may conduct research with any substance listed in Schedule I 
for which he has filed and had approved a research protocol.

[36 FR 7778, Apr. 24, 1971, as amended at 36 FR 18728, Sept. 21, 1971; 
37 FR 15918, Aug. 8, 1972; 38 FR 756, Jan. 4, 1973. Redesignated at 38 
FR 26609, Sept. 24, l973; 58 FR 31175, June 1, 1993]

    Editorial Note: For FR citations affecting Sec. 1301.22, see the 
List of CFR Sections Affected in the Finding Aids section of this 
volume.



Sec. 1301.23   Separate registrations for separate locations.

    (a) A separate registration is required for each principal place of 
business or professional practice at one general physical location where 
controlled substances are manufactured, distributed, or dispensed by a 
person.
    (b) The following locations shall be deemed not to be places where 
controlled substances are manufactured, distributed, or dispensed:
    (1) A warehouse where controlled substances are stored by or on 
behalf of a registered person, unless such substances are distributed 
directly from such warehouse to registered locations other than the 
registered location from which the substances were delivered or to 
persons not required to register by

[[Page 9]]

virtue of subsection 302(c)(2) of the Act (21 U.S.C. 822(c)(2));
    (2) An office used by agents of a registrant where sales of 
controlled substances are solicited, made, or supervised but which 
neither contains such substances (other than substances for display 
purposes or lawful distribution as samples only) nor serves as a 
distribution point for filling sales orders; and
    (3) An office used by a practitioner (who is registered at another 
location) where controlled substances are prescribed but neither 
administered nor otherwise dispensed as a regular part of the 
professional practice of the practitioner at such office, and where no 
supplies of controlled substances are maintained.

[36 FR 7778, Apr. 24, 1971, as amended at 36 FR 18728, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, l973]



Sec. 1301.24   Exemption of agents and employees; affiliated practitioners.

    (a) The requirement of registration is waived for any agent or 
employee of a person who is registered to engage in any group of 
independent activities, if such agent or employee is acting in the usual 
course of his business or employment.
    (b) An individual practitioner, as defined in section 1304.02 of 
this chapter, who is an agent or employee of another individual 
practitioner (other than a mid-level practitioner) registered to 
dispense controlled substances may, when acting in the normal course of 
business or employment, administer or dispense (other than by issuance 
of prescription) controlled substances if and to the extent that such 
individual practitioner is authorized or permitted to do so by the 
jurisdiction in which he or she practices, under the registration of the 
employer or principal practitioner in lieu of being registered him/
herself.
    (c) An individual practitioner, as defined in Sec. 1304.02 of this 
chapter, who is an agent or employee of a hospital or other institution 
may, when acting in the normal course of business or employment, 
administer, dispense, or prescribe controlled substances under the 
registration of the hospital or other institution which is registered in 
lieu of being registered him/herself, provided that:
    (1) Such dispensing, administering or prescribing is done in the 
usual course of his professional practice;
    (2) Such individual practitioner is authorized or permitted to do so 
by the jurisdiction in which he is practicing;
    (3) The hospital or other institution by whom he is employed has 
verified that the individual practitioner is so permitted to dispense, 
administer, or prescribe drugs within the jurisdiction;
    (4) Such individual practitioner is acting only within the scope of 
his employment in the hospital or institution;
    (5) The hospital or other institution authorizes the individual 
practitioner to administer, dispense or prescribe under the hospital 
registration and designates a specific internal code number for each 
individual practitioner so authorized. The code number shall consist of 
numbers, letters, or a combination thereof and shall be a suffix to the 
institution's DEA registration number, preceded by a hyphen (e.g., 
AP0123456-10 or AP0123456-A12); and
    (6) A current list of internal codes and the corresponding 
individual practitioners is kept by the hospital or other institution 
and is made available at all times to other registrants and law 
enforcement agencies upon request for the purpose of verifying the 
authority of the prescribing individual practitioner.

[36 FR 18728, Sept. 21, 1971, as amended at 37 FR 15918, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, l973, and amended at 51 FR 5319, 
Feb. 13, 1986; 58 FR 31175, June 1, 1993; 60 FR 36641, July 18, 1995]



Sec. 1301.25   Exemption of certain military and other personnel.

    (a) The requirement of registration is waived for any official of 
the U.S. Army, Navy, Marine Corps, Air Force, Coast Guard, Public Health 
Service, or Bureau of Prisons who is authorized to prescribe, dispense, 
or administer, but not to procure or purchase, controlled substances in 
the course of his official duties. Such officials shall follow 
procedures set forth in part 1306 of this chapter regarding 
prescriptions, but shall state the branch of service or

[[Page 10]]

agency (e.g., ``U.S. Army'' or ``Public Health Service'') and the 
service identification number of the issuing official in lieu of the 
registration number required on prescription forms. The service 
identification number for a Public Health Service employee is his Social 
Security identification number.
    (b) If any official exempted by this section also engages as a 
private individual in any activity or group of activities for which 
registration is required, such official shall obtain a registration for 
such private activities.

[36 FR 7778, Apr. 24, 1971, as amended at 36 FR 18729, Sept. 21, 1971; 
38 FR 756, Jan. 4, 1973. Redesignated at 38 FR 26609, Sept. 24, l973]



Sec. 1301.26   Exemption of law enforcement officials.

    (a) The requirement of registration is waived for the following 
persons in the circumstances described in this section:
    (1) Any officer or employee of the Administration, any officer of 
the U.S. Customs Service, any officer or employee of the United States 
Food and Drug Administration, and any other Federal officer who is 
lawfully engaged in the enforcement of any Federal law relating to 
controlled substances, drugs or customs, and is duly authorized to 
possess controlled substances in the course of his official duties; and
    (2) Any officer or employee of any State, or any political 
subdivision or agency thereof, who is engaged in the enforcement of any 
State or local law relating to controlled substances and is duly 
authorized to possess controlled substances in the course of his 
official duties.
    (b) Any official exempted by this section may, when acting in the 
course of his official duties, possess any controlled substance and 
distribute any such substance to any other official who is also exempted 
by this section and acting in the course of his official duties.
    (c) Any official exempted by this section may procure any controlled 
substance in the course of an inspection, in accordance with 
Sec. 1316.03(d), or in the course of any criminal investigation 
involving the person from whom the substance was procured.
    (d) In order to enable law enforcement agency laboratories to obtain 
and transfer controlled substances for use as standards in chemical 
analysis, such laboratories must obtain annually a registration to 
conduct chemical analysis. Such laboratories shall be exempted from 
payment of a fee for registration. Laboratory personnel, when acting in 
the scope of their official duties, are deemed to be officials exempted 
by this section and within the activity described in section 515(d) of 
the Act (21 U.S.C. 885(d)). For purposes of this paragraph, laboratory 
activities shall not include field or other preliminary chemical tests 
by officials exempted by this section.
    (e) Laboratories of the Administration shall obtain annually a 
registration to conduct chemical analysis in accordance with paragraph 
(d) of this section. In addition to the activities authorized under a 
registration to conduct chemical analysis pursuant to Sec. 1301.22(b) 
(4), laboratories of the Administration shall be authorized to 
manufacture or import controlled substances for any lawful purpose, to 
distribute or export such substances to any person, and to import and 
export such substances in emergencies without regard to the requirements 
of part 1312 of this chapter if a report concerning the importation or 
exportation is made to the Diversion Operations Section of the 
Administration within 30 days of such importation or exportation.

[36 FR 7778, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 46 FR 28841, May 29, 1981; 51 FR 5319, Feb. 13, 1986]



Sec. 1301.27  Exemption of civil defense officials.

    (a) The requirement of registration is waived for any official of a 
civil defense or disaster relief organization who, in the course of his 
official duties, is authorized to:
    (1) Maintain, and distribute for such maintenance, controlled 
substances held for emergency use; or
    (2) Procure controlled substances for the purpose of maintaining 
supplies for emergency use, provided that all of such procurement is 
from the U.S. General Services Administration and in

[[Page 11]]

accordance with the rules of the U.S. Office of Emergency Preparedness.
    (b) The requirement of registration is waived for any official of a 
civil defense or disaster relief organization during a state of 
emergency or disaster within his jurisdiction proclaimed by the 
President or by a concurrent resolution of the Congress, which official, 
in the course of his official duties, during such emergency or disaster, 
is authorized to:
    (1) Dispense controlled substances; or
    (2) Procure or distribute controlled substances, provided that all 
such procurement is on a special ``Civil Defense Emergency Order Form,'' 
as described in this section.
    (c) Civil Defense Emergency Order Forms shall be furnished by the 
U.S. Office of Emergency Preparedness and will contain the name of the 
civil defense or disaster relief organization. Such forms may be used 
and are valid only during a state of emergency or disaster proclaimed by 
the President or by a concurrent resolution of the Congress for the area 
in which the organization using such forms has civil defense or disaster 
relief jurisdiction, who shall state his position and the nature and 
legal designation of the emergency or disaster. Such forms may be filled 
by any person registered under the Act. The organization shall, upon the 
execution of a Civil Defense Emergency Order Form, be deemed to be 
registered under the Act for purposes of recordkeeping pursuant to part 
1304 of this chapter.



Sec. 1301.28  Registration regarding ocean vessels.

    (a) If acquired by and dispensed under the general supervision of a 
medical officer described in paragraph (b) of this section, or the 
master or first officer of the vessel under the circumstances described 
in paragraph (d) of this section, controlled substances may be held for 
stocking, be maintained in, and dispensed from medicine chests, first 
aid packets, or dispensaries:
    (1) On board any vessel engaged in international trade or in trade 
between ports of the United States and any merchant vessel belonging to 
the U.S. Government;
    (2) On board any aircraft operated by an air carrier under a 
certificate of permit issued pursuant to the Federal Aviation Act of 
1958 (49 U.S.C. 1301); and
    (3) In any other entity of fixed or transient location approved by 
the Administrator as appropriate for application of this section (e.g., 
emergency kits at field sites of an industrial firm).
    (b) A medical officer shall be:
    (1) Licensed in a state as a physician;
    (2) Employed by the owner or operator of the vessel, aircraft or 
other entity; and
    (3) Registered under the Act at either of the following locations:
    (i) The principal office of the owner or operator of the vessel, 
aircraft or other entity or
    (ii) At any other location provided that the name, address, 
registration number and expiration date as they appear on his 
Certificate of Registration (DEA Form 223) for this location are 
maintained for inspection at said principal office in a readily 
retrievable manner.
    (c) A registered medical officer may serve as medical officer for 
more than one vessel, aircraft, or other entity under a single 
registration, unless he serves as medical officer for more than one 
owner or operator, in which case he shall either maintain a separate 
registration at the location of the principal office of each such owner 
or operator or utilize one or more registrations pursuant to paragraph 
(b)(3)(ii) of this section.
    (d) If no medical officer is employed by the owner or operator of a 
vessel, or in the event such medical officer is not accessible and the 
acquisition of controlled substances is required, the master or first 
officer of the vessel, who shall not be registered under the Act, may 
purchase controlled substances from a registered manufacturer of 
distributor, or from an authorized pharmacy as described in paragraph 
(f) of this section, by following the procedure outlined below:
    (1) The master or first officer of the vessel must personally appear 
at the vendor's place of business, present proper identification (e.g., 
Seaman's photographic identification card) and a

[[Page 12]]

written requisition for the controlled substances.
    (2) The written requisition must be on the vessel's official 
stationery or purchase order form and must include the name and address 
of the vendor, the name of the controlled substance, description of the 
controlled substance (dosage form, strength and number or volume per 
container) number of containers ordered, the name of the vessel, the 
vessel's official number and country of registry, the owner or operator 
of the vessel, the port at which the vessel is located, signature of the 
vessel's officer who is ordering the controlled substances and the date 
of the requisition.
    (3) The vendor may, after verifying the identification of the 
vessel's officer requisitioning the controlled substances, deliver the 
control substances to that officer. The transaction shall be documented, 
in triplicate, on a record of sale in a format similar to that outlined 
in paragraph (d)(4) of this section. The vessel's requisition shall be 
attached to copy 1 of the record of sale and filed with the controlled 
substances records of the vendor, copy 2 of the record of sale shall be 
furnished to the officer of the vessel and retained aboard the vessel, 
copy 3 of the record of sale shall be forwarded to the nearest DEA 
Division Office within 15 days after the end of the month in which the 
sale is made.
    (4) The vendor's record of sale should be similar to, and must 
include all the information contained in, the below listed format.

                Sale of Controlled Substances to Vessels

(Name of registrant)____________________________________________________
(Address of registrant)_________________________________________________
(DEA registration number)_______________________________________________

--------------------------------------------------------------------------------------------------------------------------------------------------------
                                                               Number of                                                 Packages                       
                         Line No.                           packages ordered   Size of packages   Name of product      distributed      Date distributed
--------------------------------------------------------------------------------------------------------------------------------------------------------
1........................................................  .................  .................  .................  .................  .................
2........................................................  .................  .................  .................  .................  .................
3........................................................  .................  .................  .................  .................  .................
--------------------------------------------------------------------------------------------------------------------------------------------------------
Line numbers may be continued according to needs of the vendor.                                                                                         

Number of lines completed_______________________________________________
Name of vessel _________________________________________________________
Vessel's official number _______________________________________________
Vessel's country of registry____________________________________________
Owner or operator of the vessel_________________________________________
Name and title of vessel's officer who presented the requisition________
Signature of vessel's officer who presented the requisition_____________
    (e) Any medical officer described in paragraph (b) of this section 
shall, in addition to complying with all requirements and duties 
prescribed for registrants generally, prepare an annual report as of the 
date on which his registration expires, which shall give in detail an 
accounting for each vessel, aircraft, or other entity, and a summary 
accounting for all vessels, aircraft, or other entities under his 
supervision for all controlled substances purchased, dispensed or 
disposed of during the year. The medical officer shall maintain this 
report with other records required to be kept under the Act and, upon 
request, deliver a copy of the report to the Administration. The medical 
officer need not be present when controlled substances are dispensed, if 
the person who actually dispensed the controlled substances is 
responsible to the medical officer to justify his actions.
    (f) Any registered pharmacy which wishes to distribute controlled 
substances pursuant to this section shall be authorized to do so, 
provided that:
    (1) The registered pharmacy notifies the nearest Division Office of 
the Administration of its intention to so distribute controlled 
substances prior to the initiation of such activity. This notification 
shall be by registered mail and shall contain the name, address, and 
registration number of the pharmacy as well as the date upon which such 
activity will commence; and
    (2) Such activity is authorized by state law; and
    (3) The total number of dosage units of all controlled substances 
distributed by the pharmacy during any calendar year in which the 
pharmacy is registered to dispense does not exceed the

[[Page 13]]

limitations imposed upon such distribution by Sec. 1307.11(a)(4) and (b) 
of this chapter.
    (g) Owners or operators of vessels, aircraft, or other entities 
described in this section shall not be deemed to possess or dispense any 
controlled substance acquired, stored and dispensed in accordance with 
this section.
    (h) The Master of a vessel shall prepare a report for each calendar 
year which shall give in detail an accounting for all controlled 
substances purchased, dispensed, or disposed of during the year. The 
Master shall file this report with the medical officer emploxed by the 
owner or operator of his vessel, if any, or, if not, he shall maintain 
this report with other records required to be kept under the Act and, 
upon request, deliver a copy of the report to the Administration.
    (i) Controlled substances acquired and possessed in accordance with 
this section shall not be distributed to persons not under the general 
supervision of the medical officer employed by the owner or operator of 
the vessel, aircraft, or other entity, except in accordance with 
Sec. 1307.21 of this chapter.

[37 FR 15918, Aug. 8, 1972, as amended at 38 FR 756, Jan. 4, 1973. 
Redesignated at 38 FR 26609, Sept. 24, l973, and amended at 41 FR 9546, 
Mar. 5, 1976; 50 FR 31589, Aug. 5, 1985]



Sec. 1301.29  Provisional registration of narcotic treatment programs; compounders.

    (a) All persons currently approved by the Food and Drug 
Administration under Sec. 310.505 (formerly Sec. 130.44) of this title 
to conduct a methadone treatment program and who are registered by the 
Drug Enforcement Administration under this section will be granted a 
Provisional Narcotic Treatment Program Registration.
    (b) The provisions of Sec. 1301.45-1301.57 relating to revocation 
and suspension of registration, shall apply to a provisional 
registration.
    (c) Unless sooner revoked or suspended under paragraph (b) of this 
section, a provisional registration shall remain in effect until (1) the 
date on which such person has registered under this section or has had 
his registration denied, or (2) such date as may be prescribed by 
written notification to the person from the Drug Enforcement 
Administration for the person to become registered to conduct a narcotic 
treatment program, whichever occurs first.

[39 FR 37984, Oct. 25, 1974]

                      Applications for Registration



Sec. 1301.31  Time for application for registration; expiration date.

    (a) Any person who is required to be registered and who is not so 
registered may apply for registration at any time. No person required to 
be registered shall engage in any activity for which registration is 
required until the application for registration is granted and a 
Certificate of Registration is issued by the Administrator to such 
person.
    (b) Any person who is registered may apply to be reregistered not 
more than 60 days before the expiration date of his registration.
    (c) At the time a manufacturer, distributor, researcher, analytical 
lab, importer, exporter or narcotic treatment program is first 
registered, that business activity shall be assigned to one of twelve 
groups, which shall correspond to the months of the year. The expiration 
date of the registrations of all registrants within any group will be 
the last date of the month designated for that group. In assigning any 
of the above business activities to a group, the Administration may 
select a group the expiration date of which is less than one year from 
the date such business activity was registered. If the business activity 
is assigned to a group which has an expiration date less than three 
months from the date of which the business activity is registered, the 
registration shall not expire until one year from that expiration date; 
in all other cases, the registration shall expire on the expiration date 
following the date on which the business activity is registered.
    (d) At the time a retail pharmacy, hospital/clinic, practitioner or 
teaching institution is first registered, that business activity shall 
be assigned to one of twelve groups, which shall correspond to the 
months of the year. The expiration date of the registrations of all 
registrants within any group will be the last day of the month 
designated for that group. In assigning any of the

[[Page 14]]

above business activities to a group, the Administration may select a 
group the expiration date of which is not less than 28 months nor more 
than 39 months from the date such business activity was registered. 
After the initial registration period, the registration shall expire 36 
months from the initial expiration date.

[36 FR 7778, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, l973, and amended at 52 FR 20599, 
June 2, 1987]



Sec. 1301.32  Application forms; contents; signature.

    (a) If any person is required to be registered, and is not so 
registered and is applying for registration:
    (1) To manufacture or distribute controlled substances, he shall 
apply on DEA Form 225;
    (2) To dispense controlled substances listed in Schedules II through 
V, he shall apply on DEA Form 224;
    (3) To conduct instructional activities with controlled substances 
listed in Schedules II through V, he shall apply on DEA Form 224;
    (4) To conduct research with controlled substances listed in 
Schedules II through V (other than research described in 
Secs. 1301.22(a)(6), he shall apply on DEA Form 225;
    (5) To conduct research with narcotic drugs listed in Schedules II 
through V, as described in Sec. 1301.22(a)(6), he shall apply on DEA 
Form 225;
    (6) To conduct research with controlled substances listed in 
Schedule I, he shall apply on DEA Form 225, with three copies of a 
research protocol as described in Sec.  301.33(a) attached to the form, 
or, in the case of a clinical investigation, with three copies of a 
certificate of submission of an IND as described in Sec. 1301.33(b) 
attached to the form (the researcher also submitting to the Food and 
Drug Administration three copies of a Notice of Claimed Investigational 
Exemption for a New Drug as required in Sec. 1301.33(b) );
    (7) To conduct instructional activities with controlled substances 
listed in Schedule I, he shall apply as a researcher on DEA Form 225 
with two copies of a statement describing the nature, extent, and 
duration of such instructional activities attached to the form;
    (8) To conduct chemical analysis with controlled substances listed 
in any Schedule, he shall apply on DEA Form 225; and
    (9) To conduct a narcotic treatment program, including a compounder, 
shall apply on DEA Form 363.
    (b) If any person is registered and is applying for reregistration:
    (1) To manufacture or distribute controlled substances, he shall 
apply on DEA Form 225a;
    (2) To dispense controlled substances listed in Schedules II through 
V, he shall apply on DEA Form 224a;
    (3) To conduct instructional activities with controlled substances 
listed i Schedules II through V, he shall apply on DEA Form 224a;
    (4) To conduct research with controlled substances listed in 
Schedules II through V (other than research described in Sec. 1301.22(a) 
(6), he shall apply on DEA Form 225a;
    (5) To conduct research with narcotic drugs listed in Schedules II 
through V, as described in Sec. 1301.22(a) (6), he shall apply on DEA 
Form 225a;
    (6) To continue to conduct research with controlled substances 
listed in Schedule I under one or more approved research protocols, he 
shall apply on DEA Form 225a;
    (7) To continue to conduct instructional activities with controlled 
substances listed in Schedule I under one or more approved instructional 
statements, he shall apply as a researcher on DEA Form 225a;
    (8) To conduct chemical analysis with controlled substances listed 
in any Schedule, he shall apply on DEA Form 225a; and
    (9) To conduct a narcotic treatment program, including a compounder, 
shall apply on DEA Form 363a (Renewal Form).
    (c) DEA (or BND) Forms 224 and 225 may be obtained at any regional 
office of the Administration or by writing to the Registration Unit, 
Drug Enforcement Administration, Department of Justice, Post Office Box 
28083, Central Station, Washington, DC 20005. DEA Forms 224a, 225a and 
363a will be mailed, as applicable, to each registered person 
approximately 60 days

[[Page 15]]

before the expiration date of his registration; if any registered person 
does not receive such forms within 45 days before the expiration date of 
his registration, he must promptly give notice of such fact and request 
such forms by writing to the Registration Unit of the Administration at 
the foregoing address.
    (d) Each application for registration to handle any basic class of 
controlled substance listed in Schedule I (except to conduct chemical 
analysis with such classes) and each application for registration to 
manufacture a basic class of controlled substance listed in Schedule II 
shall include the Administration Controlled Substances Code Number, as 
set forth in part 1308 of this chapter, for each basic class to be 
covered by such registration.
    (e) Each application for registration to conduct research with any 
basic class of controlled substance listed in Schedule II shall include 
the Administration Controlled Substances Code Number, as set forth in 
part 1308 of this chapter, for each such basic class to be manufactured 
or imported as a coincident activity of that registration. A statement 
listing the quantity of each such basic class or controlled substance to 
be imported or manufactured during the registration period for which 
application is being made shall be included with each such application. 
For purposes of this paragraph only, manufacturing is defined as the 
production of a controlled substance by synthesis, extraction or by 
agricultural/horticultural means.
    (f) Each application shall include all information called for in the 
form, unless the item is not applicable, in which case this fact shall 
be indicated.
    (g) Each application, attachment, or other document filed as part of 
an application, shall be signed by the applicant, if an individual; by a 
partner of the applicant, if a partnership; or by an officer of the 
applicant, if a corporation, corporate division, association, trust or 
other entity. An applicant may authorize one or more individuals, who 
would not otherwise be authorized to do so, to sign applications for the 
applicant by filing with the Registration Unit of the Administration a 
power of attorney for each such individual. The power of attorney shall 
be signed by a person who is authorized to sign applications under this 
paragraph and shall contain the signature of the individual being 
authorized to sign applications. The power of attornex shall be valid 
until revoked by the applicant.

[36 FR 7778, Apr. 24, 1971, as amended at 36 FR 18729, Sept. 21, 1971; 
37 FR 15918, Aug. 8, 1972; 37 FR 28712, Dec. 29, 1972. Redesignated at 
38 FR 26609, Sept. 24, l973]

    Editorial Note: For FR citations affecting Sec. 1301.32, see the 
List of CFR Sections Affected in the Finding Aids section of this 
volume.



Sec. 1301.33   Research protocols.

    (a) A protocol to conduct research with controlled substances listed 
in Schedule I shall be in the following form and contain the following 
information where applicable:
    (1) Investigator:
    (i) Name, address, and DEA registration number; if any.
    (ii) Institutional affiliation.
    (iii) Qualifications, including a curriculum vitae and an 
appropriate bibliography (list of publications).
    (2) Research project:
    (i) Title of project.
    (ii) Statement of the purpose.
    (iii) Name of the controlled substances or substances involved and 
the amount of each needed.
    (iv) Description of the research to be conducted, including the 
number and species of research subjects, the dosage to be administered, 
the route and method of administration, and the duration of the project.
    (v) Location where the research will be conducted.
    (vi) Statement of the security provisions for storing the controlled 
substances (in accordance with Sec. 1301.75) and for dispensing the 
controlled substances in order to prevent diversion.
    (vii) If the investigator desires to manufacture or import any 
controlled substance listed in paragraph (a)(2)(iii) of this section, a 
statement of the quantity to be manufactured or imported and the sources 
of the chemicals to be used or the substance to be imported.
    (3) Authority:
    (i) Institutional approval.

[[Page 16]]

    (ii) Approval of a Human Research Committee for human studies.
    (iii) Indication of an approved active Notice of Claimed 
Investigational Exemption for a New Drug (number).
    (iv) Indication of an approved funded grant (number), if any.
    (b) In the case of a clinical investigation with controlled 
substances listed in Schedule I, the applicant shall submit three copies 
of a Notice of Claimed Investigational Exemption for a New Drug (IND) 
together with a statement of the security provisions (as prescribed in 
paragraph (a)(2)(v) of this section for a research protocol) to, and 
have such submission approved by, the Food and Drug Administration as 
required in 21 U.S.C. 355(i) and Sec. 130.3 of this title. Submission of 
this Notice and statement to the Food and Drug Administration shall be 
in lieu of a research protocol to the Administration as required in 
paragraph (a) of this section. The applicant, when applying for 
registration with the Administration, shall indicate that such notice 
has been submitted to the Food and Drug Administration by submitting to 
the Administration with his DEA (or BND) Form 225 three copies of the 
following certificate:

    I hereby certify that on -------- (Date), pursuant to 21 U.S.C. 
355(i) and 21 CFR 130.3, I, ------------------------------ (Name and 
Address of IND Sponsor) submitted a Notice of Claimed Investigational 
Exemption for a New Drug (IND) to the Food and Drug Administration for:

------------------------------ (Name of Investigational Drug).

------------ (Date)

------------------------------ (Signature of Applicant).

    (c) In the event that the registrant desires to increase the 
quantity of a controlled substance used for an approved research 
project, he shall submit a request to the Registration Unit, Drug 
Enforcement Administration, Post Office Box 28083, Central Station, 
Washington, DC 20005, by registered mail, return receipt requested. The 
request shall contain the following information: DEA registration 
number; name of the controlled substance or substances and the quantity 
of each authorized in the approved protocol; and the additional quantity 
of each desired. Upon return of the receipt, the registrant shall be 
authorized to purchase the additional quantity of the controlled 
substance or substances specified in the request. The Administration 
shall review the letter and forward it to the Food and Drug 
Administration together with the Administration comments. The Food and 
Drug Administration shall approve or deny the request as an amendment to 
the protocol and so notify the registrant. Approval of the letter by the 
Food and Drug Administration shall authorize the registrant to use the 
additional quantity of the controlled substance in the research project.
    (d) In the event the registrant desires to conduct research beyond 
the variations provided in the registrant's approved protocol (excluding 
any increase in the quantity of the controlled substance requested for 
his research project as outlined in paragraph (c) of this section), he 
shall submit three copies of a supplemental protocol in accordance with 
paragraph (a) of this section describing the new research and omitting 
information in the supplemental protocol which has been stated in the 
original protocol. Supplemental protocols shall be processed and 
approved or denied in the same manner as original research protocols.

[37 FR 28712, Dec. 29, 1972. Redesignated at 38 FR 26609, Sept. 24, 
l973, and amended at 51 FR 5319, Feb. 13, 1986]



Sec. 1301.34   Filing of application; joint filings.

    (a) All applications for registration shall be submitted for filing 
to the Registration Unit, Drug Enforcement Administration, Department of 
Justice, Post Office Box 28083, Central Station, Washington, DC 20005. 
The appropriate registration fee and any required attachments must 
accompany the application.
    (b) Any person required to obtain more than one registration may 
submit all applications in one package. Each application must be 
complete and should not refer to any accompanying application for 
required information.

[36 FR 7778, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 51 FR 5319, Feb. 13, 1986]

[[Page 17]]



Sec. 1301.35   Acceptance for filing; defective applications.

    (a) Applications submitted for filing are dated upon receipt. If 
found to be complete, the application will be accepted for filing. 
Applications failing to comply with the requirements of this part will 
not generally be accepted for filing. In the case of minor defects as to 
completeness, the Administrator may accept the application for filing 
with a request to the applicant for additional information. A defective 
application will be returned to the applicant within 10 days following 
its receipt with a statement of the reason for not accepting the 
application for filing. A defective application may be corrected and 
resubmitted for filing at any time; the Administrator shall accept for 
filing any application upon resubmission by the applicant, whether 
complete or not.
    (b) Accepting an application for filing does not preclude any 
subsequent request for additional information pursuant to Sec. 1301.36 
and has no bearing on whether the application will be granted.



Sec. 1301.36   Additional information.

    The Administrator may require an applicant to submit such documents 
or written statements of fact relevant to the application as he deems 
necessary to determine whether the application should be granted. The 
failure of the applicant to provide such documents or statements within 
a reasonable time after being requested to do so shall be deemed to be a 
waiver by the applicant of an opportunity to present such documents or 
facts for consideration by the Administrator in granting or denying the 
application.



Sec. 1301.37   Amendments to and withdrawal of applications.

    (a) An application may be amended or withdrawn without permission of 
the Administrator at any time before the date on which the applicant 
receives an order to show cause pursuant to Sec. 1301.48. An application 
may be amended or withdrawn with permission of the Administrator at any 
time where good cause is shown by the applicant or where the amendment 
or withdrawal is in the public interest.
    (b) After an application has been accepted for filing, the request 
by the applicant that it be returned or the failure of the applicant to 
respond to official correspondence regarding the application, when sent 
by registered or certified mail, return receipt requested, shall be 
deemed to be a withdrawal of the application.

[36 FR 7778, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
as amended at 60 FR 32101, June 20, 1995]



Sec. 1301.38   Special procedures for certain applications.

    (a) If, at the time of application for registration of a new 
pharmacy, the pharmacy has been issued a license from the appropriate 
State licensing agency, the applicant may include with his application 
an affidavit as to the existence of the State license in the following 
form:

                       Affidavit for New Pharmacy

    I, ----------, the ------------------------ (Title of officer, 
official, partner, or other position) of ------------------------ 
(Corporation, partnership, or sole proprietor), doing business as ------
---------- (Store name) at ---------------- (Number and Street), ------
---------- (City) ---------------- (State) ---------------- (Zip code), 
hereby certify that said store was issued a pharmacy permit No. -------- 
by the ------------------------ (Board of Pharmacy or Licensing Agency) 
of the State of -------------------- on ------------ (Date).

    This statement is submitted in order to obtain a Drug Enforcement 
Administration registration number. I understand that if any information 
is false, the Administration may immediately suspend the registration 
for this store and commence proceedings to revoke under 21 U.S.C. 824(a) 
because of the danger to public health and safety. I further understand 
that any false information contained in this affidavit may subject me 
personally and the above-named corporation/partnership/business to 
prosecution under 21 U.S.C. 843, the penalties for conviction of which 
include imprisonment for up to 4 years, a fine of not more than $30,000 
or both.

........................................................................
Signature (Person who signs Application for Registration)

State of ------------
County of --------------
Subscribed to and sworn before me this ---------- day of --------------, 
19----.
........................................................................
Notary Public

    (b) Whenever the ownership of a pharmacy is being transferred from 
one

[[Page 18]]

person to another, if the transferee owns at least one other pharmacy 
licensed in the same State as the one the ownership of which is being 
transferred, the transferee may apply for registration prior to the date 
of transfer. The Administrator may register the applicant and authorize 
him to obtain controlled substances at the time of transfer. Such 
registration shall not authorize the transferee to dispense controlled 
substances until the pharmacy has been issued a valid State license. The 
transferee shall include with his application the following affidavit:

                   Affidavit for Transfer of Pharmacy

    I, ----------------, the ------------------------ (Title of officer, 
official, partner or other position) of ------------------------ 
(Corporation, partnership, or sole proprietor), doing business as ------
---------- (Store name) hereby certify:
    (1) That said company was issued a pharmacy permit No. -------- by 
the ------------------------ (Board of Pharmacy of Licensing Agency) of 
the State of ---------------- and a DEA Registration Number ---------- 
for a pharmacy located at -------------------- (Number and Street) ----
------------ (City) ------------------ (State) ---------------- (Zip 
Code); and
    (2) That said company is acquiring the pharmacy business of --------
-------- (Name of Seller) doing business as ---------------- with DEA 
Registration Number ---------- on or about ---------------- (Date of 
Transfer) and that said company has applied (or will apply on ----------
------ (Date) for a pharmacy permit from the board of pharmacy (or 
licensing agency) of the State of ---------------- to do business as --
-------------- (Store name) at ---------------- (Number and Street) ----
------------ (City) ---------------- (State) ---------------- (Zip 
Code).
    This statement is submitted in order to obtain a Drug Enforcement 
Administration registration number.
    I understand that if a DEA registration number is issued, the 
pharmacy may acquire controlled substances but may not dispense them 
until a pharmacy permit or license is issued by the State board of 
pharmacy or licensing agency.
    I understand that if any information is false, the Administration 
may immediately suspend the registration for this store and commence 
proceedings to revoke under 21 U.S.C. 824(a) because of the danger to 
public health and safety. I further understand that any false 
information contained in this affidavit may subject me personally to 
prosecution under 21 U.S.C. 843, the penalties for conviction of which 
include imprisonment for up to 4 years, a fine of not more than $30,000 
or both.
........................................................................
Signature (Person who signs Application for Registration)
State of ------------
County of --------------
Subscribed to and sworn before me this ------------day of --------------
--, 19----.
........................................................................
Notary Public

    (c) The Administrator shall follow the normal procedures for 
approving an application to verify the statements in the affidavit. If 
the statements prove to be false, the Administrator may revoke the 
registration on the basis of section 1304(a)(1) of the Act (21 U.S.C. 
824(a)(1)) and suspend the registration immediately by pending 
revocation on the basis of section 1304(d) of the Act (21 U.S.C. 
824(d)). At the same time, the Administrator may seize and place under 
seal all controlled substances possessed by the applicant under section 
1304(f) of the Act (21 U.S.C. 824(f)). International misuse of the 
affidavit procedure may subject the applicant to prosecution for fraud 
under section 403(a)(4) of the Act (21 U.S.C. 843(a)(4)), and obtaining 
controlled substances under a registration fraudulently gotten may 
subject the applicant to prosecution under section 403(a)(3) of the Act 
(21 U.S.C. 843(a)(3)). The penalties for conviction of either offense 
include imprisonment for up to 4 years, a fine not exceeding $30,000 or 
both.

[38 FR 756, Jan. 4, 1973. Redesignated at 38 FR 26609, Sept. 24, l973]

  Action on Applications for Registration: Revocation or Suspension of 
                              Registration



Sec. 1301.41   Administrative review generally.

    The Administrator may inspect, or cause to be inspected, the 
establishment of an applicant or registrant, pursuant to subpart A of 
part 1316 of this chapter. The Administrator shall review, the 
application for registration and other information gathered by the 
Administrator regarding an applicant in order to determine whether the 
applicable standards of section 1303 of the Act (21 U.S.C. 823) have 
been met by the applicant.

[[Page 19]]



Sec. 1301.42   Action on applications for research in Schedule I substances.

    (a) In the case of an application for registration to conduct 
research with controlled substances listed in Schedule I, the 
Administrator shall process the application and protocol and forward a 
copy of each to the Secretary within 7 days after receipt. The Secretary 
shall determine the qualifications and competency of the applicant, as 
well as the merits of the protocol (and shall notify the Administrator 
of his determination) within 21 days after receipt of the application 
and complete protocol, except that in the case of a clinical 
investigation, the Secretary shall have 30 days to make such 
determination and notify the Administrator. The Secretary, in 
determining the merits of the protocol, shall consult with the 
Administrator as to effective procedures to safeguard adequately against 
diversion of such controlled substances from legitimate medical or 
scientific use.
    (b) An applicant whose protocol is defective shall be notified by 
the Secretary within 21 days after receipt of such protocol from the 
Administrator (or in the case of a clinical investigation within 30 
days), and he shall be requested to correct the existing defects before 
consideration shall be given to his submission.
    (c) If the Secretary determines the applicant qualified and 
competent and the research protocol meritorious, he shall notify the 
Administrator in writing of such determination. The Administrator shall 
issue a certificate of registration within 10 days after receipt of this 
notice, unless he determines that the certificate of registration should 
be denied on a ground specified in section 304(a) of the Act (21 U.S.C. 
824(a)). In the case of a supplemental protocol, a replacement 
certificate of registration shall be issued by the Administrator.
    (d) If the Secretary determines that the protocol is not meritorious 
and/or the applicant is not qualified or competent, he shall notify the 
Administrator in writing setting forth the reasons for such 
determination. If the Administrator determines that grounds exist for 
the denial of the application, he shall within 10 days issue an order to 
show cause pursuant to Sec. 1301.48 and, if requested by the applicant, 
hold a hearing on the application pursuant to Sec. 1301.51. If the 
grounds for denial of the application include a determination by the 
Secretary, the Secretary or his duly authorized agent shall furnish 
testimony and documents pertaining to his determination at such hearing.
    (e) Supplemental protocols will be processed in the same manner as 
original research protocols. If the processing of an application or 
research protocol is delayed beyond the time limits imposed by this 
section, the applicant shall be so notified in writing.

[37 FR 28712, Dec. 29, 1972. Redesignated at 38 FR 26609, Sept. 24, 
l973]



Sec. 1301.43   Application for bulk manufacture of Schedule I and II substances.

    (a) In the case of an application for registration or reregistration 
to manufacture in bulk a basic class of controlled substance listed in 
Schedule I or II, the Administrator shall, upon the filing of such 
application, publish in the Federal Register a notice naming the 
applicant and stating that such applicant has applied to be registered 
as a bulk manufacturer of a basic class of narcotic or nonnarcotic 
controlled substance, which class shall be identified. A copy of said 
notice shall be mailed simultaneously to each person registered as a 
bulk manufacturer of that basic class and to any other applicant 
therefor. Any such person may, within 60 days from the date of 
publication of the notice in the Federal Register, file with the 
Administrator written comments on or objections to the issuance of the 
proposed registration.
    (b) In order to provide adequate competition, the Administrator 
shall not be required to limit the number of manufacturers in any basic 
class to a number less than that consistent with maintenance of 
effective controls against diversion solely because a smaller number is 
capable of producing an adequate and uninterrupted supply.
    (c) This section shall not apply to the manufacture of basic classes 
of controlled substances listed in Schedules I or II as an incident to 
research or

[[Page 20]]

chemical analysis as authorized in Sec. 1301.22 (b).

[36 FR 7778, Apr. 24, 1971, as amended at 36 FR 18729, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, l973; 60 FR 32101, June 20, 1995]



Sec. 1301.44   Certificate of registration; denial of registration.

    (a) The Administrator shall issue a Certificate of Registration (DEA 
Form 223) to an applicant if the issuance of registration or 
reregistration is required under the applicable provisions of section 
303 of the Act (21 U.S.C. 823). In the event that the issuance of 
registration or reregistration is not required, the Administrator shall 
deny the application. Before denying any application, the Administrator 
shall issue an order to show cause pursuant to Sec. 1301.48 and, if 
requested by the applicant, shall hold a hearing on the application 
pursuant to Sec. 1301.51.
    (b) If a hearing is requested by an applicant for registration or 
reregistration to manufacture in bulk a basic class of controlled 
substance listed in Schedule I or II, notice that a hearing has been 
requested shall be published in the Federal Register and shall be mailed 
simultaneously to the applicant and to all persons to whom notice of the 
application was mailed. Any person entitled to file comments or 
objections to the issuance of the proposed registration pursuant to 
Sec. 1301.43(a) may participate in the hearing by filing a notice of 
appearance in accordance with Sec. 1301.54. Such persons shall have 30 
days to file a notice of appearance after the date of publication of the 
notice of a request for a hearing in the Federal Register.
    (c) The Certificate of Registration (DEA Form 223) shall contain the 
name, address, and registration ntmber of the registrant, the activity 
authorized by the registration, the schedules and/or Administration 
Controlled Substances Code Number (as set forth in part 1308 of this 
chapter) of the controlled substances which the registrant is authorized 
to handle, the amount of fee paid (or exemption), and the expiration 
date of the registration. The registrant shall maintain the certificate 
of registration at the registered location in a readily retrievable 
manner and shall permit inspection of the certificate by any official, 
agent or employee of the Administration or of any Federal, State, or 
local agency engaged in enforcement of laws relating to controlled 
substances.

[36 FR 7778, Apr. 24, 1971, as amended at 37 FR 15918, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, l973 and amended at 53 FR 4963, 
Feb. 19, 1988; 60 FR 32101, June 20, 1995]



Sec. 1301.45   Suspension or revocation of registration.

    (a) The Administrator may suspend any registration pursuant to 
section 304 (a) of the Act (21 U.S.C. 824(a)) for any period of time he 
determines.
    (b) The Administrator may revoke any registration pursuant to 
section 304 (a) of the Act (21 U.S.C. 824(a)).
    (c) Before revoking or suspending any registration, the 
Administrator shall issue an order to show cause pursuant to 
Sec. 1301.48 and, if requested by the registrant, shall hold a hearing 
pursuant to Sec. 1301.51. Notwithstanding the requirements of this 
section, however, the Administrator may suspend any registration pending 
a final order pursuant to Sec. 1301.46.
    (d) Upon service of the order of the Administrator suspending or 
revoking registration, the registrant shall immediately deliver his 
Certificate of Registration and any order forms in his possession to the 
nearest office of the Administration. The suspension or revocation of a 
registration shall suspend or revoke any individual manufacturing or 
procurement quota fixed for the registrant pursuant to part 303 of this 
chapter. Also, upon service of the order of the Administrator revoking 
or suspending registration, the registrant shall, as instructed by the 
Administrator:
    (1) Deliver all controlled substances in his possession to the 
nearest office of the Administrator or to authorized agents of the 
Administrator; or
    (2) Place all controlled substances in his possession under seal as 
described in section 304(f) of the Act (21 U.S.C. 824(f)).
    (e) In the event that revocation or suspension is limited to a 
particular controlled substance or substances, the registrant shall be 
given a new

[[Page 21]]

Certificate of Registration for all substances not affected by such 
revocation or suspension; no fee shall be required to be paid for the 
new Certificate of Registration. The registrant shall deliver the old 
Certificate of Registration and, if appropriate, any order forms in his 
possession to the nearest office of the Administration. The suspension 
or revocation of a registration, when limited to a particular basic 
class or classes of controlled substances, shall suspend or revoke any 
individual manufacturing or procurement quota fixed for the registrant 
for such class or classes pursuant to part 303 of this chapter. Also, 
upon service of the order of the Administrator revoking or suspending 
registration, the registrant shall, as instructed by the Administrator:
    (1) Deliver to the nearest office of the Administration or to 
authorized agents of the Administration all of the particular controlled 
substance or substances affected by the revocation or suspension which 
are in his possession; or
    (2) Place all of such substances under seal as described in section 
304(f) of the Act (21 U.S.C. 824(f)).

[36 FR 7778, Apr. 24, 1971, as amended at 37 FR 15919, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, l973]



Sec. 1301.46   Suspension of registration pending final order.

    (a) The Administrator may suspend any registration simultaneously 
with or at any time subsequent to the service upon the registrant of an 
order to show cause why such registration should not be revoked or 
suspended, in any case where he finds that there is an imminent danger 
to the public health or safety. If the Administrator so suspends, he 
shall serve with the order to show cause pursuant to Sec. 1301.48 an 
order of immediate suspension which shall contain a statement of his 
findings regarding the danger to public health or safety.
    (b) Upon service of the order of immediate suspension, the 
registrant shall promptly return his Certificate of Registration and any 
order forms in his possession to the nearest office of the 
Administration. The suspension of any registration under this section 
shall suspend any quota fixed for the registrant pursuant to part 1303 
of this chapter. Also, upon service of the order of the Administrator 
immediately suspending registration, the registrant shall, as instructed 
by the Administrator:
    (1) Deliver all affected controlled substances in his possession to 
the nearest office of the Administration or to authorized agents of the 
Administration; or
    (2) Place all of such substances under seal as described in section 
304(f) of the Act (21 U.S.C. 824(f)).
    (c) Any suspension shall continue in effect until the conclusion of 
all proceedings upon the revocation or suspension, including any 
judicial review thereof, unless sooner withdrawn by the Administrator or 
dissolved by a court of competent jurisdiction. Any registrant whose 
registration is suspended under this section may request a hearing on 
the revocation or suspension of his registration at a time earlier than 
specified in the order to show cause pursuant to Sec. 1301.48, which 
request shall be granted by the Administrator, who shall fix a date for 
such hearing as early as reasonably possible.



Sec. 1301.47   Extension of registration pending final order.

    In the event that an applicant for reregistration (who is doing 
business under a registration previously granted and not revoked or 
suspended) has applied for reregistration at least 45 days before the 
date on which the existing registration is due to expire, and the 
Administrator has issued no order on the application on the date on 
which the existing registration is due to expire, the existing 
registration of the applicant shall automatically be extended and 
continue in effect until the date on which the Administrator so issues 
his order. The Administrator may extend any other existing registration 
under the circumstances contemplated in this section even though the 
registrant failed to apply for reregistration at least 45 days before 
expiration of the existing registration, with or without request by the 
registrant, if the Administrator finds that such extension is not 
inconsistent with the public health and safety.

[[Page 22]]



Sec. 1301.48   Order to show cause.

    (a) If, upon examination of the application for registration from 
any applicant and other information gathered by the Administration 
regarding the applicant, the Administrator is unable to make the 
determinations required by the applicable provisions of section 303 of 
the Act (21 U.S.C. 823) to register the applicant, the Administrator 
shall serve upon the applicant an order to show cause why the 
registration should not be denied.
    (b) If, upon information gathered by the Administration regarding 
any registrant, the Administrator determines that the registration of 
such registrant is subject to suspension or revocation pursuant to 
section 304 of the Act (21 U.S.C. 824), the Administrator shall serve 
upon the registrant an order to show cause why the registration should 
not be revoked or suspended.
    (c) The order to show cause shall call upon the applicant or 
registrant to appear before the Administrator at a time and place stated 
in the order, which shall not be less than 30 days after the date of 
receipt of the order. The order to show cause shall also contain a 
statement of the legal basis for such hearing and for the denial, 
revocation, or suspension of registration and a summary of the matters 
of fact and law asserted.
    (d) Upon receipt of an order to show cause, the applicant or 
registrant must, if he desires a hearing, file a request for a hearing 
pursuant to Sec. 1301.54. If a hearing is requested, the Administrator 
shall hold a hearing at the time and place stated in the order, pursuant 
to Sec. 1301.51.
    (e) When authorized by the Administrator, any agent of the 
Administration may serve the order to show cause.

[36 FR 7778, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, l973]

                                Hearings



Sec. 1301.51   Hearings generally.

    (a) In any case where the Administrator shall hold a hearing on any 
registration or application therefor, the procedures for such hearing 
shall be governed generally by the adjudication procedures set forth in 
the Administrative Procedure Act (5 U.S.C. 551-559) and specifically by 
sections 303 and 304 of the Act (21 U.S.C. 823-824), by Secs. 1301.52-
1301.57, and by the procedures for administrative hearings under the Act 
set forth in Secs. 1316.41-1316.67 of this chapter.
    (b) Any hearing under this part shall be independent of, and not in 
lieu of, criminal prosecutions or other proceedings under the Act or any 
other law of the United States.



Sec. 1301.52   Purpose of hearing.

    If requested by a person entitled to a hearing, the Administrator 
shall hold a hearing for the purpose of receiving factual evidence 
regarding the issues involved in the denial, revocation, or suspension 
of any registration, and the granting of any application for 
registration to manufacture in bulk a basic class of controlled 
substance listed in Schedule I or II. Extensive argument should not be 
offered into evidence but rather presented in opening or closing 
statements of counsel or in memoranda or proposed findings of fact and 
conclusions of law.



Sec. 1301.53   Waiver or modification of rules.

    The Administrator or the presiding officer (with respect to matters 
pending before him) may modify or waive any rule in this part by notice 
in advance of the hearing, if he determines that no party in the hearing 
will be unduly prejudiced and the ends of justice will thereby be 
served. Such notice of modification or waiver shall be made a part of 
the record of the hearing.



Sec. 1301.54   Request for hearing or appearance; waiver.

    (a) Any person entitled to a hearing pursuant to Secs. 1301.42, 
1301.44, or 1301.45 and desiring a hearing shall, within 30 days after 
the date of receipt of the order to shown cause, file with the 
Administrator a written request for a hearing in the form prescribed in 
Sec. 1316.47 of this chapter.
    (b) Any person entitled to participate in a hearing pursuant to 
Sec. 1301.44(b) and desiring to do so shall, within 30 days of the date 
of publication of notice of the request for a hearing in the

[[Page 23]]

Federal Register, file with the Administrator a written notice of intent 
to participate in such hearing in the form prescribed in Sec. 1316.48 of 
this chapter. Any person filing a request for a hearing need not also 
file a notice of appearance.
    (c) Any person entitled to a hearing or to participate in a hearing 
pursuant to Secs. 1301.42, 1301.44, or 1301.45 may, within the period 
permitted for filing a request for a hearing or a notice of appearance, 
file with the Administrator a waiver of an opportunity for a hearing or 
to participate in a hearing, together with a written statement regarding 
such person's position on the matters of fact and law involved in such 
hearing. Such statement, if admissible, shall be made a part of the 
record and shall be considered in light of the lack of opportunity for 
cross-examination in determining the weight to be attached to matters of 
fact asserted therein.
    (d) If any person entitled to a hearing or to participate in a 
hearing pursuant to Secs. 1301.42, 1301.44, or 1301.45 fails to file a 
request for a hearing or a notice of appearance, or if such person so 
files and fails to appear at the hearing, such person shall be deemed to 
have waived the opportunity for a hearing or to participate in the 
hearing, unless such person shows good cause for such failure.
    (e) If all persons entitled to a hearing or to participate in a 
hearing waive or are deemed to waive their opportunity for the hearing 
or to participate in the hearing, the Administrator may cancel the 
hearing, if scheduled, and issue his final order pursuant to 
Sec. 1301.57 without a hearing.

[36 FR 7778, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, l973; 60 FR 32101, June 20, 1995]



Sec. 1301.55   Burden of proof.

    (a) At any hearing on an application to manufacture any controlled 
substance listed in Schedule I or II, the applicant shall have the 
burden of proving that the requirements for such registration pursuant 
to section 303(a) of the Act (21 U.S.C. 823(a)) are satisfied. Any other 
person participating in the hearing pursuant to Sec. 1301.44(b) shall 
have the burden of proving any propositions of fact or law asserted by 
such person in the hearing.
    (b) At any hearing on the granting or denial of an applicant to be 
registered to conduct a narcotic treatment program or as a compounder, 
the applicant shall have the burden of proving that the requirements for 
each registration pursuant to section 303(g) of the Act (21 U.S.C. 
823(g)) are satisfied.
    (c) At any other hearing for the denial of a registration, the 
Administration shall have the burden of proving that the requirements 
for such registration pursuant to section 303 of the Act (21 U.S.C. 823) 
are not satisfied.
    (d) At any hearing for the revocation or suspension of a 
registration, the Administration shall have the burden of proving that 
the requirements for such revocation or suspension to section 304 (a) of 
the Act (21 U.S.C. 824(a)) are satisfied.

[36 FR 7778, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 41 FR 21448, May 26, 1976; 60 FR 32102, June 20, 1995]



Sec. 1301.56   Time and place of hearing.

    The hearing will commence at the place and time designated in the 
order to show cause or notice of hearing published in the Federal 
Register (unless expedited pursuant to Sec. 1301.46(c)) but thereafter 
it may be moved to a different place and may be continued from day to 
day or recessed to a later day without notice other than announcement 
thereof by the presiding officer at the hearing.



Sec. 1301.57   Final order.

    As soon as practicable after the presiding officer has certified the 
record to the Administrator, the Administrator shall issue his order on 
the granting, denial, revocation, or suspension of registration. In the 
event that an application for registration to manufacture in bulk a 
basic class of any controlled substance listed in Schedule I or II is 
granted, or any application for registration is denied, or any 
registration is revoked or suspended, the order shall include the 
findings of fact and conclusions of law upon which the order is based. 
The order shall specify the date on which it shall take effect. The 
Administrator shall serve one copy

[[Page 24]]

of his order upon each party in the hearing.

         Modification, Transfer and Termination of Registration



Sec. 1301.61   Modification in registration.

    Any registrant may apply to modify his registration to authorize the 
handling of additional controlled substances or to change his name or 
address, by submitting a letter of request to the Registration Unit, 
Drug Enforcement Administration, Department of Justice, Post Office Box 
28083, Central Station, Washington, DC 20005. The letter shall contain 
the registrant's name, address, and registration number as printud on 
the certificate of registration, and the substances and/or schedules to 
be added to his registration or the new name or address and shall be 
signed in accordance with Sec. 1301.32(f). If the registrant is seeking 
to handle additional controlled substances listed in Schedule I for the 
purpose of research or instructional activities, he shall attach three 
copies of a research protocol describing each research project involving 
the additional substances, or two copies of a statement describing the 
nature, extent, and duration of such instructional activities, as 
appropriate. No fee shall be required to be paid for the modification. 
The request for modification shall be handled in the same manner as an 
application for registration. If the modification in registration is 
approved, the Administrator shall issue a new certificate of 
registration (DEA Form 223) to the registrant, who shall maintain it 
with the old certificate of registration until expiration.

[36 FR 18729, Sept. 21, 1971, as amended at 37 FR 15919, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, l973, and amended at 51 FR 5319, 
Feb. 13, 1986; 53 FR 4963, Feb. 19, 1988]



Sec. 1301.62   Termination of registration.

    The registration of any person shall terminate if and when such 
person dies, ceases legal existence, or discontinues business or 
professional practice. Any registrant who ceases legal existence or 
discontinues business or professional practice shall notify the 
Administrator promptly of such fact.

[37 FR 15919, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, l973]



Sec. 1301.63   Transfer of registration.

    No registration or any authority conferred thereby shall be assigned 
or otherwise transferred except upon such conditions as the 
Administrator may specifically designate and then only pursuant to his 
written consent.

                          Security Repuirements



Sec. 1301.71   Security requirements generally.

    (a) All applicants and registrants shall provide effective controls 
and procedures to guard against theft and diversion of controlled 
substances. In order to determine whether a registrant has provided 
effective controls against diversion, the Administrator shall use the 
security requirements set forth in Secs. 1301.72-1301.76 as standards 
for the physical security controls and operating procedures necessary to 
prevent diversion. Materials and construction which will provide a 
structural equivalent to the physical security controls set forth in 
Secs. 1301.72, 1301.73 and 1301.75 may be used in lieu of the materials 
and construction described in those sections.
    (b) Substantial compliance with the standards set forth in 
Secs. 1301.72-1301.76 may be deemed sufficient by the Administrator 
after evaluation of the overall security system and needs of the 
applicant or registrant. In evaluating the overall security system of a 
registrant or applicant, the Administrator may consider any of the 
following factors as he may deem relevant to the need for strict 
compliance with security requirements:
    (1) The type of activity conducted (e.g., processing of bulk 
chemicals, preparing dosage forms, packaging, labeling, cooperative 
buying, etc.);
    (2) The type and form of controlled substances handled (e.g., bulk 
liquids or dosage units, usable powders or nonusable powders);
    (3) The quantity of controlled substances handled;

[[Page 25]]

    (4) The location of the premises and the relationship such location 
bears on security needs;
    (5) The type of building construction comprising the facility and 
the general characteristics of the building or buildings;
    (6) The type of vault, safe, and secure enclosures or other storage 
system (e.g., automatic storage and retrieval system) used;
    (7) The type of closures on vaults, safes, and secure enclosures;
    (8) The adequacy of key control systems and/or combination lock 
control systems;
    (9) The adequacy of electric detection and alarm systems, if any 
including use of supervised transmittal lines and standby power sources;
    (10) The extent of unsupervised public access to the facility, 
including the presence and characteristics of perimeter fencing, if any;
    (11) The adequacy of supervision over employees having access to 
manufacturing and storage areas;
    (12) The procedures for handling business guests, visitors, 
maintenance personnel, and nonemployee service personnel;
    (13) The availability of local police protection or of the 
registrant's or applicant's security personnel, and;
    (14) The adequacy of the registrant's or applicant's system for 
monitoring the receipt, manufacture, distribution, and disposition of 
controlled substances in its operations.
    (c) When physical security controls become inadequate as a result of 
a controlled substance being transferred to a different schedule, or as 
a result of a noncontrolled substance being listed on any schedule, or 
as a result of a significant increase in the quantity of controlled 
substances in the possession of the registrant during normal business 
operations, the physical security controls shall be expanded and 
extended accordingly. A registrant may adjust physical security controls 
within the requirements set forth in Secs. 1301.72-1301.76 when the need 
for such controls decreases as a result of a controlled substance being 
transferred to a different schedule, or a result of a controlled 
substance being removed from control, or as a result of a significant 
decrease in the quantity of controlled substances in the possession of 
the registrant during normal business operations.
    (d) Any registrant or applicant desiring to determine whether a 
proposed security system substantially complies with, or is the 
structural equivalent of, the requirements set forth in Secs. 1301.72-
1301.76 may submit any plans, blueprints, sketches or other materials 
regarding the proposed security system either to the Special Agent in 
Charge in the region in which the system will be used, or to the 
Diversion Operations Section, Drug Enforcement Administration, 
Department of Justice, Washington, DC 20537.
    (e) Physical security controls of locations registered under the 
Harrison Narcotic Act or the Narcotics Manufacturing Act of 1960 on 
April 30, 1971, shall be deemed to comply substantially with the 
standards set forth in Secs. 1301.72, 1301.73 and 1301.75. Any new 
facilities or work or storage areas constructed or utilized for 
controlled substances, which facilities or work or storage areas have 
not been previously approved by the Administration, shall not 
necessarily be deemed to comply substantially with the standards set 
forth in Secs. 1301.72, 1301.73 and 1301.75, notwithstanding that such 
facilities or work or storage areas have physical security controls 
similar to those previously approved by the Administration.

[36 FR 18729, Sept. 21, 1971. Redesignated at 38 FR 26609, Sept. 24, 
l973, and amended at 46 FR 28841, May 29, 1981; 47 FR 41735, Sept. 22, 
1982; 51 FR 5319, Feb. 13, 1986]



Sec. 1301.72   Physical security controls for non-practitioners; narcotic treatment programs and compounders for narcotic treatment programs; storage areas.

    (a) Schedules I and II. Raw materials, bulk materials awaiting 
further processing, and finished products which are controlled 
substances listed in Schedule I or II shall be stored in one of the 
following secure storage areas:
    (1) Where small quantities permit, a safe or steel cabinet;
    (i) Which safe or steel cabinet shall have the following 
specifications or the equivalent: 30 man-minutes against

[[Page 26]]

surreptitious entry, 10 man-minutes against forced entry, 20 man-hours 
against lock manipulation, and 20 man-hours against radiological 
techniques;
    (ii) Which safe or steel cabinet, if it weighs less than 750 pounds, 
is bolted or cemented to the floor or wall in such a way that it cannot 
be readily removed; and
    (iii) Which safe or steel cabinet, if necessary, depending upon the 
quantities and type of controlled substances stored, is equipped with an 
alarm system which, upon attempted unauthorized entry, shall transmit a 
signal directly to a central protection company or a local or State 
police agency which has a legal duty to respond, or a 24-hour control 
station operated by the registrant, or such other protection as the 
Administrator may approve.
    (2) A vault constructed before, or under construction on, September 
1, 1971, which is of substantial construction with a steel door, 
combination or key lock, and an alarm system; or
    (3) A vault constructed after September 1, 1971:
    (i) The walls, floors, and ceilings of which vault are constructed 
of at least 8 inches of reinforced concrete or other substantial 
masonry, reinforced vertically and horizontally with \1/2\-inch steel 
rods tied 6 inches on center, or the structural equivalent to such 
reinforced walls, floors, and ceilings;
    (ii) The door and frame unit of which vault shall conform to the 
following specifications or the equivalent: 30 man-minutes against 
surreptitious entry, 10 man-minutes against forced entry, 20 man-hours 
against lock manipulation, and 20 man-hours against radiological 
techniques;
    (iii) Which vault, if operations require it to remain open for 
frequent access, is equipped with a ``day-gate'' which is self-closing 
and self-locking, or the equivalent, for use during the hours of 
operation in which the vault door is open;
    (iv) The walls or perimeter of which vault are equipped with an 
alarm, which upon unauthorized entry shall transmit a signal directly to 
a central station protection company, or a local or State police agency 
which has a legal duty to respond, or a 24-hour control station operated 
by the registrant, or such other protection as the Administrator may 
approve, and, if necessary, holdup buttons at strategic points of entry 
to the perimeter area of the vault;
    (v) The door of which vault is equipped with contact switches; and
    (vi) Which vault has one of the following: Complete electrical 
lacing of the walls, floor and ceilings; sensitive ultrasonic equipment 
within the vault; a sensitive sound accumulator system; or such other 
device designed to detect illegal entry as may be approved by the 
Administration.
    (b) Schedules III, IV and V. Raw materials, bulk materials awaiting 
further processing, and finished products which are controlled 
substances listed in Schedules III, IV and V shall be stored in the 
following secure storage areas:
    (1) A safe or steel cabinet as described in paragraph (a)(1) of this 
section;
    (2) A vault as described in paragraph (a)(2) or (3) of this section 
equipped with an alarm system as described in paragraph (b)(4)(v) of 
this section;
    (3) A building used for storage of Schedules III through V 
controlled substances with perhmeter security which limits access during 
working hours and provides security after working hours and meets the 
following specifications:
    (i) Has an electronic alarm system as described in paragraph 
(b)(4)(v) of this section,
    (ii) Is equipped with self-closing, self-locking doors constructed 
of substantial material commensurate with the type of building 
construction, provided, however, a door which is kept clored and locked 
at all times when not in use and when in use is kept under direct 
observation of a responsible employee or agent of the registrant is 
permitted in lieu of a self-closing, self-locking door. Doors may be 
sliding or hinged. Regarding hinged doors, where hinges are mounted on 
the outside, such hinges shall be sealed, welded or otherwise 
constructed to inhibit removal. Locking devices for such doors shall be 
either of the multiple-position combination or key lock type and:
    (a) In the case of key locks, shall require key control which limits 
access to a limited number of employees, or;

[[Page 27]]

    (b) In the case of combination locks, the combination shall be 
limited to a minimum number of employees and can be changed upon 
termination of employment of an employee having knowledge of the 
combination;
    (4) A cage, located within a building on the premises, meeting the 
following specifications:
    (i) Having walls constructed of not less than No. 10 gauge steel 
fabric mounted on steel posts, which posts are:
    (a) At least one inch in diameter;
    (b) Set in concrete or installed with lay bolts that are pinned or 
brazed; and
    (c) Which are placed no more than ten feet apart with horizontal one 
and one-half inch reinforcements every sixty inches;
    (ii) Having a mesh construction with openings of not more than two 
and one-half inches across the square,
    (iii) Having a ceiling constructed of the same material, or in the 
alternative, a cage shall be erected which reaches and is securely 
attached to the structural ceiling of the building. A lighter gauge mesh 
may be used for the ceilings of large enclosed areas if walls are at 
least 14 feet in height,
    (iv) Is equipped with a door constructed of No. 10 gauge steel 
fabric on a metal door frame in a metal door flange, and in all other 
respects conforms to all the requirements of 21 CFR 1301.72(b)(3)(ii), 
and
    (v) Is equipped with an alarm system which upon unauthorized entry 
shall transmit a signal directly to a central station protection agency 
or a local or state police agency, each having a legal duty to respond, 
or to a 24-hour control station operated by the registrant, or to such 
other source of protection as the Administrator may approve;
    (5) An enclosure of masonry or other material, approved in writing 
by the Administrator as providing security comparable to a cage;
    (6) A building or enclosure within a building which has been 
inspected and approved by DEA or its predecessor agency, BNDD, and 
continues to provide adequate security against the diversion of Schedule 
III through V controlled substances, of which fact written 
acknowledgment has been made by the Special Agent in Charge of DEA for 
the area in which such building or enclosure is situated;
    (7) Such other secure storage areas as may be approved by the 
Administrator after considering the factors listed in Sec. 1301.71(b), 
(1) through (14);
    (8) (i) Schedule III through V controlled substances may be stored 
with Schedules I and II controlled substances under security measures 
provided by 21 CFR 1301.72(a);
    (ii) Non-controlled drugs, substances and other materials may be 
stored with Schedule III through V controlled substances in any of the 
secure storage areas required by 21 CFR 1301.72(b), provided that 
permission for such storage of non-controlled items is obtained in 
advance, in writing, from the Special Agent in Charge of DEA for the 
area in which such storage area is situated. Any such permission 
tendered must be upon the Special Agent in Charge's written 
determination that such non-segregated storage does not diminish 
security effectiveness for Schedules III through V controlled 
substances.
    (c) Multiple storage areas. Where several types or classes of 
controlled substances are handled separately by the registrant or 
applicant for different purposes (e.g., returned goods, or goods in 
process), the controlled substances may be stored separately, provided 
that each storage area complies with the requirements set forth in this 
section.
    (d) Accessibility to storage areas. The controlled substances 
storage areas shall be accessible only to an absolute minimum number of 
specifically authorized employees. When it is necessary for employee 
maintenance personnel, nonemployee maintenance personnel, business 
guests, or visitors to be present in or pass through controlled 
substances storage areas, the registrant shall provide for adequate 
observation of the area by an employee specifically authorized in 
writing.

[36 FR 18730, Sept. 21, 1971, as amended at 37 FR 15919, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, l973]

    Editorial Note: For Federal Register citations affecting 
Sec. 1301.72, see the List of CFR Sections Affected in the Finding Aids 
section of this volume.

[[Page 28]]



Sec. 1301.73   Physical security controls for non-practitioners; compounders for narcotic treatment programs; manufacturing and compounding areas.

    All manufacturing activities (including processing, packaging and 
labeling) involving controlled substances listed in any schedule and all 
activities of compounders shall be conducted in accordance with the 
following:
    (a) All in-process substances shall be returned to the controlled 
substances storage area at the termination of the process. If the 
process is not terminated at the end of a workday (except where a 
continuous process or other normal manufacturing operation should not be 
interrupted), the processing area or tanks, vessels, bins or bulk 
containers containing such substances shall be securely locked, with 
adequate security for the area or building. If such security requires an 
alarm, such alarm, upon unauthorized entry, shall transmit a signal 
directly to a central station protection company, or local or state 
police agency which has a legal duty to respond, or a 24-hour control 
station operated by the registrant.
    (b) Manufacturing activities with controlled substances shall be 
conducted in an area or areas of clearly defined limited access which is 
under surveillance by an employee or employees designated in writing as 
responsible for the area. ``Limited access'' may be provided, in the 
absence of physical dividers such as walls or partitions, by traffic 
control lines or restricted space designation. The employee designated 
as responsible for the area may be engaged in the particular 
manufacturing operation being conducted: Provided, That he is able to 
provide continuous surveillance of the area in order that unauthorized 
persons may not enter or leave the area without his knowledge.
    (c) During the production of controlled substances, the 
manufacturing areas shall be accessible to only those employees required 
for efficient operation. When it is necessary for employee maintenance 
personnel, nonemployee maintenance personnel, business guests, or 
visitors to be present in or pass through manufacturing areas during 
production of controlled substances, the registrant shall provide for 
adequate observation of the area by an employee specifically authorized 
in writing.

[36 FR 18731, Sept. 21, 1971. Redesignated at 38 FR 26609, Sept. 24, 
l973 and amended at 39 FR 37984, Oct. 25, 1974]



Sec. 1301.74   Other security controls for non-practitioners; narcotic treatment programs and compounders for narcotic treatment programs.

    (a) Before distributing a controlled substance to any person who the 
registrant does not know to be registered to possess the controlled 
substance, the registrant shall make a good faith inquiry either with 
the Administration or with the appropriate State controlled substances 
registration agency, if any, to determine that the person is registered 
to possess the controlled substance.
    (b) The registrant shall design and operate a system to disclose to 
the registrant suspicious orders of controlled substances. The 
registrant shall inform the Field Division Office of the Administration 
in his area of suspicious orders when discovered by the registrant. 
Suspicious orders include orders of unusual size, orders deviating 
substantially from a normal pattern, and orders of unusual frequency.
    (c) The registrant shall notify the Field Division Office of the 
Administration in his area of any theft or significant loss of any 
controlled substances upon discovery of such theft or loss. The supplier 
shall be responsible for reporting in-transit losses of controlled 
substances by the common or contract carrier selected pursuant to 
Sec. 1301.74(e), upon discovery of such theft or loss. The registrant 
shall also complete DEA Form 106 regarding such theft or loss. Thefts 
must be reported whether or not the controlled substances are 
subsequently recovered and/or the responsible parties are identified and 
action taken against them.
    (d) The registrant shall not distribute any controlled substance 
listed in Schedules II through V as a complimentary sample to any 
potential or current customer (1) without the prior written request of 
the customer, (2) to be used only for satisfying the legitimate medical 
needs of patients of the customer, and (3) only in reasonable 
quantities. Such request must contain

[[Page 29]]

the name, address, and registration number of the customer and the name 
and quantity of the specific controlled substance desired. The request 
shall be preserved by the registrant with other records of distribution 
of controlled substances. In addition, the requirements of part 1305 of 
the chapter shall be complied with for any distribution of a controlled 
substance listed in Schedule II. For purposes of this paragraph, the 
term ``customer'' includes a person to whom a complimentary sample of a 
substance is given in order to encourage the prescribing or recommending 
of the substance by the person.
    (e) When shipping controlled substances, a registrant is responsible 
for selecting common or contract carriers which provide adequate 
security to guard against in-transit losses. When storing controlled 
substances in a public warehouse, a registrant is responsible for 
selecting a warehouseman which will provide adequate security to guard 
against storage losses; wherever possible, the registrant shall store 
controlled substances in a public warehouse which complies with the 
requirements set forth in Sec. 1301.72. In addition, the registrant 
shall employ precautions (e.g., assuring that shipping containers do not 
indicate that contents are controlled substances) to guard against 
storage or in-transit losses.
    (f) When distributing controlled substances through agents (e.g., 
detailmen), a registrant is responsible for providing and requiring 
adequate security to guard against theft and diversion while the 
substances are being stored or handled by the agent or agents.
    (g) Before the initial distribution of carfentanil etorphine 
hydrochloride and/or diprenorphine to any person, the registrant must 
verify that the person is authorized to handle the substances(s) by 
contacting the Drug Enforcement Administration.
    (h) The acceptance of delivery of narcotic substances by a narcotic 
treatment program shall be made only by a licensed practitioner employed 
at the facility or other authorized individuals designated in writing. 
At the time of delivery, the licensed practitioner or other authorized 
individual designated in writing (excluding persons currently or 
previously dependent on narcotic drugs), shall sign for the narcotics 
and place his specific title (if any) on any invoice. Copies of these 
signed invoices shall be kept by the distributor.
    (i) Narcotics dispensed or administered at a narcotic treatment 
program will be dispensed or administered directly to the patient by 
either (1) the licensed practitioner, (2) a registered nurse under the 
direction of the licensed practitioner, (3) a licensed practical nurse 
under the direction of the licensed practitioner, or (4) a pharmacist 
under the direction of the licensed practitioner.
    (j) Persons enrolled in a narcotic treatment program will be 
required to wait in an area physically separated from the narcotic 
storage and dispensing area. This requirement will be enforced by the 
program physician and employees.
    (k) All narcotic treatment programs must comply with standards 
established by the Secretary of Health and Human Services (after 
consultation with the Administration) respecting the quantities of 
narcotic drugs which may be provided to persons enrolled in a narcotic 
treatment program for unsupervised use.
    (l) DEA may exercise discretion regarding the degree of security 
required in narcotic treatment programs based on such factors as the 
location of a program, the number of patients enrolled in a program and 
the number of physicians, staff members and security guards. Similarly, 
such factors will be taken into consideration when evaluating existing 
security or requiring new security at a narcotic treatment program.

[36 FR 7778, Apr. 24, 1971; 36 FR 13386, July 21, 1971, as amended at 36 
FR 18731, Sept. 21, 1971. Redesignated at 38 FR 26609, Sept. 24, l973]

    Editorial Note: For Federal Register citations affecting 
Sec. 1301.74, see the List of CFR Sections Affected in the Finding Aids 
section of this volume.



Sec. 1301.75   Physical security controls for practitioners.

    (a) Controlled substances listed in Schedule I shall be stored in a 
securely

[[Page 30]]

locked, substantially constructed cabinet.
    (b) Controlled substances listed in Schedules II, III, IV, and V 
shall be stored in a securely locked, substantially constructed cabinet. 
However, pharmacies and institutional practitioners (as defined in 
Sec. 1304.02(e) of this chapter) may disperse such substances throughout 
the stock of noncontrolled substances in such a manner as to obstruct 
the theft or diversion of the controlled substances.
    (c) This section shall also apply to nonpractitioners authorized to 
conduct research or chemical analysis under another registration.
    (d) Carfentanil etorphine hydrochloride and diprenorphine shall be 
stored in a safe or steel cabinet equivalent to a U.S. Government Class 
V security container.

[39 FR 3674, Jan. 29, 1974, as amended at 39 FR 17838, May 21, 1974; 54 
FR 33674, Aug. 16, 1989]



Sec. 1301.76   Other security controls for practitioners.

    (a) The registrant shall not employ, as an agent or employee who has 
access to controlled substances, any person who has been convicted of a 
felony offense relating to controlled substances or who, at any time, 
had an application for registration with the DEA denied, had a DEA 
registration revoked or has surrendered a DEA registration for cause. 
For purposes of this subsection, the term ``for cause'' means a 
surrender in lieu of, or as a consequence of, any federal or state 
administrative, civil or criminal action resulting from an investigation 
of the individual's handling of controlled substances.
    (b) The registrant shall notify the Field Division Office of the 
Administration in his area of the theft or significant loss of any 
controlled substances upon discovery of such loss or theft. The 
registrant shall also complete DEA (or BND) Form 106 regarding such loss 
or theft.
    (c) Whenever the registrant distributes a controlled substance 
(without being registered as a distributor, as permitted in 
Sec. 1301.22(b) and/or Secs. 1307.11-1307.14), he shall comply with the 
requirements imposed on nonpractitioners in Sec. 1301.74 (a), (b), and 
(e).

[36 FR 7778, Apr. 24, 1971, as amended at 36 FR 18731, Sept. 21, 1971; 
37 FR 15919, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, l973; 
47 FR 41735, Sept. 22, 1982; 56 FR 36728, Aug. 1, 1991]

                 Employee Screening--Non- Practitioners



Sec. 1301.90   Employee screening procedures.

    It is the position of DEA that the obtaining of certain information 
by non-practitioners is vital to fairly assess the likelihood of an 
employee committing a drug security breach. The need to know this 
information is a matter of business necessity, essential to overall 
controlled substances security. In this regard, it is believed that 
conviction of crimes and unauthorized use of controlled substances are 
activities that are proper subjects for inquiry. It is, therefore, 
assumed that the following questions will become a part of an employer's 
comprehensive employee screening program:

    Question. Within the past five years, have you been convicted of a 
felony, or within the past two years, of any misdemeanor or are you 
presently formally charged with committing a criminal offense? (Do not 
include any traffic violations, juvenile offenses or military 
convictions, except by general court-martial.) If the answer is yes, 
furnish details of conviction, offense, location, date and sentence.

    Question. In the past three years, have you ever knowingly used any 
narcotics, amphetamines or barbiturates, other than those prescribed to 
you by a physician? If the answer is yes, furnish details.

    Advice. An authorization, in writing, that allows inquiries to be 
made of courts and law enforcement agencies for possible pending charges 
or convictions must be executed by a person who is allowed to work in an 
area where access to controlled substances clearly exists. A person must 
be advised that any false information or omission of information will 
jeopardize his or her position with respect to employment. The 
application for employment should inform a person that information 
furnished or recovered as a result of any inquiry will not necessarily 
preclude employment, but will be considered as part of an overall 
evaluation of the person's qualifications. The maintaining of fair 
employment practices, the protection of the person's right of privacy, 
and the assurance

[[Page 31]]

that the results of such inquiries will be treated by the employer in 
confidence will be explained to the employee.

[40 FR 17143, Apr. 17, 1975]



Sec. 1301.91   Employee responsibility to report drug diversion.

    Reports of drug diversion by fellow employees is not only a 
necessary part of an overall employee security program but also serves 
the public interest at large. It is, therefore, the position of DEA that 
an employee who has knowledge of drug diversion from his employer by a 
fellow employee has an obligation to report such information to a 
responsible security official of the employer. The employer shall treat 
such information as confidential and shall take all reasonable steps to 
protect the confidentiality of the information and the identity of the 
employee furnishing information. A failure to report information of drug 
diversion will be considered in determining the feasibility of 
continuing to allow an employee to work in a drug security area. The 
employer shall inform all employees concerning this policy.

[40 FR 17143, Apr. 17, 1975]



Sec. 1301.92   Illicit activities by employees.

    It is the position of DEA that employees who possess, sell, use or 
divert controlled substances will subject themselves not only to State 
or Federal prosecution for any illicit activity, but shall also 
immediately become the subject of independent action regarding their 
continued employment. The employer will assess the seriousness of the 
employee's violation, the position of responsibility held by the 
employee, past record of employment, etc., in determining whether to 
suspend, transfer, terminate or take other action against the employee.

[40 FR 17143, Apr. 17, 1975]



Sec. 1301.93   Sources of information for employee checks.

    DEA recommends that inquiries concerning employees' criminal records 
be made as follows:

    Local inquiries. Inquiries should be made by name, date and place of 
birth, and other identifying information, to local courts and law 
enforcement agencies for records of pending charges and convictions. 
Local practice may require such inquiries to be made in person, rather 
than by mail, and a copy of an authorization from the employee may be 
required by certain law enforcement agencies.
    DEA inquiries. Inquiries supplying identifying information should 
also be furnished to DEA Field Division Offices along with written 
consent from the concerned individual for a check of DEA files for 
records of convictions. The Regional check will result in a national 
check being made by the Field Division Office.

[40 FR 17143, Apr. 17, 1975, as amended at 47 FR 41735, Sept. 22, 1982]



PART 1302--LABELING AND PACKAGING REQUIREMENTS FOR CONTROLLED SUBSTANCES--Table of Contents




Sec.
1302.01  Scope of Part 1302.
1302.02  Definitions.
1302.03  Symbol required; exceptions.
1302.04  Location and size of symbol on label.
1302.05  Location and size of symbol on labeling.
1302.06  Effective dates of labeling requirements.
1302.07  Sealing of controlled substances.
1302.08  Labeling and packaging requirements for imported and exported 
          substances.

    Authority: 21 U.S.C. 821, 825, 871(b), 958(e).

    Source: 36 FR 7785, Apr. 24, 1971, unless otherwise noted. 
Redesignated at 38 FR 26609, Sept. 24, 1973.



Sec. 1302.01   Scope of Part 1302.

    Requirements governing the labeling and packaging of controlled 
substances pursuant to sections 1305 and 1008(d) of the Act (21 U.S.C. 
825 and 958(d)) are set forth generally by those sections and 
specifically by the sections of this part.

[36 FR 13386, July 21, 1971. Redesignated at 38 FR 26609, Sept. 24, 
l973]



Sec. 1302.02   Definitions.

    As used in this part, the following terms shall have the meanings 
specified:
    (a) The term commercial container means any bottle, jar, tube, 
ampule, or other receptacle in which a substance is held for 
distribution or dispensing to an ultimate user, and in addition, any box 
or package in which the receptacle is held for distribution or 
dispensing to an ultimate user. The term commercial

[[Page 32]]

container does not include any package liner, package insert or other 
material kept with or within a commercial container, nor any carton, 
crate, drum, or other package in which commercial containers are stored 
or are used for shipment of controlled substances.
    (b) The term label means any display of written, printed, or graphic 
matter placed upon the commercial container of any controlled substance 
by any manufacturer of such substance.
    (c) The term labeling means all labels and other written, printed, 
or graphic matter (1) upon any controlled substance or any of its 
commercial containers or wrappers, or (2) accompanying such controlled 
substance.
    (d) The term manufacture means the producing, preparation, 
propagation, compounding, or processing of a drug or other substance or 
the packaging or repackaging of such substance, or the labeling or 
relabeling of the commercial container of such substance, but does not 
include the activities of a practitioner who, as an incident to his 
administration or dispensing such substance in the course of his 
professional practice, prepares, compounds, packages or labels such 
substance. The term manufacturer means a person who manufactures a drug 
or other substance, whether under a registration as a manufacturer or 
under authority of registration as a researcher or chemical analyst.
    (e) Any term not defined in this section shall have the definition 
set forth in section 102 of the Act (21 U.S.C. 802) or Sec. 1301.02 of 
this chapter.

[36 FR 7785, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1302.03   Symbol required; exceptions.

    (a) Each commercial container of a controlled substance (except for 
a controlled substance excepted by the Administrator pursuant to 
Sec. 1308.31 of this chapter) shall have printed on the label the symbol 
designating the schedule in which such controlled substance is listed. 
Each such commercial container, if it otherwise has no label, must bear 
a label complying with the requirement of this part.
    (b) Each manufacturer shall print upon the labeling of each 
controlled substance distributed by him the symbol designating the 
schedule in which such controlled substance is listed.
    (c) The following symbols shall designate the schedule corresponding 
thereto:

                                                                        
                 Schedule                                               
                                                                        
Schedule I................................  CI or C-I.                  
Schedule II...............................  CII or C-II.                
Schedule III..............................  CIII or C-III.              
Schedule IV...............................  CIV or C-IV.                
Schedule V................................  CV or C-V.                  
                                                                        

The word ``schedule'' need not be used. No distinction need be made 
between narcotic and nonnarcotic substances.
    (d) The symbol is not required on a carton or wrapper in which a 
commercial container is held if the symbol is easily legible through 
such carton or wrapper.
    (e) The symbol is not required on a commercial container too small 
or otherwise unable to accommodate a label, if the symbol is printed on 
the box or package from which the commercial container is removed upon 
dispensing to an ultimate user.
    (f) The symbol is not required on a commercial container containing, 
or on the labeling of, a controlled substance being utilized in clinical 
research involving blind and double blind studies.

[36 FR 7785, Apr. 24, 1971, as amended at 36 FR 18731, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1302.04   Location and size of symbol on label.

    (a) The symbol shall be prominently located on the right upper 
corner of the principal panel of the label of the commercial container 
and/or the panel of the commercial container normally displayed to 
dispensers of any controlled substance listed in Schedules I through V. 
The symbol must be at least two times as large as the largest type 
otherwise printed on the label.
    (b) In lieu of locating the symbol in the corner of the label, as 
prescribed in paragraph (a) of this section, the symbol may be 
overprinted on the label, in which case the symbol must be printed at 
least one-half the height of the label and in a contrasting color 
providing clear visibility against the background color of the label.

[[Page 33]]

    (c) In all cases the symbol shall be clear and large enough to 
afford easy identification of the schedule of the controlled substance 
upon inspection without removal from the dispenser's shelf.



Sec. 1302.05   Location and size of symbol on labeling.

    The symbol shall be prominently located on all labeling other than 
labels covered by Sec. 1302.04. In all cases the symbol shall be clear 
and large enough to afford prompt identification of the controlled 
substance upon inspection of the labeling.



Sec. 1302.06   Effective dates of labeling requirements.

    (a) All labels on commercial containers of, and all labeling of, a 
controlled substance which is listed in any schedule on May 1, 1971, and 
which is packaged after December 1, 1971, shall comply with the 
requirements of Sec. 1302.03.
    (b) All labels on commercial containers of, and all labeling of, a 
controlled substance which either is listed in any schedule on May 1, 
1971, and thereafter transferred to another schedule or is added to any 
schedule after May 1, 1971, and which is packaged more than 180 days 
following the date on which the transfer or addition becomes effective, 
shall comply with the requirements of Sec. 1302.03.
    (c) The Administrator may, in the case of any controlled substance, 
require compliance with the requirements of Sec. 1302.03 within a period 
of time shorter than required by this section if he finds that public 
health or safety necessitate an earlier effective date.
    (d) Until compliance is required under this section, the label on 
commercial container containing, and the labeling of, any controlled 
substance shall comply with any requirements under Federal law as to 
labels of such containers and as to labeling of such substances existing 
prior to the effective date prescribed in this section.



Sec. 1302.07   Sealing of controlled substances.

    (a) On each bottle, multiple dose vial, or other commercial 
container of any controlled substance listed in Schedules I or II or of 
any narcotic controlled substance listed in Schedule III or IV, there 
shall be securely affixed to the stopper, cap, lid, covering, or wrapper 
or such container a seal to disclose upon inspection any tampering or 
opening of the container.
    (b) Any seal accepted for use under Federal law prior to May 1, 
1971, shall be deemed acceptable for use under this section.

[36 FR 7785, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1302.08   Labeling and packaging requirements for imported and exported substances.

    (a) The symbol requirements of Secs. 1302.03-1302.06 apply to every 
commercial container containing, and to all labeling of, controlled 
substances imported into the jurisdiction of and/or the customs 
territory of the United States, as defined in Sec. 1311.02 of this 
chapter.
    (b) The symbol requirements of Secs. 1302.03-1302.06 do not apply to 
any commercial containers containing, or any labeling of, a controlled 
substance intended for export from the jurisdiction of the United 
States, as defined in Sec. 1311.02 of this chapter.
    (c) The sealing requirements of Sec. 1302.07 apply to every bottle, 
multiple dose vial, or other commercial container of any controlled 
substance listed in schedule I or II, or of any narcotic controlled 
substance listed in schedule III or IV, imported into, exported from, or 
intended for export from, the jurisdiction of and/or the customs 
territory of the United States, as defined in Sec. 1311.02 of this 
chapter.

[36 FR 18731, Sept. 21, 1971. Redesignated at 38 FR 26609, Sept. 24, 
1973]



PART 1303--QUOTAS--Table of Contents




                           General Information

Sec.
1303.01  Scope of Part 1303.
1303.02  Definitions.

[[Page 34]]

               Aggregate Production and Procurement Quotas

1303.11  Aggregate production quotas.
1303.12  Procurement quotas.
1303.13  Adjustments of aggregate production quotas.

                     Individual Manufacturing Quotas

1303.21  Individual manufacturing quotas.
1303.22  Procedure for applying for individual manufacturing quotas.
1303.23  Procedure for fixing individual manufacturing quotas.
1303.24  Inventory allowance.
1303.25  Increase in individual manufacturing quotas.
1303.26  Reduction in individual manufacturing quotas.
1303.27  Abandonment of quota.

                                Hearings

1303.31  Hearings generally.
1303.32  Purpose of hearing.
1303.33  Waiver or modification of rules.
1303.34  Request for hearing or appearance; waiver.
1303.35  Burden of proof.
1303.36  Time and place of hearing.
1303.37  Final order.

    Authority: 21 U.S.C. 821, 826, 871(b).

                           General Information



Sec. 1303.01   Scope of Part 1303.

    Procedures governing the establishment of production and 
manufacturing quotas on basic classes of controlled substances listed in 
schedules I and II pursuant to section 306 of the Act (21 U.S.C. 826) 
are governed generally by that section and specifically by the sections 
of this part.

[36 FR 7786, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1303.02   Definitions.

    As used in this part, the following terms shall have the meanings 
specified:
    (a) The term hearing means any hearing held pursuant to this part 
regarding the determination of aggregate production quota or the 
issuance, adjustment, suspension, or denial of a procurement quota or an 
individual manufacturing quota.
    (b) The term inventory means all factory and branch stocks in 
finished form of a basic class of controlled substance manufactured or 
otherwise acquired by a registrant, whether in bulk, commercial 
containers, or contained in pharmaceutical preparations in the 
possession of the registrant (including stocks held by the registrant 
under separate registration as a manufacturer, importer, exporter, or 
distributor).
    (c) The term net disposal means, for a stated period, the quantity 
of a basic class of controlled substance distributed by the registrant 
to another person, plus the quantity of that basic class used by the 
registrant in the production of (or converted by the registrant into) 
another basic class of controlled substance or a noncontrolled 
substance, plus the quantity of that basic class otherwise disposed of 
by the registrant, less the quantity of that basic class returned to the 
registrant by any purchaser, and less the quantity of that basic class 
distributed by the registrant to another registered manufacturer of that 
basic class for purposes other than use in the production of, or 
conversion into, another basic class of controlled substance or a 
noncontrolled substance or in the manufacture of dosage forms of that 
basic class.
    (d) The term registrant means any person registered pursuant to 
section 303 of the Act (21 U.S.C. 823).
    (e) Any term not defined in this section shall have the definition 
set forth in section 102 of the Act (21 U.S.C. 802) and Sec. 1301.02 of 
this chapter.

[36 FR 7786, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971; 37 
FR 15919, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, 1973]

    Editorial Note: For an interpretation document clarifying 
Sec. 1303.02(b), see 40 FR 52844, Nov. 13, 1975.

               Aggregate Production and Procurement Quotas



Sec. 1303.11   Aggregate production quotas.

    (a) The Administrator shall determine the total quantity of each 
basic class of controlled substance listed in Schedule I or II necessary 
to be manufactured during the following calendar year to provide for the 
estimated medical, scientific, research and industrial needs of the 
United States, for lawful export requirements, and for the establishment 
and maintenance of reserve stocks.

[[Page 35]]

    (b) In making his determinations, the Administrator shall consider 
the following factors:
    (1) Total net disposal of the class by all manufacturers during the 
current and 2 preceding years;
    (2) Trends in the national rate of net disposal of the class;
    (3) Total actual (or estimated) inventories of the class and of all 
substances manufactured from the class, and trends in inventory 
accumulation;
    (4) Projected demand for such class as indicated by procurement 
quotas requested pursuant to Sec. 1303.12; and
    (5) Other factors affecting medical, scientific, research, and 
industrial needs in the United States and lawful export requirements, as 
the Administrator finds relevant, including changes in the currently 
accepted medical use in treatment with the class or the substances which 
are manufactured from it, the economic and physical availability of raw 
materials for use in manufacturing and for inventory purposes, yield and 
stability problems, potential disruptions to production (including 
possible labor strikes), and recent unforeseen emergencies such as 
floods and fires.
    (c) The Administrator shall, on or before May 1 of each year, 
publish in the Federal Register, general notice of an aggregate 
production quota for any basic class determined by him under this 
section. A copy of said notice shall be mailed simultaneously to each 
person registered as a bulk manufacturer of the basic class. The 
Administrator shall permit any interested person to file written 
comments on or objections to the proposal and shall designate in the 
notice the time during which such filings may be made. The Administrator 
may, but shall not be required to, hold a public hearing on one or more 
issues raised by the comments and objections filed with him. In the 
event the Administrator decides to hold such a hearing, he shall publish 
notice of the hearing in the Federal Register, which notice shall 
summarize the issues to be heard and shall set the time for the hearing 
which shall nnt be less than 30 days after the date of publication of 
the notice. After consideration of any comments or objections, or after 
a hearing if one is ordered by the Administrator, the Administrator 
shall issue and publish in the Federal Register his final order 
determining the aggregate production quota for the basic class of 
controlled substance. The order shall include the findings of fact and 
conclusions of law upon which the order is based. The order shall 
specify the date on which it shall take effect. A copy of said order 
shall be mailed simultaneously to each person registered as a bulk 
manufacturer of the basic class.

[36 FR 7786, Apr. 24, 1971, as amended at 37 FR 15919, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1303.12   Procurement quotas.

    (a) In order to determine the estimated needs for, and to insure an 
adequate and uninterrupted supply of, basic classes of controlled 
substances listed in Schedules I and II (except raw opium being imported 
by the registrant pursuant to an import permit) the Administrator shall 
issue procurement quotas authorizing persons to procure and use 
quantities of each basic class of such substances for the purpose of 
manufacturing such class into dosage forms or into other substances.
    (b) Any person who is registered to manufacture controlled 
substances listed in any schedule and who desires to use during the next 
calendar year any basic class of controlled substances listed in 
Schedule I or II (except raw opium being imported by the registrant 
pursuant to an import permit) for purposes of manufacturing, shall apply 
on DEA (or BND) Form 250 for a procurement quota for such basic class. A 
separate application must be made for each basic class desired to be 
procured or used. The applicant shall state whether he intends to 
manufacture the basic class himself or purchase it from another 
manufacturer. The applicant shall state separately each purpose for 
which the basic class is desired, the quantity desired for that purpose 
during the next calendar year, and the quantities used and estimated to 
be used, if any, for that purpose during the current and preceding 2 
calendar years. If the purpose is to manufacture the basic class into 
dosage form, the applicant shall state the official name, common or 
usual name, chemical

[[Page 36]]

name, or brand name of that form. If the purpose is to manufacture 
another substance, the applicant shall state the official name, common 
or usual name, chemical name, or brand name of the substance, and, if a 
controlled substance listed in any schedule, the schedule number and 
Administration Controlled Substances Code Number, as set forth in part 
1308 of this chapter, of the substance. If the purpose is to manufacture 
another basic class of controlled substance listed in Schedule I or II, 
the applicant shall also state the quantity of the other basic class 
which the applicant has applied to manufacture pursuant to Sec. 1303.22 
and the quantity of the first basic class necessary to manufacture a 
specified unit of the second basic class. DEA (or BND) Form 250 shall be 
filed on or before April 1 of the year preceding the calendar year for 
which the procurement quota is being applied. Copies of DEA (or BND) 
Form 250 may be obtained from, and shall be filed with, the Drug Control 
Section, Drug Enforcement Administration, Department of Justice, 
Washington, DC 20537.
    (c) The Administrator shall, on or before July 1 of the year 
preceding the calendar year during which the quota shall be effective, 
issue to each qualified applicant a procurement quota authorizing him to 
procure and use:
    (1) All quantities of such class necessary to manufacture all 
quantities of other basic classes of controlled substances listed in 
Schedules I and II which the applicant is authorized to manufacture 
pursuant to Sec. 1303.23; and
    (2) Such other quantities of such class as the applicant has applied 
to procure and use and are consistent with his past use, his estimated 
needs, and the total quantity of such class that will be produced.
    (d) Any person to whom a procurement quota has been issued may at 
any time request an adjustment in the quota by applying to the 
Administrator with a statement showing the need for the adjustment. Such 
application shall be filed with the Drug Control Section, Drug 
Enforcement Administration, Department of Justice, Washington, DC 20537. 
The Administrator shall increase or decrease the procurement quota of 
such person if and to the extent that he finds, after considering the 
factors enumerated in paragraph (c) of this section and any occurrences 
since the issuance of the procurement quota, that the need justifies an 
adjustment.
    (e) The following persons need not obtain a procurement quota:
    (1) Any person who is registered to manufacture a basic class of 
controlled substance listed in Schedule I or II and who uses all of the 
quantity he manufactures in the manufacture of a subsance not controlled 
under the Act;
    (2) Any person who is registered or authorized to conduct chemical 
analysis with controlled substances (for controlled substances to be 
used in such analysis only); and
    (3) Any person who is registered to conduct research with a basic 
class of controlled substance listed in Schedule I or II and who is 
authorized to manufacture a quantity of such class pursuant to 
Sec. 1301.22(b) of this chapter.
    (f) Any person to whom a procurement quota has been issued, 
authorizing that person to procure and use a quantity of a basic class 
of controlled substances listed in Schedules I or II during the current 
calendar year, shall, at or before the time of giving an order to 
another manufacturer requiring the distribution of a quantity of such 
basic class, certify in writing to such other manufacturer that the 
quantity of such basic class ordered does not exceed the person's unused 
and available procurement quota of such basic class for the current 
calendar year. The written certification shall be executed by the same 
individual who signed the DEA Form 222 transmitting the order. 
Manufacturers shall not fill an order from persons required to apply for 
a procurement quota under paragraph (b) of this section unless the order 
is accompanied by a certification as required under this section. The 
certification required by this section shall contain the following: The 
date of the certification; the name and address of the bulk manufacturer 
to whom the certification is directed; a reference to the number of the 
DEA Form 222 to which the certification applies; the name of the person 
giving the order to which the certification applies; the name of the 
basic class specified in the DEA Form 222 to

[[Page 37]]

which the certification applies; the appropriate schedule within which 
is listed the basic class specified in the DEA Form 222 to which the 
certification applies; a statement that the quantity (expressed in 
grams) of the basic class specified in the DEA Form 222 to which the 
certification applies does not exceed the unused and available 
procurement quota of such basic class, issued to the person giving the 
order, for the current calendar year; and the signature of the 
individual who signed the DEA Form 222 to which the certification 
applies.

[36 FR 7786, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971; 36 
FR 18731, Sept. 21, 1971; 37 FR 15919, Aug. 8, 1972. Redesignated at 38 
FR 26609, Sept. 24, 1973]

    Editorial Note: For FR citations affecting Sec. 1303.12, see the 
List of CFR Sections Affected in the Finding Aids section of this 
volume.



Sec. 1303.13   Adjustments of aggregate production quotas.

    (a) The Administrator may at any time increase or reduce the 
aggregate production quota for a basic class of controlled substance 
listed in Schedule I or II which he has previously fixed pursuant to 
Sec. 1303.11.
    (b) In determining to adjust the aggregate production quota, the 
Administrator shall consider the following factors:
    (1) Changes in the demand for that class, changes in the national 
rate of net disposal of the class, and changes in the rate of net 
disposal of the class by registrants holding individual manufacturing 
quotas for that class;
    (2) Whether any increased demand for that class, the national and/or 
individual rates of net disposal of that class are temporary, short 
term, or long term;
    (3) Whether any increased demand for that class can be met through 
existing inventories, increased individual manufacturing quotas, or 
increased importation, without increasing the aggregate production 
quota, taking into account production delays and the probability that 
other individual manufacturing quotas may be suspended pursuant to 
Sec. 1303.24(b);
    (4) Whether any decreased demand for that class will result in 
excessive inventory accumulation by all persons registered to handle 
that class (including manufacturers, distributors, practitioners, 
importers, and exporters), notwithstanding the possibility that 
individual manufacturing quotas may be suspended pursuant to 
Sec. 1303.24(b) or abandoned pursuant to Sec. 1303.27;
    (5) Other factors affecting medical, scientific, research, and 
industrial needs in the United States and lawful export requirements, as 
the Administrator finds relevant, including changes in the currently 
accepted medical use in treatment with the class or the substances which 
are manufactured from it, the economic and physical availability of raw 
materials for use in manufacturing and for inventory purposes, yield and 
stability problems, potential disruptions to production (including 
possible labor strikes), and recent unforeseen emergencies such as 
floods and fires.
    (c) The Administrator in the event he determines to increase or 
reduce the aggregate production quota for a basic class of controlled 
substance, shall publish in the Federal Register general notice of an 
adjustment in the aggregate production quota for that class determined 
by him under this section. A copy of said notice shall be mailed 
simultaneously to each person registered as a bulk manufacturer of the 
basic class. The Administrator shall permit any interested person to 
file written comments on or objections to the proposal and shall 
designate in the notice the time during which such filings may be made. 
The Administrator may, but shall not be required to, hold a public 
hearing on one or more issues raised by the comments and objections 
filed with him. In the event the Administrator decides to hold such a 
hearing, he shall publish notice of the hearing in the Federal Register, 
which notice shall summarize the issues to be heard and shall set the 
time for the hearing, which shall not be less than 10 days after the 
date of publication of the notice. After consideration of any comments 
or objections, or after a hearing if one is ordered by the 
Administrator, the Administrator shall issue and publish in the Federal 
Register his final order determining the aggregate production for the 
basic class of controlled

[[Page 38]]

substance. The order shall include the findings of fact and conclusions 
of law upon which the order is based. The order shall specify the date 
on which it shall take effect. A copy of said order shall be mailed 
simultaneously to each person registered as a bulk manufacturer of the 
basic class.

[37 FR 15919, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, 1973]

                     Individual Manufacturing Quotas



Sec. 1303.21   Individual manufacturing quotas.

    (a) The Administrator shall, on or before July 1 of each year, fix 
for and issue to each person who is registered to manufacture a basic 
class of controlled substance listed in Schedule I or II, and who 
applies for a manufacturing quota, an individual manufacturing quota 
authorizing that person to manufacture during the next calendar year a 
quantity of that basic class. Any manufacturing quota fixed and issued 
by the Administrator shall be subject to his authority to reduce or 
limit it at a later date pursuant to Sec. 1303.26 and to his authority 
to revoke or suspend it at any time pursuant to Secs. 1301.45 and 
1301.46 of this chapter.
    (b) No individual manufacturing quota shall be required for 
registrants listed in Sec. 1303.12(e).

[36 FR 7786, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1303.22   Procedure for applying for individual manufacturing quotas.

    Any person who is registered to manufacture any basic class of 
controlled substance listed in Schedule I or II and who desires to 
manufacture a quantity of such class shall apply on DEA (or BND) Form 
189 for a manufacturing quota for such quantity of such class. Copies of 
DEA (or BND) Form 189 may be obtained from, and shall be filed (on or 
before May 1 of the year preceding the calendar year for which the 
manufacturing quota is being applied) with, the Drug Control Section, 
Drug Enforcement Administration, Department of Justice, Washington, D.C. 
20537. A separate application must be made for each basic class desired 
to be manufactured. The applicant shall state:
    (a) The name and Administration Controlled Substances Code Number, 
as set forth in part 1308 of this chapter, of the basic class.
    (b) For the basic class in each of the current and preceding 2 
calendar years,
    (1) The authorized individual manufacturing quota, if any;
    (2) The actual or estimated quantity manufactured;
    (3) The actual or estimated net disposal;
    (4) The actual or estimated inventory allowance pursuant to 
Sec. 1303.24; and
    (5) The actual or estimated inventory as of December 31;
    (c) For the basic class in the next calendar year,
    (1) The desired individual manufacturing quota; and
    (2) Any additional factors which the applicant finds relevant to the 
fixing of his individual manufacturing quota, including the trend of 
(and recent changes in) his and the national rates of net disposal, his 
production cycle and current inventory position, the econolic and 
physical availability of raw materials for use in manufacturing and for 
inventory purposes, yield and stability problems, potential disruptions 
to production (including possible labor strikes) and recent unforeseen 
emergencies such as floods and fires.

[36 FR 7786, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971; 37 
FR 15920, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, 1973, and 
amended at 46 FR 28841, May 29, 1981; 51 FR 5319, Feb. 13, 1986]



Sec. 1303.23   Procedure for fixing individual manufacturing quotas.

    (a) In fixing individual manufacturing quotas for a basic class of 
controlled substance listed in Schedule I or II, the Administrator shall 
allocate to each applicant who is currently manufacturing such class a 
quota equal to 100 percent of the estimated net disposal of that 
applicant for the next calendar year, adjusted--
    (1) By the amount necessary to increase or reduce the estimated 
inventory of the applicant on December 31 of the current year to his 
estimated inventory allowance for the next calendar year, pursuant to 
Sec. 1303.24, and
    (2) By any other factors which the Administrator deems relevant to 
the

[[Page 39]]

fixing of the individual manufacturing quota of the applicant, including 
the trend of (and recent changes in) his and the national rates of net 
disposal, his production cycle and current inventory position, the 
economic and physical availability of raw materials for use in 
manufacturing and for inventory purposes, yield and stability problems, 
potential disruptions to production (including possible labor strikes), 
and recent unforeseen emergencies such as floods and fires.
    (b) In fixing individual manufacturing quotas for a basic class of 
controlled substance listed in Schedule I or II, the Administrator shall 
allocate to each applicant who is not currently manufacturing such class 
a quota equal to 100 percent of the reasonably estimated net disposal of 
that applicant for the next calendar year, as determined by the 
Administrator, adjusted--
    (1) By the amount necessary to provide the applicant his estimated 
inventory allowance for the next calendar year, pursuant to 
Sec. 1303.24, and
    (2) By any other factors which the Administrator deems relevant to 
the fixing of the individual manufacturing quota of the applicant, 
including the trend of (and recent changes in) the national rate of net 
disposal, his production cycle and current inventory position, the 
economic and physical availability of raw materials for use in 
manufacturing and for inventory purposes, yield and stability problems, 
potential disruptions to production (including possible labor strikes), 
and recent unforeseen emergencies such as floods and fires.
    (c) The Administrator shall, on or before March 1 of each year, 
adjust the individual manufacturing quota allocated for that year to 
each applicant in paragraph (a) of this section by the amount necessary 
to increase or reduce the actual inventory of the applicant to December 
31 of the preceding year to his estimated inventory allowance for the 
current calendar year, pursuant to Sec. 1303.24.

[36 FR 7786, Apr. 24, 1971, as amended at 37 FR 15920, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1303.24   Inventory allowance.

    (a) For the purpose of determining individual manufacturing quotas 
pursuant to Sec. 1303.23, each registered manufacturer shall be allowed 
as a part of such quota an amount sufficient to maintain an inventory 
equal to,
    (1) For current manufacturers, 50 percent of his average estimated 
net disposal for the current calendar year and the last preceding 
calendar year; or
    (2) For new manufacturers, 50 percent of his reasonably estimated 
net disposal for the next calendar year as determined by the 
Administrator.
    (b) During each calendar year each registered manufacturer shall be 
allowed to maintain an inventory of a basic class not exceeding 65 
percent of his estimated net disposal of that class for that year, as 
determined at the time his quota for that year was determined. At any 
time the inventory of a basic class held by a manufacturer exceeds 65 
percent of his estimated net disposal, his quota for that class is 
automatically suspended and shall remain suspended until his inventory 
is less than 60 percent of his estimated net disposal. The Administrator 
may, upon application and for good cause shown, permit a manufacturer 
whose quota is, or is likely to be, suspended pursuant to this paragraph 
to continue manufacturing and to accumulate an inventory in excess of 65 
percent of his estimated net disposal, upon such conditions and within 
such limitations as the Administrator may find necessary or desirable.
    (c) If, during a calendar year, a registrant has manufactured the 
entire quantity of a basic class allocated to him under an individual 
manufacturing quota, and his inventory of that class is less than 40 
percent of his estimated net disposal of that class for that year, the 
Administrator may, upon application pursuant to Sec. 1303.25, increase 
the quota of such registrant sufficiently to allow restoration of the 
inventory to 50 percent of the estimated net disposal for that year.

[36 FR 7786, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]

[[Page 40]]



Sec. 1303.25   Increase in individual manufacturing quotas.

    (a) Any registrant who holds an individual manufacturing quota for a 
basic class of controlled substance listed in Schedule I or II may file 
with the Administrator an application on Administration Form 189 for an 
increase in such quota in order for him to meet his estimated net 
disposal, inventory and other requirements during the remainder of such 
calendar year.
    (b) The Administrator, in passing upon a registrant's application 
for an increase in his individual manufacturing quota, shall take into 
consideration any occurrences since the filing of such registrant's 
initial quota application that may require an increased manufacturing 
rate by such registrant during the balance of the calendar year. In 
passing upon such application the Administrator may also take into 
consideration the amount, if any, by which his determination of the 
total quantity for the basic class of controlled substance to be 
manufactured under Sec. 1303.11 exceeds the aggregate of all the 
individual manufacturing quotas for the basic class of controlled 
substance, and the equitable distribution of such excess among other 
registrants.

[36 FR 7786, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1303.26   Reduction in individual manufacturing quotas.

    The Administrator may at any time reduce an individual manufacturing 
quota for a basic class of controlled substance listed in Schedule I or 
II which he has previously fixed in order to prevent the aggregate of 
the individual manufacturing quotas and import permits outstanding or to 
be granted from exceeding the aggregate production quota which has been 
established for that class pursuant of Sec. 1303.11, as adjusted 
pursuant to Sec. 1303.13. If a quota assigned to a new manufacturer 
pursuant to Sec. 1303.23(b), or if a quota assigned to any manufacturer 
is increased pursuant to Sec. 1303.24(c), or if an import permit issued 
to an importer pursuant to part 1312 of this chapter, causes the total 
quantity of a basic class to be manufactured and imported during the 
year to exceed the aggregate production quota which has been established 
for that class pursuant to Sec. 1303.11, as adjusted pursuant to 
Sec. 1303.13, the Administrator may proportionately reduce the 
individual manufacturing quotas and import permits of all other 
registrants to keep the aggregate production quota within the limits 
originally established, or, alternatively, the Administrator may reduce 
the individual manufacturing quota of any registrant whose quota is 
suspended pursuant to Sec. 1303.24(b) or Sec. 1301.45 or Sec. 1301.46 of 
this chapter, or is abandoned pursuant to Sec. 1303.27.

[36 FR 7786, Apr. 24, 1971, as amended at 37 FR 15920, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1303.27   Abandonment of quota.

    Any manufacturer assigned an individual manufacturing quota for any 
basic class pursuant to Sec. 1303.23 may at any time abandon his right 
to manufacture all or any part of such quota by filing with the Drug 
Control Section a written notice of such abandonment, stating the name 
and Administration Controlled Substances Code Number, as set forth in 
part 1308 of this chapter, of the substance and the amount which he has 
chosen not to manufacture. The Administrator may, in his discretion, 
allocate such amount among the other manufacturers in proportion to 
their respective quotas.

[36 FR 7786, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 46 FR 28841, 
May 29, 1981; 51 FR 5319, Feb. 13, 1986]

                                Hearings



Sec. 1303.31   Hearings generally.

    (a) In any case where the Administrator shall hold a hearing 
regarding the determination of an aggregate production quota pursuant to 
Sec. 1303.11(c), or regarding the adjustment of an aggregate production 
quota pursuant to Sec. 1303.13(c), the procedures for such hearing shall 
be governed generally by the rule making procedures set forth in the 
Administrative Procedure Act (5 U.S.C. 551-559) and specifically by 
section 306 of the Act (21 U.S.C. 826), by Secs. 1303.32-1303.37, and by 
the procedures for administrative hearings under the

[[Page 41]]

Act set forth in Secs. 1316.41-1316.67 of this chapter.
    (b) In any case where the Administrator shall hold a hearing 
regarding the issuance, adjustment, suspension, or denial of a 
procurement quota pursuant to Sec. 1303.12, or the issuance, adjustment, 
suspension, or denial of an individual manufacturing quota pursuant to 
Secs. 1303.21-1303.27, the procedures for such hearing shall be governed 
generally by the adjudication procedures set forth in the Administrative 
Procedures Act (5 U.S.C. 551-559) and specifically by section 306 of the 
Act (21 U.S.C. 826), by Secs. 1303.32-1303.37, and by the procedures for 
administrative hearings under the Act set forth in Secs. 1316.41-1316.67 
of this chapter.

[36 FR 7786, Apr. 24, 1971, as amended at 37 FR 15920, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1303.32   Purpose of hearing.

    (a) The Administrator may, in his sole discretion, hold a hearing 
for the purpose of receiving factual evidence regarding any one or more 
issues (to be specified by him) involved in the determination or 
adjustment of any aggregate production quota.
    (b) If requested by a person applying for or holding a procurement 
quota or an individual manufacturing quota, the Administrator shall hold 
a hearing for the purpose of receiving factual evidence regarding the 
issues involved in the issuance, adjustment, suspension, or denial of 
such quota to such person, but the Administrator need not hold a hearing 
on the suspension of a quota pursuant to Sec. 1301.45 or Sec. 1301.46 of 
this chapter separate from a hearing on the suspension of registration 
pursuant to those sections.
    (c) Extensive argument should not be offered into evidence but 
rather presented in opening or closing statements of counsel or in 
memoranda or proposed findings of fact and conclusions of law.

[36 FR 7786, Apr. 24, 1971, as amended at 37 FR 15920, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1303.33   Waiver or modification of rules.

    The Administrator or the presiding officer (with respect to matters 
pending before him) may modify or waive any rule in this part by notice 
in advance of the hearing, if he determines that no party in the hearing 
will be unduly prejudiced and the ends of justice will thereby be 
served. Such notice of modification or waiver shall be made a part of 
the record of the hearing.

[36 FR 7786, Apr. 24,1971. Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1303.34   Request for hearing or appearance; waiver.

    (a) Any applicant or registrant who desires a hearing on the 
issuance, adjustment, suspension, or denial of his procurement and/or 
individual manufacturing quota shall, within 30 days after the date of 
receipt of the issuance, adjustment, suspension, or denial of such 
quota, file with the Administrator a written request for a hearing in 
the form prescribed in Sec. 1316.47 of this chapter. Any interested 
person who desires a hearing on the determination of an aggregate 
production quota shall, within the time prescribed in Sec. 1303.11(c), 
file with the Administrator a written request for a hearing in the form 
prescribed in Sec. 1316.47 of this chapter, including in the request a 
statement of the grounds for a hearing.
    (b) Any interested person who desires to participate in a hearing on 
the determination or adjustment of an aggregate production quota, which 
hearing is ordered by the Administrator pursuant to Sec. 1303.11(c) or 
Sec. 1303.13(c) may do so by filing with the Administrator, within 30 
days of the date of publication of notice of the hearing in the Federal 
Register, a written notice of his intention to participate in such 
hearing in the form prescribed in Sec. 1316.48 of this chapter.
    (c) Any person entitled to a hearing or to participate in a hearing 
pursuant to paragraph (b) of this section, may, within the period 
permitted for filing a request for a hearing of notice of appearance, 
file with the Administrator a waiver of an opportunity for a hearing or 
to participate in a hearing, together with a written statement regarding 
his position on the matters of fact and law involved in such hearing. 
Such statement, if admissible, shall be made a part of the record and 
shall be considered in light of the lack of opportunity for

[[Page 42]]

cross-examination in determining the weight to be attached to matters of 
fact asserted therein.
    (d) If any person entitled to a hearing or to participate in a 
hearing pursuant to paragraph (b) of this section, fails to file a 
request for a hearing or notice of appearance, or if he so files and 
fails to appear at the hearing, he shall be deemed to have waived his 
opportunity for the hearing or to participate in the hearing, unless he 
shows good cause for such failure.
    (e) If all persons entitled to a hearing or to participate in a 
hearing waive or are deemed to waive their opportunity for the hearing 
or to participate in the hearing, the Administrator may cancel the 
hearing, if scheduled, and issue his final order pursuant to 
Sec. 1303.37 without a hearing.

[36 FR 7786, Apr. 24, 1971, as amended at 36 FR 18731, Sept. 21, 1971; 
37 FR 15920, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1303.35   Burden of proof.

    (a) At any hearing regarding the determination or adjustment of an 
aggregrate production quota, each interested person participating in the 
hearing shall have the burden of proving any propositions of fact or law 
asserted by him in the hearing.
    (b) At any hearing regarding the issuance, adjustment, suspension, 
or denial of a procurement or individual manufacturing quota, the 
Administration shall have the burden of proving that the requirements of 
this part for such issuance, adjustment, suspension, or denial are 
satisfied.

[36 FR 7786, Apr. 24, 1971, as amended at 37 FR 15920, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1303.36   Time and place of hearing.

    (a) If any applicant or registrant requests a hearing on the 
issuance, adjustment, suspension, or denial of his procurement and/or 
individual manufacturing quota pursuant to Sec. 1303.34, the 
Administrator shall hold such hearing. Notice of the hearing shall be 
given to the applicant or registrant of the time and place at least 30 
days prior to the hearing, unless the applicant or registrant waives 
such notice and requests the hearing be held at an earlier time, in 
which case the Administrator shall fix a date for such hearing as early 
as reasonably possible.
    (b) The hearing will commence at the place and time designated in 
the notice given pursuant to paragraph (a) of this section or in the 
notice of hearing published in the Federal Register pursuant to 
Sec. 1303.11(c) or Sec. 1303.13 (c), but thereafter it may be moved to a 
different place and may be continued from day to day or recessed to a 
later day without notice other than announcement thereof by the 
presiding officer at the hearing.

[36 FR 7786, Apr. 24, 1971, as amended at 37 FR 15920, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1303.37   Final order.

    As soon as practicable after the presiding officer has certified the 
record to the Administrator, the Administrator shall issue his order on 
the determination or adjustment of the aggregate production quota or on 
the issuance, adjustment, suspension, or denial of the procurement quota 
or individual manufacturing quota, as case may be. The order shall 
include the findings of fact and conclusions of law upon which the order 
is based. The order shall specify the date on which it shall take 
effect. The Administrator shall serve one copy of his order upon each 
party in the hearing.

[36 FR 7786, Apr. 24, 1971, as amended at 37 FR 15920, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



PART 1304--RECORDS AND REPORTS OF REGISTRANTS--Table of Contents




                           General Information

Sec.
1304.01  Scope of Part 1304.
1304.02  Definitions.
1304.03  Persons required to keep records and file reports.
1304.04  Maintenance of records and inventories.

                         Inventory Requirements

1304.11  General requirements for inventories.
1304.12  Initial inventory date.
1304.13  Biennial inventory date.
1304.14  Inventory date for newly controlled substances.

[[Page 43]]

1304.15  Inventories of manufacturers.
1304.16  Inventories of distributors.
1304.17  Inventories of dispensers and researchers.
1304.18  Inventories of importers and exporters.
1304.19  Inventories of chemical analysts.

                           Continuing Records

1304.21  General requirements for continuing records.
1304.22  Records for manufacturers.
1304.23  Records for distributors.
1304.24  Records for dispensers and researchers.
1304.25  Records for importers.
1304.26  Records for exporters.
1304.27  Records for chemical analysts.
1304.28  Records for maintenance treatment programs and detoxification 
          treatment programs.
1304.29  Records for treatment programs which compound narcotics for 
          treatment programs and other locations.

                                 Reports

1304.31  Reports from manufacturers importing opium.
1304.32  Reports of manufacturers importing medicinal coca leaves.
1304.33  Reports from manufacturers importing special coca leaves.
1304.34  Reports generally.
1304.35  Reports from manufacturers of bulk materials or dosage units.
1304.36  Reports from packagers and labelers.
1304.37  Reports from distributors.
1304.38  Reports from manufacturers importing poppy straw or concentrate 
          of poppy straw.

    Authority: 21 U.S.C. 821, 827, 871(b), 958(d), 965, unless otherwire 
noted.

                           General Information



Sec. 1304.01   Scope of Part 1304.

    Inventory and other records and reports required under section 307 
or section 1008(d) of the Act (21 U.S.C. 827 and 958(d)) shall be in 
accordance with, and contain the information required by, those sections 
and by the sections of this part.

[36 FR 7789, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1304.02   Definitions.

    As used in this part, the following terms shall have the meanings 
specified:
    (a) The term Act means the Controlled Substances Act (84 Stat. 1242; 
21 U.S.C. 801) and/or the Controlled Substances Import and Export Act 
(84 Stat. 1285; 21 U.S.C. 951).
    (b) The term commercial container means any bottle, jar, tube, 
ampule, or other receptacle in which a substance is held for 
distribution or dispensing to an ultimate user, and in addition, any box 
or package in which the receptacle is held for distribution or 
dispensing to an ultimate user. The term commercial container does not 
include any package liner, package insert of other material kept with or 
within a commercial container, nor any carton, crate, drum, or other 
package in which commercial containers are stored or are used for 
shipment of controlled substances.
    (c) The term dispenser means an individual practitioner, 
institutional practitioner, pharmacy or pharmacist who dispenses a 
controlled substance.
    (d) The term individual practitioner means a physician, dentist, 
veterinarian, or other individual licensed, registered, or otherwise 
permitted, by the United States or the jurisdiction in which he 
practices, to dispense a controlled substance in the course of 
professional practice, but does not include a pharmacist, a pharmacy, or 
an institutional practitioner.
    (e) The term institutional practitioner means a hospital or other 
person (other than an individual) licensed, registered, or otherwise 
permitted, by the United States or the jurisdiction in which it 
practices, to dispense a controlled substance in the course of 
professional practice, but does not include a pharmacy.
    (f) The term mid-level practitioner means an individual practitioner 
(as defined in Sec. 1304.02(d)), other than a physician, dentist, 
veterinarian, or podiatrist, who is licensed, registered, or otherwise 
permitted by the United States or the jurisdiction in which he/she 
practices, to dispense a controlled substance in the course of 
professional practice. Examples of mid-level practitioners include, but 
are not limited to, health care providers such as nurse practitioners, 
nurse midwives, nurse anesthetists, clinical nurse specialists and 
physician assistants who are authorized to dispense controlled 
substances by the state in which they practice.

[[Page 44]]

    (g) The term name means the official name, common or usual name, 
chemical name, or brand name of a substance.
    (h) The term pharmacist means any pharmacist licensed by a State to 
dispense controlled substances, and shall include any other person 
(e.g., pharmacist intern) authorized by a State to dispense controlled 
substances under the supervision of a pharmacist licensed by such State.
    (i) The term readily retrievable means that certain records are kept 
by automatic data processing systems or other electronic or mechanized 
recordkeeping systems in such a manner that they can be separated out 
from all other records in a reasonable time and/or records are kept on 
which certain items are asterisked, redlined, or in some other manner 
visually identifiable apart from other items appearing on the records.
    (j) Any term not defined in this section shall have the definition 
set forth in sections 102 and 1001 of the Act (21 U.S.C. 802 and 951) 
and in Secs. 1301.02 and 1311.02 of this chapter.

[36 FR 7789, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973; 58 FR 31175, June 1, 1993]



Sec. 1304.03   Persons required to keep records and file reports.

    (a) Each registrant shall maintain the records and inventories and 
shall file the reports required by this part, except as exempted by this 
section. Any registrant who is authorized to conduct other activities 
without being registered to conduct those activities, either pursuant to 
Sec. 1301.22(b) of this chapter or pursuant to Secs. 1307.11-1307.15 of 
this chapter, shall maintain the records and inventories and shall file 
the reports required by this part for persons registered to conduct such 
activities. This latter requirement should not be construed as requiring 
stocks of controlled substances being used in various activities under 
one registration to be stored separately, nor that separate records are 
required for each activity. The intent of the Administration is to 
permit the registrant to keep one set of records which are adapted by 
the registrant to account for controlled substances used in any 
activity. Also, the Administration does not wish to acquire separate 
stocks of the same substance to be purchased and stored for separate 
activities. Otherwise, there is no advantage gained by permitting 
several activities under one registration. Thus, when a researcher 
manufactures a controlled item, he must keep a record of the quantity 
manufactured; when he distributes a quantity of the item, he must use 
and keep invoices or order forms to document the transfer; when he 
imports a substance, he keeps as part of his records the documentation 
required of an importer; and when substances are used in chemical 
analysis, he need not keep a record of this because such a record would 
not be required of him under a registration to do chemical analysis. All 
of these records may be maintained in one consolidated record system. 
Similarly, the researcher may store all of his controlled items in one 
place, and every two years take inventory of all items on hand, 
regardless of whether the substances were manufactured by him, imported 
by him, or purchased domestically by him, of whether the substances will 
be administered to subjects, distributed to other researchers, or 
destroyed during chemical analysis.
    (b) A registered individual practitioner is required to keep 
records, as described in Sec. 1304.04, of controlled substances in 
Schedules II, III, IV, and V which are dispensed, other than by 
prescribing or administering in the lawful course of professional 
practice.
    (c) A registered individual practitioner is not required to keep 
records of controlled substances in Schedules II, III, IV, and V which 
are prescribed in the lawful course of professional practice, unless 
such substances are prescribed in the course of maintenance or 
detoxification treatment of an individual.
    (d) A registered individual practitioner is not required to keep 
records of controlled substances listed in Schedules II, III, IV and V 
which are administered in the lawful course of professional practice 
unless the practitioner regularly engages in the dispensing or 
administering of controlled substances and charges patients, either 
separately or together with charges for

[[Page 45]]

other professional services, for substances so dispensed or 
administered. Records are required to be kept for controlled substances 
administered in the course of maintenance or detoxification treatment of 
an individual.
    (e) Each registered mid-level practitioner shall maintain in a 
readily retrievable manner those documents required by the state in 
which he/she practices which describe the conditions and extent of his/
her authorization to dispense controlled substances and shall make such 
documents available for inspection and copying by authorized employees 
of the Administration. Examples of such documentation include protocols, 
practice guidelines or practice agreements.
    (f) A registered person using any controlled substance in research 
conducted in conformity with an exemption granted under section 505(i) 
or 512(j) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 355(i) 
or 360b(j)) at a registered establishment which maintains records in 
accordance with either of those sections is not required to keep records 
if he notifies the Administration of the name, address, and registration 
number of the establishment maintaining such records.
    (g) A registered person using any controlled substance in 
preclinical research or in teaching at a registered establishment which 
maintains records with respect to such substances is not required to 
keep records if he notifies the Administration of the name, address, and 
registration number of the establishment maintaining such records.
    (h) Notice required by paragraphs (f) and (g) of this section shall 
be given at the time the person applies for registration or 
reregistration and shall be made in the form of an attachment to the 
application, which shall be filed with the application.

[36 FR 7790, Apr. 24, 1971, as amended at 36 FR 18731, Sept. 21, 1971; 
37 FR 15920, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 50 FR 40523, Oct. 4, 1985; 51 FR 5320, Feb. 13, 1986; 51 
FR 26154, July 21, 1986; 58 FR 31175, June 1, 1993]



Sec. 1304.04  Maintenance of records and inventories.

    (a) Every inventory and other records required to be kept under this 
part shall be kept by the registrant and be available, for at least 2 
years from the date of such inventory or records, for inspection and 
copying by authorized employees of the Administration, except that 
financial and shipping records (such as invoices and packing slips but 
not excuted order forms subject to Sec. 1305.13 of this chapter) may be 
kept at a central location, rather than at the registered location, if 
the registrant has notified the Administration of his intention to keep 
central records. Written notification must be submitted by registered or 
certified mail, return receipt requested, in triplicate, to the Special 
Agent in Charge of the Administration in the area in which the 
registrant is located. Unless the registrant is informed by the Special 
Agent in Charge that permission to keep central records is denied, the 
registrant may maintain central records commencing 14 days after receipt 
of his notification by the Special Agent in Charge.

All notifications must include:
    (1) The nature of the records to be kept centrally.
    (2) The exact location where the records will be kept.
    (3) The name, address, DEA registration number and type of DEA 
registration of the registrant whose records are being maintained 
centrally.
    (4) Whether central records will be maintained in a manual, or 
computer readable form.
    (b) All registrants that are authorized to maintain a central 
recordkeeping system shall be subject to the following conditions:
    (1) The records to be maintained at the central record location 
shall not include executed order forms, prescriptions and/or inventories 
which shall be maintained at each registered location.
    (2) If the records are kept on microfilm, computer media or in any 
form requiring special equipment to render the records easily readable, 
the registrant shall provide access to such equipment with the records. 
If any

[[Page 46]]

code system is used (other than pricing information), a key to the code 
shall be provided to make the records understandable.
    (3) The registrant agrees to deliver all or any part of such records 
to the registered location within two business days upon receipt of a 
written request from the Administration for such records, and if the 
Administration chooses to do so in lieu of requiring delivery of such 
records to the registered location, to allow authorized employees of the 
Administration to inspect such records at the central location upon 
request by such employees without a warrant of any kind.
    (4) In the event that a registrant fails to comply with these 
conditions, the Special Agent in Charge may cancel such central 
recordkeeping authorization, and all other central recordkeeping 
authorizations held by the registrant without a hearing or other 
procedures. In the event of a cancellation of central recordkeeping 
authorizations under this paragraph the registrant shall, within the 
time specified by the Special Agent in Charge, comply with the 
requirements of this section that all records be kept at the registered 
location.
    (c) Registrants need not notify the Special Agent in Charge or 
obtain central recordkeeping approval in order to maintain records on an 
in-house computer system.
    (d) ARCOS participants who desire authorization to report from other 
than their registered locations must obtain a separate central reporting 
identifier. Request for central reporting identifiers will be submitted 
to: ARCOS Unit, P.O. Box 28293, Central Station, Washington, DC 20005.
    (e) All central recordkeeping permits previously issued by the 
Administration will expire on September 30, 1980. Registrants who desire 
to continue maintaining central records will make notification to the 
local Special Agent in Charge as provided in paragraph (a) of this 
section.
    (f) Each registered manufacturer, distributor, importer, exporter, 
narcotic treatment program and compounder for narcotic treatment program 
shall maintain inventories and records of controlled substances as 
follows:
    (1) Inventories and records of controlled substances listed in 
Schedules I and II shall be maintained separately from all of the 
records of the registrant; and
    (2) Inventories and records of controlled substances listed in 
Schedules III, IV, and V shall be maintained either separately from all 
other records of the registrant or in such form that the information 
required is readily retrievable from the ordinary business records of 
the registrant.
    (g) Each registered individual practitioner required to keep records 
and institutional practitioner shall maintain inventories and records of 
controlled substances in the manner prescribed in paragraph (f) of this 
section.
    (h) Each registered pharmacy shall maintain the inventories and 
records of controlled substances as follows:
    (1) Inventories and records of all controlled substances listed in 
Schedules I and II shall be maintained separately from all other records 
of the pharmacy, and prescriptions for such substances shall be 
maintained in a separate prescription file; and
    (2) Inventories and records of controlled substances listed in 
Schedules III, IV, and V shall be maintained either separately from all 
other records of the pharmacy or in such form that the information 
required is readily retrievable from ordinary business records of the 
pharmacy, and prescriptions for such substances shall be maintained 
either in separate prescription file for controlled substances listed in 
Schedules III, IV, and V only or in such form that they are readily 
retrievable from the other prescription records of the pharmacy. 
Prescriptions will be deemed readily retrievable if, at the time they 
are initially filed, the face of the prescription is stamped in red ink 
in the lower right corner with the letter ``C'' no less than 1-inch high 
and filed either in the prescription file for controlled substances 
listed in

[[Page 47]]

Schedules I and II or in the usual consecutively numbered prescription 
file for non-controlled substances.

(21 U.S.C. 821 and 871(b); 28 CFR 0.100)

[36 FR 7790, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, l973, and amended at 39 FR 37985, 
Oct. 25, 1974; 45 FR 44266, July 1, 1980; 47 FR 41735, Sept. 22, 1982; 
51 FR 5320, Feb. 13, 1986]

                         Inventory Requirements



Sec. 1304.11   General requirements for inventories.

    (a) Each inventory shall contain a complete and accurate record of 
all controlled substances on hand on the date the inventory is taken. 
Controlled substances shall be deemed to be ``on hand'' if they are in 
the possession of or under the control of the registrant, including 
substances returned by a customer, substances ordered by a customer but 
not yet invoiced, substances stored in a warehouse on behalf of the 
registrant, and substances in the possession of employees of the 
registrant and intended for distribution as complimentary samples.
    (b) A separate inventory shall be made by a registrant for each 
registered location. In the event controlled substances in the 
possession or under the control of the registrant at a location for 
which he is not registered, the substances shall be included in the 
inventory of the registered location to which they are subject to 
control or to which the person possessing the substance is responsible. 
Each inventory for a registered location shall be kept at the registered 
location.
    (c) A separate inventory shall be made by a registrant for each 
independent activity for which he is registered, except as provided in 
Sec. 1304.18.
    (d) A registrant may take an inventory on a date that is within 4 
days of his biennial inventory date pursuant to Sec. 1304.13 if he 
notifies in advance the Special Agent in Charge of the Administration in 
his area of the date on which he will take the inventory. A registrant 
may take an inventory either as of the opening of business or as of the 
close of business on the inventory date. The registrant shall indicate 
on the inventory records whether the inventory is taken as of the 
opening or as of the close of business and the date the inventory is 
taken.
    (e) An inventory must be maintained in a written, typewritten or 
printed form. An inventory taken by use of an oral recording device must 
be promptly transcribed.

[36 FR 7790, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, l973, 
and amended at 47 FR 41735, Sept. 22, 1982]



Sec. 1304.12   Initial inventory date.

    (a) Every person required to keep records who is provisionally 
registered on May 1, 1971, shall take an inventory of all stocks of 
controlled substances on hand on that date in accordance with 
Secs. 1304.15-1304.19, as applicable.
    (b) Every person required to keep records who is registered after 
May 1, 1971, and who was not provisionally registered on that date, 
shall take an inventory of all stocks of controlled substances on hand 
on the date he first engages in the manufacture, distribution, or 
dispensing of controlled substances, in accordance with Secs. 1304.15-
1304.19, as applicable. In the event a person commences business with no 
controlled substances on hand, he shall record this fact as his initial 
inventory.

[36 FR 7791, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971; 37 
FR 15920, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1304.13   Biennial inventory date.

    Every 2 years following the date on which the initial inventory is 
taken by a registrant pursuant to Sec. 1304.12, the registrant shall 
take a new inventory of all stocks of controlled substances on hand. The 
biennial inventory may be taken (a) on the day of the year on which the 
initial inventory was taken or (b) on the registrant's regular general 
physical inventory date, if any, which is nearest to and does not vary 
by more than 6 months from the biennial date that would otherwise apply 
or (c) on any other fixed date which does not vary by more than 6 months 
from the biennial date that would otherwise apply. If the registrant 
elects to take the biennial inventory on his regular

[[Page 48]]

general physical inventory date or another fixed date, he shall notify 
the Administration of this election and of the date on which the 
biennial inventory will be taken.

[36 FR 7791, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1304.14   Inventory date for newly controlled substances.

    On the effective date of a rule by the Administrator pursuant to 
Secs. 1308.48-1308.49, or Sec. 1308.50 of this chapter adding a 
substance to any schedule of controlled substances, which substance was, 
immediately prior to that date, not listed on any such schedule, every 
registrant required to keep records who possesses that substance shall 
take an inventory of all stocks of the substance on hand. Thereafter 
such substance shall be included in each inventory made by the 
registrant pursuant to Sec. 1304.13.

[36 FR 7791, Apr. 24, 1971, as amended at 36 FR 18732, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1304.15   Inventories of manufacturers.

    Each person registered or authorized (by Sec. 1301.22(b), 
Sec. 1307.12, or Sec. 1307.15 of this chapter) to manufacture controlled 
substances shall include the following information in his inventory:
    (a) For each controlled substance in bulk form to be used in (or 
capable of use in) the manufacture of the same or other controlled or 
non-controlled substances in finished form:
    (1) The name of the substance; and
    (2) The total quantity of the substance to the nearest metric unit 
weight consistent with unit size (except that for inventories made in 
1971, avoirdupois weights may be utilized where metric weights are not 
readily available).
    (b) For each controlled substance in the process of manufacture on 
the inventory date:
    (1) The name of the substance;
    (2) The quantity of the substance in each batch and/or stage of 
manufacture, identified by the batch number or other appropriate 
identifying number;
    (3) The physical form which the substance is to take upon completion 
of the manufacturing process (e.g., granulations, tablets, capsules, or 
solutions), identified by the batch number or other appropriate 
identifying number, and if possible the finished form of the substance 
(e.g., 10-milligram tablet or 10-milligram concentration per fluid ounce 
or milliliter) and the number or volume thereof; and
    (c) For each controlled substance in finished form:
    (1) The name of the substance;
    (2) Each finished form of the substance (e.g., 10-milligram tablet 
or 10-milligram concentration per fluid ounce or milliliter);
    (3) The number of units or volume of each finished form in each 
commercial container (e.g., 100-tablet bottle or 3-milliliter vial); and
    (4) The number of commercial containers of each such finished form 
(e.g. four 100-tablet bottles or six 3-milliliter vials).
    (d) For each controlled substance not included in paragraphs (a), 
(b) or (c) of this section (e.g., damaged, defective or impure 
substances awaiting disposal, substances held for quality control 
purposes, or substances maintained for extemporaneous compoundings):
    (1) The name of the substance;
    (2) The total quantity of the substance to the nearest metric unit 
weight or the total number of units of finished form; and
    (3) The reason for the substance being maintained by the registrant 
and whether such substance is capable of use in the manufacture of any 
controlled substance in finished form.

[36 FR 7791, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971; 36 
FR 18732, Sept. 21, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1304.16   Inventories of distributors.

    Each person registered or authorized (by Secs. 1301.22(b) or 
Secs. 1307.11-1307.14 of this chapter) to distribute controlled 
substances shall include in his inventory the same information required 
of manufacturers pursuant to Sec. 1304.15 (c) and (d).

[36 FR 7791, Apr. 24, 1971, as amended at 36 FR 18732, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]

[[Page 49]]



Sec. 1304.17   Inventories of dispensers and researchers.

    Each person registered or authorized (by Sec. 1301.22(b) of this 
chapter) to dispense or conduct research with controlled substances and 
required to keep records pursuant to Sec. 1304.03 shall include in his 
inventory the same information required of manufacturers pursuant to 
Sec. 1304.15 (c) and (d). In determining the number of units of each 
finished form of a controlled substance in a commercial container which 
has been opened, the dispenser shall do as follows:
    (a) If the substance is listed in Schedule I or II, he shall make an 
exact count or measure of the contents; and
    (b) If the substance is listed in Schedule III, IV, or V, he shall 
make an estimated count or measure of the contents, unless the container 
holds more than 1,000 tablets or capsules in which case he must make an 
exact count of the contents.

[36 FR 7791, Apr. 24, 1971, as amended at 36 FR 18732, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1304.18   Inventories of importers and exporters.

    Each person registered or authorized (by Sec. 1301.22(b) of this 
chapter) to import or export controlled substances shall include in his 
inventory the same information required of manufacturers pursuant to 
Sec. 1304.15 (a), (c), and (d). Each such person who is also registered 
as a manufacturer or as a distributor shall include in his inventory as 
an importer or exporter only those stocks of controlled substances that 
are actually separated from his stocks as a manufacturer or as a 
distributor (e.g., in transit or in storage for shipment).

[36 FR 7791, Apr. 24, 1971, as amended at 36 FR 18732, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1304.19   Inventories of chemical analysts.

    Each person registered or authorized (by Sec. 1301.22(b) of this 
chapter) to conduct chemical analysis with controlled substances shall 
include in his inventory the same information required of manufacturers 
pursuant to Sec. 1305.15 (a), (c), and (d) as to substances which have 
been manufactured, imported, or received by such person. If less than 1 
kilogram of any controlled substance (other than a hallucinogenic 
controlled substance listed in Schedule I), or less than 20 grams of a 
hallucinogenic substance listed in Schedule I (other than lysergic acid 
diethylamide), or less than 0.5 gram of lysergic acid diethylamide, is 
on hand at the time of inventory, that substance need not be included in 
the inventory. Laboratories of the Administrator may possess up to 150 
grams of any hallucinogenic substance in Schedule I without regard to a 
need for an inventory of those substances. No inventory is required of 
known or suspected controlled substances received as evidentiary 
materials for analysis.

[36 FR 7791, Apr. 24, 1971, as amended at 36 FR 18732, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]

                           Continuing Records



Sec. 1304.21   General requirements for continuing records.

    (a) On and after May 1, 1971, every registrant required to keep 
records pursuant to Sec. 1304.03 shall maintain on a current basis a 
complete and accurate record of each such substance manufactured, 
imported, received, sold, delivered, exported, or otherwise disposed of 
by him, except that no registrant shall be required to maintain a 
perpetual inventory.
    (b) Separate records shall be maintained by a registrant for each 
registered location except as provided in Sec. 1304.04 (a). In the event 
controlled substances are in the possession or under the control of a 
registrant at a location for which he is not registered, the substances 
shall be included in the records of the registered location to which 
they are subject to control or to which the person possessing the 
substance is responsible.
    (c) Separate records shall be maintained by a registrant for each 
independent activity for which he is registered, except as provided in 
Secs. 1304.25 and 1304.26.
    (d) In recording dates of receipt, importation, distribution, 
exportation, or other transfers, the date on which the

[[Page 50]]

controlled substances are actually received, imported, distributed, 
exported, or otherwise transferred shall be used as the date of receipt 
or distribution of any documents of transfer (e.g., invoices or packing 
slips).

[36 FR 7792, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1304.22   Records for manufacturers.

    Each person registered or authorized (by Sec. 1301.22(b) or 
Sec. 1307.15 of this chapter) to manufacture controlled substances shall 
maintain records with the following information:
    (a) For each controlled substance in bulk form to be used in, or 
capable of use in, or being used in, the manufacture of the same or 
other controlled or noncontrolled substances in finished form,
    (1) The name of the substance;
    (2) The quantity manufactured in bulk form by the registrant, 
including the date, quantity and batch or other identifying number of 
each batch manufactured;
    (3) The quantity received from other persons, including the date and 
quantity of each receipt and the name, address, and registration number 
of the other person from whom the substance was received;
    (4) The quantity imported directly by the registrant (under a 
registration as an importer) for use in manufacture by him, including 
the date, quantity, and import permit or declaration number for each 
importation;
    (5) The quantity used to manufacture the same substance in finished 
form, including:
    (i) The date and batch or other identifying number of each 
manufacture;
    (ii) The quantity used in the manufacture;
    (iii) The finished form (e.g., 10-milligram tablets or 10-milligram 
concentration per fluid ounce or milliliter);
    (iv) The number of units of finished form manufactured;
    (v) The quantity used in quality control;
    (vi) The quantity lost during manufacturing and the causes therefor, 
if known;
    (vii) The total quantity of the substance contained in the finished 
form;
    (viii) The theoretical and actual yields; and
    (ix) Such other information as is necessary to account for all 
controlled substances used in the manufacturing process;
    (6) The quantity used to manufacture other controlled and 
noncontrolled substances, including the name of each substance 
manufactured and the information required in paragraph (a)(5) of this 
section;
    (7) The quantity distributed in bulk form to other persons, 
including the date and quantity of each distribution and the name, 
address, and registration number of each person to whom a distribution 
was made;
    (8) The quantity exported directly by the registrant (under a 
registration as an exporter), including the date, quantity, and export 
permit or declaration number of each exportation;
    (9) The quantity distributed or disposed of in any other manner by 
the registrant (e.g., by distribution of complimentary samples or by 
destruction), including the date and manner of distribution or disposal, 
the name, address, and registration number of the person to whom 
distributed, and the quantity distributed or disposed;
    (10) The originals of all written certifications of available 
procurement quotas submitted by other persons (as required by 
Sec. 1303.12(f) of this chapter) relating to each order requiring the 
distribution of a basic class of controlled substance listed in Schedule 
I or II.
    (b) For each controlled substance in finished form,
    (1) The name of the substance;
    (2) Each finished form (e.g., 10-milligram tablet or 10-milligram 
concentration per fluid ounce or milliliter) and the number of units or 
volume of finished form in each commercial container (e.g., 100-tablet 
bottle or 3-milliliter vial);
    (3) The number of containers of each such commercial finished form 
manufactured from bulk form by the registrant, including the information 
required pursuant to paragraph (a)(5) of this section;

[[Page 51]]

    (4) The number of units of finished forms and/or commercial 
containers received from other persons, including the date of and number 
of units and/or commercial containers in each receipt and the name, 
address, and registration number of the person from whom the units were 
received;
    (5) The number of units of finished forms and/or commercial 
containers imported directly by the person (under a registration or 
authorization to import), including the date of, the number of units 
and/or commercial containers in, and the import permit or declaration 
number for, each importation;
    (6) The number of units and/or commercial containers manufactured by 
the registrant from units in finished form received from others or 
imported, including:
    (i) The date and batch or other identifying number of each 
manufacture;
    (ii) The operation performed (e.g., repackaging or relabeling);
    (iii) The number of units of finished form used in the manufacture, 
the number manufactured and the number lost during manufacture, with the 
causes for such losses, if known; and
    (iv) Such other information as is necessary to account for all 
controlled substances used in the manufacturing process;
    (7) The number of commercial containers distributed to other 
persons, including the date of and number of containers in each 
distribution, and the name, address, and registration number of the 
person to whom the containers were distributed;
    (8) The number of commercial containers exported directly by the 
registrant (under a registration as an exporter), including the date, 
number of containers and export permit or declaration number for each 
exportation; and
    (9) The number of units of finished forms and/or commercial 
containers distributed or disposed of in any other manner by the 
registrant (e.g., by distribution of complimentary samples or by 
destruction), including the date and manner of distribution or disposal, 
the name, address, and registration number of the person to whom 
distributed, and the quantity in finished form distributed or disposed.

[36 FR 7792, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971; 36 
FR 18732, Sept. 21, 1971; 37 FR 15920, Aug. 8, 1972. Redesignated at 38 
FR 26609, Sept. 24, 1973]

    Editorial Note: For FR citations affecting Sec. 1304.22, see the 
List of CFR Sections Affected in the Finding Aids section of this 
volume.



Sec. 1304.23   Records for distributors.

    Each person registered or authorized (by Sec. 1301.22(b) or 
Secs. 1307.11-1307.14 of this chapter) to distribute controlled 
substances shall maintain records with the following information for 
each controlled substance:
    (a) The name of the substance;
    (b) Each finished form (e.g., 10-milligram tablet or 10-milligram 
concentration per fluid ounce or milliliter) and the number of units or 
volume of finished form in each commercial container (e.g., 100-tablet 
bottle or 3-milliliter vial);
    (c) The number of commercial containers of each such finished form 
received from other persons, including the date of and number of 
containers in each receipt and the name, address, and registration 
number of the person from whom the containers were received;
    (d) The number of commercial containers or each such finished form 
imported directly by the person (under a registration or authorization 
to import), including the date of, the number of commercial containers 
in, and the import permit or declaration number for, each importation;
    (e) The number of commercial containers of each such finished form 
distributed to other persons, including the date of and number of 
containers in each distribution and the name, address, and registration 
number of the person to whom the containers were distributed;
    (f) The number of commercial containers of each such finished form 
exported directly by the person (under a registration or authorization 
to export), including the date of, the number of commercial containers 
in, and the export permit or declaration number for, each exportation; 
and

[[Page 52]]

    (g) The number of units or volume of finished forms and/or 
commercial containers distributed or disposed of in any other manner by 
the person (e.g., by distribution as complimentary samples or by 
destruction) including the date and manner of distribution or disposal, 
the name, address, and registration number of the person to whom 
distributed, and the quantity of the substance in finished form 
distributed or disposed.

[36 FR 7792, Apr. 24, 1971, as amended at 36 FR 18732, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1304.24   Records for dispensers and researchers.

    Each person registered or authorized (by Sec. 1301.22(b) of this 
chapter) to dispense or conduct research with controlled substances and 
required to keep records pursuant to Sec. 1304.03 shall maintain records 
with the following information for each controlled substance:
    (a) The name of the substance;
    (b) Each finished form (e.g., 10-milligram tablet or 10-milligram 
concentration per fluid ounce or milliliter) and the number of units or 
volume of finished form in each commercial container (e.g., 100-tablet 
bottle or 3-milliliter vial);
    (c) The number of commercial containers of each such finished form 
received from other persons, including the date of and number of 
containers in each receipt and the name, address, and registration 
number of the person from whom the containers were received;
    (d) The number of units or volume of such finished form dispensed, 
including the name and address of the person to whom it was dispensed, 
the date of dispensing, the number of units or volume dispensed, and the 
written or typewritten name or initials of the individual who dispensed 
or administered the substance on behalf of the dispenser; and
    (e) The number of units or volume of such finished forms and/or 
commercial containers disposed of in any other manner by the registrant, 
including the date and manner of disposal and the quantity of the 
substance in finished form disposed.

[36 FR 7793, Apr. 24, 1971, as amended at 36 FR 18732, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1304.25   Records for importers.

    Each person registered or authorized (by Sec. 1301.22(b) of this 
chapter) to import controlled substances shall maintain records with the 
following information for each controlled substance:
    (a) The name of the substance;
    (b) The quantity (or number of units or volume in finished form) 
imported, including the date, quantity (or number of units or volume), 
and import permit or declaration number for each importation;
    (c) The quantity (or number of units or volume in finished form) 
distributed to other persons, including the date and quantity (or number 
of units or volume) of each distribution and the name, address, and 
registration number of each person to whom a distribution was made; and
    (d) The quantity disposed of in any other manner by the registrant 
(except quantities used in manufacturing by an importer under a 
registration as a manufacturer, which quantities are to be recorded 
pursuant to Sec. 1304.22(a) (4) or (b) (5)), including the date and 
manner of disposal and the quantity disposed.

[36 FR 7793, Apr. 24, 1971, as amended at 36 FR 18732, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1304.26   Records for exporters.

    Each person registered or authorized (by Sec. 1301.22(b) of this 
chapter) to export controlled substances shall maintain records with the 
following information for each controlled substance:
    (a) The name of the substance;
    (b) The quantity (or number of units or volume in finished form) 
received from other persons, including the date and quantity (or number 
of units or volume) of each receipt and the name, address, and 
registration number of each person from whom the substance was received;
    (c) The quantity (or number of units or volume in finished form) 
exported, including the date, quantity (or number of units or volume), 
and the export

[[Page 53]]

permit or declaration number for each exportation, but excluding all 
quantities (and numbers of units and volumes) manufactured by an 
exporter under a registration as a manufacturer, which quantities (and 
numbers of units and volumes) are to be recorded pursuant to 
Sec. 1304.22 (a) (8) or (b) (8); and
    (d) The quantity disposed of in any other manner by the registrant, 
including the date and manner of disposal and the quantity disposed.

[36 FR 7793, Apr. 24, 1971, as amended at 36 FR 18732, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1304.27   Records for chemical analysts.

    (a) Each person registered or authorized (by Sec. 1301.22(b) of this 
chapter) to conduct chemical analysis with controlled substances shall 
maintain records with the following information (to the extent known and 
reasonably ascertainable by him) for each controlled substance:
    (1) The name of the substance;
    (2) The form or forms in which the substance is received, imported, 
or manufactured by the registrant (e.g., powder, granulation, tablet, 
capsule, or solution) and the concentration of the substance in such 
form (e.g., C.P., U.S.P., N.F., 10-milligram tablet or 10-milligram 
concentration per milliliter);
    (3) The total number of the forms received, imported or manufactured 
(e.g., 100 tablets, thirty 1-milliliter vials, or 10 grams of powder), 
including the date and quantity of each receipt, importation, or 
manufacture and the name, address, and registration number, if any, of 
the person from whom the substance was received;
    (4) The quantity distributed, exported, or destroyed in any manner 
by the registrant (except quantities used in chemical analysis or other 
laboratory work), including the date and manner of distribution, 
exportation, or destruction, and the name, address, and registration 
number, if any, of each person to whom the substance was distributed or 
exported.
    (b) Records of controlled substances used in chemical analysis or 
other laboratory work are not required.
    (c) Records relating to known or suspected controlled substances 
received as evidentiary material for analysis are not required under 
paragraph (a) of this section.

[36 FR 7793, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971; 36 
FR 18732, Sept. 21, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1304.28   Records for maintenance treatment programs and detoxification treatment programs.

    (a) Each person registered or authorized (by Sec. 1301.22 of this 
chapter) to maintain and/or detoxify controlled substance users in a 
narcotic treatment program shall maintain records with the following 
information for each narcotic controlled substance:
    (1) Name of substance;
    (2) Strength of substance;
    (3) Dosage form;
    (4) Date dispensed;
    (5) Adequate identification of patient (consumer);
    (6) Amount consumed;
    (7) Amount and dosage form taken home by patient; and
    (8) Dispenser's initials.
    (b) The records required by paragraph (a) of this section will be 
maintained in a dispensing log at the narcotic treatment program site 
and will be maintained in compliance with Sec. 1304.24 without reference 
to Sec. 1304.03.
    (c) All sites which compound a bulk narcotic solution from bulk 
narcotic powder to liquid for on-site use must keep a separate batch 
record of the compounding.
    (d) Records of identity, diagnosis, prognosis, or treatment of any 
patients which are maintained in connection with the performance of a 
narcotic treatment program shall be confidential, except that such 
records may be disclosed for purposes and under the circumstances 
authorized by part 310 and part 1401 of this title.

[39 FR 37985, Oct. 25, 1974]



Sec. 1304.29   Records for treatment programs which compound narcotics for treatment programs and other locations.

    Each person registered or authorized by Sec. 1301.22 of this chapter 
to compound

[[Page 54]]

narcotic drugs for off-site use in a narcotic treatment program shall 
maintain records which include the following information for each 
narcotic drug:
    (a) For each narcotic controlled substance in bulk form to be used 
in, or capable of use in, or being used in, the compounding of the same 
or other noncontrolled substances in finished form:
    (1) The name of the substance;
    (2) The quantity compounded in bulk form by the registrant, 
including the date, quantity and batch or other identifying number of 
each batch compounded;
    (3) The quantity received from other persons, including the date and 
quantity of each receipt and the name, address and registration number 
of the other person from whom the substance was received;
    (4) The quantity imported directly by the registrant (under a 
registration as an importer) for use in compounding by him, including 
the date, quantity and import permit or declaration number of each 
importation;
    (5) The quantity used to compound the same substance in finished 
form, including:
    (i) The date and batch or other identifying number of each 
compounding;
    (ii) The quantity used in the compound;
    (iii) The finished form (e.g., 10-milligram tablets or 10-milligram 
concentration per fluid ounce or milliliter;
    (iv) The number of units of finished form compounded;
    (v) The quantity used in quality control;
    (vi) The quantity lost during compounding and the causes therefore, 
if known;
    (vii) The total quantity of the substance contained in the finished 
form;
    (viii) The theoretical and actual yields; and
    (ix) Such other information as is necessary to account for all 
controlled substances used in the compounding process;
    (6) The quantity used to manufacture other controlled and non-
controlled substances; including the name of each substance manufactured 
and the information required in paragraph (a)(5) of this section;
    (7) The quantity distributed in bulk form to other programs, 
including the date and quantity of each distribution and the name, 
address and registration number of each program to whom a distribution 
was made;
    (8) The quantity exported directly by the registrant (under a 
registration as an exporter), including the date, quantity, and export 
permit or declaration number of each exploration; and
    (9) The quantity disposed of by destruction, including the reason, 
date and manner of destruction. All other destruction of narcotic 
controlled substances will comply with Sec. 1307.22.
    (b) For each narcotic controlled substance in finished form:
    (1) The name of the substance;
    (2) Each finished form (e.g., 10-milligram tablet or 10 milligram 
concentration per fluid ounce or milliliter) and the number of units or 
volume or finished form in each commercial container (e.g., 100-tablet 
bottle or 3-milliliter vial);
    (3) The number of containers of each such commercial finished form 
compounded from bulk form by the registrant, including the information 
required pursuant to paragraph (a)(5) of this section;
    (4) The number of units of finished forms and/or commercial 
containers received from other persons, including the date of and number 
of units and/or commercial containers in each receipt and the name, 
address and registration number of the person from whom the units were 
received;
    (5) The number of units of finished forms and/or commercial 
containers imported directly by the person (under a registration or 
authorization to import), including the date of, the number of units 
and/or commercial containers in, and the import permit or declaration 
number for, each importation;
    (6) The number of units and/or commercial containers compounded by 
the registrant from units in finished form received from others or 
imported, including:
    (i) The date and batch or other identifying number of each 
compounding;
    (ii) The operation performed (e.g., repackaging or relabeling);

[[Page 55]]

    (iii) The number of units of finished form used in the compound, the 
number compounded and the number lost during compounding, with the 
causes for such losses, if known; and
    (iv) Such other information as is necessary to account for all 
controlled substances used in the compounding process;
    (7) The number of containers distributed to other programs, 
including the date, the number of containers in each distribution, and 
the name, address and registration number of the program to whom the 
containers were distributed;
    (8) The number of commercial containers exported directly by the 
registrant (under a registration as an exporter), including the date, 
number of containers and export permit or declaration number for each 
exportation; and
    (9) The number of units of finished forms and/or commercial 
containers destroyed in any manner by the registrant, including the 
reason, the date and manner of destruction. All other destruction of 
narcotic controlled substances will comply with Sec. 1307.22.

[39 FR 37985, Oct. 25, 1974]

                                 Reports



Sec. 1304.31  Reports from manufacturers importing opium.

    (a) Every manufacturer importing crude opium shall submit, in 
addition to the report on DEA (or BND) Form 234 and its supplements, DEA 
(or BND) Form 247 and its supplements, 247a and 247b, accounting for the 
importation and for all manufacturing operations performed between 
importation and the production in bulk of finished marketable products, 
standardized in accordance with the U.S. Pharmacopeia, National 
Formulary, or other recognized medical standards. Subsequent manufacture 
from such products, including bottling or packaging operations, shall be 
accounted for in the quarterly returns on DEA (or BND) Form 234 and its 
supplements. DEA (or BND) Form 247 and its supplements shall be 
submitted quarterly to the Drug Control Section, Drug Enforcement 
Administration, Department of Justice, Washington, DC 20537, on or 
before the 15th day of the month immediately following the period for 
which it is submitted.
    (b) The report of manufacture from crude opium shall consist of 
summaries (DEA (or BND) Forms 247 and 247a) with supporting detail 
sheets (on DEA (or BND) Form 247b) accounting for original manufacture 
from crude opium, production from morphine for further manufacture and 
production from manufacturing opium, and also accounting for stocks of 
crude opium, manufacturing opium, morphine for further manufacture and 
other crude alkaloids.
    (c) The detail sheets (DEA (or BND) Form 247b) supporting the 
summary of original manufacture from crude opium shall show separately 
the crude opium used for the manufacture of opium tinctures and 
extracts, crude opium used for the extraction of alkaloids, crude opium 
used for the manufacture of controlled substances listed in Schedule V, 
and crude opium used for the production of manufacturing opium; and 
shall show separately the medicinal opium, alkaloids and salts, opium 
tinctures and extracts, controlled substances listed in Schedule V, and 
manufacturing opium produced.
    (d) Importation of opium shall be reported in summarized entries in 
the debit summary of the quarterly report (DEA (or BND) Form 234) and 
shall be immediately reported by similar summarized entries in the 
credit summary of the quarterly report (DEA (or BND) Form 234) as 
transferred to importing manufacturer's report. Such importations shall 
further be reported in summary (DEA (or BND) Form 247) and supporting 
detail sheets (DEA (or BND) Form 247b). Products manufactured therefrom 
shall be reported as produced in accordance with paragraphs (b) and (c) 
of this section and, with the exception of manufacturing opium, morphine 
for further manufacture, and other crude or unfinished alkaloids, shall 
be transferred to the quarterly report (DEA (or BND) Form 234) when 
reported produced.
    (e) Upon importation of crude opium, samples will be selected and 
assays made by the importing manufacturer in the manner and according to 
the

[[Page 56]]

method specified in the U.S. Pharmacopoeia. These assays shall be 
accounted for in terms of its anhydrous morphine alkaloid content. Where 
final assay data is not determined at the time of rendering report, the 
report shall be made on the basis of the best data available, subject to 
adjustment, and the necessary adjusting entries shall be made on the 
next report.
    (f) Upon withdrawal of crude opium from customs custody, the 
importing manufacturer shall assign to each container an identification 
mark or number by which the opium will be associated with the lot assay 
and identified in reports.
    (g) Where factory procedure is such that partial withdrawals of 
opium are made from individual containers, there shall be attached to 
each container a stock record card on which shall be kept a complete 
record of all withdrawals therefrom.
    (h) Opium products and derivatives which are produced for exclusive 
use in further manufacturing purposes shall be reported produced when 
they come into existence in that form in which they are to be so used. 
Medicinal opium, morphine and its salts, or other alkaloids or 
derivatives produced exclusively for distribution shall be reported as 
produced when manufacture has actually been completed and the finished 
marketable product ready for packaging and distribution. Such products 
shall be regarded as ready for packaging and distribution as soon as all 
processing other than mere packaging has been completed. Medicinal 
opium, tinctures, extracts, or other products manufactured partly for 
distribution and partly for use in further manufacture will be reported 
produced as soon as manufacture is complete and they are ready either 
for use in further manufacture or for packaging for distribution.
    (i) Subject to Sec. 1303.24(c) of this chapter, no accumulations of 
morphine or other narcotic controlled substances in their pure or near-
pure states shall be permitted to remain inactively in process for an 
unreasonable time in light of efficient industrial practices. All such 
products nearing completion of their respective processes and 
approaching a condition of purity shall be carefully protected, promptly 
completed, and immediately transferred to finished stocks, and reported 
as produced.
    (j) In making conversions of opium alkaloids and their salts to 
anhydrous morphine the quantity of the particular alkaloid or salt in 
avoirdupois ounces shall be multipled by a conversion factor arrived at 
by ascertaining the ratio, carried to the fourth decimal place, between 
the respective molecular weight of such alkaloid or salt and the 
molecular weight of anhydrous morphine (285.16), such weights being 
computed to the third decimal place from the chemical formulae of the 
substances and the atomic weights of elements, as adopted by the 
International Committee on Chemical Elements and published in the latest 
edition of the U.S. Pharmacopoeia.

[36 FR 7794, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973. 
Redesignated and amended at 51 FR 5319, 5320, Feb. 13, 1986]



Sec. 1304.32  Reports of manufacturers importing medicinal coca leaves.

    (a) Every manufacturer importing raw coca leaves for the manufacture 
of medicinal products shall submit, in addition to the report on DEA (or 
BND) Form 234 and its supplements, DEA (or BND) Form 168 and its 
supplements, 168a and 168b, accounting for the importation and for all 
manufacturing operations performed between the importation and the 
manufacture of bulk or finished products standardized in accordance with 
U.S. Pharmacopoeia, National Formulary, or other recognized standards. 
Subsequent manufacture from such products, including bottling or 
packaging operations, shall be accounted for in quarterly reports on DEA 
(or BND) Form 234 and its supplements. Reports on Form 168 and its 
supplements shall be submitted quarterly to the Drug Control Section, 
Drug Enforcement Administration, Department of Justice, Washington, DC 
20537, on or before the 15th day of the month immediately following the 
period for which it is submitted.
    (b) The report of manufacture from medicinal coca leaves shall 
consist of summaries (DEA (or BND) Forms 168 and 168a) with supporting 
detail sheets (DEA (or BND) Form 168b) accounting for original 
manufacture from such

[[Page 57]]

leaves, conversions or production from manufacturing coca extracts, and 
also accounting for stocks of raw coca leaves, manufacturing coca 
extracts, and other crude coca alkaloids.
    (c) The detail sheets (DEA (or BND) Form 168b) supporting the 
summary of original manufacture from medicinal coca leaves, shall show 
separately the coca leaves used for the manufacture of manufacturing 
coca extracts, coca leaves used for the direct manufacture of marketable 
coca tinctures and extracts, and coca leaves used for the extraction of 
alkaloids, and shall show separately the coca alkaloids and salts, coca 
tinctures and extracts, and manufacturing coca extracts produced.
    (d) Importations of medicinal coca leaves shall be reported in 
summarized entries in the debit summary of the quarterly report (DEA (or 
BND) Form 234) and shall be immediately reported by similar summarized 
entries in the credit summary of the quarterly report (DEA (or BND) Form 
234) as transferred to importing manufacturer's report. Such 
importations shall further be reported in summary (DEA (or BND) Form 
168) and supporting detail sheets (DEA (or BND) Form 168b). Products 
manufactured therefrom shall be reported as produced in accordance with 
paragraph (h) of this section and, with the exception of manufacturing 
coca extracts, residues or bases for further manufacture, and other 
crude or unfinished alkaloids, shall be transferred to the quarterly 
report (DEA (or BND) Form 234) when reported produced.
    (e) Upon importation of medicinal coca leaves, samples will be 
selected and assays made by the importing manufacturer in accordance 
with recognized chemical procedures. These assays shall form the basis 
of accounting for such coca leaves, which shall be accounted for in 
terms of their cocaine alkaloid content or equivalency or their total 
anhydrous coca alkaloid content. Where final assay data is not 
determined at the time of submitting the report, the report shall be 
made on the basis of the best data available, subject to adjustment, and 
the necessary adjusting entries shall be made on the next report.
    (f) Upon withdrawal of medicinal coca leaves from customs custody, 
the importing manufacturer shall assign to each bale or container an 
identification mark or number by which the coca leaves will be 
associated with the lot assay and identified in reports.
    (g) Where factory procedure is such that partial withdrawals of 
medicinal coca leaves are made from individual containers, there shall 
be attached to the container a stock record card on which shall be kept 
a complete record of withdrawals therefrom.
    (h) Manufacturing coca extracts shall be reported as produced when 
they come into existence in that form in which they are intended for 
exclusive use in further manufacture. Cocaine and its salts, ecgonine 
and its salts, or other alkaloids or derivatives produced exclusively 
for distribution shall be reported as produced when manufacture has 
actually been completed and the finished marketable product is ready for 
packaging and distribution. Such products shall be regarded as ready for 
packaging and distribution as soon as all processing other than mere 
packaging has been completed. Tinctures, extracts, or other products 
manufactured partly for distribution and partly for use in further 
manufacture shall be reported produced as soon as manufacture is 
complete and they are ready either for use in further manufacture or for 
packaging for distribution.
    (i) No accumulations of cocaine or ecgonine or other narcotic 
controlled substances in their pure or near-pure states shall be 
permitted to remain inactively in process. All such products nearing 
completion of their respective processes and approaching a condition of 
purity shall be carefully protected, promptly completed, and immediately 
transferred to finished stocks and reported as produced.
    (j) In making conversions of coca alkaloids and their salts to 
cocaine alkaloid and to anhydrous ecgonine alkaloid, the quantity of the 
particular alkaloid or salt in avoirdupois ounces shall be multiplied by 
a conversion factor arrived at by ascertaining the ratio, carried to the 
fourth decimal place, between the molecular weight of such alkaloid or 
salt and the molecular weight of cocaine alkaloid (303.172) or anhydrous 
ecgonine alkaloid (185.125), as the case may be, such weights being

[[Page 58]]

computed to the third decimal place from the chemical formulae of the 
substances and the atolic weights of elements, as adopted by the 
International Committee on Chemical Elements and published in the latest 
edition of the U.S. Pharmacopoeia.

[36 FR 7795, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973. 
Redesignated and amended at 51 FR 5319, 5320, Feb. 13, 1986]



Sec. 1304.33  Reports from manufacturers importing special coca leaves.

    (a) Every manufacturer using special coca leaves imported into the 
United States shall submit a quarterly report (DEA (or BND) Form 249) 
accounting for all transactions involving such leaves or substances 
derived therefrom which contain cocaine or ecgonine, or any salts, 
derivatives, or preparations from which cocaine or ecgonine may be 
synthesized or made. This report shall be submitted to the Drug Control 
Section, Drug Enforcement Administration, Department of Justice, 
Washington, DC 20537, on or before the 15th day of the month following 
the period for which the report is made. Such report shall include a 
report of all importations of special coca leaves (DEA (or BND) Form 
249a), a report of all materials entered into the processes of 
manufacture (DEA (or BND) Form 249b), a report of the various substances 
produced therefrom (DEA (or BND) Forms 249c, 249d, and 249e), a report 
of all such substances destroyed (DEA (or BND) Form 249f), and a summary 
of operations (DEA (or BND) Form 249g).
    (b) The report of importations shall provide in appropriate columns 
the following data as to each importation:
    (1) The date of the import permit;
    (2) The serial number of the import permit;
    (3) The name of the foreign consignor;
    (4) The address of the foreign consignor;
    (5) The foreign port of export;
    (6) The number of bales imported;
    (7) The serial numbers of the bales imported; and
    (8) The quantity imported in avoirdupois pounds.
    (c) The report of materials entered into the process of manufacture 
shall provide in appropriate columns the following information as to 
each lot of leaves dumped:
    (1) The lot number of specification, a specification to be assigned 
to each dump for identification purposes in order to avoid repeating the 
serial numbers of the bales when the lot is subsequently referred to;
    (2) The date the leaves entered into the process of manufacture;
    (3) The number of bales dumped;
    (4) The serial numbers of the bales;
    (5) The quantity of leaves entered into the process of manufacture, 
stated in avoirdupois pounds;
    (6) The quantity of alcohol used for each extraction or wash of the 
leaves;
    (7) The quantity of water used for each water extraction or 
dilution;
    (8) The quantity of any other or additional substance introduced at 
any stage into the process of manufacture; and
    (9) The dry weight of any filter cloth or other absorbent material 
to be later removed from the process after saturation.
    (d) The reports of substances produced from special coca leaves 
shall provide in columns the following information as to each production 
lot or dump:
    (1) The lot number;
    (2) The quantity of ground leaves entered into process, in terms of 
avoirdupois ounces and the quantity, in ounces and grains, of alkaloid 
contained therein as determined by analysis;
    (3) The quantity of substance in process after each distinct step in 
the manufacturing process and the total alkaloid contained in each, 
stated in ounces and grains;
    (4) The quantity of exhausted or spent leaves and the quantity of 
each residue removed from process, and the total alkaloid contained in 
each, stated in ounces and grains;
    (5) The weight of the used filter cloth or other absorbent material 
removed after saturation; and
    (6) The quantity, in gallons, of finished extract produced.
    (e) The report of substances destroyed, shall provide in appropriate 
columns the following data as to each lot destroyed:
    (1) The lot number;

[[Page 59]]

    (2) The quantity of spent leaves, residues, and saturated materials 
destroyed, stated separately for each; and
    (3) The name of the Government officer witnessing the destruction.
    (f) The summary shall include a complete accounting for all 
transactions in raw leaves, leaves in process, and residues removed from 
production processes.
    (1) The summary of raw coca leaves shall include:
    (i) The quantity of special coca leaves on hand at the beginning of 
the quarter;
    (ii) The quantity of special coca leaves imported during the 
quarter;
    (iii) The quantity of special coca leaves entered into the process 
of manufacture during the quarter;
    (iv) The quantity of special coca leaves on hand at the end of the 
quarter; and
    (v) Any other transaction during the quarter which increased or 
decreased the quantity of raw coca leaves on hand.
    (2) The summary of coca leaves in process shall include:
    (i) The quantity of special coca leaves in process at the beginning 
of the quarter;
    (ii) The quantity of such leaves placed in the process during the 
quarter;
    (iii) The quantity of such leaves represented by lots completed 
during the quarter;
    (iv) The quantity of such leaves represented by lots in process at 
the end of the quarter; and
    (v) Any other transaction during the quarter which increased or 
decreased the quantity of leaves in process.
    (3) The summary of residues removed from production processes shall 
provide in appropriate columns, separately as to spent leaves, each 
residue and saturated material, the following information:
    (i) The quantity of each, on hand at the beginning of the quarter, 
awaiting destruction;
    (ii) The quantity of each removed from process during the quarter;
    (iii) The quantity of each destroyed during the quarter;
    (iv) The quantity of each on hand at the end of the quarter; and
    (v) Any other transaction during the quarter affecting the quantity 
of such residues on hand.

[36 FR 7795, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 46 FR 28841, May 29, 1981. Redesignated and amended at 51 
FR 5319, Feb. 13, 1986]



Sec. 1304.34  Reports generally.

    (a) All reports required by Secs. 1304.35--1304.38 shall be filed 
with the ARCOS Unit, P.O. Box 28293, Central Station, Washington, DC. 
20005.
    (b) Reports required by Secs. 1304.35--1304.38 shall be filed on DEA 
(or BND) Form 333, or on media which contains the data required by DEA 
(or BND) Form 333 and which is acceptable to the ARCOS Unit.
    (c) References to DEA (or BND) Form 234 in Secs. 1304.33 and 1304.34 
shall be deemed to refer equally to DEA (or BND) Form 333.

[37 FR 28714, Dec. 29, 1972. Redesignated at 38 FR 26609, Sept. 24, 
1973, and amended at 46 FR 28841, May 29, 1981. Redesignated and amended 
at 51 FR 5319, 5320, Feb. 13, 1986]



Sec. 1304.35  Reports from manufacturers of bulk materials or dosage units.

    Each person who is registered to manufacture controlled substances 
in bulk or dosage form shall report as follows:
    (a) Substance covered.  Reports shall include data on each 
controlled substance listed in Schedules I and II, on each narcotic 
controlled substance listed in Schedules III, IV and V, and on each 
psychotropic controlled substance listed in Schedules III and IV as 
identified below:

                              Schedule III

    (1) Benzphetamine;
    (2) Cyclobarbital;
    (3) Glutethimide;
    (4) Methylprylon; and
    (5) Phendimetrazine.

                               Schedule IV

    (1) Barbital;
    (2) Diethylproprion (Amfepramone);
    (3) Ethchlovynol;
    (4) Ethinamate;
    (5) Lefetamine (SPA);
    (6) Mazindol;
    (7) Meprobamate;
    (8) Methylphenobarbital;
    (9) Phenobarbital;

[[Page 60]]

    (10) Phentermine; and
    (11) Pipradrol.

Data shall be presented in such a manner as to identify the particular 
form, strength, and trade name, if any, of the product containing the 
controlled substance for which the report is being made. For this 
purpose, persons filing reports shall utilize the National Drug Code 
Number assigned to the product under the National Drug Code System of 
the Food and Drug Administration.
    (b) Transactions reported. Reports shall provide data on each 
acquisition to inventory (identifying whether it is, e.g., by purchase 
or transfer, return from a customer, recovery of waste material, 
manufacture from other materials, or supplied by the Federal Government) 
and each reduction from inventory (identifying whether it is, e.g., by 
sale or transfer, sampling, use in production, loss through 
nonrecoverable waste, theft, destruction, or seizure by Government 
agencies). These reports shall be filed every month not later than the 
15th day of the month succeeding the month for which it is submitted; 
except that a registrant may be given permission to file more frequently 
or less frequently (but not less than quarterly), depending on the 
number of transactions being reported each time by that registrant.
    (c) Inventories reported. Reports shall provide data on the stocks 
of each reported controlled substance on hand as of the close of 
business on December 31 of each year, indicating whether the substance 
is in storage or in process of manufacturing. These reports shall be 
filed no later than January 15 of the following year.
    (d) Registrants manufacturing etorphine hydrochloride or 
diprenorphine shall, on a weekly basis, forward a copy of the order 
forms received for these substances to the Administration.

(Approved by the Office of Management and Budget under control number 
1117-0003)

[37 FR 28714, Dec. 29, 1972. Redesignated at 38 FR 26609, Sept. 24, 
1973, and amended at 39 FR 17838, May 21, 1974; 49 FR 37060, Sept. 21, 
1984. Redesignated and amended at 51 FR 5320, Feb. 13, 1986]



Sec. 1304.36   Reports from packagers and labelers.

    Each person who is registered to manufacture controlled substances 
and who only packages, repackages, labels, or relabels such substances 
shall report as follows:
    (a) Substances covered. Reports shall include data on each 
controlled substance listed in Schedule I and II and on each narcotic 
controlled substance listed in Schedule III (but not on any material, 
compound, mixture, or preparation containing a quantity of a substance 
having a stimulant effect on the central nervous system, which material, 
compound, mixture, or preparation is listed in Schedule III or on any 
narcotic controlled substance listed in Schedule V). Data shall be 
presented in such a manner as to identify the particular form, strength, 
and trade name, if any, of the product containing the controlled 
substance for which the report is being made. For this purpose, persons 
filing reports shall utilize the National Drug Code Number assigned to 
the product under the National Drug Code System of the Food and Drug 
Administration.
    (b) Transactions reported. Reports shall provide data on each 
acquisition to inventory (identifying whether it is, e.g., by purchase 
or transfer, return from a customer, or supply by the Federal Government 
and each reduction from inventory (identifying whether it is, e.g., by 
sale or transfer, sampling, theft, destruction, or seizure by Government 
agencies). These reports shall be filed every month not later than the 
15th day of the month succeeding the month for which it is submitted; 
except that a registrant may be given permission to file more frequently 
or less frequently (but not less than quarterly), depending on the 
number of transactions being reported each time by that registrant.
    (c) Inventories reported. Reports shall provide data on the stocks 
of each reported controlled substance on hand as of the close of 
business on December 31 of each year. These reports shall be filed no 
later than January 15 of the following year.
    (d) Exceptions. A registered institutional practitioner who 
repackages or relabels exclusively for distribution to and

[[Page 61]]

dispensing by agents, employees, or affiliated institutional 
practitioners of the registrant may be exempted from filing reports 
under this section by applying to the ARCOS Unit of the Administration.

(Approved by the Office of Management and Budget under control number 
1117-0003)

[37 FR 28714, Dec. 29, 1972. Redesignated at 38 FR 26609, Sept. 24, 
1973, and amended at 38 FR 34998, Dec. 21, 1973; 46 FR 28841, May 29, 
1981; 49 FR 37060, Sept. 21, 1984. Redesignated at 51 FR 5320, Feb. 13, 
1986]



Sec. 1304.37   Reports from distributors.

    Each person who is registered to distribute controlled substances 
shall report as follows:
    (a) Substances covered. Reports shall include data on each 
controlled substance listed in Schedules I and II and on each narcotic 
controlled substance listed in Schedule III (but not on any material, 
compound, mixture or preparation containing a quantity of a substance 
having a stimulant effect on the central nervous system, which material, 
compound, mixture or preparation is listed in Schedule III or on any 
narcotic controlled substance listed in Schedule V). Data shall be 
presented in such a manner as to identify the particular form, strength, 
and trade name, if any, of the product containing the controlled 
substance for which the report is being made. For this purpose, persons 
filing reports shall utilize the National Drug Code Number assigned to 
the product under the National Drug Code System of the Food and Drug 
Administration.
    (b) Transactions reported. Reports shall provide data on each 
acquisition to inventory (identifying whether it is, e.g., by purchase 
or transfer, return from a customer, or supply by the Federal 
Government) and each reduction from inventory (identifying whether it 
is, e.g., by sale or transfer, sampling, theft, destruction, or seizure 
by Government agencies). These reports shall be filed every month not 
later than the 15th day of the month succeeding the month for which it 
is submitted: except that a registrant may be given permission to file 
more frequently or less frequently (but not less than quarterly), 
depending on the number of transactions being reported each time by that 
registrant.
    (c) Inventories reported. Reports shall provide data on the stocks 
of each reported controlled substance on hand as of the close of 
business on December 31 of each year. These reports shall be filed no 
later than January 15 of the following year.
    (d) Exceptions. A registered institutional practitioner which 
distributes exclusively to (for dispensing by) agents, employees, or 
affiliated institutional practitioners of the registrant may be exempted 
from filing reports under this section by applying to the ARCOS Unit of 
the Administration.

[37 FR 28714, Dec. 29, 1972. Redesignated at 38 FR 26609, Sept. 24, 
1973, and amended at 38 FR 34998, Dec. 21, 1973; 46 FR 28841, May 29, 
1981. Redesignated at 49 FR 37060, Sept. 21, 1984. Redesignated at 51 FR 
5320, Feb. 13, 1986]



Sec. 1304.38   Reports from manufacturers importing poppy straw or concentrate of poppy straw.

    (a) Every manufacturer importing poppy straw or concentrate of poppy 
straw shall submit in addition to Form 333, Form DEA 247(c) accounting 
for the importation and for all manufacturing operations performed 
between importation and the production in bulk of finished marketable 
products, standardized in accordance with the U.S. Pharmacopeia, 
National Formulary, or other recognized medical standards. Subsequent 
manufacture from such products, including bottling or packaging 
operations, shall be accounted for in the returns on DEA Form 333 
(Sec. 1304.38) and its supplements. DEA Form 247(c) shall be submitted 
quarterly to the Drug Control Section, Drug Enforcement Administration, 
Department of Justice, Washington, DC 20537, on or before the 15th day 
of the month immediately following the period for which it is submitted.
    (b) The report of manufacture from poppy straw or concentrate of 
poppy straw shall consist of summaries with supporting detail sheets 
accounting for original manufacture from poppy straw to concentrate, and 
from concentrate of poppy straw, production from morphine for further 
manufacture and also accounting for all stocks of poppy

[[Page 62]]

straw, concentrate of poppy straw, morphine for further manufacture and 
other crude alkaloids.
    (c) The detail sheets (DEA 247(c)) supporting the summary of 
manufacture from poppy straw or concentrate of poppy straw shall show 
separately the amount of poppy straw or concentrate imported, the poppy 
straw used for production of concentrate, the concentrate used for 
extraction of alkaloids, subsequent manufacture from those alkaloids and 
the inventory of poppy straw and concentrate of poppy straw at the close 
of the reporting period.
    (d) Upon importation of poppy straw or concentrate of poppy straw, 
samples will be selected and assays made by the importing manufacturer 
in a manner and according to a method previously approved by DEA. Where 
final assay data is not determined at the time of rendering report, the 
report shall be made on the basis of the best data available, subject to 
adjustment, and the necessary adjusting entries shall be made on the 
next report.
    (e) Upon withdrawal of poppy straw or concentrate of poppy straw 
from Customs custody, the importing manufacturer shall assign to each 
lot or container an identification number by which the poppy straw or 
concentrate will be associated with the lot assay and identified in 
reports.
    (f) Where factory procedure is such that partial withdrawals of 
poppy straw or concentrate are made from individual containers, there 
shall be attached to each container a stock record card on which shall 
be kept a complete record of all withdrawals therefrom.
    (g) Concentrate of poppy straw and derivatives produced for 
exclusive use in further manufacturing purposes shall be reported 
produced when they come into existence in that form in which they are to 
be so used. Alkaloids or derivatives produced exclusively for 
distribution shall be reported as produced when manufacture has actually 
been completed and the finished marketable product ready for packaging 
and distribution. Such products shall be regarded as ready for packaging 
and distribution as soon as all processing other than mere packaging has 
been completed. Products manufactured partly for distribution and partly 
for use in further manufacture will be reported produced as soon as 
manufacture is complete and they are ready either for use in further 
manufacture or for packaging for distribution.
    (h) Subject to Sec. 1303.24(c) of this chapter, no accumulations of 
morphine or other narcotic controlled substances in their pure or near-
pure states shall be permitted to remain inactively in process for an 
unreasonable time in light of efficient industrial practices. All such 
products nearing completion of their respective processes and 
approaching a condition of purity shall be carefully protected, promptly 
completed, and immediately transferred to finished stocks, and reported 
as produced.
    (i) In making conversions of concentrate of poppy straw alkaloids 
and their salts to anhydrous morphine the quantity of the particular 
alkaloid or salt in avoirdupois ounces shall be multiplied by a 
conversion factor arrived at by ascertaining the ratio, carried to the 
fourth decimal place, between the respective molecular weight of such 
alkaloid or salt and the molecular weight of anhydrous morphine 
(285.16), such weights being computed to the third decimal place from 
the chemical formulae of the substances and the atomic weights of 
elements, as adopted by the International Committee on Chemical Elements 
and published in the latest edition of the U.S. Pharmacopoeia.

[40 FR 6779, Feb. 14, 1975, as amended at 40 FR 42866, Sept. 17, 1975; 
46 FR 28841, May 29, 1981. Redesignated at 49 FR 37060, Sept. 21, 1984. 
Redesignated and amended at 51 FR 5319, 5320, Feb. 13, 1986]



PART 1305--ORDER FORMS--Table of Contents




Sec.
1305.01  Scope of Part 1305.
1305.02  Definitions.
1305.03  Distributions requiring order forms.
1305.04  Persons entitled to obtain and execute order forms.
1305.05  Procedure for obtaining order forms.
1305.06  Procedure for executing order forms.
1305.07  Power of attorney.
1305.08  Persons entitled to fill order forms.
1305.09  Procedure for filling order forms.
1305.10  Procedure for endorsing order forms.
1305.11  Unaccepted and defective order forms.
1305.12  Lost and stolen order forms.

[[Page 63]]

1305.13  Preservation of order forms.
1305.14  Return of unused order forms.
1305.15  Cancellation and voiding of order forms.
1305.16  Special procedure for filling certain order forms.

    Authority: 21 U.S.C. 821, 828, 871(b), unless otherwise noted.

    Source: 36 FR 7796, Apr. 24, 1971, unless otherwise noted. 
Redesignated at 38 FR 26609, Sept. 24, 1973.



Sec. 1305.01   Scope of Part 1305.

    Procedures governing the issuance, use, and preservation of order 
forms pursuant to section 1308 of the Act (21 U.S.C. 828) are set forth 
generally by that section and specifically by the sections of this part.



Sec. 1305.02   Definitions.

    As used in this part, the following terms shall have the meanings 
specified:
    (a) The term Act means the Controlled Substances Act (84 Stat. 1242; 
21 U.S.C. 801) and/or the Controlled Substances Import and Export Act 
(84 Stat. 1285; 21 U.S.C. 951).
    (b) The term purchaser means any registered person entitled to 
obtain and execute order forms pursuant to Sec. 1305.04 and 
Sec. 1305.06.
    (c) The term supplier means any registered person entitled to fill 
order forms pursuant to Sec. 1305.08.
    (d) Any term not defined in this section shall have the definition 
set forth in section 102 of the Act (21 U.S.C. 802) and Secs. 1301.02 
and 1302.02 of this chapter.



Sec. 1305.03   Distributions requiring order forms.

    An order form (DEA Form 222) is required for each distribution of a 
controlled substance listed in Schedule I or II, except for the 
following:
    (a) The exportation of such substances from the United States in 
conformity with the Act;
    (b) The delivery of such substances to or by a common or contract 
carrier for carriage in the lawful and usual course of its business, or 
to or by a warehouseman for storage in the lawful and usual course of 
its business (but excluding such carriage or storage by the owner of the 
substance in connection with the distribution to a third person);
    (c) The procurement of a sample of such substances by an exempt law 
enforcement official pursuant to Sec. 1301.26(b) of this chapter, 
provided that the receipt required by that section is used and is 
preserved in the manner prescribed in this part for order forms;
    (d) The procurement of such substances by a civil defense or 
disaster relief organization, pursuant to Sec. 1301.27 of this chapter, 
provided that the Civil Defense Emergency Order Form required by that 
section is used and is preserved with other records of the registrant; 
and
    (e) The purchase of such sustances by the master or first officer of 
a vessel pursuant to Sec. 1301.28 of this chapter: Provided, That copies 
of the record of sale are generated, distributed and preserved by the 
vendor according to that section.
    (f) The delivery of such substances to a registered analytical 
laboratory, or its agent approved by DEA, from an anonymous source for 
the analysis of the drug sample, provided the laboratory has obtained a 
written waiver of the order form requirement from the Special Agent in 
Charge of the Area in which the laboratory is located, which waiver may 
be granted upon agreement of the laboratory to conduct its activities in 
accordance with Administration guidelines.

[36 FR 7796, Apr. 24, 1971, as amended at 37 FR 15920, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 39 FR 15031, 
Apr. 30, 1974; 47 FR 41735, Sept. 22, 1982; 50 FR 31590, Aug. 5, 1985; 
51 FR 5320, Feb. 13, 1986; 53 FR 4963, Feb. 19, 1988]



Sec. 1305.04   Persons entitled to obtain and execute order forms.

    (a) Order forms may be obtained only by persons who are registered 
under section 303 of the Act (21 U.S.C. 823) to handle controlled 
substances listed in Schedules I and II, and by persons who are 
registered under section 1008 of the Act (21 U.S.C. 958) to export such 
substances. Persons not registered to handle controlled substances 
listed in Schedule I or II and persons registered only to import 
controlled substances listed in any schedule are not entitled to obtain 
order forms.

[[Page 64]]

    (b) An order form may be executed only on behalf of the registrant 
named thereon and only if his registration as to the substances being 
purchased has not expired or been revoked or suspended.



Sec. 1305.05   Procedure for obtaining order forms.

    (a) Order Forms are issued in mailing envelopes containing either 
seven or fourteen forms, each form containing an original duplicate and 
triplicate copy (respectively, Copy 1, Copy 2, and Copy 3). A limit, 
which is based on the business activity of the registrant, will be 
imposed on the number of order forms which will be furnished on any 
requisition unless additional forms are specifically requested and a 
reasonable need for such additional forms is shown.
    (b) Any person applying for a registration which would entitle him 
to obtain order forms may requisition such forms by so indicating on the 
application form; order forms will be supplied upon the registration of 
the applicant. Any person holding a registration entitling him to obtain 
order forms may requisition such forms for the first time by contacting 
any Division Office or the Registration Unit of the Administration. Any 
person already holding order forms may requisition additional forms on 
DEA Form 222a which is mailed to a registrant approximately 30 days 
after each shipment of order forms to that registrant or by contacting 
any Division Office or the Registration Unit of the Administration. All 
requisition forms (DEA Form 222a) shall be submitted to the Registration 
Unit, Drug Enforcement Administration, Department of Justice, Post 
Office Box 28083, Central Station, Washington, DC 20005.
    (c) Each requisition shall show the name, address, and registration 
number of the registrant and the number of books of order forms desired. 
Each requisition shall be signed and dated by the same person who signed 
the most recent application for registration or for reregistration, or 
by any person authorized to obtain and execute order forms by a power of 
attorney pursuant to Sec. 1305.07.
    (d) Order forms will be serially numbered and issued with the name, 
address and registration number of the registrant, the authorized 
activity and schedules of the registrant. This information cannot be 
altered or changed by the registrant; any errors must be corrected by 
the Registration Unit of the Administration by returning the forms with 
notification of the error.

[36 FR 7796, Apr. 24, 1971, as amended at 36 FR 18732, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 51 FR 5319, 
Feb. 13, 1986; 53 FR 4963, Feb. 19, 1988]



Sec. 1305.06   Procedure for executing order forms.

    (a) Order forms shall be prepared and executed by the purchaser 
simultaneously in triplicate by means of interleaved carbon sheets which 
are part of the DEA Form 222. Order forms shall be prepared by use of a 
typewriter, pen, or indelible pencil.
    (b) Only one item shall be entered on each numbered line. There are 
ten lines on each order form. If one order form is not sufficient to 
include all items in an order, additional forms shall be used. Order 
forms for carfentanil etorphine hydrochloride and diprenorphine shall 
contain only these substances. The total number of items ordered shall 
be noted on that form in the space provided.
    (c) An item shall consist of one or more commercial or bulk 
containers of the same finished or bulk form and quantity of the same 
substance; a separate item shall be made for each commercial or bulk 
container of different finished or bulk form, quantity or substance. For 
each item the form shall show the name of the article ordered, the 
finished or bulk form of the article (e.g., 10-milligram tablet, 10-
milligram concentration per fluid ounce or milliliter, or U.S.P.), the 
number of units or volume in each commercial or bulk container (e.g., 
100-tablet bottle or 3-milliliter vial) or the quantity or volume of 
each bulk container (e.g., 10 kilograms), the number of commercial or 
bulk containers ordered, and the name and quantity per unit of the 
controlled substance or substances contained in the article if not in 
pure

[[Page 65]]

form. The catalogue number of the article may be included at the 
discretion of the purchaser.
    (d) The name and address of the supplier from whom the controlled 
substances are being ordered shall be entered on the form. Only one 
supplier may be listed on any one form.
    (e) Each order form shall be signed and dated by a person authorized 
to sign a requisition for order forms on behalf of the purchaser 
pursuant to Sec. 1305.05(c). The name of the purchaser, if different 
from the individual signing the order form, shall also be inserted in 
the signature space. Unexecuted order forms may be kept and may be 
executed at a location other than the registered location printed on the 
form, provided that all unexecuted forms are delivered promptly to the 
registered location upon an inspection of such location by any officer 
authorized to make inspections, or to enforce, any Federal, State, or 
local law regarding controlled substances.

[36 FR 7796, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 39 FR 17838, 
May 21, 1974; 53 FR 4963, Feb. 19, 1988; 54 FR 33674, Aug. 16, 1989]



Sec. 1305.07   Power of attorney.

    Any purchaser may authorize one or more individuals, whether or not 
located at the registered location of the purchaser, to obtain and 
execute order forms on his behalf by executing a power of attorney for 
each such individual. The power of attorney shall be signed by the same 
person who signed (or was authorized to sign, pursuant to 
Sec. 1301.32(f) of this chapter or Sec. 1311.32(f) of this chapter) the 
most recent application for registration or reregistration and by the 
individual being authorized to obtain and execute order forms. The power 
of attorney shall be filed with the executed order forms of the 
purchaser, and shall be retained for the same period as any order form 
bearing the signature of the attorney. The power of attorney shall be 
available for inspection together with other order form records. Any 
power of attorney may be revoked at any time by executing a notice of 
revocation, signed by the person who signed (or was authorized to sign) 
the power of attorney or by a successor, whoever signed the most recent 
application for registration or reregistration, and filing it with the 
power of attorney being revoked. The form for the power of attorney and 
notice of revocation shall be similar to the following:

                  Power of Attorney for DEA Order Forms

 -------------------- (Name of registrant) -------------------- (Address 
of registrant) -------------------- (DEA registration number)
    I, ------------------------ (name of person granting power), the 
undersigned, who is authorized to sign the current application for 
registration of the above-named registrant under the Controlled 
Substances Act or Controlled Substances Import and Export Act, have 
made, constituted, and appointed, and by these presents, do make, 
constitute, and appoint ------------------------ (name of attorney-in-
fact), my true and lawful attorney for me in my name, place, and stead, 
to execute applications for books of official order forms and to sign 
such order forms in requisition for Schedule I and II controlled 
substances, in accordance with section 308 of the Controlled Substances 
Act (21 U.S.C. 828) and part 305 of Title 21 of the Code of Federal 
Regulations. I hereby ratify and confirm all that said attorney shall 
lawfully do or cause to be done by virtue hereof.
........................................................................
(Signature of person granting power)
    I, ---------------------- (name of attorney-in-fact), hereby affirm 
that I am the person named herein as attorney-in-fact and that the 
signature affixed hereto is my signature.
........................................................................
(Signature of attorney-in-fact)
    Witnesses:
    1. ------------------------.
    2. -----------------------.
    Signed and dated on the ------ day of ----------------, 19----, at 
----------------.

                          Notice of Revocation

    The foregoing power of attorney is hereby revojed by the 
undersigned, who is authorized to sign the current application for 
registration of the above-named registrant under the Controlled 
Substances Act of the Controlled Substances Import and Export Act. 
Written notice of this revocation has been given to the attorney-in-fact 
---------------- this same day.
........................................................................
(Signature of person revoking power)
    Witnesses:
    1. ------------------------.
    2. ------------------------.

[[Page 66]]

    Signed and dated on the ------ day of ----------------, 19----, at 
----------------.

[37 FR 15921, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1305.08   Persons entitled to fill order forms.

    An order form may be filled only by a person registered as a 
manufacturer or distributor of controlled substances listed in Schedule 
I or II under section 303 of the Act (21 U.S.C. 823) or as an importer 
of such substances under section 1008 of the Act (21 U.S.C. 958), except 
for the following:
    (a) A person registered to dispense such substances under section 
303 of the Act, or to export such substances under section 1008 of the 
Act, if he is discontinuing business or if his registration is expiring 
without reregistration, may dispose of any controlled substances listed 
in Schedule I or II in his possession pursuant to order forms in 
accordance with Sec. 1307.14 of this chapter;
    (b) A person who has obtained any controlled substance in Schedule I 
or II by order form may return such substance, or portion thereof, to 
the person from whom he obtained the substance or the manufacturer of 
the substance pursuant to the order form of the latter person;
    (c) A person registered to dispense such substances may distribute 
such substances to another dispenser pursuant to, and only in the 
circumstances described in, Sec. 1307.11 of this chapter; and
    (d) A person registered or authorized to conduct chemical analysis 
or research with controlled substances may distribute a controlled 
substance listed in Schedule I or II to another person registered or 
authorized to conduct chemical analysis, instructional activities, or 
research with such substances pursuant to the order form of the latter 
person, if such distribution is for the purpose of furthering such 
chemical analysis, instructional activities, or research.
    (e) A person registered as a compounder of narcotic substances for 
use at off-site locations in conjunction with a narcotic treatment 
program at the compounding location, who is authorized to handle 
Schedule II narcotics, is authorized to fill order forms for 
distribution of narcotic drugs to off-site narcotic treatment programs 
only.

[36 FR 7796, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971; 36 
FR 18732, Sept. 21, 1971; 37 FR 15921, Aug. 8, 1972. Redesignated at 38 
FR 26609, Sept. 24, 1973]

    Editorial Note: For FR citations affecting Sec. 1305.08, see the 
List of CFR Sections Affected in the Finding Aids section of this 
volume.



Sec. 1305.09   Procedure for filling order forms.

    (a) The purchaser shall submit Copy 1 and Copy 2 of the order form 
to the supplier, and retain Copy 3 in his own files.
    (b) The supplier shall fill the order, if possible and if he desires 
to do so, and record on Copies 1 and 2 the number of commercial or bulk 
containers furnished on each item and the date on which such containers 
are shipped to the purchaser. If an order cannot be filled in its 
entirety, it may be filled in part and the balance supplied by 
additional shipments within 60 days following the date of the order 
form. No order form shall be valid more than 60 days after its execution 
by the purchaser, except as specified in paragraph (f) of this section.
    (c) The controlled substances shall only be shipped to the purchaser 
and at the location printed by the Administration on the order form, 
except as specified in paragraph (f) of this section.
    (d) The supplier shall retain Copy 1 of the order form for his ovn 
files and forward Copy 2 to the Special Agent in Charge of the Drug 
Enforcement Administration in the area in which the supplier is located. 
Copy 2 shall be forwarded at the close of the month during which the 
order is filled; if an order is filled by partial shipments, Copy 2 
shall be forwarded at the close of the month during which the final 
shipment is made or during which the 60-day validity period expires.
    (e) The purchaser shall record on Copy 3 of the order form the 
number of commercial or bulk containers furnished on each item and the 
dates on which such containers are received by the purchaser.

[[Page 67]]

    (f) Order forms submitted by registered procurement officers of the 
Defense Personnel Support Center of Defense Supply Agency for delivery 
to armed services establishments within the United States may be shipped 
to locations other than the location printed on the order form, and in 
partial shipments at different times not to exceed six months from the 
date of the order, as designated by the procurement officer when 
submitting the order.

[36 FR 7796, Apr. 24, 1971, as amended at 36 FR 18732, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 47 FR 41735, 
Sept. 22, 1982]



Sec. 1305.10   Procedure for endorsing order forms.

    (a) An order form made out to any supplier who cannot fill all or a 
part of the order within the time limitation set forth in Sec. 1305.09 
may be endorsed to another supplier for filling. The endorsement hall be 
made only by the supplier to whom the order form was first made, shall 
state (in the spaces provided on the reverse sides of Copies 1 and 2 of 
the order form) the name and address of the second supplier, and shall 
be signed by a person authorized to obtain and execute order forms on 
behalf of the first supplier. The first supplier may not fill any part 
of an order on an endorsed form. The second supplier shall fill the 
order, if possible and if he desires to do so, in accordance with 
Sec. 1305.09 (b), (c), and (d), including shipping all substances 
directly to the purchaser.
    (b) Distributions made on endorsed order forms shall be reported by 
the second supplier in the same manner as all other distributions except 
that where the name of the supplier is requested on the reporting form, 
the second supplier shall record the name, address and registration 
number of the first supplier.



Sec. 1305.11   Unaccepted and defective order forms.

    (a) No order form shall be filled if it:
    (1) Is not complete, legible, or properly prepared, executed, or 
endorsed; or
    (2) Shows any alteration, erasure, or change of any description.
    (b) If an order form cannot be filled for any reason under this 
section, the supplier shall return Copies 1 and 2 to the purchaser with 
a statement as to the reason (e.g., illegible or altered). A supplier 
may for any reason refuse to accept any order and if a supplier refuses 
to accept the order, a statement that the order is not accepted shall be 
sufficient for purposes of this paragraph.
    (c) When received by the purchaser, Copies 1 and 2 of the order form 
and the statement shall be attached to Copy 3 and retained in the files 
of the purchaser in accordance with Sec. 1305.13. A defective order form 
may not be corrected; it must be replaced by a new order form in order 
for the order to be filled.



Sec. 1305.12   Lost and stolen order forms.

    (a) If a purchaser ascertains that an unfilled order form has been 
lost, he shall execute another in triplicate and a statement containing 
the serial number and date of the lost form, and stating that the goods 
covered by the first order form were not received through loss of that 
order form. Copy 3 of the second form and a copy of the statement shall 
be retained with Copy 3 of the order form first executed. A copy of the 
statement shall be attached to Copies 1 and 2 of the second order form 
sent to the supplier. If the first order form is subsequently received 
by the supplier to whom it was directed, the supplier shall mark upon 
the face thereof ``Not accepted'' and return Copies 1 and 2 to the 
purchaser, who shall attach it to Copy 3 and the statement.
    (b) Whenever any used or unused order forms are stolen from or lost 
(otherwise than in the course of transmission) by any purchaser or 
supplier, he shall immediately upon discovery of such theft or loss, 
report the same to the Registration Unit, Drug Enforcement 
Administration, Department of Justice, Post Office Box 28083, Central 
Station, Washington, DC 20005, stating the serial number of each form 
stolen or lost. If the theft or loss includes any original order forms 
received from purchasers and the supplier is unable to state the serial 
numbers of such order forms, he shall report the date or approximate 
date of receipt thereof and the names and addresses of the purchasers. 
If an entire book of order

[[Page 68]]

forms is lost or stolen, and the purchaser is unable to state the serial 
numbers of the order forms contained therein, he shall report, in lieu 
of the numbers of the forms contained in such book, the date or 
approximate date of issuance thereof. If any unused order form reported 
stolen or lost is subsequently recovered or found, the Registration 
Branch of the Administration shall immediately be notified.

[36 FR 7796, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 51 FR 5319, 
Feb. 13, 1986]



Sec. 1305.13   Preservation of order forms.

    (a) The purchaser shall retain Copy 3 of each order form which has 
been filled. He shall also retain in his files all copies of each 
unaccepted or defective order form and each statement attached thereto.
    (b) The supplier shall retain Copy 1 of each order form which he has 
filled.
    (c) Order forms must be maintained separately from all other records 
of the registrant. Order forms are required to be kept available for 
inspection for a period of 2 years. If a purchaser has several 
registered locations, he must retain Copy 3 of the executed order forms 
and any attached statements or other related documents (not including 
unexecuted order forms which may be kept elsewhere pursuant to 
Sec. 1305.06(e)) at the registered location printed on the order form.
    (d) The supplier of carfentanil etorphine hydrochloride and 
diprenorphine shall maintain order forms for these substances separately 
from all other order forms and records required to be maintained by the 
registrant.

[36 FR 7796, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 39 FR 17839, May 21, 1974; 54 FR 33674, Aug. 16, 1989]



Sec. 1305.14   Return of unused order forms.

    If the registration of any purchaser terminates (because the 
purchaser dies, ceases legal existence, discontinues business or 
professional practice, or changes his name or address as shown on his 
registration) or is suspended or revoked pursuant to Secs. 1301.45 or 
1301.46 of this chapter as to all controlled substances listed in 
Schedules I and II for which he is registered, he shall return all 
unused order forms for such substance to the nearest office of the 
Administration.

[36 FR 7796, Apr. 24, 1971, as amended at 36 FR 18732, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1305.15   Cancellation and voiding of order forms.

    (a) A purchaser may cancel part or all of an order on an order form 
by notifying the supplier in writing of such cancellation. The supplier 
shall indicate the cancellation on Copies 1 and 2 of the order form by 
drawing a line through the canceled items and printing ``canceled'' in 
the space provided for number of items shipped.
    (b) A supplier may void part or all of an order on an order form by 
notifying the purchaser in writing of such voiding. The supplier shall 
indicate the voiding in the manner prescribed for cancellation in 
paragraph (a) of this section.
    (c) No cancellation or voiding permitted by this section shall 
affect in any way contract rights of either the purchaser or the 
supplier.

[36 FR 7796, Apr. 24, 1971, as amended at 36 FR 13386, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1305.16   Special procedure for filling certain order forms.

    (a) The purchaser of carfentanil etorphine hydrochloride or 
diprenorphine shall submit copy 1 and 2 of the order form to the 
supplier and retain copy 3 in his own files.
    (b) The supplier, if he determines that the purchaser is a 
veterinarian engaged in zoo and exotic animal practice, wildlife 
management programs and/or research and authorized by the Administrator 
to handle these substances shall fill the order in accordance with the 
procedures set forth in Sec. 1305.09 except that:
    (1) Order forms for carfentanil etorphine hydrochloride and 
diprenorphine shall only contain these substances in reasonable 
quantities and (2) the substances shall only be shipped to the purchaser 
at the location printed by the Administration

[[Page 69]]

upon the order form under secure conditions using substantial packaging 
material with no markings on the outside which would indicate the 
content.

[39 FR 17839, May 21, 1974, as amended at 54 FR 33674, Aug. 16, 1989]



PART 1306--PRESCRIPTIONS--Table of Contents




                           General Information

Sec.
1306.01  Scope of Part 1306.
1306.02  Definitions.
1306.03  Persons entitled to issue prescriptions.
1306.04  Purpose of issue of prescription.
1306.05  Manner of issuance of prescriptions.
1306.06  Persons entitled to fill prescriptions.
1306.07  Administering or dispensing of narcotic drugs.

               Controlled Substances Listed in Schedule II

1306.11  Requirement of prescription.
1306.12  Refilling prescriptions.
1306.13  Partial filling of prescriptions.
1306.14  Labeling of substances.
1306.15  Filing of prescriptions.

          Controlled Substances Listed in Schedules III and IV

1306.21  Requirement of prescription.
1306.22  Refilling of prescriptions.
1306.23  Partial filling of prescriptions.
1306.24  Labeling of substances.
1306.25  Filing prescriptions.
1306.26  Transfer between pharmacies of presription information for 
          Schedules III, IV, and V controlled substances for refill 
          purposes.

               Controlled Substances Listed in Schedule V

1306.31  Requirement of prescription.
1306.32  Dispensing without prescription.

    Authority: 21 U.S.C. 821, 829, 871(b), unless otherwise noted.

    Source: 36 FR 7799, Apr. 24, 1971; 36 FR 13386, July 21, 1971, 
unless otherwise noted. Redesignated at 38 FR 26609, Sept. 24, 1973.

                           General Information



Sec. 1306.01   Scope of Part 1306.

    Rules governing the issuance, filling and filing of prescriptions 
pursuant to section 309 of the Act (21 U.S.C. 829) are set forth 
generally in that section and specifically by the sections of this part.



Sec. 1306.02   Definitions.

    As used in this part, the following terms shall have the meanings 
specified:
    (a) The term Act means the Controlled Substances Act (84 Stat. 1242; 
21 U.S.C. 801).
    (b) The term individual practitioner means a physician, dentist, 
veterinarian, or other individual licensed, registered, or otherwise 
permitted, by the United States or the jurisdiction in which he 
practices, to dispense a controlled substance in the course of 
professional practice, but does not include a pharmacist, a pharmacy, or 
an institutional practitioner.
    (c) The term institutional practitioner means a hospital or other 
person (other than an individual) licensed, registered, or otherwise 
permitted, by the United States or the jurisdiction in which it 
practices, to dispense a controlled substance in the course of 
professional practice, but does not include a pharmacy.
    (d) The term pharmacist means any pharmacist licensed by a State to 
dispense controlled substances, and shall include any other person 
(e.g., a pharmacist intern) authorized by a State to dispense controlled 
substances under the supervision of a pharmacist licensed by such State.
    (e) A Long Term Care Facility (LTCF) means a nursing home, 
retirement care, mental care or other facility or institution which 
provides extended health care to resident patients.
    (f) The term prescription means an order for medication which is 
dispensed to or for an ultimate user but does not include an order for 
medication which is dispensed for immediate administration to the 
ultimate used. (e.g., an order to dispense a drug to a bed patient for 
immediate administration in a hospital is not a prescription.)
    (g) The terms register and registered refer to registration required 
and permitted by section 303 of the Act (21 U.S.C. 823).
    (h) The term home infusion pharmacy means a pharmacy which compounds 
solutions for direct administration to a patient in a private residence, 
Long Term Care Facility or hospice setting by means of parenteral, 
intravenous,

[[Page 70]]

intramuscular, subcutaneous or intraspinal infusion.
    (i) Any term not defined in this section shall have the definition 
set forth in section 102 of the Act (21 U.S.C. 802) or Sec. 1301.02 of 
this chapter.

(21 U.S.C. 801, et seq.)

[36 FR 7799, Apr. 24, 1971, as amended at 36 FR 18732, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and further amended at 45 
FR 54330, July 15, 1980; 59 FR 26111, May 19, 1994]



Sec. 1306.03   Persons entitled to issue prescriptions.

    (a) A prescription for a controlled substance may be issued only by 
an individual practitioner who is:
    (1) authorized to prescribe controlled substances by the 
jurisdiction in which he is licensed to practice his profession and
    (2) either registered or exempted from registration pursuant to 
Secs. 1301.24(c) and 1301.25 of this chapter.
    (b) A prescription issued by an individual practitioner may be 
communicated to a pharmacist by an employee or agent of the individual 
practitioner.

[36 FR 7799, Apr. 24, 1971, as amended at 36 FR 18732, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1306.04   Purpose of issue of prescription.

    (a) A prescription for a controlled substance to be effective must 
be issued for a legitimate medical purpose by an individual practitioner 
acting in the usual course of his professional practice. The 
responsibility for the proper prescribing and dispensing of controlled 
substances is upon the prescribing practitioner, but a corresponding 
responsibility rests with the pharmacist who fills the prescription. An 
order purporting to be a prescription issued not in the usual course of 
professional treatment or in legitimate and authorized research is not a 
prescription within the meaning and intent of section 309 of the Act (21 
U.S.C. 829) and the person knowingly filling such a purported 
prescription, as well as the person issuing it, shall be subject to the 
penalties provided for violations of the provisions of law relating to 
controlled substances.
    (b) A prescription may not be issued in order for an individual 
practitioner to obtain controlled substances for supplying the 
individual practitioner for the purpose of general dispensing to 
patients.
    (c) A prescription may not be issued for the dispensing of narcotic 
drugs listed in any schedule for ``detoxification treatment'' or 
``maintenance treatment'' as defined in Section 102 of the Act (21 
U.S.C. 802).

[36 FR 7799, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 39 FR 37986, Oct. 25, 1974]



Sec. 1306.05   Manner of issuance of prescriptions.

    (a) All prescriptions for controlled substances shall be dated as 
of, and signed on, the day when issued and shall bear the full name and 
address of the patient, the drug name, strength, dosage form, quantity 
prescribed, directions for use and the name, address and registration 
number of the practitioner. A practitioner may sign a prescription in 
the same manner as he would sign a check or legal document (e.g., J.H. 
Smith or John H. Smith). Where an oral order is not permitted, 
prescriptions shall be written with ink or indelible pencil or 
typewriter and shall be manually signed by the practitioner. The 
prescriptions may be prepared by the secretary or agent for the 
signature of a practitioner, but the prescribing practitioner is 
responsible in case the prescription does not conform in all essential 
respects to the law and regulations. A corresponding liability rests 
upon the pharmacist who fills a prescription not prepared in the form 
prescribed by these regulations.
    (b) An individual practitioner exempted from registration under 
Sec. 1301.24(c) of this chapter shall include on all prescriptions 
issued by him or her the registration number of the hospital or other 
institution and the special internal code number assigned to him or her 
by the hospital or other institution as provided in Sec. 1301.24(c) of 
this chapter, in lieu of the registration number of the practitioner 
required by this section. Each written prescription shall have the name 
of the physician stamped, typed, or handprinted on it,

[[Page 71]]

as well as the signature of the physician.
    (c) An official exempted from registration under Sec. 1301.25 shall 
include on all prescriptions issued by him his branch of service or 
agency (e.g., ``U.S. Army'' or ``Public Health Service'') and his 
service identification number, in lieu of the registration number of the 
practitioner required by this section. The service identification number 
for a Public Health Service employee is his Social Security 
identification number. Each prescription shall have the name of the 
officer stamped, typed, or handprinted on it, as well as the signature 
of the officer.

[36 FR 7799, Apr. 24, 1971, as amended at 36 FR 18733, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 56 FR 25026, 
June 3, 1991; 60 FR 36641, July 18, 1995]



Sec. 1306.06   Persons entitled to fill prescriptions.

    A prescription for controlled substances may only be filled by a 
pharmacist acting in the usual course of his professional practice and 
either registered individually or employed in a registered pharmacy or 
registered institutional practitioner.



Sec. 1306.07   Administering or dispensing of narcotic drugs.

    (a) The administering or dispensing directly (but not prescribing) 
of narcotic drugs listed in any schedule to a narcotic drug dependent 
person for ``detoxification treatment'' or ``maintenance treatment'' as 
defined in section 102 of the Act (21 U.S.C. 802) shall be deemed to be 
within the meaning of the term ``in the course of his professional 
practice or research'' in section 308(e) and section 102(20) of the Act 
(21 U.S.C. 828 (e)): Provided, That the practitioner is separately 
registered with the Attorney General as required by section 303(g) of 
the Act (21 U.S.C. 823(g)) and then thereafter complies with the 
regulatory standards imposed relative to treatment qualification, 
security, records and unsupervised use of drugs pursuant to such Act.
    (b) Nothing in this section shall prohibit a physician who is not 
specifically registered to conduct a narcotic treatment program from 
administering (but not prescribing) narcotic drugs to a person for the 
purpose of relieving acute withdrawal symptoms when necessary while 
arrangements are being made for referral for treatment. Not more than 
one day's medication may be administered to the person or for the 
person's use at one time. Such emergency treatment may be carried out 
for not more than three days and may not be renewed or extended.
    (c) This section is not intended to impose any limitations on a 
physician or authorized hospital staff to administer or dispense 
narcotic drugs in a hospital to maintain or detoxify a person as an 
incidental adjunct to medical or surgical treatment of conditions other 
than addiction, or to administer or dispense narcotic drugs to persons 
with intractable pain in which no relief or cure is possible or none has 
been found after reasonable efforts.

[39 FR 37986, Oct. 25, 1974]

               Controlled Substances Listed in Schedule II



Sec. 1306.11   Requirement of prescription.

    (a) A pharmacist may dispense directly a controlled substance in 
Schedule II, which is a prescription drug as determined by the Federal 
Food, Drug and Cosmetic Act, only pursuant to a written prescription 
signed by the practitioner, except as provided in paragraph (d) of this 
section. A prescription for a Schedule II controlled substance may be 
transmitted by the practitioner or the practitioner's agency to a 
pharmacy via facsimile equipment, provided the original written, signed 
prescription is presented to the pharmacist for review prior to the 
actual dispensing of the controlled substance, except as noted in 
paragraph (e) or (f) of this section. The original prescription shall be 
maintained in accordance with Sec. 1304.04(h).
    (b) An individual practitioner may administer or dispense directly a 
controlled substance listed in Schedule II in the course of his 
professional practice without a prescription, subject to Sec. 1306.07.
    (c) An institutional practitioner may administer or dispense 
directly (but not prescribe) a controlled substance listed in Schedule 
II only pursuant to a

[[Page 72]]

written prescription signed by the prescribing individual practitioner 
or to an order for medication made by an individual practitioner which 
is dispensed for immediate administration to the ultimate user.
    (d) In the case of an emergency situation, as defined by the 
Secretary in Sec. 290.10 of this title, a pharmacist may dispense a 
controlled substance listed in Schedule II upon receiving oral 
authorization of a prescribing individual practitioner, provided that:
    (1) The quantity prescribed and dispensed is limited to the amount 
adequate to treat the patient during the emergency period (dispensing 
beyond the emergency period must be pursuant to a written prescription 
signed by the prescribing individual practitioner);
    (2) The prescription shall be immediately reduced to writing by the 
pharmacist and shall contain all information required in Sec. 1306.05, 
except for the signature of the prescribing individual practitioner;
    (3) If the prescribing individual practitioner is not known to the 
pharmacist, he must make a reasonable effort to determine that the oral 
authorization came from a registered individual practitioner, which may 
include a callback to the prescribing individual practitioner using his 
phone number as listed in the telephone directory and/or other good 
faith efforts to insure his identity; and
    (4) Within 72 hours after authorizing an emergency oral 
prescription, the prescribing individual practitioner shall cause a 
written prescription for the emergency quantity prescribed to be 
delivered to the dispensing pharmacist. In addition to conforming to the 
requirements of Sec. 1306.05, the prescription shall have written on its 
face ``Authorization for Emergency Dispensing,'' and the date of the 
oral order. The written prescription may be delivered to the pharmacist 
in person or by mail, but if delivered by mail it must be postmarked 
within the 72-hour period. Upon receipt, the dispensing pharmacist shall 
attach this prescription to the oral emergency prercription which had 
earlier been reduced to writing. The pharmacist shall notify the nearest 
office of the Administration if the prescribing individual practitioner 
fails to deliver a written prescription to him; failure of the 
pharmacist to do so shall void the authority conferred by this paragraph 
to dispense without a written prescription of a prescribing individual 
practitioner.
    (e) A prescription prepared in accordance with Sec. 1306.05 written 
for a Schedule II narcotic substance to be compounded for the direct 
administration to a patient by parenteral, intravenous, intramuscular, 
subcutaneous or intraspinal infusion may be transmitted by the 
practitioner or the practitioner's agent to the home infusion pharmacy 
by facsimile. The facsimile serves as the original written prescription 
for purposes of this paragraph (e) and it shall be maintained in 
accordance with Sec. 1304.04(h).
    (f) A prescription prepared in accordance with Sec. 1306.05 written 
for Schedule II substance for a resident of a Long Term Care Facility 
may be transmitted by the practitioner or the practitioner's agent to 
the dispensing pharmacy by facsimile. The facsimile serves as the 
original written prescription for purposes of this paragraph (f) and it 
shall be maintained in accordance with Sec. 1304.04(h).

[36 FR 7799, Apr. 24, 1971, as amended at 36 FR 18733, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973 and amended at 53 FR 4964, 
Feb. 19, 1988; 59 FR 26111, May 19, 1994; 59 FR 30832, June 15, 1994]



Sec. 1306.12   Refilling prescriptions.

    The refilling of a prescription for a controlled substance listed in 
Schedule II is prohibited.



Sec. 1306.13   Partial filling of prescriptions.

    (a) The partial filling of a prescription for a controlled substance 
listed in Schedule II is permissible, if the pharmacist is unable to 
supply the full quantity called for in a written or emergency oral 
prescription and he makes a notation of the quantity supplied on the 
face of the written prescription (or written record of the emergency 
oral prescription). The remaining portion of the prescription may be 
filled within 72 hours of the first partial filling; however, if the 
remaining portion is not or cannot be filled within the 72-hour period, 
the

[[Page 73]]

pharmacist shall so notify the prescribing individual practitioner. No 
further quantity may be supplied beyond 72 hours without a new 
prescription.
    (b) A prescription for a Schedule II controlled substance written 
for a patient in a Long Term Care Facility (LTCF) or for a patient with 
a medical diagnosis documenting a terminal illness may be filled in 
partial quantities to include individual dosage units. If there is any 
question whether a patient may be classified as having a terminal 
illness, the pharmacist must contract the practitioner prior to 
partially filling the prescription. Both the pharmacist and the 
prescribing practitioner have a corresponding responsibility to assure 
that the controlled substance is for a terminally ill patient. The 
pharmacist must record on the prescription whether the patient is 
``terminally ill'' or an ``LTCF patient.'' A prescription that is 
partially filled and does not contain the notation ``terminally ill'' or 
``LTCF patient'' shall be deemed to have been filled in violation of the 
Act. For each partial filling, the dispensing pharmacist shall record on 
the back of the prescription (or on another appropriate record, 
uniformly maintained, and readily retrievable) the date of the partial 
filling, quantity dispensed, remaining quantity authorized to be 
dispensed, and the identification of the dispensing pharmacist. Prior to 
any subsequent partial filling the pharmacist is to determine that the 
additional partial filling is necessary. The total quantity of Schedule 
II controlled substances dispensed in all partial fillings must not 
exceed the total quantity prescribed. Schedule II prescriptions for 
patients in a LTCF or patients with a medical diagnosis documenting a 
terminal illness shall be valid for a period not to exceed 60 days from 
the issue date unless sooner terminated by the discontinuance of 
medication.
    (c) Information pertaining to current Schedule II prescriptions for 
patients in a LTCF or for patients with a medical diagnosis documenting 
a terminal illness may be maintained in a computerized system if this 
system has the capability to permit:
    (1) Output (display or printout) of the original prescription 
number, date of issue, identification of prescribing individual 
practitioner, identification of patient, address of the LTCF or address 
of the hospital or residence of the patient, identification of 
medication authorized (to include dosage, form, strength and quantity), 
listing of the partial fillings that have been dispensed under each 
prescription and the information required in Sec. 1306.13(b).
    (2) Immediate (real time) updating of the prescription record each 
time a partial filling of the prescription is conducted.
    (3) Retrieval of partially filled Schedule II prescription 
information is the same as required by Sec. 1306.22(b) (4) and (5) for 
Schedule III and IV prescription refill information.

(21 U.S.C. 801, et seq.)

[36 FR 7799, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 45 FR 54330, July 15, 1980; 56 FR 25027, June 3, 1991]



Sec. 1306.14   Labeling of substances.

    (a) The pharmacist filling a written or emergency oral prescription 
for a controlled substance listed in Schedule II shall affix to the 
package a label showing date of filling, the pharmacy name and address, 
the serial number of the prescription, the name of the patient, the name 
of the prescribing practitioner, and directions for use and cautionary 
statements, if any, contained in such prescription or required by law.
    (b) The requirements of paragraph (a) of this section do not apply 
when a controlled substance listed in Schedule II is prescribed for 
administration to an ultimate user who is institutionalized: Provided, 
That:
    (1) Not more than 7-day supply of the controlled substance listed in 
Schedule II is dispensed at one time;
    (2) The controlled substance listed in Schedule II is not in the 
possession of the ultimate user prior to the administration;
    (3) The institution maintains appropriate safeguards and records 
regarding the proper administration, control, dispensing, and storage of 
the controlled substance listed in Schedule II; and
    (4) The system employed by the pharmacist in filling a prescription 
is adequate to identify the supplier, the

[[Page 74]]

product, and the patient, and to set forth the directions for use and 
cautionary statements, if any, contained in the prescription or required 
by law.

[36 FR 13368, July 21, 1971, as amended at 37 FR 15921, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1306.15   Filing of prescriptions.

    All written prescriptions and written records of emergency oral 
prescriptions shall be kept in accordance with requirements of 
Sec. 1304.04(h) of this chapter.

[36 FR 7799, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 51 FR 5320, Feb. 13, 1986]

          Controlled Substances Listed in Schedules III and IV



Sec. 1306.21   Requirement of prescription.

    (a) A pharmacist may dispense directly a controlled substance listed 
in Schedule III or IV, which is a prescription drug as determined under 
the Federal Food, Drug and Cosmetic Act, only pursuant to either a 
written prescription signed by a practitioner or a facsimile of a 
written, signed prescription transmitted by the practitioner or the 
practitioner's agent to the pharmacy or pursuant to an oral prescription 
made by an individual practitioner and promptly reduced to writing by 
the pharmacist containing all information required in Sec. 1306.05, 
except for the signature of the practitioner.
    (b) An individual practitioner may administer or dispense directly a 
controlled substance listed in Schedule III or IV in the course of his 
professional practice without a prescription, subject to Sec. 1306.07.
    (c) An institutional practitioner may administer or dispense 
directly (but not prescribe) a controlled substance listed in Schedules 
III or IV only pursuant to written prescription signed by an individual 
practitioner, or pursuant to a facsimile of a written prescription or 
order for medication transmitted by the practitioner or the 
practitioner's agent to the institutional practitioner-pharmacist, or 
pursuant to an oral prescription made by an individual practitioner and 
promptly reduced to writing by the pharmacist (containing all 
information required in Sec. 1306.05 except for the signature of the 
individual practitioner), or pursuant to an order for medication made by 
an individual practitioner which is dispensed for immediate 
administration to the ultimate user, subject to Sec. 1306.07.

[36 FR 7799, Apr. 24, 1971, as amended at 36 FR 18733, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973; 59 FR 26112, May 19, 1994]



Sec. 1306.22   Refilling of prescriptions.

    (a) No prescription for a controlled substance listed in Schedule 
III or IV shall be filled or refilled more than six months after the 
date on which such prescription was issued and no such prescription 
authorized to be refilled may be refilled more than five times. Each 
refilling of a prescription shall be entered on the back of the 
prescription or on another appropriate document. If entered on another 
document, such as a medication record, the document must be uniformly 
maintained and readily retrievable. The following information must be 
retrievable by the prescription number consisting of the name and dosage 
form of the controlled substance, the date filled or refilled, the 
quantity dispensed, initials of the dispensing pharmacist for each 
refill, and the total number of refills for that prescription. If the 
pharmacist merely initials and dates the back of the prescription it 
shall be deemed that the full face amount of the prescription has been 
dispensed. The prescribing practitioner may authorize additional refills 
of Schedule III or IV controlled substances on the original prescription 
through an oral refill authorization transmitted to the pharmacist 
provided the following conditions are met:
    (1) The total quantity authorized, including the amount of the 
original prescription, does not exceed five refills nor extend beyond 
six months from the date of issue of the original prescription.
    (2) The pharmacist obtaining the oral authorization records on the 
reverse of the original prescription the date, quantity of refill, 
number of additional refills authorized, and initials the prescription 
showing who received the authorization from the prescribing

[[Page 75]]

practioner who issued the original prescription.
    (3) The quantity of each additional refill authorized is equal to or 
less than the quantity authorized for the initial filling of the 
original prescription.
    (4) The prescribing practitioner must execute a new and separate 
prescription for any additional quantities beyond the five refill, six-
month limitation.
    (b) As an alternative to the procedures provided by subsection (a), 
an automated data processing system may be used for the storage and 
retrival of refill information for prescription orders for controlled 
substances in Schedule III and IV, subject to the following conditions:
    (1) Any such proposed computerized system must provide on-line 
retrieval (via CRT display or hard-copy printout) of original 
prescription order information for those prescription orders which are 
currently authorized for refilling. This shall include, but is not 
limited to, data such as the original prescription number, date of 
issuance of the original prescription order by the practitioner, full 
name and address of the patient, name, address, and DEA registration 
number of the practitioner, and the name, strength, dosage form, 
quantity of the controlled substance prescribed (and quantity dispensed 
if different from the quantity prescribed), and the total number of 
refills authorized by the prescribing practitioner.
    (2) Any such proposed computerized system must also provide on-line 
retrieval (via CRT display or hard-copy printout) of the current refill 
history for Schedule III or IV controlled substance prescription orders 
(those authorized for refill duing the past six months.) This refill 
history shall include, but is not limited to, the name of the controlled 
substance, the date of refill, the quantity dispensed, the 
identification code, or name or initials of the dispensing pharmacist 
for each refill and the total number of refills dispensed to date for 
that prescription order.
    (3) Documentation of the fact that the refill information entered 
into the computer each time a pharmacist refills an original 
prescription order for a Schedule III or IV controlled substance is 
correct must be provided by the individual pharmacist who makes use of 
such a system. If such a system provides a hard-copy printout of each 
day's controlled substance prescription order refill data, that printout 
shall be verified, dated, and signed by the individual pharmacist who 
refilled such a prescription order. The individual pharmacist must 
verify that the data indicated is correct and then sign this document in 
the same manner as he would sign a check or legal document (e.g., J. H. 
Smith, or John H. Smith). This document shall be maintained in a 
separate file at that pharmacy for a period of two years from the 
dispensing date. This printout of the day's controlled substance 
prescription order refill data must be provided to each pharmacy using 
such a computerized system within 72 hours of the date on which the 
refill was dispensed. It must be verified and signed by each pharmacist 
who is involved with such dispensing. In lieu of such a printout, the 
pharmacy shall maintain a bound log book, or separate file, in which 
each individual pharmacist involved in such dispensing shall sign a 
statement (in the manner previously described) each day, attesting to 
the fact that the refill information entered into the computer that day 
has been reviewed by him and is correct as shown. Such a book or file 
must be maintained at the pharmacy employing such a system for a period 
of two years after the date of dispensing the appropriately authorized 
refill.
    (4) Any such computerized system shall have the capability of 
producing a printout of any refill data which the user pharmacy is 
responsible for maintaining under the Act and its implementing 
regulations. For example, this would include a refill-by-refill audit 
trail for any specified strength and dosage form of any controlled 
substance (by either brand or generic name or both). Such a printout 
must include name of the prescribing practitioner, name and address of 
the patient, quantity dispensed on each refill, date of dispensing for 
each refill, name or identification code of the dispensing pharmacist, 
and the number of the original prescription order. In any computerized 
system employed by a

[[Page 76]]

user pharmacy the central recordkeeping location must be capable of 
sending the printout to the pharmacy within 48 hours, and if a DEA 
Special Agent or Compliance Investigator requests a copy of such 
printout from the user pharmacy, it must, if requested to do so by the 
Agent or Investigator, verify the printout transmittal capability of its 
system by documentation (e.g., postmark).
    (5) In the event that a pharmacy which employs such a computerized 
system experiences system down-time, the pharmacy must have an auxiliary 
procedure which will be used for documentation of refills os Schedule 
III and IV controlled substance prescription orders. This auxiliary 
procedure must insure that refills are authorized by the original 
prescription order, that the maximum number of refills has not been 
exceeded, and that all of the appropriate data is retained for on-line 
data entry as soon as the computer system is available for use again.
    (c) When filing refill information for original prescription orders 
for Schedule III or IV controlled substances, a pharmacy may use only 
one of the two systems described in paragraphs (a) or (b) of this 
section.

[36 FR 7799, Apr. 24, 1971; 36 FR 13386, July 21, 1971. Redesignated at 
38 FR 26609, Sept. 24, 1973, and amended at 42 FR 28878, June 6, 1977; 
45 FR 44266, July 1, 1980; 52 FR 3605, Feb. 5, 1987]



Sec. 1306.23   Partial filling of prescriptions.

    The partial filling of a prescription for a controlled substance 
listed in Schedule III or IV is permissible, provided that:
    (a) Each partial filling is recorded in the same manner as a 
refilling,
    (b) The total quantity dispensed in all partial fillings does not 
exceed the total quantity prescribed, and
    (c) No dispensing occurs after 6 months after the date on which the 
prescription was issued.

[36 FR 18733, Sept. 21, 1971. Redesignated at 38 FR 26609, Sept. 24, 
1973, and amended at 51 FR 5320, Feb. 13, 1986]



Sec. 1306.24   Labeling of substances.

    (a) The pharmacist filling a prescription for a controlled substance 
listed in Schedule III or IV shall affix to the package a label showing 
the pharmacy name and address, the serial number and date of initial 
filling, the name of the patient, the name of the practitioner issuing 
the prescription, and directions for use and cautionary statements, if 
any, contained in such prescription as required by law.
    (b) The requirements of paragraph (a) of this section do not apply 
when a controlled substance listed in Schedule III or IV is prescribed 
for administration to an ultimate user who is institutionalized: 
Provided, That:
    (1) Not more than a 34-day supply or 100 dosage units, whichever is 
less, of the controlled substance listed in Schedule III or IV is 
dispensed at one time;
    (2) The controlled substance listed in Schedule III or IV is not in 
the possession of the ultimate user prior to administration;
    (3) The institution maintains appropriate safeguards and records the 
proper administration, control, dispensing, and storage of the 
controlled substance listed in Schedule III or IV; and
    (4) The system employed by the pharmacist in filling a prescription 
is adequate to identify the supplier, the product and the patient, and 
to set forth the directions for use and cautionary statements, if any, 
contained in the prescription or required by law.

[36 FR 7799, Apr. 24, 1971. Redesignated at 36 FR 18733, Sept. 21, 1971, 
and amended at 37 FR 15921, Aug. 8, 1972]



Sec. 1306.25   Filing prescriptions.

    All prescriptions for controlled substances listed in Schedules III 
and IV shall be kept in accordance with Sec. 1304.04(h) of this chapter.

[36 FR 7799, Apr. 24, 1971. Redesignated at 36 FR 18733, Sept. 21, 1971, 
and amended at 51 FR 5320, Feb. 13, 1986]



Sec. 1306.26  Transfer between pharmacies of prescription information for Schedules III, IV, and V controlled substances for refill purposes.

    (a) The transfer of original prescription information for a 
controlled substance listed in Schedules III, IV or V for the purpose of 
refill dispensing is permissible between pharmacies on a

[[Page 77]]

one time basis subject to the following requirements:
    (1) The transfer is communicated directly between two licensed 
pharmacists and the transferring pharmacist records the following 
information:
    (i) Write the word ``VOID'' on the face of the invalidated 
prescription.
    (ii) Record on the reverse of the invalidated prescription the name, 
address and DEA registration number of the pharmacy to which it was 
transferred and the name of the pharmacist receiving the prescription 
information.
    (iii) Record the date of the transfer and the name of the pharmacist 
transferring the information.
    (b) The pharmacist receiving the transferred prescription 
information shall reduce to writing the following:
    (1) Write the word ``transfer'' on the face of the transferred 
prescription.
    (2) Provide all information required to be on a prescription 
pursuant to 21 CFR 1306.05 and include:
    (i) Date of issuance of original prescription;
    (ii) Original number of refills authorized on original prescription;
    (iii) Date of original dispensing;
    (iv) Number of valid refills remaining and date of last refill;
    (v) Pharmacy's name, address, DEA registration number and original 
prescription number from which the prescription information was 
transferred;
    (vi) Name of transferor pharmacist.
    (3) Both the original and transferred prescription must be 
maintained for a period of two years from the date of last refill.
    (c) Pharmacies electronically accessing the same prescription record 
must satisfy all information requirements of a manual mode for 
prescription transferral.
    (d) The procedure allowing the transfer of prescription information 
for refill purposes is permissible only if allowable under existing 
state or other applicable law.

[46 FR 48919, Oct. 5, 1981]

               Controlled Substances Listed in Schedule V



Sec. 1306.31   Requirement of prescription.

    (a) A pharmacist may dispense directly a controlled substance listed 
in Schedule V pursuant to a prescription as required for controlled 
substances listed in Schedules III and IV in Sec. 1306.21. A 
prescription for a controlled substance listed in Schedule V may be 
refilled only as expressly authorized by the prescribing individual 
practitioner on the prescription; if no such authorization is given, the 
prescription may not be refilled. A pharmacist dispensing such substance 
pursuant to a prescription shall label the substance in accordance with 
Sec. 1306.24 and file the prescription in accordance with Sec. 1306.25.
    (b) An individual practitioner may administer or dispense directly a 
controlled substance listed in Schedule V in the course of his 
professional practice without a prescription, subject to Sec. 1306.07.
    (c) An institutional practitioner may administer or dispense 
directly (but not prescribe) a controlled substance listed in Schedule V 
only pursuant to a written prescription signed by an individual 
practitioner, or pursuant to a facsimile of a written prescription 
transmitted by the practitioner or the practitioner's agent to the 
institutional practitioner--pharmacist, or pursuant to an oral 
prescription made by an individual practitioner and promptly reduced to 
writing by the pharmacist (containing all information required in 
Sec. 1306.05 except for the signature of the individual practitioner), 
or pursuant to an order for medication made by an individual 
practitioner which is dispensed for immediate administration to the 
ultimate user, subject to Sec. 1306.07.

[36 FR 7799, Apr. 24, 1971, as amended at 36 FR 18733, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 51 FR 5320, 
Feb. 13, 1986; 59 FR 26112, May 19, 1994; 59 FR 30832, June 15, 1994]

[[Page 78]]



Sec. 1306.32   Dispensing without prescription.

    A controlled substance listed in Schedule V, and a controlled 
substance listed in Schedule II, III, or IV which is not a prescription 
drug as determined under the Federal Food, Drug, and Cosmetic Act, may 
be dispensed by a pharmacist without a prescription to a purchaser at 
retail, provided that:
    (a) Such dispensing is made only by a pharmacist (as defined in 
Sec. 1306.02(d)), and not by a nonpharmacist employee even if under the 
supervision of a pharmacist (although after the pharmacist has fulfilled 
his professional and legal responsibilities set forth in this section, 
the actual cash, credit transaction, or delivery, may be completed by a 
nonpharmacist);
    (b) Not more than 240 cc. (8 ounces) of any such controlled 
substance containing opium, nor more than 120 cc. (4 ounces) of any 
other such controlled substance nor more than 48 dosage units of any 
such controlled substance containing opium, nor more than 24 dosage 
units of any other such controlled substance may be dispensed at retail 
to the same purchaser in any given 48-hour period;
    (c) The purchaser is at least 18 years of age;
    (d) The pharmacist requires every purchaser of a controlled 
substance under this section not known to him to furnish suitable 
identification (including proof of age where appropriate);
    (e) A bound record book for dispensing of controlled substances 
under this section is maintained by the pharmacist, which book shall 
contain the name and address of the purchaser, the name and quantity of 
controlled substance purchased, the date of each purchase, and the name 
or initials of the pharmacist who dispensed the substance to the 
purchaser (the book shall be maintained in accordance with the 
recordkeeping requirement of Sec. 1304.04 of this chapter); and
    (f) A prescription is not required for distribution or dispensing of 
the substance pursuant to any other Federal, State or local law.

[36 FR 7799, Apr. 24, 1971, as amended at 36 FR 18733, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



PART 1307--MISCELLANEOUS--Table of Contents




                           General Information

Sec.
1307.01  Definitions.
1307.02  Application of State law and other Federal law.
1307.03  Exceptions to regulations.

   Special Exceptions for Manufacture and Distribution of Controlled 
                               Substances

1307.11  Distribution by dispenser to another practitioner.
1307.12  Manufacture and distribution of narcotic solutions and 
          compounds by a pharmacist.
1307.13  Distribution to supplier.
1307.14  Distribution upon discontinuance or transfer of business.
1307.15  Incidental manufacture of controlled substances.

                    Disposal of Controlled Substances

1307.21  Procedure for disposing of controlled substances.
1307.22  Disposal of controlled substances by the Administration.

                         Special Exempt Persons

1307.31  Native American Church.

    Authority: 21 U.S.C. 821, 822(d), 871(b), unless otherwise noted.

    Source: 36 FR 7801, Apr. 24, 1971, unless otherwise noted. 
Redesignated at 38 FR 26609, Sept. 24, 1973.

                           General Information



Sec. 1307.01   Definitions.

    As used in this part, the following terms shall have the meanings 
specified:
    (a) The term Act means the Controlled Substances Act (84 Stat. 1242; 
21 U.S.C. 801) and/or the Controlled Substances Import and Export Act 
(84 Stat. 1285; 21 U.S.C. 951).
    (b) Any term not defined in this section shall have the definition 
set forth in section 102 and 1001 of the Act (21 U.S.C. 802 and 951) and 
in Sec. 1301.02 of this chapter.



Sec. 1307.02   Application of State law and other Federal law.

    Nothing in parts 1301-1308, 1311, 1312, or 1316 of this chapter 
shall be construed as authorizing or permitting any person to do any act 
which such person is not authorized or permitted

[[Page 79]]

to do under other Federal laws or obligations under international 
treaties, conventions or protocols, or under the law of the State in 
which he desires to do such act nor shall compliance with such parts be 
construed as compliance with other Federal or State laws unless 
expressly provided in such other laws.



Sec. 1307.03  Exceptions to regulations.

    Any person may apply for an exception to the application of any 
provision of parts 1301-1313, or 1316 of this chapter by filing a 
written request stating the reasons for such exception. Requests shall 
be filed with the Administrator, Drug Enforcement Administration, 
Department of Justice, Washington, D.C. 20537. The Administrator may 
grant an exception in his discretion, but in no case shall he be 
required to grant an exception to any person which is not otherwise 
required by law or the regulations cited in this section.

[60 FR 32454, June 22, 1995]

   Special Exceptions for Manufacture and Distribution of Controlled 
                               Substances



Sec. 1307.11   Distribution by dispenser to another practitioner.

    (a) A practitioner who is registered to dispense a controlled 
substance may distribute (without being registered to distribute) a 
quantity of such substance to another practitioner for the purpose of 
general dispensing by the practitioner to his or its patients: Provided, 
That:
    (1) The practitioner to whom the controlled substance is to be 
distributed is registered under the Act to dispense that controlled 
substance;
    (2) The distribution is recorded by the distributing practitioner in 
accordance with Sec. 1304.24(e) of this chapter and by the receiving 
practitioner in accordance with Sec. 1304.24(c) of this chapter;
    (3) If the substance is listed in Schedule I or II, an order form is 
used as required in part 1305 of this chapter;
    (4) The total number of dosage units of all controlled substances 
distributed by the practitioner pursuant to this section and 
Sec. 1301.28 of this chapter during each calendar year in which the 
practitioner is registered to dispense does not exceed 5 percent of the 
total number of dosage units of all controlled substances distributed 
and dispensed by the practitioner during the same calendar year.
    (b) If, during any calendar year in which the practitioner is 
registered to dispense, the practitioner has reason to believe that the 
total number of dosage units of all controlled substances which will be 
distributed by him pursuant to this section and Sec. 1301.28 of this 
chapter will exceed 5 percent of the total number of dosage units of all 
controlled substances distributed and dispensed by him during that 
calendar year, the practitioner shall obtain a registration to 
distribute controlled substances.

[36 FR 18733, Sept. 21, 1971. Redesignated at 38 FR 26609, Sept. 24, 
1973, and amended at 50 FR 31590, Aug. 5, 1985]



Sec. 1307.12   Manufacture and distribution of narcotic solutions and compounds by a pharmacist.

    As an incident to a distribution under Sec. 1307.11, a pharmacist 
may manufacture (without being registered to manufacture) an aqueous or 
oleaginous solution or solid dosage form containing a narcotic 
controlled substance in a proportion not exceeding 20 percent of the 
complete solution, compound, or mixture.

[36 FR 18733, Sept. 21, 1971. Redesignated at 38 FR 26609, Sept. 24, 
1973]



Sec. 1307.13   Distribution to supplier.

    Any person lawfully in possession of a controlled substance listed 
in any schedule may distribute (without being registered to distribute) 
that substance to the person from whom he obtained it or to the 
manufacturer of the substance, provided that a written record is 
maintained which indicates the date of the transaction, the name, form 
and quantity of the substance, the name, address, and registration 
number, if any, of the person making the distribution, and the name, 
address, and registration number, if known, of the supplier or 
manufacturer. In the case of returning a controlled substance listed in 
Schedule I or II, an order form shall be used in the manner prescribed 
in part 1305 of this chapter and be maintained as the written record of 
the

[[Page 80]]

transaction. Any person not required to register pursuant to sections 
302(c) or 1007(b)(1) of the Act (21 U.S.C. 823(c) or 957(b)(1)) shall be 
exempt from maintaining the records required by this section.

[36 FR 7801, Apr. 24, 1971, as amended at 36 FR 18733, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1307.14   Distribution upon discontinuance or transfer of business.

    (a) Any registrant desiring to discontinue business activities 
altogether or with respect to controlled substances (without 
transferring such business activities to another person) shall return 
for cancellation his certificate of registration, and any unexecuted 
order forms in his possession, to the Registration Unit, Drug 
Enforcement Administration, Department of Justice, Post Office Box 
28083, Central Station, Washington, DC 20005. Any controlled substances 
in his possession may be disposed of in accordance with Sec. 1307.21.
    (b) Any registrant desiring to discontinue business activities 
altogether or with respect to controlled substance (by transferring such 
business activities to another person) shall submit in person or by 
registered or certified mail, return receipt requested, to the Special 
Agent in Charge in his area, at least 14 days in advance of the date of 
the proposed transfer (unless the Special Agent in Charge waives this 
time limitation in individual instances), the following information:
    (1) The name, address, registration number, and authorized business 
activity of the registrant discontinuing the business (registrant-
transferor);
    (2) The name, address, registration number, and authorized business 
activity of the person acquiring the business (registrant-transferee);
    (3) Whether the business activities will be continued at the 
location registered by the person discontinuing business, or moved to 
another location (if the latter, the address of the new location should 
be listed);
    (4) Whether the registrant-transferor has a quota to manufacture or 
procure any controlled substance listed in Schedule I or II (if so, the 
basic class or class of the substance should be indicated); and
    (5) The date on which the transfer of controlled substances will 
occur.
    (c) Unless the registrant-transferor is informed by the Regional 
Administrator, before the date on which the transfer was stated to 
occur, that the transfer may not occur, the registrant-transferor may 
distribute (without being registered to distribute) controlled 
substances in his possession to the registrant-transferee in accordance 
with the following:
    (1) On the date of transfer of the controlled substances, a complete 
inventory of all controlled substances being transferred shall be taken 
in accordance with Secs. 1304.11-1304.19 of this chapter. This inventory 
shall serve as the final inventory of the registrant-transferor and the 
initial inventory of the registrant-transferee, and a copy of the 
inventory shall be included in the records of each person. It shall not 
be necessary to file a copy of the inventory with the Administration 
unless requested by the Regional Administrator. Transfers of any 
substances listed in Schedule I or II shall require the use of order 
forms in accordance with part 1305 of this chapter.
    (2) On the date of transfer of the controlled substances, all 
records required to be kept by the registrant-transferor with reference 
to the controlled substances being transferred, under part 1304 of this 
chapter, shall be transferred to the registrant-transferee. 
Responsibility for the accuracy of records prior to the date of transfer 
remains with the transferor, but responsibility for custody and 
maintenance shall be upon the transferee.
    (3) In the case of registrants required to make reports pursuant to 
part 1304 of this chapter, a report marked ``Final'' will be prepared 
and submitted by the registrant-transferor showing the disposition of 
all the controlled substances for which a report is required; no 
additional report will be required from him, if no further transactions 
involving controlled substances are consummated by him. The initial 
report of the registrant-transferee shall account for transactions 
beginning with the day next succeeding the date of discontinuance or 
transfer of

[[Page 81]]

business by the transferor-registrant and the substances transferred to 
him shall be reported as receipts in his initial report.

[37 FR 15921, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 47 FR 41735, Sept. 22, 1982; 51 FR 5319, Feb. 13, 1986]



Sec. 1307.15   Incidental manufacture of controlled substances.

    Any registered manufacturer who, incidentally but necessarily, 
manufactures a controlled substance as a result of the manufacture of a 
controlled substance or basic class of controlled substance for which he 
is registered and has been issued an individual manufacturing quota 
pursuant to part 1303 of this chapter (if such substance or class is 
listed in Schedule I or II) shall be exempt from the requirement of 
registration pursuant to part 1301 of this chapter and, if such 
incidentally manufactured substance is listed in Schedule I or II, shall 
be exempt from the requirement of an individual manufacturing quota 
pursuant to part 1303 of this chapter, if such substances are disposed 
of in accordance with Sec. 1307.21.

                    Disposal of Controlled Substances



Sec. 1307.21   Procedure for disposing of controlled substances.

    (a) Any person in possession of any controlled substance and 
desiring or required to dispose of such substance may request the 
Special Agent in Charge of the Administration in the area in which the 
person is located for authority and instructions to dispose of such 
substance. The request should be made as follows:
    (1) If the person is a registrant required to make reports pursuant 
to part 1304 of this chapter, he shall list the controlled substance or 
substances which he desires to dispose of on the ``b'' subpart of the 
report normally filed by him, and submit three copies of that subpart to 
the Special Agent in Charge of the Administration in his area.
    (2) If the person is a registrant not required to make reports 
pursuant to part 1304 of this chapter, he shall list the controlled 
substance or substances which he desires to dispose of on DEA Form 41, 
and submit three copies of that form to the Special Agent in Charge in 
his area; and
    (3) If the person is not a registrant, he shall submit to the 
Special Agent in Charge a letter stating:
    (i) The name and address of the person;
    (ii) The name and quantity of each controlled substance to be 
disposed of;
    (iii) How the applicant obtained the substance, if known; and
    (iv) The name, address, and registration number, if known, of the 
person who possessed the controlled substances prior to the applicant, 
if known.
    (b) The Special Agent in Charge shall authorize and instruct the 
applicant to dispose of the controlled substance in one of the following 
manners:
    (1) By transfer to person registered under the Act and authorized to 
possess the substance;
    (2) By delivery to an agent of the Administration or to the nearest 
office of the Administration;
    (3) By destruction in the presence of an agent of the Administration 
or other authorized person; or
    (4) By such other means as the Special Agent in Charge may determine 
to assure that the substance does not become available to unauthorized 
persons.
    (c) In the event that a registrant is required regularly to dispose 
of controlled substances, the Special Agent in Charge may authorize the 
registrant to dispose of such substances, in accordance with paragraph 
(b) of this section, without prior approval of the Administration in 
each instance, on the condition that the registrant keep records of such 
disposals and file periodic reports with the Special Agent in Charge 
summarizing the disposals made by the registrant. In granting such 
authority, the Special Agent in Charge may place such conditions as he 
deems proper on the disposal of controlled substances, including the 
method of disposal and the frequency and detail of reports.
    (d) This section shall not be construed as affecting or altering in 
any way the disposal of controlled substances through procedures 
provided in

[[Page 82]]

laws and regulations adopted by any State.

[36 FR 7801, Apr. 24, 1971, as amended at 37 FR 15922, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 47 FR 41735, 
Sept. 22, 1982]



Sec. 1307.22   Disposal of controlled substances by the Administration.

    Any controlled substance delivered to the Administration under 
Sec. 1307.21 or forfeited pursuant to section 511 of the Act (21 U.S.C. 
881) may be delivered to any department, bureau, or other agency of the 
United States or of any State upon proper application addressed to the 
Administrator, Drug Enforcement Administration, Department of Justice, 
Washington, DC 28083. The application shall show the name, address, and 
official title of the person or agency to whom the controlled drugs are 
to be delivered, including the name and quantity of the substances 
desired and the purpose for which intended. The delivery of such 
controlled drugs shall be ordered by the Administrator, if, in his 
opinion, there exists a medical or scientific need therefor.

                         Special Exempt Persons



Sec. 1307.31   Native American Church.

    The listing of peyote as a controlled substance in Schedule I does 
not apply to the nondrug use of peyote in bona fide religiots ceremonies 
of the Native American Church, and members of the Native American Church 
so using peyote are exempt from registration. Any person who 
manufactures peyote for or distributes peyote to the Native American 
Church, however, is required to obtain registration annually and to 
comply with all other requirements of law.



PART 1308--SCHEDULES OF CONTROLLED SUBSTANCES--Table of Contents




                           General Information

Sec.
1308.01  Scope of Part 1308.
1308.02  Definitions.
1308.03  Administration Controlled Substances Code Number.
1308.04  Submission of information by manufacturers.

                                Schedules

1308.11  Schedule I.
1308.12  Schedule II.
1308.13  Schedule III.
1308.14  Schedule IV.
1308.15  Schedule V.

                     Excluded Nonnarcotic Substances

1308.21  Application for exclusion of a nonnarcotic substance.
1308.22  Excluded substances.

                      Exempt Chemical Preparations

1308.23  Exemption of certain chemical preparations; application.
1308.24  Exemption chemical preparations.

          Excluded Veterinary Anabolic Steroid Implant Products

1308.25  Exclusion of a veterinary anabolic steroid implant product; 
          application.
1308.26  Excluded veterinary anabolic steroid implant products.

                     Exempted Prescription Products

1308.31  Application for exemption of a nonnarcotic prescription 
          product.
1308.32  Exempted prescription products.

                    Exempt Anabolic Steroid Products

1308.33  Exemption of certain anabolic steroid products; application.
1308.34  Exempt anabolic steroid products.

                                Hearings

1308.41  Hearings generally.
1308.42  Purpose of hearing.
1308.43  Waiver or modification of Rules.
1308.44  Initiation of proceedings for rule-making.
1308.45  Request for hearing or appearance; waiver.
1308.46  Burden of proof.
1308.47  Time and place of hearing.
1308.48  Final order.
1308.49  Control required under international treaty.
1308.50  Control of immediate precursors.
1308.51  Pending proceedings.
1308.52  Emergency sheduling.

    Authority: 21 U.S.C. 811, 812, 871(b), unless otherwise noted.

    Source: 38 FR 8254, Mar. 30, 1973, unless otherwise noted. 
Redesignated at 38 FR 26609, Sept. 24, 1973.

                           General Information



Sec. 1308.01   Scope of Part 1308.

    Schedules of controlled substances established by section 202 of the 
Act (21

[[Page 83]]

U.S.C. 812), as they are changed, updated, and republished from time to 
time, are set forth in this part.



Sec. 1308.02   Definitions.

    As used in this part, the following terms shall have the meanings 
specified:
    (a) The term Act means the Controlled Substance Act (84 Stat. 1242; 
21 U.S.C. 801) and/or the Controlled Substances Import and Export Act 
(84 Stat. 1285; 21 U.S.C. 951).
    (b) The term anabolic steroid means any drug or hormonal substance, 
chemically and pharmacologically related to testosterone (other than 
estrogens, progestins, and corticosteroids) that promotes muscle growth, 
and includes:
    (1) Boldenone;
    (2) Chlorotestosterone (4-chlortestosterone);
    (3) Clostebol;
    (4) Dehydrochlormethyltestosterone;
    (5) Dihydrotestosterone (4-dihydrotestosterone);
    (6) Drostanolone;
    (7) Ethylestrenol;
    (8) Fluoxymesterone;
    (9) Formebulone (formebolone);
    (10) Mesterolone;
    (11) Methandienone;
    (12) Methandranone;
    (13) Methandriol;
    (14) Methandrostenolone;
    (15) Methenolone;
    (16) Methyltestosterone;
    (17) Mibolerone;
    (18) Nandrolone;
    (19) Norethandrolone;
    (20) Oxandrolone;
    (21) Oxymesterone;
    (22) Oxymetholone;
    (23) Stanolone;
    (24) Stanozolol;
    (25) Testolactone;
    (26) Testosterone;
    (27) Trenbolone; and
    (28) Any salt, ester, or isomer of a drug or substance described or 
listed in this paragraph, if that salt, ester, or isomer promotes muscle 
growth. Except such term does not include an anabolic steroid which is 
expressly intended for administration through implants to cattle or 
other nonhuman species and which has been approved by the Secretary of 
Health and Human Services for such administration. If any person 
prescribes, dispenses, or distributes such steroid for human use, such 
person shall be considered to have prescribed, dispensed, or distributed 
an anabolic steroid within the meaning of this paragraph.
    (c) The term hearing means any hearing held pursuant to this part 
for the issuance, amendment, or repeal of any rule issuable pursuant to 
section 201 of the Act.
    (d) The term isomer means the optical isomer, except as used in 
Sec. 1308.11(d) and Sec. 1308.12(b)(4). As used in Sec. 1308.11(d), the 
term isomer means the optical, positional, or geometric isomer. As used 
in Sec. 1308.12(b)(4), the term isomer means the optical or geometric 
isomer.
    (e) The term interested person means any person adversely affected 
or aggrieved by any rule or propored rule issuable pursuant to section 
201 of the Act.
    (f) The term narcotic drug means any of the following whether 
produced directly or indirectly by extraction from substances of 
vegetable origin or independently by means of chemical synthesis or by a 
combination of extraction and chemical synthesis:
    (1) Opium, opiates, derivatives of opium and opiates, including 
their isomers, esters, ethers, salts, and salts of isomers, esters, and 
ethers whenever the existence of such isomers, esters, ethers and salts 
is possible within the specific chemical designation. Such term does not 
include the isoquinoline alkaloids of opium.
    (2) Poppy straw and concentrate of poppy straw.
    (3) Coca leaves, except coco leaves and extracts of coca leaves from 
which cocaine, ecgonine and derivatives of ecgonine or their salts have 
been removed.
    (4) Cocaine, its salts, optical and geometric isomers, and salts of 
isomers.
    (5) Ecgonine, its derivatives, their salts, isomers and salts of 
isomers.
    (6) Any compotnd, mixture, or preparation which contains any 
quantity of any of the substances referred to in subparagraphs (1) 
through (5).

[[Page 84]]

    (g) The term proceeding means all actions taken for the issuance, 
amendment, or repeal of any rule issued pursuant to section 201 of the 
Act, commencing with the publication by the Administrator of the 
proposed rule, amended rule, or repeal in the Federal Register.
    (h) Any term not defined in this section shall have the definition 
set forth in section 102 and 1001 of the Act (21 U.S.C. 802 and 951) and 
Sec. 1301.02 of this chapter.

[38 FR 8254, Mar. 30, 1973. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 51 FR 15317, Apr. 23, 1986; 56 FR 5754, Feb. 13, 1991]



Sec. 1308.03   Administration Controlled Substances Code Number.

    (a) Each controlled substance, or basic class thereof, has been 
assigned an ``Administration Controlled Substances Code Number'' for 
purposes of identification of the substances or class on certain 
Certificates of Registration issued by the Administration pursuant to 
Secs. 1301.44 and 1311.43 of this chapter and on certain order forms 
issued by the Administration pursuant to Sec. 1305.05(d) of this 
chapter. Applicants for procurement and/or individual manufacturing 
quotas must include the appropriate code number on the application as 
required in Secs. 1303.12(b) and 1303.22(a) of this chapter. Applicants 
for import and export permits must include the appropriate code number 
on the application as required in Secs. 1312.12(a) and 1312.22(a) of 
this chapter. Authorized registrants who desire to import or export a 
controlled substance for which an import or export permit is not 
required must include the appropriate Administration Controlled 
Substances Code Number beneath or beside the name of each controlled 
substance listed on the DEA Form 236 (Controlled Substance Import/Export 
Declaration) which is executed for such importation or exportation as 
required in Secs. 1312.18(c) and 1312.27(b) of this chapter.
    (b) Except as stated in paragraph (a) of this section, no applicant 
or registrant is required to use the Administration Controlled 
Substances Code Number for any purpose.

[38 FR 8254, Mar. 30, 1973. Redesignated at 38 FR 26609, Sept. 24, 1973 
and amended at 51 FR 15318, Apr. 23, 1986]



Sec. 1308.04   Submission of information by manufacturers.

    (a) Each person who manufactures, packages, repackages, labels, 
relabels, or distributes under his own label any product (including any 
compound, mixture, or preparation, diagnostic, reagent, buffer, or 
biological) containing any quantity of any controlled substance (whether 
such product is itself controlled or is excepted, exempted, or excluded 
from some or all controls pursuant to Sec. 1308.21-24 or Sec. 1308.31-
32) shall submit information required in paragraph (b) of this section 
for each such product being manufactured or sold on July 1, 1972. The 
information should be submitted by registered mail, return receipt 
requested, to the Regulatory Support Section, Attention: Project Label, 
Drug Enforcement Administration, Department of Justice, Washington, DC 
20537, by August 31, 1972. In the case of new products manufactured 
after July 1, 1972, or new dosage forms or other unit forms manufactured 
after July 1, 1972, or changes in information submitted by August 31, 
1972, the registrant shall submit the information regarding such item 
within 30 days after the date on which the manufacture commences or 
information change occurs. In the case of products, the manufacture of 
which is discontinued after July 1, 1972, the registrant shall submit 
notice of such discontinuance within 30 days after the date on which 
manufacture ceases. In the case of products the manufacture of which was 
discontinued before July 1, 1972, which are still being sold, the 
registrant shall submit a notice of such discontinuance with his initial 
submission.
    (b) Two labels or other documents reflecting the following 
information shall be submitted with reference to each dosage form or 
other unit form of each item containing any quantity of any controlled 
substance:
    (1) The trade name, brand name, or other commercial name of the 
product;

[[Page 85]]

    (2) The generic or chemical name and quantity of each active 
ingredient, including both controlled and noncontrolled substances (if 
any of this information is a proprietary trade secret, please indicate 
those portions);
    (3) The National Drug Code Number assigned to the product, if any; 
and
    (4) The weight (in metric measure) of each dosage unit or the weight 
(in metric measure) of the controlled substance per 100 grams of 
finished product for all items containing any quantity of any narcotic 
controlled substance in solid dosage forms.

(21 U.S.C. 821 and 871(b))

[38 FR 8254, Mar. 30, 1973. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 46 FR 28841, May 29, 1981]

                                Schedules



Sec. 1308.11   Schedule I.

    (a) Schedule I shall consist of the drugs and other substances, by 
whatever official name, common or usual name, chemical name, or brand 
name designated, listed in this section. Each drug or substance has been 
assigned the DEA Controlled Substances Code Number set forth opposite 
it.
    (b) Opiates. Unless specifically excepted or unless listed in 
another schedule, any of the following opiates, including their isomers, 
esters, ethers, salts, and salts of isomers, esters and ethers, whenever 
the existence of such isomers, esters, ethers and salts is possible 
within the specific chemical designation (for purposes of paragraph 
(b)(34) only, the term isomer includes the optical and geometric 
isomers):


(1) Acetyl-alpha-methylfentanyl (N-[1-(1-methyl-2-phenethyl)-4-         
 piperidinyl]-N-phenylacetamide).................................   9815
(2) Acetylmethadol...............................................   9601
(3) Allylprodine.................................................   9602
(4) Alphacetylmethadol (except levo-alphacetylmethadol also known       
 as levo-alpha-acetylmethadol, levomethadyl acetate, or LAAM)....   9603
(5) Alphameprodine...............................................   9604
(6) Alphamethadol................................................   9605
(7) Alpha-methylfentanyl (N-[1-(alpha-methyl-beta-phenyl)ethyl-4-       
 piperidyl] propionanilide; 1-(1-methyl-2-phenylethyl)-4-(N-            
 propanilido) piperidine)........................................   9814
(8) Alpha-methylthiofentanyl (N-[1-methyl-2-(2-thienyl)ethyl-4-         
 piperidinyl]-N-phenylpropanamide)...............................   9832
(9) Benzethidine.................................................   9606
(10) Betacetylmethadol...........................................   9607
(11) Beta-hydroxyfentanyl (N-[1-(2-hydroxy-2-phenethyl)-4-              
 piperidinyl]-N-phenylpropanamide)...............................   9830
(12) Beta-hydroxy-3-methylfentanyl (other name: N-[1-(2-hydroxy-2-      
 phenethyl)-3-methyl-4-piperidinyl]-N-phenylpropanamide..........   9831
(13) Betameprodine...............................................   9608
(14) Betamethadol................................................   9609
(15) Betaprodine.................................................   9611
(16) Clonitazene.................................................   9612
(17) Dextromoramide..............................................   9613
(18) Diampromide.................................................   9615
(19) Diethylthiambutene..........................................   9616
(20) Difenoxin...................................................   9168
(21) Dimenoxadol.................................................   9617
(22) Dimepheptanol...............................................   9618
(23) Dimethylthiambutene.........................................   9619
(24) Dioxaphetyl butyrate........................................   9621
(25) Dipipanone..................................................   9622
(26) Ethylmethylthiambutene......................................   9623
(27) Etonitazene.................................................   9624
(28) Etoxeridine.................................................   9625
(29) Furethidine.................................................   9626
(30) Hydroxypethidine............................................   9627
(31) Ketobemidone................................................   9628
(32) Levomoramide................................................   9629
(33) Levophenacylmorphan.........................................   9631
(34) 3-Methylfentanyl (N-[3-methyl-1-(2-phenylethyl)-4-piperidyl]-      
 N-phenylpropanamide)............................................   9813
(35) 3-methylthiofentanyl (N-[(3-methyl-1-(2-thienyl)ethyl-4-           
 piperidinyl]-N-phenylpropanamide)...............................   9833
(36) Morpheridine................................................   9632
(37) MPPP (1-methyl-4-phenyl-4-propionoxypiperidine).............   9661
(38) Noracymethadol..............................................   9633
(39) Norlevorphanol..............................................   9634
(40) Normethadone................................................   9635
(41) Norpipanone.................................................   9636
(42) Para-fluorofentanyl (N-(4-fluorophenyl)-N-[1-(2-phenethyl)-4-      
 piperidinyl] propanamide........................................   9812
(43) PEPAP (1-(-2-phenethyl)-4-phenyl-4-acetoxypiperidine........   9663
(44) Phenadoxone.................................................   9637
(45) Phenampromide...............................................   9638
(46) Phenomorphan................................................   9647
(47) Phenoperidine...............................................   9641
(48) Piritramide.................................................   9642
(49) Proheptazine................................................   9643
(50) Properidine.................................................   9644
(51) Propiram....................................................   9649
(52) Racemoramide................................................   9645
(53) Thiofentanyl (N-phenyl-N-[1-(2-thienyl)ethyl-4-piperidinyl]-       
 propanamide.....................................................   9835
(54) Tilidine....................................................   9750
(55) Trimeperidine...............................................   9646
                                                                        

    (c) Opium derivatives. Unless specifically excepted or unless listed 
in another schedule, any of the following opium derivatives, its salts, 
isomers, and salts of isomers whenever the existence of such salts, 
isomers, and salts of isomers is possible within the specific chemical 
designation:


(1) Acetorphine..................................................   9319
(2) Acetyldihydrocodeine.........................................   9051
(3) Benzylmorphine...............................................   9052
(4) Codeine methylbromide........................................   9070
(5) Codeine-N-Oxide..............................................   9053
(6) Cyprenorphine................................................   9054
(7) Desomorphine.................................................   9055
(8) Dihydromorphine..............................................   9145
(9) Drotebanol...................................................   9335
(10) Etorphine (except hydrochloride salt).......................   9056
(11) Heroin......................................................   9200
(12) Hydromorphinol..............................................   9301
(13) Methyldesorphine............................................   9302
(14) Methyldihydromorphine.......................................   9304
(15) Morphine methylbromide......................................   9305
(16) Morphine methylsulfonate....................................   9306

[[Page 86]]

                                                                        
(17) Morphine-N-Oxide............................................   9307
(18) Myrophine...................................................   9308
(19) Nicocodeine.................................................   9309
(20) Nicomorphine................................................   9312
(21) Normorphine.................................................   9313
(22) Pholcodine..................................................   9314
(23) Thebacon....................................................   9315
                                                                        
                                                                        

    (d) Hallucinogenic substances. Unless specifically excepted or 
unless listed in another schedule, any material, compound, mixture, or 
preparation, which contains any quantity of the following hallucinogenic 
substances, or which contains any of its salts, isomers, and salts of 
isomers whenever the existence of such salts, isomers, and salts of 
isomers is possible within the specific chemical designation (for 
purposes of this paragraph only, the term ``isomer'' includes the 
optical, position and geometric isomers):


(1) Alpha-ethyltryptamine........................................   7249
  Some trade or other names: etryptamine; Monase; -ethyl-      
   1H-indole-3-ethanamine; 3-(2-aminobutyl) indole; -ET;       
   and AET.                                                             
(2) 4-bromo-2,5-dimethoxy-amphetamine............................   7391
  Some trade or other names: 4-bromo-2,5-dimethoxy--           
   methylphenethylamine; 4-bromo-2,5-DMA                                
(3) 4-Bromo-2,5-dimethoxyphenethylamine..........................   7392
  Some trade or other names: 2-(4-bromo-2,5-dimethoxyphenyl)-1-         
   aminoethane; alpha-desmethyl DOB; 2C-B, Nexus.                       
(4) 2,5-dimethoxyamphetamine.....................................   7396
  Some trade or other names: 2,5-dimethoxy--                   
   methylphenethylamine; 2,5-DMA                                        
(5) 2,5-dimethoxy-4-ethylamphet-amine............................   7399
  Some trade or other names: DOET                                       
(6) 4-methoxyamphetamine.........................................   7411
  Some trade or other names: 4-methoxy--                       
   methylphenethylamine; paramethoxyamphetamine, PMA                    
(7) 5-methoxy-3,4-mdthylenedioxy-amphetamine.....................   7401
(8) 4-methyl-2,5-dimethoxy-amphetamine...........................   7395
  Some trade and other names: 4-methyl-2,5-dimethoxy--         
   methylphenethylamine; ``DOM''; and ``STP''                           
(9) 3,4-methylenedioxy amphetamine...............................   7400
(10) 3,4-methylenedioxymethamphetamine (MDMA)....................   7405
(11) 3,4-methylenedioxy-N-ethylamphetamine (also known as N-ethyl-      
 alpha-methyl-3,4(methylenedioxy)phenethylamine, N-ethyl MDA,           
 MDE, MDEA.......................................................   7404
(12) N-hydroxy-3,4-methylenedioxyamphetamine (also known as N-          
 hydroxy-alpha-methyl-3,4(methylenedioxy)phenethylamine, and N-         
 hydroxy MDA.....................................................   7402
(13) 3,4,5-trimethoxy amphetamine................................   7390
(14) Bufotenine..................................................   7433
  Some trade and other names: 3-(-Dimethylaminoethyl)-5-       
   hydroxyindole; 3-(2-dimethylaminoethyl)-5-indolol; N, N-             
   dimethylserotonin; 5-hydroxy-N,N-dimethyltryptamine; mappine         
(15) Diethyltryptamine...........................................   7434
  Some trade and other names: N,N-Diethyltryptamine; DET                
(16) Dimethyltryptamine..........................................   7435
  Some trade or other names: DMT                                        
(17) Ibogaine....................................................   7260
  Some trade and other names: 7-Ethyl-6,6,7,8,9,10,12,13-      
   octahydro-2-methoxy-6,9-methano-5H-pyrido [1', 2':1,2] azepino       
   [5,4-b] indole; Tabernanthe iboga                                    
(18) Lysergic acid diethylamide..................................   7315
(19) Marihuana...................................................   7360
(20) Mescaline...................................................   7381
(21) Parahexyl--7374; some trade or other names: 3-Hexyl-1-             
 hydroxy-7,8,9,10-tetrahydro-6,6,9-trimethyl-6H-                        
 dibenzo[b,d]pyran; Synhexyl.                                           
(22) Peyote......................................................   7415
  Meaning all parts of the plant presently classified botanically       
   as Lophophora williamsii Lemaire, whether growing or not, the        
   seeds thereof, any extract from any part of such plant, and          
   every compound, manufacture, salts, derivative, mixture, or          
   preparation of such plant, its seeds or extracts                     
  (Interprets 21 USC 812(c), Schedule I(c) (12))                        
(23) N-ethyl-3-piperidyl benzilate...............................   7482
(24) N-methyl-3-piperidyl benzilate..............................   7484
(25) Psilocybin..................................................   7437
(26) Psilocyn....................................................   7438
(27) Tetrahydrocannabinols.......................................   7370
  Synthetic equivalents of the substances contained in the plant,       
   or in the resinous extractives of Cannabis, sp. and/or               
   synthetic substances, derivatives, and their isomers with            
   similar chemical structure and pharmacological activity such         
   as the following:                                                    
  1 cis or trans tetrahydrocannabinol, and their optical       
   isomers                                                              
  6 cis or trans tetrahydrocannabinol, and their optical       
   isomers                                                              
  3,4 cis or trans tetrahydrocannabinol, and its optical       
   isomers                                                              
  (Since nomenclature of these substances is not internationally        
   standardized, compounds of these structures, regardless of           
   numerical designation of atomic positions covered.)                  
(28) Ethylamine analog of phencyclidine..........................   7455
  Some trade or other names: N-ethyl-1-phenylcyclohexylamine, (1-       
   phenylcyclohexyl)ethylamine, N-(1-phenylcyclohexyl)ethylamine,       
   cyclohexamine, PCE                                                   
(29) Pyrrolidine analog of phencyclidine.........................   7458
  Some trade or other names: 1-(1-phenylcyclohexyl)-pyrrolidine,        
   PCPy, PHP                                                            
(30) Thiophene analog of phencyclidine...........................   7470
  Some trade or other names: 1-[1-(2-thienyl)-cyclohexyl]-              
   piperidine, 2-thienylanalog of phencyclidine, TPCP, TCP              
(31) 1-[1-(2-thienyl)cyclohexyl]pyrrolidine......................   7473
  Some other names: TCPy                                                
                                                                        

    (e) Depressants. Unless specifically excepted or unless listed in 
another schedule, any material, compound, mixture, or preparation which 
contains any quantity of the following substances having a depressant 
effect on the central nervous system, including its salts, isomers, and 
salts of isomers whenever the existence of such salts, isomers, and 
salts of isomers is possible within the specific chemical designation:

(1) Mecloqualone.................................................   2572
(2) Methaqualone.................................................   2565
                                                                        

    (f) Stimulants. Unless specifically excepted or unless listed in 
another schedule, any material, compound,

[[Page 87]]

mixture, or preparation which contains any quantity of the following 
substances having a stimulant effect on the central nervous system, 
including its salts, isomers, and salts of isomers:


(1) Aminorex (Some other names: aminoxaphen; 2-amino-5-phenyl-2-        
 oxazoline; or 4,5-dihydro-5-phenly-2-oxazolamine)...............   1585
(2) Cathinone....................................................   1235
  Some trade or other names: 2-amino-1-phenyl-1-propanone, alpha-       
   aminopropiophenone, 2-aminopropiophenone, and norephedrone           
(3) Fenethylline.................................................   1503
(4) Methcathinone (Some other names: 2-(methylamino)-                   
 propiophenone; alpha-(methylamino)propiophenone; 2-(methylamino)-      
 1-phenylpropan-1-one; alpha-N-methylaminopropiophenone;                
 monomethylpropion; ephedrone; N-methylcathinone;                       
 methylcathinone; AL-464; AL-422; AL-463 and UR1432), its salts,        
 optical isomers and salts of optical isomers....................   1237
(5) ()cis-4-methylaminorex (()cis-4,5-          
 dihydro-4-methyl-5-phenyl-2-oxazolamine)........................   1590
(6) N-ethylamphetamine...........................................   1475
(7) N,N-dimethylamphetamine (also known as N,N-alpha-trimethyl-         
 benzeneethanamine; N,N-alpha-trimethylphenethylamine)...........   1480
                                                                        
                                                                        

    (g) Temporary listing of substances subject to emergency scheduling. 
Any material, compound, mixture or preparation which contains any 
quantity of the following substances:


(1) N-[1-benzyl-4-piperidyl]-N-phenylpropanamide                        
 (benzylfentanyl), its optical isomers, salts and salts of              
 isomers.........................................................   9818
(2) N-[1-(2-thienyl)methyl-4-piperidyl]-N-phenylpropanamide             
 (thenylfentanyl), its optical isolers, salts and salts of              
 isomers.........................................................   9834
                                                                        


[39 FR 22141, June 20, 1974]

    Editorial Note: For Federal Register citations affecting 
Sec. 1308.11, see the List of CFR Sections Affected in the Finding Aids 
section of this volume.



Sec. 1308.12   Schedule II.

    (a) Schedule II shall consist of the drugs and other substances, by 
whatever official name, common or usual name, chemical name, or brand 
name designated, listed in this section. Each drug or substance has been 
assigned the Controlled Substances Code Number set forth opposite it.
    (b) Substances, vegetable origin or chemical synthesis. Unless 
specifically excepted or unless listed in another schedule, any of the 
following substances whether produced directly or indirectly by 
extraction from substances of vegetable origin, or independently by 
means of chemical synthesis, or by a combination of extraction and 
chemical synthesis:
    (1) Opium and opiate, and any salt, compound, derivative, or 
preparation of opium or opiate excluding apomorphine, thebaine-derived 
butorphanol, dextrorphan, nalbuphine, nalmefene, naloxone, and 
naltrexone, and their respective salts, but including the following:


(1) Raw opium....................................................   9600
(2) Opium extracts...............................................   9610
(3) Opium fluid..................................................   9620
(4) Powdered opium...............................................   9639
(5) Granulated opium.............................................   9640
(6) Tincture of opium............................................   9630
(7) Codeine......................................................   9050
(8) Ethylmorphine................................................   9190
(9) Etorphine hydrochloride......................................   9059
(10) Hydrocodone.................................................   9193
(11) Hydromorphone...............................................   9150
(12) Metopon.....................................................   9260
(13) Morphine....................................................   9300
(14) Oxycodone...................................................   9143
(15) Oxymorphone.................................................   9652
(16) Thebaine....................................................   9333
                                                                        

    (2) Any salt, compound, derivative, or preparation thereof which is 
chemically equivalent or identical with any of the substances referred 
to in paragraph (b) (1) of this section, except that these substances 
shall not include the isoquinoline alkaloids of opium.
    (3) Opium poppy and poppy straw.
    (4) Coca leaves (9040) and any salt, compound, derivative or 
preparation of coca leaves (including cocaine (9041) and ecgonine (9180) 
and their salts, isomers, derivatives and salts of isomers and 
derivatives), and any salt, compound, derivative, or preparation thereof 
which is chemically equivalent or identical with any of these 
substances, except that the substances shall not include decocainized 
coca leaves or extraction of coca leaves, whhch extractions do not 
contain cocaine or ecgonine.
    (5) Concentrate of poppy straw (the crude extract of poppy straw in 
either liquid, solid or powder form which contains the phenanthrene 
alkaloids of the opium poppy), 9670.
    (c) Opiates. Unless specifically excepted or unless in another 
schedule any of the following opiates, including its isomers, esters, 
ethers, salts and salts of isomers, esters and ethers

[[Page 88]]

whenever the existence of such isomers, esters, ethers, and salts is 
possible within the specific chemical designation, dextrorphan and 
levopropoxyphene excepted:


(1) Alfentanil...................................................   9737
(2) Alphaprodine.................................................   9010
(3) Anileridine..................................................   9020
(4) Bezitramide..................................................   9800
(5) Bulk dextropropoxyphene (non-dosage forms)...................   9273
(6) Carfentanil..................................................   9743
(7) Dihydrocodeine...............................................   9120
(8) Diphenoxylate................................................   9170
(9) Fentanyl.....................................................   9801
(10) Isomethadone................................................   9226
(11) Levo-alphacetylmethadol.....................................   9648
  [Some other names: levo-alpha-acetylmethadol, levomethadyl            
   acetate, LAAM]                                                       
(12) Levomethorphan..............................................   9210
(13) Levorphanol.................................................   9220
(14) Metazocine..................................................   9240
(15) Methadone...................................................   9250
(16) Methadone-Intermediate, 4-cyano-2-dimethylamino-4,4-diphenyl       
 butane..........................................................   9254
(17) Moramide-Intermediate, 2-methyl-3-morpholino-1, 1-                 
 diphenylpropane-carboxylic acid.................................   9802
(18) Pethidine (meperidine)......................................   9230
(19) Pethidine-Intermediate-A, 4-cyano-1-methyl-4-                      
 phenylpiperidine................................................   9232
(20) Pethidine-Intermediate-B, ethyl-4-phenylpiperidine-4-              
 carboxylate.....................................................   9233
(21) Pethidine-Intermediate-C, 1-methyl-4-phenylpiperidine-4-           
 carboxylic acid.................................................   9234
(22) Phenazocine.................................................   9715
(23) Piminodine..................................................   9730
(24) Racemethorphan..............................................   9732
(25) Racemorphan.................................................   9733
(26) Sufentanil..................................................   9740
                                                                        

    (d) Stimulants. Unless specifically excepted or unless listed in 
another schedule, any material, compound, mixture, or preparation which 
contains any quantity of the following substances having a stimulant 
effect on the central nervous system:


(1) Amphetamine, its salts, optical isomers, and salts of its           
 optical isomers.................................................   1100
(2) Methamphetamine, its salts, isomers, and salts of its isomers   1105
(3) Phenmetrazine and its salts..................................   1631
(4) Methylphenidate..............................................   1724
                                                                        

    (e) Depressants. Unless specifically excepted or unless listed in 
another schedule, any material, compound, mixture, or preparation which 
contains any quantity of the following substances having a depressant 
effect on the central nervous system, including its salts, isomers, and 
salts of isomers whenever the existence of such salts, isomers, and 
salts of isomers is possible within the specific chemical designation:


(1) Amobarbital..................................................   2125
(2) Glutethimide.................................................   2550
(3) Pentobarbital................................................   2270
(4) Phencyclidine................................................   7471
(5) Secobarbital.................................................   2315
                                                                        

    (f) Hallucinogenic substances.


(1) Dronabinol (synthetic) in sesame oil and encapsulated in a          
 soft gelatin capsule in a U.S. Food and Drug Administration            
 approved drug product...........................................   7369
  [Some other names for dronabinol: (6aR-trans)-6a,7,8,10a-             
   tetrahydro-6,6,9-trimethyl-3-pentyl-6H-dibenzo[b,d]pyran-1-ol,       
   or (-)-delta-9-(trans)-tetrahydrocannabinol]                         
(2) Nabilone.....................................................   7379
  [Another name for nabilone: ()-trans-3-(1,1-              
   dimethylheptyl)-6,6a,7,8,10,10a-hexahydro-1-hydroxy-6,6-             
   dimethyl-9H-dibenzo[b,d]pyran-9-one]                                 
                                                                        

    (g) Immediate prectrsors. Unless specifically excepted or unless 
listed in another schedule, any material, compound, mixture, or 
preparation which contains any quantity of the following substances:
    (1) Immediate precursor to amphetamine and methamphetamine:


(i) Phenylacetone................................................   8501
  Some trade or other names: phenyl-2-propanone; P2P; benzyl            
   methyl ketone; methyl benzyl ketone;                                 
                                                                        


    (2) Immediate precursors to phencyclidine (PCP):


(i) 1-phenylcyclohexylamine......................................   7460
(ii) 1-piperidinocyclohexanecarbonitrile (PCC)...................   8603
                                                                        

[39 FR 22142, June 20, 1974]

    Editorial Note: For Federal Register citations affecting 
Sec. 1308.12, see the List of CFR Sections Affected in the Finding Aids 
section of this volume.



Sec. 1308.13   Schedule III.

    (a) Schedule III shall consist of the drugs and other substances, by 
whatever official name, common or usual name, chemical name, or brand 
name designated, listed in this section. Each drug or substance has been 
assigned the DEA Controlled Substances Code Number set forth opposite 
it.
    (b) Stimulants. Unless specifically excepted or unless listed in 
another schedule, any material, compound, mixture, or preparation which 
contains any quantity of the following substances having a stimulant 
effect on the central nervous sxstem, including its salts, isomers 
(whether optical, position, or geometric), and salts of such isomers 
whenever the existence of such salts, isomers, and salts of isomers is

[[Page 89]]

possible within the specific chemical designation:


(1) Those compounds, mixtures, or preparations in dosage unit           
 form containing any stimulant substances lirted in schedule II         
 which compounds, mixtures, or preparations were listed on August       
 25, 1971, as excepted compounds under Sec.  308.32, and any            
 other drug of the quantitive composition shown in that list for        
 those drugs or which is the same except that it contains a             
 lesser quantity of controlled substances........................   1405
(2) Benzphetamine................................................   1228
(3) Chlorphentermine.............................................   1645
(4) Clortermine..................................................   1647
(5) Phendimetrazine..............................................   1615
                                                                        

    (c) Depressants. Unless specifically excepted or unless listed in 
another schedule, any material, compound, mixture, or preparation which 
contains any quantity of the following substances having a depressant 
effect on the central nervous system:


(1) Any compound, mixture or preparation containing:                    
    (i) Amobarbital..............................................   2126
    (ii) Secobarbital............................................   2316
    (iii) Pentobarbital..........................................   2271
  or any salt thereof and one or more other active medicinal            
   ingredients which are not listed in any schedule.                    
(2) Any suppository dosage form containing:                             
    (i) Amobarbital..............................................   2126
    (ii) Secobarbital............................................   2316
    (iii) Pentobarbital..........................................   2271
  or any salt of any of these drugs and approved by the Food and        
   Drug Administration for marketing only as a suppository.             
(3) Any substance which contains any quantity of a derivative of        
 barbituric acid or any salt thereof.............................   2100
(4) Chlorhexadol.................................................   2510
(5) Lysergic acid................................................   7300
(6) Lysergic acid amide..........................................   7310
(7) Methyprylon..................................................   2575
(8) Sulfondiethylmethane.........................................   2600
(9) Sulfonethylmethane...........................................   2605
(10) Sulfonmethane...............................................   2610
(11) Tiletamine and zolazepam or any salt thereof................   7295
  Some trade or other names for a tiletamine-zolazepam                  
   combination product:                                                 
    Telazol......................................................       
  Some trade or other names for tiletamine:                             
    2-(ethylamino)-2-(2-thienyl)-cyclohexanone...................       
  Some trade or other names for zolazepam:                              
    4-(2-fluorophenyl)-6,8-dihydro-1,3,8-trimethylpyrazolo-[3,4-        
     e] [1,4]-diazepin-7(1H)-one, flupyrazapon...................       
                                                                        

    (d) Nalorphine 9400.
    (e) Narcotic Drugs. Unless specifically excepted or unless listed in 
another schedule, any material, compound, mixture, or preparation 
containing any of the following narcotic drugs, or their salts 
calculated as the free anhydrous base or alkaloid, in limited quantities 
as set forth below:


(1) Not more than 1.8 grams of codeine per 100 milliliters or not       
 more than 90 milligrams per dosage unit, with an equal or              
 greater quantity of an isoquinoline alkaloid of opium...........   9803
(2) Not more than 1.8 grams of codeine per 100 milliliters or not       
 more than 90 milligrams per dosage unit, with one or more              
 active, nonnarcotic ingredients in recognized therapeutic              
 amounts.........................................................   9804
(3) Not more than 300 milligrams of dihydrocodeinone                    
 (hydrocodone) per 100 milliliters or not more than 15 milligrams       
 per dosage unit, with a fourfold or greater quantity of an             
 isoquinoline alkaloid of opium..................................   9805
(4) Not more than 300 milligrams of dihydrocodeinone                    
 (hydrocodone) per 100 milliliters or not more than 15 milligrams       
 per dosage unit, with one or more active nonnarcotic ingredients       
 in recognized therapeutic amounts...............................   9806
(5) Not more than 1.8 grams of dihydrocodeine per 100 milliliters       
 or not more than 90 milligrams per dosage unit, with one or more       
 active nonnarcotic ingredients in recognized therapeutic amounts   9807
(6) Not more than 300 milligrams of ethylmorphine per 100               
 milliliters or not more than 15 milligrams per dosage unit, with       
 one or more active, nonnarcotic ingredients in recognized              
 therapeutic amounts.............................................   9808
(7) Not more than 500 milligrams of opium per 100 milliliters or        
 per 100 grams or not more than 25 milligrams per dosage unit,          
 with one or more active, nonnarcotic ingredients in recognized         
 therapeutic amounts.............................................   9809
(8) Not more than 50 milligrams of morphine per 100 milliliters         
 or per 100 grams, with one or more active, nonnarcotic                 
 ingredients in recognized therapeutic amounts...................   9810
                                                                        

    (f) Anabolic steroids. Unless specifically excepted or unless listed 
in another schedule, any material, compound, mixture, or preparation 
containing any quantity of the following substances, including its 
salts, isomers, and salts of isomers whenever the existence of such 
salts of isomers is possible within the specific chemical designation:

(1) Anabolic Steroids...............................................4000

[39 FR 22142, June 20, 1974, as amended at 41 FR 43401, Oct. 1, 1976; 43 
FR 3359, Jan. 25, 1978; 44 FR 40888, July 13, l979; 46 FR 52334, Oct. 
27, 1981; 51 FR 5320, Feb. 13, 1986; 52 FR 2222, Jan. 21, 1987; 52 FR 
5952, Feb. 27, 1987; 56 FR 5754, Feb. 13, 1991; 56 FR 11932, Mar. 21, 
1991]



Sec. 1308.14   Schedule IV.

    (a) Schedule IV shall consist of the drugs and other substances, by 
whatever official name, common or usual name, chemical name, or brand 
name designated, listed in this section. Each drug or substance has been 
assigned the DEA Controlled Substances Code Number set forth opposite 
it.
    (b) Narcotic drugs. Unless specifically excepted or unless listed in 
another schedule, any material, compound, mixture, or preparation 
containing any

[[Page 90]]

of the following narcotic drugs, or their salts calculated as the free 
anhydrous base or alkaloid, in limited quantities as set forth below:


(1) Not more than 1 milligram of difenoxin and not less than 25         
 micrograms of atropine sulfate per dosage unit..................   9167
(2) Dextropropoxyphene (alpha-(+)-4-dimethylamino-1,2-diphenyl-3-       
 methyl-2-propionoxybutane)......................................   9278
                                                                        

    (c) Depressants. Unless specifically excepted or unless listed in 
another schedule, any material, compound, mixture, or preparation which 
contains any quantity of the following substances, including its salts, 
isomers, and salts of isomers whenever the existence of such salts, 
isomers, and salts of isomers is possible within the specific chemical 
designation:


(1)  Alprazolam.................................................    2882
(2)  Barbital...................................................    2145
(3)  Bromazepam.................................................    2748
(4)  Camazepam..................................................    2749
(5)  Chloral betaine............................................    2460
(6)  Chloral hydrate............................................    2465
(7)  Chlordiazepoxide...........................................    2744
(8)  Clobazam...................................................    2751
(9)  Clonazepam.................................................    2737
(10) Clorazepate................................................    2768
(11) Clotiazepam................................................    2752
(12) Cloxazolam.................................................    2753
(13) Delorazepam................................................    2754
(14) Diazepam...................................................    2765
(15) Estazolam..................................................    2756
(16) Ethchlorvynol..............................................    2540
(17) Ethinamate.................................................    2545
(18) Ethyl loflazepate..........................................    2758
(19) Fludiazepam................................................    2759
(20) Flunitrazepam..............................................    2763
(21) Flurazepam.................................................    2767
(22) Halazepam..................................................    2762
(23) Haloxazolam................................................    2771
(24) Ketazolam..................................................    2772
(25) Loprazolam.................................................    2773
(26) Lorazepam..................................................    2885
(27) Lormetazepam...............................................    2774
(28) Mebutamate.................................................    2800
(29) Medazepam..................................................    2836
(30) Meprobamate................................................    2820
(31) Methohexital...............................................    2264
(32) Methylphenobarbital (mephobarbital)........................    2250
(33) Midazolam..................................................    2884
(34) Nimetazepam................................................    2837
(35) Nitrazepam.................................................    2834
(36) Nordiazepam................................................    2838
(37) Oxazepam...................................................    2835
(38) Oxazolam...................................................    2839
(39) Paraldehyde................................................    2585
(40) Petrichloral...............................................    2591
(41) Phenobarbital..............................................    2285
(42) Pinazepam..................................................    2883
(43) Prazepam...................................................    2764
(44) Quazepam...................................................    2881
(45) Temazepam..................................................    2925
(46) Tetrazepam.................................................    2886
(47) Triazolam..................................................    2887
(48) Zolpidem...................................................    2783
                                                                        

    (d) Fenfluramine. Any material, compound, mixture, or preparation 
which contains any quantity of the following substances, including its 
salts, isomers (whether optical, position, or geometric), and salts of 
such isomers, whenever the existence of such salts, isomers, and salts 
of isomers is possible:


(1) Fenfluramine.................................................   1670
                                                                        

    (e) Stimulants. Unless specifically excepted or unless listed in 
another schedule, any material, compound, mixture, or preparation which 
contains any quantity of the following substances having a stimulant 
effect on the central nervous system, including its salts, isomers and 
salts of isomers:


(1) Cathine ((+)-norpseudoephedrine).............................   1230
(2) Diethylpropion...............................................   1610
(3) Fencamfamin..................................................   1760
(4) Fenproporex..................................................   1575
(5) Mazindol.....................................................   1605
(6) Mefenorex....................................................   1580
(7) Pemoline (including organometallic complexes and chelates           
 thereof)........................................................   1530
(8) Phentermine..................................................   1640
(9) Pipradrol....................................................   1750
(10) SPA ((-)-1-dimethylamino-1,2-diphenylethane)................   1635
                                                                        

    (f) Other substances. Unless specifically excepted or unless listed 
in another schedule, any material, compound, mixture or preparation 
which contains any quantity of the following substances, including its 
salts:

(1) Pentazocine..................................................   9709
                                                                        

[39 FR 22143, June 20, 1974]

    Editorial Note: For Federal Register citations affecting 
Sec. 1308.14, see the List of CFR Sections Affected in the Finding Aids 
section of this volume.



Sec. 1308.15   Schedule V.

    (a) Schedule V shall consist of the drugs and other substances, by 
whatever official name, common or usual name, chemical name, or brand 
name designated, listed in this section.
    (b) Narcotic drugs. Unless specifically excepted or unless listed in 
another schedule, any material, compound, mixture, or preparation 
containing any of the following narcotic drugs and their salts, as set 
forth below:

(1) Buprenorphine................................................   9064
                                                                        

    (c) Narcotic drugs containing non-narcotic active medicinal 
ingredients. Any compound, mixture, or preparation containing any of the 
following

[[Page 91]]

narcotic drugs, or their salts calculated as the free anhydrous base or 
alkaloid, in limited quantities as set forth below, which shall include 
one or more non-narcotic active medicinal ingredients in sufficient 
proportion to confer upon the compound, mixture, or preparation valuable 
medicinal qualities other than those possessed by narcotic drugs alone:
    (1) Not more than 200 milligrams of codeine per 100 milliliters or 
per 100 grams.
    (2) Not more than 100 milligrams of dihydrocodeine per 100 
milliliters or per 100 grams.
    (3) Not more than 100 milligrams of ethylmorphine per 100 
milliliters or per 100 grams.
    (4) Not more than 2.5 milligrams of diphenoxylate and not less than 
25 micrograms of atropine sulfate per dosage unit.
    (5) Not more than 100 milligrams of opium per 100 milliliters or per 
100 grams.
    (6) Not more than 0.5 milligram of difenoxin and not less than 25 
micrograms of atropine sulfate per dosage unit.
    (d) Stimulants. Unless specifically exempted or excluded or unless 
listed in another schedule, any material, compound, mixture, or 
preparation which contains any quantity of the following substances 
having a stimulant effect on the central nervous system, including its 
salts, isomers and salts of isomers:

(1) Pyrovalerone...................................................1485.
(2)  [Reserved]

[39 FR 22143, June 20, 1974, as amended at 43 FR 38383, Aug. 28, 1978; 
44 FR 40888, July 13, 1979; 47 FR 49841, Nov. 3, 1982; 50 FR 8108, Feb. 
28, 1985; 52 FR 5952, Feb. 27, 1987; 53 FR 10870, Apr. 4, 1988; 56 FR 
61372, Dec. 3, 1991]

                     Excluded Nonnarcotic Substances



Sec. 1308.21   Application for exclusion of a nonnarcotic substance.

    (a) Any person seeking to have any nonnarcotic substance which may, 
under the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 301), be 
lawfully sold over the counter without a prescription, excluded from any 
schedule, pursuant to section 201(g) (1) of the Act (21 U.S.C. 811 (g) 
(1)), may apply to the Administrator, Drug Enforcement Administration, 
Department of Justice, Washington, DC 20537.
    (b) An application for an exclusion under this section shall contain 
the following information:
    (1) The name and address of the applicant;
    (2) The name of the substance for which exclusion is sought; and
    (3) The complete quantitative composition of the substance.
    (c) Within a reasonable period of time after the receipt of an 
application for an exclusion under this section, the Administrator shall 
notify the applicant of his acceptance or nonacceptance of his 
application, and if not accepted, the reason therefore. The 
Administrator need not accept an application for filing if any of the 
requirements prescribed in paragraph (b) of this section is lacking or 
is not set forth as to be readily understood. If the applicant desires, 
he may amend the application to meet the requirements of paragraph (b) 
of this section. If the application is accepted for filing, the 
Administrator shall issue and publish in the Federal Register his order 
on the application, which shall include a reference to the legal 
authority under which the order is issued and the findings of fact and 
conclusions of law upon which the order is based. This order shall 
specify the date on which it shall take effect. The Administrator shall 
permit any interested person to file written comments on or objections 
to the order within 60 days of the date of publication of his order in 
the Federal Register. If any such comments or objections raise 
significant issues regarding any finding of fact or conclusion of law 
upon which the order is based, the Administrator shall immediately 
suspend the effectiveness of the order until he may reconsider the 
application in light of the comments and objections filed. Thereafter, 
the Administrator shall reinstate, revoke, or amend his original order 
as he determines appropriate.
    (d) The Administrator may at any time revoke any exclusion granted 
pursuant to section 201(g) of the Act (21 U.S.C. 811(g)) by following 
the procedures set forth in paragraph (c) of this section for handling 
an application for

[[Page 92]]

an exclusion which has been accepted for filing.



Sec. 1308.22   Excluded substances.

    The following nonnarcotic substances which may, under the Federal 
Food, Drug, and Cosmetic Act (21 U.S.C. 301), be lawfully sold over the 
counter without a prescription, are excluded from all schedules pursuant 
to section 201(g) (1) of the Act (21 U.S.C. 811(g) (1)):

                                          Excluded Nonarcotic Products                                          
----------------------------------------------------------------------------------------------------------------
                                                                                     Controlled       (mg or mg/
            Company                  Trade name         NDC code        Form          substance          ml)    
----------------------------------------------------------------------------------------------------------------
Bioline Laboratories...........  Theophed..........      00719-1945  TB          Phenobarbital.....         8.00
Goldline Laboratories..........  Guiaphed Elixir...      00182-1377  EL          Phenobarbital.....         4.00
Goldline Laboratories..........  Tedrigen Tablets..      00182-0134  TB          Phenobarbital.....         8.00
Hawthorne Products Inc.........  Choate's Leg        ..............  LQ          Chloral hydrate...       246.67
                                  Freeze.                                                                       
Parke-Davis & Co...............  Tedral............      00071-0230  TB          Phenobarbital.....         8.00
Parke-Davis & Co...............  Tedral Elixir.....      00071-0242  EX          Phenobarbital.....        40.00
Parke-Davis & Co...............  Tedral S.A........      00071-0231  TB          Phenobarbital.....         8.00
Parke-Davis & Co...............  Tedral Suspension.      00071-0237  SU          Phenobarbital.....        80.00
Parmed Pharmacy................  Asma-Ese..........      00349-2018  TB          Phenobarbital.....         8.10
Rondex Labs....................  Azma-Aids.........      00367-3153  TB          Phenobarbital.....         8.00
Smith Kline Consumer...........  Benzedrex.........      49692-0928  IN          Propylhexedrine...       250.00
Sterling Drug, Inc.............  Bronkolixir.......      00057-1004  EL          Phenobarbital.....         0.80
Sterling Drug, Inc.............  Bronkotabs........      00057-1005  TB          Phenobarbital.....         8.00
Vicks Chemical Co..............  Vicks Inhaler.....      23900-0010  IN          I-Desoxyephedrine.       113.00
White Hall Labs................  Primatene (P-           00573-2940  TB          Phenobarbital.....         8.00
                                  tablets).                                                                     
----------------------------------------------------------------------------------------------------------------

[38 FR 8255, Mar. 30, 1973. Redesignated at 38 FR 26609, Sept. 24, l973, 
and amended at 41 FR 16553, Apr. 20, 1976; 41 FR 53477, Dec. 7, 1976; 46 
FR 51603, Oct. 21, 1981; 47 FR 45867, Oct. 14, 1982; 54 FR 2100, Jan. 
19, 1989; 55 FR 12162, Mar. 30, 1990]

                      Exempt Chemical Preparations



Sec. 1308.23   Exemption of certain chemical preparations; application.

    (a) The Administrator may, by regulation, exempt from the 
application of all or any part of the Act any chemical preparation or 
mixture containing one or more controlled substances listed in any 
schedule, which preparation or mixture is intended for laboratory, 
industrial, educational, or special research purposes and not for 
general administration to a human being or other animal, if the 
preparation or mixture either:
    (1) Contains no narcotic controlled substance and is packaged in 
such a form or concentration that the packaged quantity does not present 
any significant potential for abuse (the type of packaging and the 
history of abuse of the same or similar preparations may be considered 
in determining the potential for abuse of the preparation or mixture); 
or
    (2) Contains either a narcotic or nonnarcotic controlled substance 
and one or more adulterating or denaturing agents in such a manner, 
combination, quantity, proportion, or concentration, that the 
preparation or mixture does not present any potential for abuse. If the 
preparation or mixture contains a narcotic controlled substance, the 
preparation or mixture must be formulated in such a manner that it 
incorporates methods of denaturing or other means so that the 
preparation or mixture is not liable to be abused or have ill effects, 
if abused, and so that the narcotic substance cannot in practice be 
removed.
    (b) Any person seeking to have any preparation or mixture containing 
a controlled substance and one or more noncontrolled substances exempted 
from the application of all or any part of the Act, pursuant to 
paragraph (a) of this section, may apply to the Administrator, Drug 
Enforcement Administration, Department of Justice, Washington, DC 20537.
    (c) An application for an exemption under this section shall contain 
the following information:
    (1) The name, address, and registration number, if any, of the 
applicant;
    (2) The name, address, and registration number, if any, of the 
manufacturer or importer of the preparation or mixture, if not the 
applicant;

[[Page 93]]

    (3) The exact trade name or other designation of the preparation or 
mixture;
    (4) The complete qualitative and quantitative composition of the 
preparation or mixture (including all active and inactive ingredients 
and all controlled and noncontrolled substances);
    (5) The form of the immediate container in which the preparation or 
mixture will be distributed with sufficient descriptive detail to 
identify the preparation or mixture (e.g., bottle, packet, vial, soft 
plastic pillow, agar gel plate, etc.);
    (6) The dimensions or capacity of the immediate container of the 
preparation or mixture;
    (7) The label and labeling, as defined in Sec. 1302.01 of this 
chapter, of the immediate container and the commercial containers, if 
any, of the preparation or mixture;
    (8) A brief statement of the facts which the applicant believes 
justify the granting of an exemption under this paragraph, including 
information on the use to which the preparation or mixture will be put;
    (9) The date of the application; and
    (10) Which of the information submitted on the application, if any, 
is deemed by the applicant to be a trade secret or otherwise 
confidential and entitled to protection under subsection 402(a)(8) of 
the Act (21 U.S.C. 842(a) (8)) or any other law restricting public 
disclosure of information.
    (d) The Administrator may require the applicant to submit such 
documents or written statements of fact relevant to the application as 
he deems necessary to determine whether the application should be 
granted.
    (e) Within a reasonable period of time after the receipt of an 
application for an exemption under this section, the Administrator shall 
notify the applicant of his acceptance or nonacceptance of his 
application, and if not accepted, the reason therefor. The Administrator 
need not accept an application for filing if any of the requirements 
prescribed in paragraph (c) or requested pursuant to paragraph (d) is 
lacking or is not set forth as to be readily understood. If the 
applicant desires, he may amend the application to meet the requirements 
of paragraphs (c) and (d) of this section. If the application is 
accepted for filing, the Administrator shall issue and publish in the 
Federal Register his order on the application, which shall include a 
reference to the legal authority under which the order is based. This 
order shall specify the date on which it shall take effect. The 
Administrator shall permit any interested person to file written 
comments on or objections to the order within 60 days of the date of 
publication of his order in the Federal Register. If any such comments 
or objections raise significant issues regarding any finding of fact or 
conclusion of law upon which the order is based, the Administrator shall 
immediately suspend the effectiveness of the order until he may 
reconsider the application in light of the comments and objections 
filed. Thereafter, the Administrator shall reinstate, revoke, or amend 
his original order as he determines appropriate.
    (f) The Administrator may at any time revoje or modify any exemption 
granted pursuant to this section by following the procedures set forth 
in paragraph (e) of this section for handling an application for an 
exemption which has been accepted for filing. The Administrator may also 
modify or revoke the criteria by which exemptions are granted (and 
thereby modify or revoke all preparations and mixtures granted under the 
old criteria) and modify the scope of exemptions at any time.

[38 FR 8254, Mar. 30, 1973. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 46 FR 28841, May 29, 1981]



Sec. 1308.24   Exempt chemical preparations.

    (a) The chemical preparations and mixtures set forth in paragraph 
(i) of this section have been exempted by the Administrator from 
application of sections 302, 303, 305, 306, 307, 308, 309, 1002, 1003 
and 1004 of the Act (21 U.S.C. 822-3, 825-9, 952-4) and Sec. 1301.74 of 
this chapter, to the extent described in paragraphs (b) to (h) of this 
section. Substances set forth in paragraph (j) shall be exempt from the 
application of sections 305, 306, 307, 308, 309, 1002, 1003 and 1004 of 
the Act (21 U.S.C. 825-9, 952-4) and Secs. 1301.71-1301.73 and 
1301.74(a), (b),

[[Page 94]]

(d), (e) and (f) of this chapter to the extent as hereinafter may be 
provided.
    (b) Registration and security: Any person who manufactures an exempt 
chemical preparation or mixture must be registered under the Act and 
comply with all relevant security requirements regarding controlled 
substances being used in the manufacturing process until the preparation 
or mixture is in the form described in paragraph (i) of this section. 
Any other person who handles an exempt chemical preparation after it is 
in the form described in paragraph (i) of this section is not required 
to be registered under the Act to handle that preparation, and the 
preparation is not required to be stored in accordance with security 
requirements regarding controlled substances.
    (c) Labeling: In lieu of the requirements set forth in part 1302 of 
this chapter, the label and the labeling of an exempt chemical 
preparation must be prominently marked with its full trade name or other 
description and the name of the manufacturer or supplier as set forth in 
paragraph (i) of this section, in such a way that the product can be 
readily identified as an exempt chemical preparation. The label and 
labeling must also include in a prominent manner the statement ``For 
industrial use only'' or ``For chemical use only'' or ``For in vitro use 
only--not for human or animal use'' or ``Diagnostic reagent--for 
professional use only'' or a comparable statement warning the person 
reading it that human or animal use is not intended. The symbol 
designating the schedule of the controlled substance is not required on 
either the label or the labeling of the exempt chemical preparation, nor 
is it necessary to list all ingredients of the preparation.
    (d) Records and reports: Any person who manufactures an exempt 
chemical preparation or mixture must keep complete and accurate records 
and file all reports required under part 1304 of this chapter regarding 
all controlled substances being used in the manufacturing process until 
the preparation or mixture is in the form described in paragraph (i) of 
this section. In lieu of records and reports required under part 1304 of 
this chapter regarding exempt chemical preparations, the manufacturer 
need only record the name, address, and registration number, if any, of 
each person to whom the manufacturer distributes any exempt chemical 
preparation. Each importer or exporter of an exempt narcotic chemical 
preparation must submit a semiannual report of the total quantity of 
each substance imported or exported in each calendar half-year within 30 
days of the close of the period to the Drug Control Section, Drug 
Enforcement Administration, Department of Justice, Washington, DC 20537. 
Any other person who handles an exempt chemical preparation after it is 
in the form described in paragraph (i) of this section is not required 
to maintain records or file reports.
    (e) Quotas, order forms, prescriptions, import, export, and 
transshipment requirements: Once an exempt chemical preparation is in 
the form described in paragraph (i) of this section, the requirements 
regarding quotas, order forms, prescriptions, import permits and 
declarations, export permit and declarations, and transshipment and 
intransit permits and declarations do not apply. These requirements do 
apply, however, to any controlled substances used in manufacturing the 
exempt chemical preparation before it is in the form described in 
paragraph (i) of this section.
    (f) Criminal penalties: No exemption granted pursuant to 
Sec. 1308.23 affects the criminal liability for illegal manufacture, 
distribution, or possession of controlled substances contained in the 
exempt chemical preparation. Distribution, possession, and use of an 
exempt chemical preparation are lawful for registrants and 
nonregistrants only as long as such distribution, possession, or use is 
intended for laboratory, industrial, or educational purposes and not for 
immediate or subsequent administration to a human being or other animal.
    (g) Bulk materials: For materials exempted in bulk quantities, the 
Administrator may prescribe requirements other than those set forth in 
paragraphs (b) through (e) of this section on a case-by-case basis.
    (h) Changes in chemical preparations: Any change in the quantitative 
or

[[Page 95]]

qualitative composition of the preparation or mixture after the date of 
application, or change in the trade name or other designation of the 
preparation or mixture, set forth in paragraph (i) of this section, 
requires a new application for exemption.
    (i) The following preparations and mixtures, in the form and 
quantity listed in the application submitted (indicated as the ``date of 
application'') are designated as exempt chemical preparations for the 
purposes set forth in this section:

                                          Exempt Chemical Preparations                                          
----------------------------------------------------------------------------------------------------------------
                Supplier                           Product name                      Form                Date   
----------------------------------------------------------------------------------------------------------------
Aalto Scientific, LTD..................  Therapeutic Drug Monitoring      Vial: 5ml................      4/09/91
                                          Control Level I, II, III                                              
                                          Freeze Dried.                                                         
Abbott Laboratories....................  125I Cholylglycyltyrosine        Plastic Bottle: 20ml.....      4/07/78
                                          Reagent Solution, No. 7816.                                           
Abbott Laboratories....................  ADx Benzoylecgonine Fluorescein  Bottle: 3.2 ml...........     12/02/86
                                          Tracer Solution.                                                      
Abbott Laboratories....................  ADx Cannabinoids Fluorescein     Bottle: 3.2ml............     12/02/86
                                          Tracer Solution.                                                      
Abbott Laboratories....................  ADx Cannabinoids Reagent Pack    Reagent Pack: 50 tests...     12/02/86
                                          (No. 9671-55).                                                        
Abbott Laboratories....................  ADx Cocaine Metabolite           Vial: 3.2ml, Kit: 100          4/18/89
                                          Fluorescein Tracer Solution,     vials.                               
                                          No. 9670-T, No. 9670T0013.                                            
Abbott Laboratories....................  ADx Cocaine Metabolite Reagent   50 Test Unit.............      4/18/89
                                          Pack, No. 9670-55.                                                    
Abbott Laboratories....................  ADx Opiates Fluorescein Tracer   Vial: 3.2ml, Kit: 100          4/18/89
                                          Solution, No. 9673-T, No.        vials.                               
                                          9673T0013.                                                            
Abbott Laboratories....................  ADx Opiates Reagent Pack, No.    50 Test Unit.............      4/18/89
                                          9673-55.                                                              
Abbott Laboratories....................  ADx Propoxyphene Fluorescein     Box: 100 bottles or less.     11/30/90
                                          Tracer Solutions Item No.                                             
                                          9675T0011.                                                            
Abbott Laboratories....................  ADx Propoxyphene Reagent Pack    Kit: 50 test.............     11/30/90
                                          Item No.9675-55.                                                      
Abbott Laboratories....................  Advisor (4 Track); Code 9A18-21  Kit: 40 Discs............      3/25/94
Abbott Laboratories....................  Advisor Cannabinoids Bulk        Flasks: 6L, 4L, 2L, 1L,        4/10/92
                                          Tracer No.76224.                 500ml, 250ml, 200ml,                 
                                                                           100ml; Bottles: 950ml,               
                                                                           500ml, 100ml, 50ml, 5ml;             
                                                                           Amp: 20ml, 10ml, 5ml,                
                                                                           2ml.                                 
Abbott Laboratories....................  Advisor Card & Cover No.07A15..  Box: 2000 Cards..........      4/10/92
Abbott Laboratories....................  Advisor Card & Tracer No.07A14.  Box: 2000 Cards..........      4/10/92
Abbott Laboratories....................  Advisor Card with Cover; Code #  Box: 2000 Cards..........      3/25/94
                                          05B08.                                                                
Abbott Laboratories....................  Advisor Card with Tracer; Code   Box: 2000 Cards..........      3/25/94
                                          # 05B07.                                                              
Abbott Laboratories....................  Advisor Cocaine Bulk Tracer (in- Flasks: 6L, 4L, 2L, 1L,        6/08/92
                                          process) No.77458A.              500ml, 250ml, 200ml,                 
                                                                           100ml; Bottles: 950ml,               
                                                                           500ml, 100ml, 50ml, 5ml;             
                                                                           Amp: 20ml, 10ml, 5ml,                
                                                                           2ml.                                 
Abbott Laboratories....................  Advisor Cocaine Bulk Tracer      Flasks: 6L, 4L, 2L, 1L,        4/10/92
                                          No.77458.                        500ml, 250ml, 200ml,                 
                                                                           100ml; Bottles: 950ml,               
                                                                           500ml, 100ml, 50ml, 5ml;             
                                                                           Amp: 20ml, 10ml, 5ml,                
                                                                           2ml.                                 
Abbott Laboratories....................  Advisor Controls, Code # 6A63-   Kit: 2 Bottles...........      1/25/94
                                          10.                                                                   
Abbott Laboratories....................  Advisor Drug of Abuse Screening  Kit: 10 Discs............      4/10/92
                                          System No.6A60-10.                                                    
Abbott Laboratories....................  Advisor Drug of Abuse Screening  Kit: 40 Discs............      4/10/92
                                          System No.6A60-21.                                                    
Abbott Laboratories....................  Advisor Opiates Bulk Tracer (in- Flasks: 6L, 4L, 2L, 1L,        6/08/92
                                          process) No.78692A.              500ml, 250ml, 200ml,                 
                                                                           100ml; Bottles: 950ml,               
                                                                           500ml, 100ml, 50ml, 5ml;             
                                                                           Amp: 20ml, 10ml, 5ml,                
                                                                           2ml.                                 
Abbott Laboratories....................  Advisor Opiates Bulk Tracer      Flasks: 6L, 4L, 2L, 1L,        4/10/92
                                          No.78692.                        500ml, 250ml, 200ml,                 
                                                                           100ml; Bottles: 950ml,               
                                                                           500ml, 100ml, 50ml, 5ml;             
                                                                           Amp: 20ml, 10ml, 5ml,                
                                                                           2ml.                                 
Abbott Laboratories....................  Advisor Positive Control, Bulk,  Carboy: 50, 45, 20, 10L;       1/25/94
                                          Code # 82979.                    Flask: 6, 4, 2, 1L; 500,             
                                                                           250, 200, 125, 100,                  
                                                                           50ml; Bottle: 8, 4, 2,               
                                                                           1L; 500, 250, 125, 50,               
                                                                           30, 10, 5ml.                         
Abbott Laboratories....................  Advisor Positive Control, Code   Bottle: 5ml..............      1/25/94
                                          # 6A63P.                                                              
Abbott Laboratories....................  Advisor Positive Control, In-    Box: 100 Bottles.........      1/25/94
                                          Process, Code # 6A63P001.                                             

[[Page 96]]

                                                                                                                
Abbott Laboratories....................  Advisor Reaction Disc No.6A60B.  Disc: 1 Card.............      4/10/92
Abbott Laboratories....................  Advisor Reaction Discs (4        Inner Carton: 20 Discs...      3/25/94
                                          Track); Code # 9A18.                                                  
Abbott Laboratories....................  Advisor Reaction Discs No.6A60.  Carton: 20 Discs.........      4/10/92
Abbott Laboratories....................  Amphetamine Bulk Calibrators, B- Carboy: 10L Flask: 6L,        10/09/85
                                          F.                               2L, 1L, 250ml, 200ml.                
Abbott Laboratories....................  Amphetamine Bulk Controls, L     Flask: 2 liter...........     12/09/85
                                          and H.                                                                
Abbott Laboratories....................  Amphetamine Class Bulk           50L, 45L, 20L, 10L, 8L,        3/01/88
                                          Calibrator B-F.                  6L, 4L, 2L, 1L, 500ml,               
                                                                           250ml, 200ml, 125ml,                 
                                                                           100ml, 50ml, 30ml, 20ml,             
                                                                           15ml, 10ml, 5ml, 2ml.                
Abbott Laboratories....................  Amphetamine Class Bulk Control   50L, 45L, 20L, 10L, 8L,        3/01/88
                                          L and H.                         6L, 4L, 2L, 1L, 500ml,               
                                                                           250ml, 200ml, 125ml,                 
                                                                           100ml, 50ml, 30ml, 20ml,             
                                                                           15ml, 5ml, .2ml.                     
Abbott Laboratories....................  Amphetamine Class Bulk Tracer:   50L, 45L, 20L, 10L, 8L,        3/01/88
                                          No. 94699.                       6L, 4L, 2L, 1L, 500ml,               
                                                                           250ml, 200ml, 125ml,                 
                                                                           100ml, 50ml, 30ml, 20ml,             
                                                                           15ml, 10ml, 5ml, 2ml.                
Abbott Laboratories....................  Amphetamine Class QC Primary B-  Carboy: 10L Flask: 4L,        11/22/88
                                          F, L, M, H No. 9667 (B-F, L,     2L, 1L, 500 ml, 250 ml,              
                                          M, H) QC.                        200 ml, 100 ml Bottle:               
                                                                           5ml.                                 
Abbott Laboratories....................  Amphetamine Class Stock Tracer:  Bottle: 30 ml............      3/01/88
                                          No. 94700.                                                            
Abbott Laboratories....................  Amphetamine Stock Standard No.   Carboy: 20L, 10L Flask:       11/22/88
                                          97072, 97072 A-B.                4L, 2L, 1L, 500 ml, 250              
                                                                           ml, 200 ml, 100 ml                   
                                                                           Bottle: 950ml, 500ml,                
                                                                           100ml, 5ml.                          
Abbott Laboratories....................  Amphetamine Stock Standard, No.  Bottle: 125ml............      9/30/85
                                          97072.                                                                
Abbott Laboratories....................  Amphetamine/ Methamphetamine II  5 ML Vial................      8/26/88
                                          Controls (L, M, H) No. 1A99-L,                                        
                                          M, H.                                                                 
Abbott Laboratories....................  Amphetamine/ Methamphetamine II  Kit: 3 Vials.............      8/26/88
                                          Controls No. 1A99-10.                                                 
Abbott Laboratories....................  Amphetamine/ Methamphetamine QC  Carboy: 10L Flask: 4L,        11/22/88
                                          Primary B-F, L, M, H No. 9668    2L, 1L, 500 ml, 250 ml,              
                                          (B-F, L, M, H) QC.               200 ml, 100 ml Bottle:               
                                                                           5ml.                                 
Abbott Laboratories....................  Amphetamine/ Methamphetamine QC  Bottle: 5 ml.............     11/10/87
                                          Primary Standard Control M,                                           
                                          No. 9668-M.                                                           
Abbott Laboratories....................  Amphetamine/Metamphetamine QC    Flasks: 1 liter, 250 ml,      11/10/87
                                          Primary Bulk Control M, No.      and 200 ml.                          
                                          9668-M.                                                               
Abbott Laboratories....................  Amphetamine/Methamphetamine      Carboy: 10L Flask: 4L,        11/22/88
                                          (II) QC Primary B-F, L, M, H     2L, 1L, 500 ml, 250 ml,              
                                          No. 1A99 (B-F, L, M, H) QC.      200 ml, 100 ml Bottle:               
                                                                           5ml.                                 
Abbott Laboratories....................  Amphetamine/Methamphetamine II   Carboy: 20L, 10L, 6L, 2L,      7/14/89
                                          Bulk Calibrator B, C, D, E, F;   1L, 250ml, 200ml.                    
                                          No. 01A99-B, C, D, E, F.                                              
Abbott Laboratories....................  Amphetamine/Methamphetamine II   50L, 45.5L, 20 L, 19L,         8/26/88
                                          Bulk Calibrators B-F Code No.    13.25L, 13L, 10 L, 9.5L,             
                                          1A99 (B-F).                      9L Carboy; 6 L, 4L, 2 L,             
                                                                           1 L, 250 ml, 200 ml                  
                                                                           Flask.                               
Abbott Laboratories....................  Amphetamine/Methamphetamine II   Carboy: 20L, 10L, Flask:       7/14/89
                                          Bulk Control L, M, H, ; No.      6L, 2L, 1L, 250ml, 200ml.            
                                          01A99-L, M, H.                                                        
Abbott Laboratories....................  Amphetamine/Methamphetamine II   50L, 45.5L, 20 L, 19L,         8/26/88
                                          Bulk Controls (L, M, H) Code     13.25L, 13L, 10 L, 9.5L,             
                                          No. 1A99 (L, M, H).              9L Carboy; 6 L, 4L, 2 L,             
                                                                           1 L, 250 ml, 200 ml                  
                                                                           Flask.                               
Abbott Laboratories....................  Amphetamine/Methamphetamine II   Carboy: 20L, 10L, Flask:       1/19/89
                                          Bulk Controls, No. 1A99X, Y, Z.  6L, 2L, 1L, 250ml, 200ml.            
Abbott Laboratories....................  Amphetamine/Methamphetamine II   Carboys: 50, 45, 20, 10L;      6/12/95
                                          Bulk Master Calibrator W, 3B27-  Flasks: 6, 4, 2, 1L;                 
                                          W.                               500, 250, 200, 125, 100,             
                                                                           50ml.                                
Abbott Laboratories....................  Amphetamine/Methamphetamine II   5 ml Vial................      8/26/88
                                          Calibrators B-F No. 1A99 B-F.                                         

[[Page 97]]

                                                                                                                
Abbott Laboratories....................  Amphetamine/Methamphetamine II   Kit: 100 vials...........      1/19/89
                                          Control X, Y, Z; No. 1A99-02,                                         
                                          03, 04.                                                               
Abbott Laboratories....................  Amphetamine/Methamphetamine II   Vial: 5ml................      1/19/89
                                          Control X, Y, Z; No. 1A99X, Y,                                        
                                          Z.                                                                    
Abbott Laboratories....................  Amphetamine/Methamphetamine II   Carboy: 20, 10L; Flask:        2/20/91
                                          QC Primary 2-6 QT, NG, CO, PS    6, 4, 2, 1L, 500, 250,               
                                          No. 1A99 2-6 QT-QC & NG/CO/PS-   200, 100ml; Bottle: 950,             
                                          QC.                              500, 100, 50, 5ml;                   
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  Amphetamine/Methamphetamine II   Carboy: 20L, 10L; Flask:      10/25/91
                                          QC Primary 8QT No. 1A998QT-QC.   6, 4, 2, 1L, 500, 250,               
                                                                           200, 100ml; Bottle: 950,             
                                                                           500, 100, 50, 5ml;                   
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  AxSYM Amphetamine/               Bottle: 5ml..............      6/12/95
                                          Methamphetamine II Master                                             
                                          Calibrator 2.                                                         
Abbott Laboratories....................  AxSYM Amphetamine/               Kit: 2 Bottles, 5ml each.      6/12/95
                                          Methamphetamine II Master                                             
                                          Calibrators, 3B27-30.                                                 
Abbott Laboratories....................  AxSYM Barbiturates II U Master   Bottle: 5ml..............      5/10/95
                                          Calibrator 2.                                                         
Abbott Laboratories....................  AxSYM Barbiturates II U Master   Kit: 2 Bottles...........      5/10/95
                                          Calibrators.                                                          
Abbott Laboratories....................  AxSYM Benzodiazepines Master     Bottle: 5ml..............      5/10/95
                                          Calibrator 2.                                                         
Abbott Laboratories....................  AxSYM Benzodiazepines Master     Kit: 2 Bottles...........      5/10/95
                                          Calibrators.                                                          
Abbott Laboratories....................  AxSYM Cannabinoids Fluorescin    Bottles: 35, 20, 15ml;         6/02/94
                                          Tracer; Code 3B28T0001.          Box: 100 vials; Tray:                
                                                                           200vials.                            
Abbott Laboratories....................  AxSYM Cannabinoids Master        Bottle: 5ml..............      5/10/95
                                          Calibrator 2.                                                         
Abbott Laboratories....................  AxSYM Cannabinoids Master        Kit: 2 Bottles...........      5/10/95
                                          Calibrators.                                                          
Abbott Laboratories....................  AxSYM Cannabinoids Reagent Pack  Kit: 100 Tests...........      7/27/94
Abbott Laboratories....................  AxSYM Cocaine Metabolite         Kit: 100 Tests...........      7/27/94
                                          Reagent Pack.                                                         
Abbott Laboratories....................  AxSYM Cocaine Metabolite         Bottles: 35, 20, 15ml;         6/02/94
                                          Fluorescin Tracer Solution;      Box: 100 vials; Tray:                
                                          Code 3B24T0001.                  200 vials.                           
Abbott Laboratories....................  AxSYM Cocaine Metabolite Master  Bottle: 5ml..............      5/10/95
                                          Calibrator 2.                                                         
Abbott Laboratories....................  AxSYM Cocaine Metabolite Master  Kit: 2 Bottles...........      5/10/95
                                          Calibrators.                                                          
Abbott Laboratories....................  AxSYM Methadone Master           Bottle: 5ml..............      6/12/95
                                          Calibrator 2.                                                         
Abbott Laboratories....................  AxSYM Methadone Master           Kit: 2 Bottles, 5ml each.      6/12/95
                                          Calibrators, 3B31-30.                                                 
Abbott Laboratories....................  AxSYM Opiates Fluorescin Tracer  Bottles: 35, 20, 15ml;         6/02/94
                                          Solution; Code 3B25T0001.        Box: 100 vials; Tray:                
                                                                           200 vials.                           
Abbott Laboratories....................  AxSYM Opiates Master Calibrator  Bottle: 5ml..............      5/10/95
                                          2.                                                                    
Abbott Laboratories....................  AxSYM Opiates Master             Kit: 2 Bottles...........      5/10/95
                                          Calibrators.                                                          
Abbott Laboratories....................  AxSYM Opiates Reagent Pack.....  Kit: 100 Tests...........      7/27/94
Abbott Laboratories....................  AxSYM Phencyclidine Master       Bottle: 5ml..............      6/12/95
                                          Calibrator 2.                                                         
Abbott Laboratories....................  AxSYM Phencyclidine Master       Kit: 2 Bottles, 5ml each.      6/12/95
                                          Calibrators, 3B26-30.                                                 
Abbott Laboratories....................  AxSYM Phenobarbital Calibrator   Vial: 5ml................      1/25/94
                                          B, Code # 7A70-B.                                                     
Abbott Laboratories....................  AxSYM Phenobarbital Calibrator   Vial: 5ml................      1/25/94
                                          C, Code # 7A70-C.                                                     
Abbott Laboratories....................  AxSYM Phenobarbital Calibrator   Vial: 5ml................      1/25/94
                                          D, Code # 7A70-D.                                                     
Abbott Laboratories....................  AxSYM Phenobarbital Calibrator   Vial: 5ml................      1/25/94
                                          E, Code 7A70-E.                                                       
Abbott Laboratories....................  AxSYM Phenobarbital Calibrator   Vial: 5ml................      1/25/94
                                          F, Code 7A70-F.                                                       
Abbott Laboratories....................  AxSYM Phenobarbital Calibrators  Kit: 6 Vials.............      1/25/94
                                          (B-F), Code # 7A70-01.                                                
Abbott Laboratories....................  AxSYM Phenobarbital Control H,   Vial: 10ml...............      1/25/94
                                          Code # 7A70-H.                                                        
Abbott Laboratories....................  AxSYM Phenobarbital Control M,   Vial: 10ml...............      1/25/94
                                          7A70-M.                                                               
Abbott Laboratories....................  AxSYM Phenobarbital Controls     Kit: 3 Vials.............      1/25/94
                                          (L, M, H), Code # 7A70-L.                                             
Abbott Laboratories....................  Barbital Buffer, 0.06 M;         Plastic Bottle: 2.5ml....      4/07/78
                                          Reagent Solution No. 7824.                                            
Abbott Laboratories....................  Barbiturate II U Control L, M,   Bottle: 5 ml.............     10/17/89
                                          H; No. 9669 L, M, H-11.                                               
Abbott Laboratories....................  Barbiturates Bulk Calibrator B-  Carboy: 50L, 45.5L, 20L,       7/01/88
                                          F; No. 9669 B-F.                 19L, 13.25L, 13L, 10L,               
                                                                           9.5L, 9L, 6L, 4L, 2L,                
                                                                           1L, 250ml, 200ml.                    
Abbott Laboratories....................  Barbiturates Bulk Control L, H;  Carboy: 50L, 45.5L, 20L,       7/01/88
                                          No. 9669 L, H.                   19L, 13.25L, 13L, 10L,               
                                                                           9.5, 9L, 6L, 4L, 2L, 1L,             
                                                                           250ml, 200ml.                        
Abbott Laboratories....................  Barbiturates Bulk Controls, No.  Carboy: 20L, 10L, Flask:       1/19/89
                                          9669X, Y, Z.                     6L, 2L, 1L, 250ml, 200ml.            
Abbott Laboratories....................  Barbiturates Control X, Y, Z;    Vial: 5ml................      1/19/89
                                          No. 9669X, Y, Z.                                                      

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Abbott Laboratories....................  Barbiturates II QC Primary NG,   Carboy: 20, 10L; Flask:        2/20/91
                                          CO, PS; No. 9669 NG/CO/PS-11-    6, 4, 2, 1L, 500, 250,               
                                          QC.                              200, 100ml; Bottle: 950,             
                                                                           500, 100, 50, 5ml;                   
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  Barbiturates II U Bulk           Carboy: 50L, 45.5L, 20L,      10/17/89
                                          Calibrators B-F; No. 9669 B-F-   19L, 13.25L, 13L, 10L,               
                                          05.                              9.5L, 9L, 6L, 4L, 2L,                
                                                                           1L, Flask: 250ml, 200ml.             
Abbott Laboratories....................  Barbiturates II U Bulk Controls  Carboy: 50L, 45.5L, 20L,      10/17/89
                                          L, M, H; No. 9669 L, M, H-11.    19L, 13.25L, 13L, 10L,               
                                                                           9.5L, 9L, 6L, 4L, 2L,                
                                                                           1L, Flask: 250ml, 200ml.             
Abbott Laboratories....................  Barbiturates II U Bulk Master    Carboys: 50, 45, 20, 10L;      5/10/95
                                          Calibrator W.                    Flasks: 6, 4, 2, 1L;                 
                                                                           500, 250, 200, 125, 100,             
                                                                           50ml.                                
Abbott Laboratories....................  Barbiturates II U Calibrators B- Bottle: 5 ml.............     10/17/89
                                          F; No. 9669 B-F-05.                                                   
Abbott Laboratories....................  Barbiturates II U Controls L,    Kit: 3 vials.............     10/17/89
                                          M, H; No. 9661-11.                                                    
Abbott Laboratories....................  Barbiturates II U QC Primary B-  Carboy: 10L, Flask: 4L,       10/17/89
                                          F; No. 9669 B-F-05 QC.           2L, 1L, 500ml, 250ml,                
                                                                           200ml, 100ml, Bottle:                
                                                                           950ml, 500ml, 100ml, 5ml.            
Abbott Laboratories....................  Barbiturates II U QC Primary L,  Carboy: 10L, Flask: 4L,       10/17/89
                                          M, H; No. 9669 L, M, H-11 QC.    2L, 1L, 500ml, 250ml,                
                                                                           200ml, 100ml, Bottle:                
                                                                           950ml, 500ml, 100ml, 5ml.            
Abbott Laboratories....................  Barbiturates QC Primary B-F, L,  Carboy: 10L Flask: 4L,        11/22/88
                                          M, H No. 9669 (B-F, L, M, H)     2L, 1L, 500 ml, 250 ml,              
                                          QC.                              200 ml, 100 ml Bottle: 5             
                                                                           ml.                                  
Abbott Laboratories....................  Barbiturates QC Primary Bulk     Flasks: 1 liter, 250 ml,      11/10/87
                                          Control M, No. 9669-M.           and 200 ml.                          
Abbott Laboratories....................  Barbiturates QC Primary          Bottle: 5 ml.............     11/10/87
                                          Standard Control M, No. 9669-M.                                       
Abbott Laboratories....................  Barbiturates QC Primary X, No.   Carboy: 10L, Flask: 4L,        6/05/89
                                          9669X-QC.                        2L, 1L, 500ml, 250ml,                
                                                                           200ml, 100ml, Bottle:                
                                                                           5ml.                                 
Abbott Laboratories....................  Barbiturates Serum Bulk          Carboy, Flask, Bottle or       1/03/89
                                          Calibrator B-F, No. 9679 B-F.    Ampule: 50, 45, 20, 10,              
                                                                           8, 6, 4, 2, 1-(L); 500,              
                                                                           250, 200, 125, 100, 50,              
                                                                           30, 20, 15, 10, 5, 2-                
                                                                           (ml).                                
Abbott Laboratories....................  Barbiturates Serum Bulk Control  Carboy: 20L, 10L, Flask:       1/03/89
                                          L, M, H; No. 9676 L, M, H.       6L, 2L, 1L, 250ml, 200ml.            
Abbott Laboratories....................  Barbiturates Serum Calibrators   Kit: 6 vials.............      1/03/89
                                          B-F, No. 9679-01.                                                     
Abbott Laboratories....................  Barbiturates Serum Calibrators   Bottle: 5ml..............      1/03/89
                                          B/F, No. 9679 B/F.                                                    
Abbott Laboratories....................  Barbiturates Serum Controls L,   Bottle: 5ml..............      1/03/89
                                          M, H; No. 9679 L, M, H.                                               
Abbott Laboratories....................  Barbiturates Serum Controls L,   Kit: 3 vials.............      1/03/89
                                          M, H; No. 9679-10.                                                    
Abbott Laboratories....................  Barbiturates Serum QC Primary B- Carboy: 10L, Flask: 4L,        1/03/89
                                          F, L, M, H; No. 9679 (B-F, L,    2L, 1L, 500ml, 250ml,                
                                          M, H)-QC.                        200ml, 100ml, Bottle:                
                                                                           5ml.                                 
Abbott Laboratories....................  Benzodiazepine Serum QC Primary  Carboy: 10L Flask: 4L,        11/22/88
                                          B-F, L, M, H No. 9682 (B-F, L,   2L, 1L, 500 ml, 250 ml,              
                                          M, H)-QC.                        200 ml, 100 ml Bottle: 5             
                                                                           ml.                                  
Abbott Laboratories....................  Benzodiazepines Bulk Calibrator  Carboy: 50L, 45.5L, 20L,       7/18/88
                                          No. 9674 B-F.                    l9.5L, 19L, 13.25L, 13L,             
                                                                           10L, 9L, 6L, 4L, 2L, 1L,             
                                                                           250ml, 200ml.                        
Abbott Laboratories....................  Benzodiazepines Bulk Control L,  Carboy: 50L, 45.5L, 20L,       7/18/88
                                          H No. 9674 L, H.                 19L, 13.25zl, 13L, 10L,              
                                                                           9.5, 9L, 6L, 4L, 2L, 1L,             
                                                                           250ml, 200ml,.                       
Abbott Laboratories....................  Benzodiazepines Bulk Master      Carboys: 50, 45, 20, 10L;      5/10/95
                                          Calibrator W.                    Flasks: 6, 4, 2, 1L;                 
                                                                           500, 250, 200, 125, 100,             
                                                                           50ml.                                

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Abbott Laboratories....................  Benzodiazepines QC Primary Bulk  Flasks: 1 liter, 250 ml,      11/10/87
                                          Control M, No. 9674-M.           and 200 ml.                          
Abbott Laboratories....................  Benzodiazepines QC Primary Bulk  Flasks: 1 liter, 250 ml,      11/10/87
                                          Control M, No. 9674-M.           and 200 ml.                          
Abbott Laboratories....................  Benzodiazepines QC Primary NG,   Carboy: 20, 10L; Flask:        2/20/91
                                          CO, PS No. 9674NG/CO/PS-QC.      6, 4, 2, 1L, 500, 250,               
                                                                           200, 100ml; Bottle: 950,             
                                                                           500, 100, 50, 5ml;                   
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  Benzodiazepines QC Primary, B-   Carboy: 10L Flask: 4L,        11/22/88
                                          F, L, M, H No. 9674 (B-F, L,     2L, 1L, 500 ml, 250 ml,              
                                          M, H) QC.                        200 ml, 100 ml Bottle:               
                                                                           5ml.                                 
Abbott Laboratories....................  Benzodiazepines Serum Bulk       Carboy: 10 liter; Flask:      12/07/87
                                          Calibrators B-F: Code No. 9682   6 liter, 2 liter.                    
                                          B-F.                                                                  
Abbott Laboratories....................  Benzodiazepines Serum Bulk       Carboy: 20 liters, 10          5/02/88
                                          Calibrators: No. 9682 B-F.       liters; Flask: 6 liters,             
                                                                           2 liters, 1 liter.                   
Abbott Laboratories....................  Benzodiazepines Serum Bulk       Carboy: 10 liter; Flask:      12/07/88
                                          Controls L, M, & H: Code No.     6 liter, 2 liter.                    
                                          9682 L, M, & H.                                                       
Abbott Laboratories....................  Benzodiazepines Serum Bulk       Carboy: 20 liters, 10          5/02/88
                                          Controls: No. 9682 L, M, H.      liters; Flask: 6 liters,             
                                                                           2 liters, 1 liter, 250               
                                                                           ml, 200 ml.                          
Abbott Laboratories....................  Benzoylecgonine Stock Standard   Carboy: 20L, 10L Flask:       11/23/88
                                          No. 97182, 97182 A-B.            4L, 2L, 1L, 500 ml, 250              
                                                                           ml, 200 ml, 100 ml,                  
                                                                           Bottle: 950ml, 500ml,                
                                                                           100ml, 5ml.                          
Abbott Laboratories....................  Benzoylecgonine Stock Standard,  Bottle: 125ml............     11/21/85
                                          No. 97182.                                                            
Abbott Laboratories....................  CG RIA Diagnostic Kit No. 7815.  Kit: 100 tests...........      4/07/78
Abbott Laboratories....................  Cannabinoids--GS Bulk Controls,  Carboy: 20L, 10L, Flask:       1/19/89
                                          No. 3897X, Y, Z.                 6L, 2L, 1L, 250ml, 200ml.            
Abbott Laboratories....................  Cannabinoids--GS Control X, Y,   Kit: 100 vials...........      1/19/89
                                          Z; No. 3897-02, 03, 04.                                               
Abbott Laboratories....................  Cannabinoids--GS Control X, Y,   Vial: 5ml................      1/19/89
                                          Z; No. 3897X, Y, Z.                                                   
Abbott Laboratories....................  Cannabinoids Bulk Calibrators B- Carboy: 50L, 45.5L, 20L,      10/24/86
                                          F, No. 9671 (B02-F02).           19L, 13.25L, 13L, 10L,               
                                                                           9.5L, 9L Flask: 6L, 4L,              
                                                                           2L, 1L, 250ml, 200ml.                
Abbott Laboratories....................  Cannabinoids Bulk Controls L,    Carboy: 50L, 45.5L, 20L,      10/24/86
                                          M, H; No. 9671 (L11, M11H11).    19L, 13.25L, 13L, 10L,               
                                                                           9.5L, 9L Flask: 6L, 4L,              
                                                                           2L, 1L, 250ml, 200ml.                
Abbott Laboratories....................  Cannabinoids Bulk Master         Carboys: 50, 45, 20, 10L;      5/10/95
                                          Calibrator W.                    Flasks: 6, 4, 2, 1L;                 
                                                                           500, 250, 200, 125, 100,             
                                                                           50ml.                                
Abbott Laboratories....................  Cannabinoids Bulk Tracer (No.    Carboy: 50L, 45.5L, 20L,      10/27/86
                                          94192).                          19L, 13.25L, 13L, 10L,               
                                                                           9.5L, 9L Flask: 6L, 4L,              
                                                                           2L, 1L, 250ml, 200ml.                
Abbott Laboratories....................  Cannabinoids Bulk Tracer; Code   Sizes: 50, 45, 20, 10, 8,      6/02/94
                                          3B28T.                           6, 4, 2, 1L; 500, 250,               
                                                                           200, 125, 100, 50, 35,               
                                                                           30, 20, 15, 10, 5ml;                 
                                                                           Ampules: 50, 20, 15, 10,             
                                                                           5, 2ml.                              
Abbott Laboratories....................  Cannabinoids QC Primary 2-6 QT,  Carboy: 20, 10L; Flask:        2/20/91
                                          NG, CO, PS No. 9671-11 2-6 QT-   6, 4, 2, 1L, 500, 250,               
                                          QC & NG/CO/PS-QC.                200, 100ml; Bottle: 950,             
                                                                           500, 100, 50, 5ml;                   
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  Cannabinoids QC Primary 8QT No.  Carboy: 20, 10L; Flask:       10/25/91
                                          9671-11 8QT-QC.                  6, 4, 2, 1L, 500, 250,               
                                                                           200, 100ml; Bottle: 950,             
                                                                           500, 100, 50, 5ml;                   
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  Cannabinoids QC Primary NBS, B-  Carboy: 10L, Flask: 4L,       12/27/88
                                          F, L, M, H; No. 9671-02[NBS, B-  2L, 500ml, 250ml, 100ml,             
                                          F]-QC; No. 9671-11[L, M, H]-QC.  200ml, Bottle: 5ml.                  

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Abbott Laboratories....................  Cannabinoids QC Primary NBS, B-  Carboy: 10L, Flask: 4L,       12/27/88
                                          F, L, M, H; No. 9671 (NBS, B-    2L, 1L, 500ml, 250ml,                
                                          F, L, M, H)-QC.                  200ml, 100ml, Bottle:                
                                                                           5ml.                                 
Abbott Laboratories....................  Cannabinoids Stock Standard      Bottle: 125 ml...........      6/19/87
                                          (94568).                                                              
Abbott Laboratories....................  Cannabinoids Stock Standard      Bottle: 125 ml...........     10/24/86
                                          (No. 94193).                                                          
Abbott Laboratories....................  Cannabinoids Stock Standard      Carboy: 20L, 10L, Flask:      12/27/89
                                          10mcg/ml-No. 94568, 5mcg/ml-     4L, 2L, 1L, 500ml,                   
                                          NO. 94568A, 1mcg/ml-No. 94568B.  250ml, 200ml, 100ml,                 
                                                                           bottle: 950ml, 500ml,                
                                                                           100ml, 5ml.                          
Abbott Laboratories....................  Cannabinoids Stock Standard;     Carboy: 20L, 10L, Flask:      12/27/88
                                          10mcg/ml-No. 94193, 5mcg/ml-     4L, 2L, 1L, 500ml,                   
                                          No. 94193A, 1mcg/ml-No. 94193B.  250ml, 200ml, 100ml,                 
                                                                           bottle: 950ml, 500ml,                
                                                                           100ml, 5ml.                          
Abbott Laboratories....................  Cannabinoids Stock Tracer (No.   Flasks: 6L, 4L, 2L, 1L,       10/27/86
                                          94194).                          500ml, 250ml, 200ml,                 
                                                                           100ml; Bottles: 950ml,               
                                                                           500ml, 100ml, 50ml,                  
                                                                           30ml, 5ml; Amp: 20, 10,              
                                                                           5, 2ml.                              
Abbott Laboratories....................  Cannabinoids--GS Bulk            20 L, 10 L Carboy; 6 L, 2      7/28/88
                                          Calibrators B-F No. 3897 B-F.    L, 1 L, 250 ml, 200 ml               
                                                                           Flask.                               
Abbott Laboratories....................  Cannabinoids--GS Bulk Controls   20 L, 10 L Carboy; 6 L, 2      7/28/88
                                          (L, M, H) Code No. 3897 (L, M,   L, 1 L, 250 ml, 200 ml               
                                          H).                              Flask.                               
Abbott Laboratories....................  Cannabinoids--GS Bulk Tracer     10 L Carboy; 6 L, 2 L          7/28/88
                                          Code No. 95826.                  Flask.                               
Abbott Laboratories....................  Cannabinoids--GS Calibrators B-  5 ml Vial................      7/28/88
                                          F No. 3897 B-F.                                                       
Abbott Laboratories....................  Cannabinoids--GS Calibrators     Kit: 6 Vials.............      7/28/88
                                          No. 3897-01.                                                          
Abbott Laboratories....................  Cannabinoids--GS Controls (L,    5 ml Vial................      7/28/88
                                          M, H) No. 3897-L, M, H.                                               
Abbott Laboratories....................  Cannabinoids--GS Controls No.    Kit: 3 Vials.............      7/28/88
                                          3897-10.                                                              
Abbott Laboratories....................  Cannabinoids--GS QC Primary      Carboy: 10L, Flask: 4L,       12/27/88
                                          NBS, B-F, L, M, H; No. 3897      2L, 1L, 500ml, 250ml,                
                                          (NBS, B-F, L, M, H)-QC.          200ml, 100ml, Bottle:                
                                                                           5ml.                                 
Abbott Laboratories....................  Cannabinoids--GS Reagent Pack    Kit: 100 Tests...........      7/28/88
                                          100 Test No. 3897-20.                                                 
Abbott Laboratories....................  Cannabinoids--GS Reagent Pack    Kit: 100 Tests...........      9/22/89
                                          100 Test, No. 3897-19.                                                
Abbott Laboratories....................  Cannabinoids--GS Tracer Code     5 ml Vial................      7/28/88
                                          No. 3897-T.                                                           
Abbott Laboratories....................  Cholylglycine Antiserum          Plastic Bottle: 20ml.....      4/07/78
                                          (Rabbit) Reagent Solution No.                                         
                                          7817.                                                                 
Abbott Laboratories....................  Cocaine Metabolite Bulk          Carboy: 9.5, 19 L........      7/07/88
                                          Calibrator B-F No. 9670 B-F.                                          
Abbott Laboratories....................  Cocaine Metabolite Bulk          Carboy: 20L, 10L; Flask:      10/28/85
                                          Calibrator, B-F No. 9670.        6L, 4L, 2L, 1L, 250ml,               
                                                                           200ml.                               
Abbott Laboratories....................  Cocaine Metabolite Bulk          Carboy: 9.5, 19 L........      7/07/88
                                          Controls L, H No. 9670-L, H.                                          
Abbott Laboratories....................  Cocaine Metabolite Bulk          Carboy: 20L, 10L, Flask:      10/28/85
                                          Controls, L and H No. 9670.      6L, 4L, 2L, 1L, 250ml,               
                                                                           200ml.                               
Abbott Laboratories....................  Cocaine Metabolite Bulk          Carboy: 20L, 10L, Flask:       1/19/89
                                          Controls, No. 9670X, Y, Z.       6L, 2L, 1L, 250ml, 200ml.            
Abbott Laboratories....................  Cocaine Metabolite Bulk Master   Carboys: 50, 45, 20, 10L;      5/10/95
                                          Calibrator W.                    Flasks: 6, 4, 2, 1L;                 
                                                                           500, 250, 200, 125, 100,             
                                                                           50ml.                                
Abbott Laboratories....................  Cocaine Metabolite Bulk Tracer,  Carboy: 50L, 45.5L, 20L,      10/30/85
                                          No. 97075.                       13.25L, 13L, 10L, 9L;                
                                                                           Flask: 6L, 4L, 2L, 1L,               
                                                                           250ml, 200ml.                        
Abbott Laboratories....................  Cocaine Metabolite Control X,    Vial: 5ml................      1/19/89
                                          Y, Z; No. 9670X, Y, Z.                                                
Abbott Laboratories....................  Cocaine Metabolite QC Primary 2- Carboy: 20, 10L; Flask:        2/20/91
                                          6 QT, NG, CO, PS No. 9670 2-6    6, 4, 2, 1L, 500, 250,               
                                          QT-QC & NG/CO/PS-QC.             200, 100ml; Bottle: 950,             
                                                                           500, 100, 50, 5ml;                   
                                                                           Ampule: 20, 10, 5, 2ml.              

[[Page 101]]

                                                                                                                
Abbott Laboratories....................  Cocaine Metabolite QC Primary 2- Carboy: 20, 10L; Flask:       10/28/91
                                          6 QT-C, 8QT-C No. 9670 2-6 QTC-  6, 4, 2, 1L, 500, 250,               
                                          QC, 9670 8QTC-QC.                200, 100ml; Bottle: 950,             
                                                                           500, 100, 50, 5ml;                   
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  Cocaine Metabolite QC Primary    Carboy: 20, 10L; Flask:       10/25/91
                                          8QT No. 9670 8QT-QC.             6, 4, 2, 1L, 500, 250,               
                                                                           200, 100ml; Bottle: 950,             
                                                                           500, 100, 50, 5ml;                   
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  Cocaine Metabolite QC Primary B- Carboy: 10L; Flask: 4L,       11/23/88
                                          F, L, M. H, No. 9670 (B-F, L,    2L, 1L, 500 ml, 250 ml,              
                                          M, H)-QC.                        200 ml, 100 ml, Bottle:              
                                                                           5 ml.                                
Abbott Laboratories....................  Cocaine Metabolite QC Primary    Flasks: 1 liter, 250 ml,      11/10/87
                                          Bulk Control M, No. 9670-M.      and 200 ml.                          
Abbott Laboratories....................  Cocaine Metabolite QC Primary    Bottle: 5 ml.............     11/10/87
                                          Standard Control M, No. 9670-M.                                       
Abbott Laboratories....................  Cocaine Metabolite QC Primary    Carboy: 10L; Flask: 4L,        6/05/89
                                          X, No. 9670X-QC; Primary Z,      2L, 1L, 500ml, 250ml,                
                                          No. 9670Z-QC.                    200ml, 100ml; Bottle:                
                                                                           5ml.                                 
Abbott Laboratories....................  Cocaine Metabolite Stock         Flasks: 6L, 4L, 2L, 1L,       10/30/85
                                          Tracer, No. 97156.               500ml, 250ml, 200ml,                 
                                                                           100ml; Bottles: 950ml,               
                                                                           500ml, 100ml, 50ml,                  
                                                                           30ml, 5ml; Amp: 20, 10,              
                                                                           5, 2ml.                              
Abbott Laboratories....................  Codeine Metabolite Bulk Tracer;  Sizes: 50, 45, 20, 10, 8,      6/02/94
                                          Code 3B48T.                      6, 4, 2, 1L; 500, 250,               
                                                                           200, 125, 100, 50, 35,               
                                                                           30, 20, 15, 10, 5ml;                 
                                                                           Ampules: 50, 20, 15, 10,             
                                                                           5, 2ml.                              
Abbott Laboratories....................  High Multiconstituent (9) Stock  Carboy: 50, 20, 10L;           7/02/91
                                          Standard Cat. No. 92622.         Flask: 6, 4, 2, 1L, 500,             
                                                                           250, 200, 100ml; Bottle:             
                                                                           950, 500, 100, 50, 5ml;              
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  Low Multiconstituent (9) Stock   Carboy: 50, 20, 10L;           7/02/91
                                          Standard Cat. No. 92620.         Flask: 6, 4, 2, 1L, 500,             
                                                                           250, 200, 100ml; Bottle:             
                                                                           950, 500, 100, 50, 5ml;              
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  Low, Medium, High                Carboy: 10, 20L; Flask:       10/06/89
                                          Multiconstituent Stock           6, 4, 2, 1L, 500, 250,               
                                          Standards, No. 90967, 90968,     200, 100ml; Bottle: 950,             
                                          90969.                           500, 100, 50, 5ml;                   
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  Medium Multiconstituent (9)      Carboy: 50, 20, 10L;           7/02/91
                                          Stock Standard Cat. No. 92621.   Flask: 6, 4, 2, 1L, 500,             
                                                                           250, 200, 100ml; Bottle:             
                                                                           950, 500, 100, 50, 5ml;              
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  Methadone Bulk Calibrators (B-   20 L, 10 L Carboy; 6 L, 2      9/02/88
                                          F) Code No. 9676 (B-F).          L, 1 L, 250 ml, 200 ml               
                                                                           Flask.                               
Abbott Laboratories....................  Methadone Bulk Calibrators (L,   20 L, 10 L Carboy; 6 L, 2      9/02/88
                                          M, H) Code No. 9676 (L, M, H).   L, 1 L, 250 ml, 200 ml               
                                                                           Flask.                               
Abbott Laboratories....................  Methadone Bulk Master            Carboys: 50, 45, 20, 10L;      6/12/95
                                          Calibrator W, 3B31-W.            Flasks: 6, 4, 2, 1L;                 
                                                                           500, 250, 200, 125, 100,             
                                                                           50ml.                                
Abbott Laboratories....................  Methadone Bulk Stock Standard    10 L Carboy; 6 L, 2 L, 1       9/02/88
                                          Code No. 95952.                  L Flask.                             
Abbott Laboratories....................  Methadone Calibrators B-F No.    5 ml Vial................      9/02/88
                                          9676 B-F.                                                             
Abbott Laboratories....................  Methadone Controls L, M, H No.   5 ml Vial................      9/02/88
                                          9676-L, M, H.                                                         
Abbott Laboratories....................  Methadone Controls No. 9676-10.  Kit: 3 Vials.............      9/02/88

[[Page 102]]

                                                                                                                
Abbott Laboratories....................  Methadone QC Primary NG, CO, PS  Carboy: 20, 10L; Flask:        2/20/91
                                          No. 9676 NG/CO/PS-QC.            6, 4, 2, 1L, 500, 250,               
                                                                           200, 100ml; Bottle: 950,             
                                                                           500, 100, 50, 5ml;                   
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  Methadone Stock Standard Code    1 L, 500 ml, 100 ml            9/02/88
                                          No. 95720.                       Bottle.                              
Abbott Laboratories....................  Morphine Stock Standard, No.     Vial: 125ml..............     10/16/85
                                          97291.                                                                
Abbott Laboratories....................  Morphine Stock Standard, No.     Carboy: 20L, 10L Flask:       11/22/88
                                          97291 A-B.                       4L, 2L, 1L, 500 ml, 250              
                                                                           ml, 200 ml, 100 ml                   
                                                                           Bottle: 950ml, 500ml,                
                                                                           100ml, 5ml.                          
Abbott Laboratories....................  Multiconstituent (9) QC Control  Carboy: 50, 20, 10L;           7/02/91
                                          H Cat. No. 92625.                Flask: 6, 4, 2, 1L, 500,             
                                                                           250, 200, 100ml; Bottle:             
                                                                           950, 500, 100, 50, 5ml;              
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  Multiconstituent (9) QC Control  Carboy: 50, 20, 10L;           7/02/91
                                          L Cat. No. 92623.                Flask: 6, 4, 2, 1L, 500,             
                                                                           250, 200, 100ml; Bottle:             
                                                                           950, 500, 100, 50, 5ml;              
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  Multiconstituent (9) QC Control  Carboy: 50, 20, 10L;           7/02/91
                                          M Cat. No. 92624.                Flask: 6, 4, 2, 1L, 500,             
                                                                           250, 200, 100ml; Bottle:             
                                                                           950, 500, 100, 50, 5ml;              
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  Multiconstituent Bulk Controls   Carboy: 20L, 10L, Flask:       9/03/87
                                          L, M, H (No. 9687-L, M, H).      10L, 6L, 4L, 2L, 1L,                 
                                                                           250ml, 200ml.                        
Abbott Laboratories....................  Multiconstituent Control for     Carboy: 20L, 10L, 19L,        10/06/89
                                          Abused Drug Assays Bulk L, M,    9.5L, 6L, 4L, 1L, Flask:             
                                          H; No. 9687-L, M, H.             250ml, 200ml.                        
Abbott Laboratories....................  Multiconstituent Control for     Vial: 5 ml...............     10/06/89
                                          Abused Drug Assays L, M, H;                                           
                                          No. 9687-L, M, H.                                                     
Abbott Laboratories....................  Multiconstituent Control for     Carboy: 10L, Flask: 4L,       10/06/89
                                          Abused Drug Assays QC            2L, 1L, 500ml, 250ml,                
                                          Primaries L, M, H; No. 9687-L,   200ml, 100ml, Bottle:                
                                          H, H-QC.                         950ml, 500ml, 100ml, 5ml.            
Abbott Laboratories....................  Nordiazepam Serum Bulk Stock     Carboy: 10 liters; Flask:      5/02/88
                                          Standard No. 94941.              6 liters, 2 liters, 1                
                                                                           liter.                               
Abbott Laboratories....................  Nordiazepam Serum Bulk Stock     Carboy: 10 liter; Flask:      12/07/87
                                          Standard: Code No. 94941.        6 liter, 2 liter.                    
Abbott Laboratories....................  Nordiazepam Serum Stock          Carboy: 20L, 10L Flask:       11/22/88
                                          Standard No. 94941, 94941 A, B.  4L, 2L, 1L, 500 ml, 250              
                                                                           ml, 200 ml, 100 ml                   
                                                                           Bottle: 950 ml, 500 ml,              
                                                                           100 ml, 5 ml.                        
Abbott Laboratories....................  Nordiazepam Serum Stock          Bottle: 125 ml...........     12/07/87
                                          Standard: Code No. 94941.                                             
Abbott Laboratories....................  Nordiazepam Serum Stock          Bottle: 125 ml...........      5/02/88
                                          Standard: No. 94941.                                                  
Abbott Laboratories....................  Nordiazepam Stock Standard No.   Carboy: 20L, 10L Flask:       11/22/88
                                          97757, 97757 A, B.               4L, 2L, 1L, 500 ml, 250              
                                                                           ml, 200 ml, 100 ml                   
                                                                           Bottle: 950ml, 500ml,                
                                                                           100ml, 5ml.                          
Abbott Laboratories....................  Nordiazepam Stock Standard, No.  Bottle: 125ml............      4/21/86
                                          97757.                                                                
Abbott Laboratories....................  Opiate Bulk Calibrators, B-F,    Carboy: 50L, 45.5L, 20L,       5/07/86
                                          No. 9673 B-F.                    19L, 13.25L, 13L, 10L,               
                                                                           9.5L, 9L Flask: 6L, 4L,              
                                                                           2L, 1L, 250ml, 200ml.                
Abbott Laboratories....................  Opiate Bulk Controls, L and H    Carboy: 50L, 45.5L, 20L,       5/07/86
                                          No. 9673 L and H.                19L, 13.25L, 13L, 10L,               
                                                                           9.5L, 9L Flask: 6L, 4L,              
                                                                           2L, 1L, 250ml, 200ml.                
Abbott Laboratories....................  Opiates Bulk Controls, No.       Carboy: 20L, 10L, Flask:       1/19/89
                                          9673X, Y, Z.                     6L, 2L, 1L, 250ml, 200ml.            

[[Page 103]]

                                                                                                                
Abbott Laboratories....................  Opiates Bulk Master Calibrator   Carboys: 50, 45, 20, 10L;      5/10/95
                                          W.                               Flasks: 6, 4, 2, 1L;                 
                                                                           500, 250, 200, 125, 100,             
                                                                           50ml.                                
Abbott Laboratories....................  Opiates Bulk Tracer, No. 97458.  Carboy: 50L, 45.5L, 20L,       5/07/86
                                                                           19L, 13.25L, 13L, 10L,               
                                                                           9.5L, 9L Flask: 6L, 4L,              
                                                                           2L, 1L, 250ml, 200ml.                
Abbott Laboratories....................  Opiates Bulk Tracer; Code #      Sizes: 50, 45, 20, 10, 8,      6/02/94
                                          3B25T.                           6, 4, 2, 1L; 500, 250,               
                                                                           200, 125, 100, 50, 35,               
                                                                           30, 20, 15, 10, 5ml;                 
                                                                           Ampules: 50, 20, 15, 10,             
                                                                           5, 2ml.                              
Abbott Laboratories....................  Opiates Control X, Y, Z; No.     Vial: 5ml................      1/19/89
                                          9673X, Y, Z.                                                          
Abbott Laboratories....................  Opiates QC Primary (B-F, L, M,   Carboy: 10L Flask: 4L,        11/22/88
                                          H) QC No. 9673 (B-F, L, M, H)    2L, 1L, 500 ml, 250 ml,              
                                          QC.                              200 ml, 100 ml Bottle:               
                                                                           5ml.                                 
Abbott Laboratories....................  Opiates QC Primary 2-6 QT, NG,   Carboy: 20, 10L; Flask:        2/20/91
                                          CO, PS No. 9673 2-6 QT-QC & NG/  6, 4, 2, 1L, 500, 250,               
                                          CO/PS-QC.                        200, 100ml; Bottle: 950,             
                                                                           500, 100, 50, 5ml;                   
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  Opiates QC Primary 8QT No. 9673  Carboy: 20, 10L; Flask:       10/25/91
                                          8QT-QC.                          6, 4, 2, 1L, 500, 250,               
                                                                           200, 100ml; Bottle: 950,             
                                                                           500, 100, 50, 5ml;                   
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  Opiates QC Primary Bulk Control  Flasks: 1 liter, 250 ml,      11/10/87
                                          M, No. 9673-M.                   and 200 ml.                          
Abbott Laboratories....................  Opiates QC Primary Standard      Bottle: 5 ml.............     11/10/87
                                          Control M, No. 9673-M.                                                
Abbott Laboratories....................  Opiates QC Primary X, No. 9673X- Carboy: 10L, Flask: 4L,        6/05/89
                                          QC; Primary Y, No. 9673Y-QC;     2L, 1L, 500ml, 250ml,                
                                          PrimaryZ, No. 9673Z-QC.          200ml, 100ml, Bottle:                
                                                                           5ml.                                 
Abbott Laboratories....................  Opiates Stock Tracer, No. 98718  Flasks: 6L, 4L, 2L, 1L,        5/07/86
                                                                           500ml, 250ml, 200ml,                 
                                                                           100ml; Bottles: 950ml,               
                                                                           500ml, 100ml, 50ml,                  
                                                                           30ml, 5ml; Amp: 20, 10,              
                                                                           5, 2ml.                              
Abbott Laboratories....................  Phencyclidine Bulk Calibrator,   Carboy: 50L, 45.5L, 20L,       3/21/86
                                          B-F No. 9672 B-F.                13.25L, 13L, 10L, 9L                 
                                                                           Flask: 6L, 4L, 2L, 1L,               
                                                                           250ml, 200ml.                        
Abbott Laboratories....................  Phencyclidine Bulk Control M,    Carboy: 50L, 45.5L, 20L,       9/26/86
                                          No. 9672 M.                      13.25L, 13L, 10L, 9L                 
                                                                           Flask: 6L, 4L, 2L, 1L,               
                                                                           250ml, 200ml.                        
Abbott Laboratories....................  Phencyclidine Bulk Controls, L   Carboy: 50L, 45.5L, 20L,       3/21/86
                                          and H No. 9672 L and H.          13.25L, 13L, 10L, 9L                 
                                                                           Flask: 6L, 4L, 2L, 1L,               
                                                                           250ml, 200ml.                        
Abbott Laboratories....................  Phencyclidine Bulk Controls,     Carboy: 20L, 10L, Flask:       1/19/89
                                          No. 9672X, Y, Z.                 6L, 2L, 1L, 250ml, 200ml.            
Abbott Laboratories....................  Phencyclidine Bulk Master        Carboys: 50, 45, 20, 10L;      6/12/95
                                          Calibrator W, 3B26-W.            Flasks: 6, 4, 2, 1L;                 
                                                                           500, 250, 200, 125, 100,             
                                                                           50ml.                                
Abbott Laboratories....................  Phencyclidine Control X, Y, Z;   Vial: 5ml................      1/19/89
                                          No. 9672X, Y, Z.                                                      
Abbott Laboratories....................  Phencyclidine QC Primary (B-F,   Carboy: 10L Flask: 4L,        11/22/88
                                          L, M, H) QC No. 9672 (B-F, L,    2L, 1L, 500 ml, 250 ml,              
                                          M, H) QC.                        200 ml, 100 ml Bottle:               
                                                                           5ml.                                 
Abbott Laboratories....................  Phencyclidine QC Primary 2-6 QT  Carboy: 20, 10L; Flask:        2/20/91
                                          NG, CO, PS No. 9672 2-6 QT-QC    6, 4, 2, 1L, 500, 250,               
                                          & NG/CO/PS-QC.                   200, 100ml; Bottle: 950,             
                                                                           500, 100, 50, 5ml;                   
                                                                           Ampule: 20, 10, 5, 2ml.              

[[Page 104]]

                                                                                                                
Abbott Laboratories....................  Phencyclidine QC Primary 8QT     Carboy: 20, 10L; Flask:       10/25/91
                                          No. 9672 8QT-QC.                 6, 4, 2, 1L, 500, 250,               
                                                                           200, 100ml; Bottle: 950,             
                                                                           500, 100, 50, 5ml;                   
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  Phencyclidine QC Primary X, No.  Carboy: 10L, Flask: 4L,        6/05/89
                                          9672X-QC; Primary Z, No. 9672Z-  2L, 1L, 500ml, 250ml,                
                                          QC.                              200ml, 100ml, Bottle:                
                                                                           5ml.                                 
Abbott Laboratories....................  Phencyclidine Stock Standard     Carboy: 20L, 10L Flask:       11/22/88
                                          No. 97158, 97158 A-B.            4L, 2L, 1L, 500 ml, 250              
                                                                           ml, 200 ml, 100 ml                   
                                                                           Bottle: 950ml, 500ml,                
                                                                           100ml, 5ml.                          
Abbott Laboratories....................  Phencyclidine Stock Standard,    Flask: 100ml, 200ml,           4/18/89
                                          No. 95356.                       250ml, 500ml, 1L, 2L,                
                                                                           4L, Bottle: 5ml, 100ml,              
                                                                           500ml, 950 ml, Carboys:              
                                                                           10L, 20L.                            
Abbott Laboratories....................  Phencyclidine Stock Standard,    Bottle: 125ml............     11/21/85
                                          No. 97158.                                                            
Abbott Laboratories....................  Phenobarbital Bulk Calibrators   Carboy: 50L, 45.5L, 19L,       6/16/88
                                          No. 9500 B-F.                    13.25L, 13L, 9.5L, 9L;               
                                                                           Flask: 6L, 4L, 2L, 1L,               
                                                                           250ml, 200ml.                        
Abbott Laboratories....................  Phenobarbital Bulk Controls No.  Carboy: 50L, 45.5L, 19L,       6/16/88
                                          9500 L, M, H.                    13.25L, 13L, 9.5L, 9L;               
                                                                           Flask: 6L, 4L, 2L, 1L,               
                                                                           250ml, 200ml.                        
Abbott Laboratories....................  Phenobarbital Control L, Code #  Vial: 10ml...............      1/25/94
                                          7A70-L.                                                               
Abbott Laboratories....................  Phenobarbital Enzyme Inhibitor   Vial: 2ml................      1/20/84
                                          Stock.                                                                
Abbott Laboratories....................  Phenobarbital QC Primary B-F,    Carboy: 20, 10L; Flask:        1/04/91
                                          L, M, H Item No. 9500B-F, L,     6, 4, 2, 1L, 500, 250,               
                                          M, H.                            200, 100ml; Bottles:                 
                                                                           950, 500, 100, 50, 5ml;              
                                                                           Ampules: 20, 10, 5, 2ml.             
Abbott Laboratories....................  Phenobarbital Stock Solution 1   Plastic Bottle: 125 ml...      3/23/87
                                          mg/ml Code No. 94312.                                                 
Abbott Laboratories....................  Phenobarbital Stock Solution 10  Plastic Bottle: 125 ml...      3/23/87
                                          mg/ml Code No. 94313.                                                 
Abbott Laboratories....................  Phenobarbital Stock Standard     Carboy: 50, 20, 10L;           1/04/91
                                          500 ug/ml Item No. 99259.        Flask: 6, 4, 2, 1L, 500,             
                                                                           250, 200, 100ml;                     
                                                                           Bottles: 950, 500, 100,              
                                                                           50, 5ml; Ampules: 20,                
                                                                           10, 5, 2ml.                          
Abbott Laboratories....................  Phenobarbital Stock Standard     Bottle: 1 liter..........      8/12/82
                                          Solution.                                                             
Abbott Laboratories....................  Polyethylene Glycol 8000, 16%    Plastic Bottle: 300 ml,        9/21/77
                                          Solution in 0.09 M Barbital      150 ml.                              
                                          Buffer, No. 7541.                                                     
Abbott Laboratories....................  Polyethylene Glycol 8000, 18%    Stainless Steel Tank:          3/09/88
                                          Solution in 0.09M Barbital       1000 liters.                         
                                          Buffer: No. 07602.                                                    
Abbott Laboratories....................  Progesterone Buffer No. 2242J..  Bottle: 30ml.............      3/11/92
Abbott Laboratories....................  Progesterone Buffer No.          Box: 100 Bottles/30ml....      3/11/92
                                          2242J0001.                                                            
Abbott Laboratories....................  Progesterone Bulk Buffer No.     Carboy: 50L, 25L, 20L,         5/11/92
                                          12918.                           19L, 15L, 13L, 10L, 9L;              
                                                                           Bottle: 950ml, 500ml,                
                                                                           100ml, 50ml, 30ml, 20ml;             
                                                                           Amp: 20ml, 10ml, 5ml,                
                                                                           2ml.                                 
Abbott Laboratories....................  Progesterone Reagent Pack No.    Kit: 4 Bottles...........      3/11/92
                                          2242-20.                                                              
Abbott Laboratories....................  Propoxyphene Bulk Calibrator B-  Carboys or Flasks: 50L,       11/30/90
                                          F No. 9675 B-F.                  45.5L, 20L, 19L, 13.25L,             
                                                                           13L, 10L, 9.5L, 9L, 6L,              
                                                                           4L, 2L, 1L, 250ml, 200ml.            
Abbott Laboratories....................  Propoxyphene Bulk Control L, M,  Carboys or Flasks: 50L,       11/30/90
                                          H No. 9675 L, M, H.              45.5L, 20L, 19L, 13.25L,             
                                                                           13L, 10L, 9.5L, 9L, 6L,              
                                                                           4L, 2L, 1L, 250ml, 200ml.            

[[Page 105]]

                                                                                                                
Abbott Laboratories....................  Propoxyphene Bulk Tracer Item    Carboys or Flasks: 50L,       11/30/90
                                          No. 92003.                       45.5L, 20L, 19L, 13.25L,             
                                                                           13L, 10L, 9.5L, 9L, 6L,              
                                                                           4L, 2L, 1L, 250ml, 200ml.            
Abbott Laboratories....................  Propoxyphene Calibrators Item    Kit: 5 vials.............     11/30/90
                                          No. 9675-01.                                                          
Abbott Laboratories....................  Propoxyphene Calibrators Item    Vial: 5ml................     11/30/90
                                          No. 9675B-F.                                                          
Abbott Laboratories....................  Propoxyphene Controls Item No.   Kit: 3 vials.............     11/30/90
                                          9675-10.                                                              
Abbott Laboratories....................  Propoxyphene Controls Item No.   Vial: 5ml................     11/30/90
                                          9675L, M, H.                                                          
Abbott Laboratories....................  Propoxyphene QC Primary B-F, L,  Carboy: 20, 10L Flasks:       11/30/90
                                          M, H, Z Item No. 9675(B-F, L,    6, 4, 2, 1L, 500, 250,               
                                          M, H, Z)-QC.                     200, 100ml Bottles: 950,             
                                                                           500, 100, 50, 5ml                    
                                                                           Ampules: 20, 10, 5, 2ml.             
Abbott Laboratories....................  Propoxyphene QC Primary NG, CO,  Carboy: 20, 10L; Flask:        2/20/91
                                          PS No. 9675 NG/CO/PS-QC.         6, 4, 2, 1L, 500, 250,               
                                                                           200, 100ml; Bottle:                  
                                                                           950ml, 500, 100, 50,                 
                                                                           5ml; Ampule: 20, 10, 5,              
                                                                           2ml.                                 
Abbott Laboratories....................  Propoxyphene Stock Standard,     Carboys: 20, 10L Flasks:      11/30/90
                                          100 mcg/ml Item No. 92005.       6, 4, 2, 1L, 500, 250,               
                                                                           200, 100ml Bottles: 950,             
                                                                           500, 100, 50, 5ml                    
                                                                           Ampules: 20, 10, 5, 2ml.             
Abbott Laboratories....................  Propoxyphene Stock Tracer Item   Bottle: 12ml.............     11/30/90
                                          No. 92001.                                                            
Abbott Laboratories....................  Propoxyphene Tracer Item No.     Bottles: 3.2ml, 5ml......     11/30/90
                                          9675-T.                                                               
Abbott Laboratories....................  Secobarbital Bulk Calibrator, B- Carboy: 20L, 10L, Flask:       3/21/86
                                          F No. 9669.                      6L, 4L, 2L, 1L, 250ml,               
                                                                           200ml.                               
Abbott Laboratories....................  Secobarbital Bulk Controls, L    Carboy: 20L, 10L, Flask:       3/21/86
                                          and H No. 9669.                  6L, 4L, 2L, 1L, 250ml,               
                                                                           200ml.                               
Abbott Laboratories....................  Secobarbital Stock Standard      Carboy: 20L, 10L, Flask:       1/03/89
                                          1000mcg/ml-No. 90107, 500mcg/    4L, 2L, 1L, 500ml,                   
                                          ml-No. 90107A, 200mcg/ml-No.     250ml, 200ml, 100ml,                 
                                          90107B.                          Bottle: 950ml, 500ml,                
                                                                           100ml, 5ml.                          
Abbott Laboratories....................  Secobarbital Stock Standard No.  Carboy: 20L, 10L Flask:       11/22/88
                                          97171, 97171 A, B.               4L, 2L, 1L, 500 ml, 250              
                                                                           ml, 200 ml, 100 ml                   
                                                                           Bottle: 950 ml, 500 ml,              
                                                                           100 ml, 5 ml.                        
Abbott Laboratories....................  Secobarbital Stock Standard,     Bottle: 125ml............     11/21/85
                                          No. 97171.                                                            
Abbott Laboratories....................  Spectrum Phenobarbital           Bottle: 4ml..............     10/03/85
                                          Calibrator II-VI, Nos. 9755,                                          
                                          9757, 9759, 9761, 9763.                                               
Abbott Laboratories....................  Spectrum Phenobarbital Control,  Bottle: 4ml..............     10/03/85
                                          Nos. 9876, 9878, 9880. (L, M,                                         
                                          H).                                                                   
Abbott Laboratories....................  TDx Amphetamine Class            Kit containing 6 vials...      3/01/88
                                          Calibrators 9667-01.                                                  
Abbott Laboratories....................  TDx Amphetamine Class            Bottle: 5 ml.............      3/01/88
                                          Calibrators B-F.                                                      
Abbott Laboratories....................  TDx Amphetamine Class Control L  Bottle: 5 ml.............      3/01/88
                                          and H.                                                                
Abbott Laboratories....................  TDx Amphetamine Class Controls   Kit containing 2 vials...      3/01/88
                                          9667-10.                                                              
Abbott Laboratories....................  TDx Amphetamine Class Reagent    Kit containing 1 vial....      3/01/88
                                          Pack, No. 9667-60.                                                    
Abbott Laboratories....................  TDx Amphetamine Class Tracer     Bottle: 5 ml.............      3/01/88
                                          Solution, No. 9667T.                                                  
Abbott Laboratories....................  TDx Amphetamine/Methamphetamine  Bottles: 4ml.............      8/23/85
                                          Calibrator, No. 9668-01.                                              
Abbott Laboratories....................  TDx Amphetamine/Methamphetamine  Bottles: 4ml.............      8/23/85
                                          Controls, No. 9668-10.                                                
Abbott Laboratories....................  TDx Barbiturates Calibrators     5 ml Vial................      7/01/88
                                          No. 9669 B-F.                                                         
Abbott Laboratories....................  TDx Barbiturates Calibrators     Kit: 5 Vials, 5 ml each..      7/01/88
                                          No. 9669-01.                                                          
Abbott Laboratories....................  TDx Barbiturates Calibrators, B- Bottle: 4 ml.............     10/08/85
                                          F No. 9669.                                                           
Abbott Laboratories....................  TDx Barbiturates Control L, H    5 ml Vial................      7/01/88
                                          No. 9669 L, H.                                                        
Abbott Laboratories....................  TDx Barbiturates Control, L and  Bottle: 4ml..............     10/08/85
                                          H No. 9669.                                                           
Abbott Laboratories....................  TDx Barbiturates Controls No.    Kit: 2 Vials, 5 ml each..      7/01/88
                                          9669-10.                                                              
Abbott Laboratories....................  TDx Benzodiazepines Calibrator   5 ml Vial................      7/18/88
                                          No. 9674 B-F.                                                         
Abbott Laboratories....................  TDx Benzodiazepines              Bottles: 4ml.............      4/21/86
                                          Calibrators, No. 9674-01.                                             
Abbott Laboratories....................  TDx Benzodiazepines Controls L,  5 ml Vial................      7/18/88
                                          H No. 9674 L, H.                                                      
Abbott Laboratories....................  TDx Benzodiazepines Controls L,  Kit: 2 Vials, 5 ml each..      7/18/88
                                          H No. 9674-10.                                                        
Abbott Laboratories....................  TDx Benzodiazepines Controls,    Bottles: 4ml.............      4/21/86
                                          No. 9674-10.                                                          
Abbott Laboratories....................  TDx Benzodiazepines Serum        Bottle: 4 ml.............      5/02/88
                                          Calibrator No. 9682 B-F.                                              
Abbott Laboratories....................  TDx Benzodiazepines Serum        Bottle: 4ml, 5ml.........     12/07/88
                                          Calibrators B-F: Code No. 9682                                        
                                          B-F.                                                                  

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Abbott Laboratories....................  TDx Benzodiazepines Serum        Kit......................     12/07/88
                                          Calibrators: Code No. 9682-01.                                        
Abbott Laboratories....................  TDx Benzodiazepines Serum        Kit containing 6 vials...      5/02/88
                                          Calibrators: No. 9682-01.                                             
Abbott Laboratories....................  TDx Benzodiazepines Serum        Bottle: 4 ml.............     12/07/87
                                          Controls L, M, & H: No. 9682                                          
                                          L, M, H.                                                              
Abbott Laboratories....................  TDx Benzodiazepines Serum        Bottle: 4 ml.............      5/02/88
                                          Controls L, M, H: No. 9682 L,                                         
                                          M, H.                                                                 
Abbott Laboratories....................  TDx Benzodiazepines Serum        Kit......................     12/07/88
                                          Controls: Code No. 9682-10.                                           
Abbott Laboratories....................  TDx Benzodiazepines Serum        Kit containing 3 vials...      5/02/88
                                          Controls: No. 9682-10.                                                
Abbott Laboratories....................  TDx Cannabinoids Calibrators B-  Bottles: 5 ml............     10/24/86
                                          F (No. 9671-01).                                                      
Abbott Laboratories....................  TDx Cannabinoids Controls L, M,  Bottle: 5 ml.............      6/19/87
                                          and H (9671-11).                                                      
Abbott Laboratories....................  TDx Cannabinoids Controls L, M,  Bottles: 5 ml............     10/24/86
                                          H (No. 9671-10).                                                      
Abbott Laboratories....................  TDx Cannabinoids Fluorescein     Bottle: 5 ml.............     10/27/86
                                          Tracer Solution (No. 9671-T).                                         
Abbott Laboratories....................  TDx Cannabinoids Reagent Pack    100 tests................     10/27/86
                                          (No. 9671-20).                                                        
Abbott Laboratories....................  TDx Cocaine Metabolite           5 ml Vial................      7/07/88
                                          Calibrator B-F No. 9670 B-F.                                          
Abbott Laboratories....................  TDx Cocaine Metabolite           Bottle: 4ml..............     10/02/85
                                          Calibrator, B-F No. 9670.                                             
Abbott Laboratories....................  TDx Cocaine Metabolite Control   5 ml Vial................      7/07/88
                                          L, H No. 9670 L, H.                                                   
Abbott Laboratories....................  TDx Cocaine Metabolite Control,  Bottle: 4ml..............     10/02/85
                                          L and H No. 9669.                                                     
Abbott Laboratories....................  TDx Cocaine Metabolite Controls  Kit: 2 Vials, 5 ml each..      7/07/88
                                          No. 9670-10.                                                          
Abbott Laboratories....................  TDx Cocaine Metabolite           Kit: 100 Vials, 5 ml Each      7/07/88
                                          Fluorescein Tracer Solution                                           
                                          No. 9670 T0001.                                                       
Abbott Laboratories....................  TDx Cocaine Metabolite           Box: 5 ml Vial...........      7/07/88
                                          Fluorescein Tracer Solution                                           
                                          No. 9670-T.                                                           
Abbott Laboratories....................  TDx Cocaine Metabolite Reagent   Reagent well: 5ml........     10/02/85
                                          Pack.                                                                 
Abbott Laboratories....................  TDx Cocaine Metabolite Reagent   Kit: 100 Tests...........      7/07/88
                                          Pack No. 9670-20.                                                     
Abbott Laboratories....................  TDx Multiconstituent Controls    Bottle: 5 ml.............      9/03/87
                                          L, M, H (No. 9687-L, M, H).                                           
Abbott Laboratories....................  TDx Opiates Calibrators B-F:     Kit: 6 Vials.............      2/29/88
                                          No. 9673-01.                                                          
Abbott Laboratories....................  TDx Opiates Calibrators, B-F     5 ml Vial................      5/07/86
                                          No. 9673.                                                             
Abbott Laboratories....................  TDx Opiates Controls L and H,    Kit: 2 Vials.............      2/29/88
                                          No. 9673-10.                                                          
Abbott Laboratories....................  TDx Opiates Controls L and H:    Vial: 5 ml...............      2/29/88
                                          No. 9673 L, H.                                                        
Abbott Laboratories....................  TDx Opiates Controls, L and H    Vials: 5ml...............      5/07/86
                                          No. 9673.                                                             
Abbott Laboratories....................  TDx Opiates Fluorescein Tracer   Box: 10 Vials, 5 ml each.      7/08/88
                                          Solution No. 9673 T0001.                                              
Abbott Laboratories....................  TDx Opiates Fluorescein Tracer   Vial: 5 ml...............      2/29/88
                                          Solution: No. 9673-T.                                                 
Abbott Laboratories....................  TDx Opiates Reagent Pack No.     Kit: 100 tests...........      5/07/86
                                          9673-20, 100 tests.                                                   
Abbott Laboratories....................  TDx Phencyclidine Bulk           5 ml Vial................      7/18/88
                                          Calibrator B-F No. 9672 B-F.                                          
Abbott Laboratories....................  TDx Phencyclidine Bulk           Carboy: 9.5, 19 L........      7/18/88
                                          Calibrator B-F No. 9672 B-F.                                          
Abbott Laboratories....................  TDx Phencyclidine Bulk Control   Carboy: 9.5, 19 L........      7/18/88
                                          L, M, H No. 9672 L, M, H.                                             
Abbott Laboratories....................  TDx Phencyclidine Calibrators,   Bottle: 4ml..............     10/09/85
                                          B-F No. 9672.                                                         
Abbott Laboratories....................  TDx Phencyclidine Control M No.  Bottle: 4ml..............      9/26/86
                                          9672.                                                                 
Abbott Laboratories....................  TDx Phencyclidine Controls L,    5 ml Vial................      7/18/88
                                          M, H No. 9672 L, M, H.                                                
Abbott Laboratories....................  TDx Phencyclidine Controls No.   Kit: 3 Vials, 5 ml each..      7/18/88
                                          9672-10.                                                              
Abbott Laboratories....................  TDx Phencyclidine Controls, L    Bottle: 4ml..............     10/09/85
                                          and H No. 9672.                                                       
Abbott Laboratories....................  TDx Phenobarbital Calibrator-    Kit ctg: 6 vials.........      8/31/81
                                          0.0, 5.0, 10.0, 20.0, 40.0,                                           
                                          and 80.0 mcg/ml.                                                      
Abbott Laboratories....................  TDx Phenobarbital Calibrators B- 5 ml Vial................      6/16/88
                                          F No. 9500 B-F.                                                       
Abbott Laboratories....................  TDx Phenobarbital Calibrators    Kit: 6 Vials, 5 ml each..      6/16/88
                                          No. 9500-01 (9500 B-F).                                               
Abbott Laboratories....................  TDx Phenobarbital Controls No.   5 ml Vial................      6/16/88
                                          9500 L, M, H.                                                         
Abbott Laboratories....................  TDx Phenobarbital Controls No.   Kit: 3 Vials, 5 ml each..      6/16/88
                                          9500-10 (9500 L, M, H).                                               
Abbott Laboratories....................  TDx Phenobarbital Controls-      Kit ctg: 3 vials.........      8/31/81
                                          15.0, 30.0, 50.0 mcg/ml.                                              
Abbott Laboratories....................  TDx Propoxyphene Reagent Pack    Kit: 100 tests...........     11/30/90
                                          Item No. 9675-20.                                                     
Abbott Laboratories....................  TDx Systems Multiconstituent     Kit: 6 Bottles...........      9/03/87
                                          Controls for Abused Drug (No.                                         
                                          9687-10).                                                             
Abbott Laboratories....................  TDx or TDx/TDxFLx Propoxyphene   Box: 100 bottles or less.     11/30/90
                                          Fluorescein Tracer Solution                                           
                                          Item No. 9675T0001.                                                   
Abbott Laboratories....................  TDx, ADx Amphetamine Class       Kit: 100 tests...........      3/01/88
                                          Reagent Pack, No. 9667-20, No.                                        
                                          9667-55.                                                              
Abbott Laboratories....................  TDx/TDxFLx Propoxyphene Reagent  Kit: 100 tests...........     11/30/90
                                          Pack Item No. 9675-60.                                                
Abbott Laboratories....................  Thyroxine Binding Globulin,      Glass Bottle: 13ml.            4/22/76
                                          Thyroxine I 125.                 Plastic Bottle: 250ml.               
Abbott Laboratories....................  TrakPak Five Drug Control 2-6    Carboy: 20, 10L Flask: 6,     10/19/90
                                          QT Nos. 92212-92216.             4, 2, 1L, 500, 250, 200,             
                                                                           100ml Bottle: 950, 500,              
                                                                           100, 50, 5ml Ampule: 20,             
                                                                           10, 5, 2ml.                          

[[Page 107]]

                                                                                                                
Abbott Laboratories....................  TrakPak Five Drug Control 8QT    Carboy: 20, 10L; FlaskL:      10/25/91
                                          No. 93349.                       6, 4, 2, 1L, 500, 250,               
                                                                           200, 100ml; Bottle: 950,             
                                                                           500, 100, 50, 5ml;                   
                                                                           Ampule: 20, 10, 5, 2ml.              
Abbott Laboratories....................  TrakPak Five Drug Control Stock  Carboy: 20, 10L Flask: 6,     10/19/90
                                          No. 92210.                       4, 2, 1L, 500, 250, 200,             
                                                                           100ml Bottle: 950, 500,              
                                                                           100, 50, 5ml Ampule: 20,             
                                                                           10, 5, 2ml.                          
Abbott Laboratories....................  Trakpak Card w/Cover Code        Box: 2000 cards w/cover..      3/08/91
                                          #01249.                                                               
Abbott Laboratories....................  Trakpak Card w/Tracers Code      Box: 2000 cards..........      3/08/91
                                          #01248.                                                               
Abbott Laboratories....................  Trakpak Cocaine Tracer Code      Flasks: 6, 4, 2, 1L, 500,      3/08/91
                                          #92199.                          250, 200, 100ml;                     
                                                                           Bottles: 950, 500, 100,              
                                                                           50, 5ml; Ampules: 20,                
                                                                           10, 5, 2ml.                          
Abbott Laboratories....................  Trakpak Drug of Abuse Screening  Kit: 40 cartridges.......      3/08/91
                                          System (40 test kit) Code                                             
                                          #04A74.                                                               
Abbott Laboratories....................  Trakpak Negative Control Code    Vial: 5ml................      3/08/91
                                          #04A74C.                                                              
Abbott Laboratories....................  Trakpak Opiates Tracer Code      Flasks: 6, 4, 2, 1L, 500,      3/08/91
                                          #92198.                          250, 200, 100ml;                     
                                                                           Bottles: 950, 5, 00,                 
                                                                           100, 50, 5ml; Ampules:               
                                                                           20, 10, 5, 2ml.                      
Abbott Laboratories....................  Trakpak Reaction Cartridge Code  Cartridge: 1 card........      3/08/91
                                          #04A74B.                                                              
Abbott Laboratories....................  Trakpak THC Tracer Code #92200.  Flasks: 6, 4, 2, 1L, 500,      3/08/91
                                                                           250, 200, 100ml;                     
                                                                           Bottles: 950, 500, 100,              
                                                                           50, 5ml; Ampules: 20,                
                                                                           10, 5, 2ml.                          
Abbott Laboratories....................  X Systems Amphetamine/           Vial: 5 ml...............      7/14/89
                                          Methamphetamine II Calibrator                                         
                                          B, C, D, E, F; No. 01A99-B, C,                                        
                                          D, E, F.                                                              
Abbott Laboratories....................  X Systems Amphetamine/           Kit: 6 vials.............      7/14/89
                                          Methamphetamine II                                                    
                                          Calibrators, No. 01A99-01.                                            
Abbott Laboratories....................  X Systems Amphetamine/           Vial: 5 ml...............      7/14/89
                                          Methamphetamine II Control L,                                         
                                          M, H; No. 01A99-L, M, H.                                              
Abbott Laboratories....................  X Systems Amphetamine/           Kit: 3 vials.............      7/14/89
                                          Methamphetamine II Controls,                                          
                                          No. 01A99-10.                                                         
Abbott Laboratories....................  X Systems Methadone Calibrators  Bottle: 5ml..............      5/15/92
                                          B-F.                                                                  
Abbott Laboratories....................  X Systems Methadone Calibrators  Kit: 6 Bottles...........      5/12/92
                                          B-F.                                                                  
Abbott Laboratories....................  X Systems Methadone Controls L,  Kit: 3 Bottles...........      5/15/92
                                          M, H, No. 9676-10.                                                    
Abbott Laboratories....................  X Systems Methadone Controls L,  Bottle: 5ml..............      5/15/92
                                          M, H; No. 9676 L, M, H.                                               
Abbott Laboratories....................  XSYSTEMS Amphetamine/            Kit: 6 Vials.............      8/26/88
                                          Methamphetamine II Calibrators                                        
                                          No. 1A99-06.                                                          
Abbott Laboratories....................  XSYSTEMS Barbiturates II U       Kit: 6 vials.............     10/17/89
                                          Calibrators , No. 9669-07.                                            
Abbott Laboratories....................  XSYSTEMS Benzodiazepines         Kit: 5 Vials, 5 ml each..      7/18/88
                                          Calibrators, No. 9674-02.                                             
Abbott Laboratories....................  XSYSTEMS Cannabinoids            Bottle: 5 ml.............      6/19/87
                                          Calibrators, No. 9671-04.                                             
Abbott Laboratories....................  XSYSTEMS Cocaine Metabolite      Kit: 5 Vials, 5 ml each..      7/07/88
                                          Calibrators No. 9670-06.                                              
Abbott Laboratories....................  XSYSTEMS Methadone Calibrators   Kit: 6 Vials.............      9/02/88
                                          No. 9676-02.                                                          
Abbott Laboratories....................  XSYSTEMS Multiconstituent        Kit: 6 vials.............     10/06/89
                                          Controls, No. 9687-12.                                                
Abbott Laboratories....................  XSYSTEMS Opiates Calibrators,    Vial: 5 ml...............      2/29/88
                                          No. 9673-06.                                                          
Abbott Laboratories....................  XSYSTEMS Phencyclidine           Kit: 5 Vials, 5 ml each..      7/18/88
                                          Calibrators, No. 9672-06.                                             
Abbott Laboratories....................  d-Amphetamine (II) Bulk Stock    10 L Carboy; 6 L, 2 L, 1       8/26/88
                                          Standard Code No. 95947.         L Flask.                             
Abbott Laboratories....................  d-Amphetamine (II) Stock         1 L, 500 ml, 100 ml            8/26/88
                                          Standard Code No. 95934.         Bottle.                              
Abbott Laboratories....................  d-Amphetamine (II) Stock         Carboy: 20L, 10L Flask:       11/22/88
                                          Standard No. 95934, 95934 A-B.   4L, 2L, 1L, 500 ml, 250              
                                                                           ml, 200 ml, 100 ml                   
                                                                           Bottle: 950ml, 500ml,                
                                                                           100ml, 5ml.                          
Adri/Technam...........................  3-Ortho-Carboxymethylmorphine..  Screw Cap Vial...........      5/03/73
Adri/Technam...........................  5-Ethyl-5-(1-Carboxy-n-propyl)   Screw Cap Vial...........      5/03/73
                                          Barbituric Acid.                                                      
Adri/Technam...........................  5-Ethyl-5-(1-Carboxy-n-propyl)   Vaccine Vial: 10ml.......      5/03/73
                                          Barbituric Acid-Bovine Serum                                          
                                          Albumin.                                                              
Adri/Technam...........................  5-Ethyl-5-(1-Carboxy-n-propyl)   Vaccine Vial: 10ml.......      5/03/73
                                          Barbituric Acid-Rabbit Serum                                          
                                          Albumin.                                                              
Adri/Technam...........................  Barbiturate Standard...........  Screw-cap vial: 10ml.....      7/17/76

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Adri/Technam...........................  Barbituric Acid Sensitized Red   Vaccine Vial: 50ml.......      5/03/73
                                          Blood Cells.                                                          
Adri/Technam...........................  Benzoyl Ecgonine...............  Screw-cap vial: 10ml.....      4/18/74
Adri/Technam...........................  Benzoyl Ecgonine Sensitized Red  Vaccine Vial: 50ml.......      5/03/73
                                          Blood Cells.                                                          
Adri/Technam...........................  Benzoyl Ecgonine Standard......  Screw-cap vial: 10ml.....      7/17/76
Adri/Technam...........................  Benzoyl Ecgonine-BSA...........  Vaccine Vial.............      7/21/75
Adri/Technam...........................  Benzoyl Ecgonine-RSA...........  Vaccine Vial.............      7/21/75
Adri/Technam...........................  CMM-BSA and CMM-RSA              Vaccine Vial: 10ml.......      5/03/73
                                          (Carboxymethylmorphine Bovine                                         
                                          Serum Albumin or                                                      
                                          Carboxymethylmorphine Rabbit                                          
                                          Serum Albumin).                                                       
Adri/Technam...........................  Cannabuse Cannabidiol Standard.  Disks: 25/package........      5/03/85
Adri/Technam...........................  Cannabuse Delta 8 THC            Disks: 25/package........      9/19/84
                                          Carboxylic Acid Standard.                                             
Adri/Technam...........................  Cannabuse Delta 8 THC            Vial: 6 ml...............      9/19/84
                                          Carboxylic Acid Standard.                                             
Adri/Technam...........................  Cannabuse Delta 9 THC            Vial: 6 ml...............      9/19/84
                                          Carboxylic Acid Standard.                                             
Adri/Technam...........................  Cannabuse Delta 9 THC            Disks: 25/package........      9/19/84
                                          Carboxylic Acid Standard.                                             
Adri/Technam...........................  Cannabuse Delta 9 THC Standard.  Disks: 25/package........      9/19/84
Adri/Technam...........................  Cannabuse Delta 9 THC Standard.  Vial: 6 ml...............      9/19/84
Adri/Technam...........................  Drug Standards, Acid/Neutral     Disks: 25/package........     11/15/85
                                          Mixture A and B.                                                      
Adri/Technam...........................  Drug Standards, Basic Mixture A  Disks: 25/package........     11/15/85
                                          and B.                                                                
Adri/Technam...........................  Methadone Standard.............  Screw-cap vial: 10ml.....      7/17/76
Adri/Technam...........................  Morphine Sensitized Red Blood    Vaccine Vial: 50ml.......      5/03/73
                                          Cells.                                                                
Adri/Technam...........................  Morphine Standard (in distilled  Screw-cap vial: 10ml.....      7/17/77
                                          water).                                                               
Adri/Technam...........................  Tropinecarboxylic Acid           Screw-cap Bottle: 10ml...      5/03/73
                                          (ecgonine).                                                           
Alltech-Applied Science Laboratories...  (D)-Norpseudoephedrine HCL.....  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  4-Chlorotestosterone...........  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  4-Methylaminorex...............  Vial: 1 ml...............      6/16/89
Alltech-Applied Science Laboratories...  6-Acetylcodeine................  Vial: 1 ml...............      6/16/89
Alltech-Applied Science Laboratories...  6-Monoacetylmorphine HCl.......  Vial: 1 ml...............      3/30/88
Alltech-Applied Science Laboratories...  Allylisobutylbarbituric Acid...  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Alphaprodine HCL...............  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Alphenal.......................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Alprazolam.....................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Amobarbital....................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Amphetamine HCL................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Antidepressants Mix............  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Aprobarbital...................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Barbital.......................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Barbiturates, Mixture 4........  Vial: 10ml...............     10/04/72
Alltech-Applied Science Laboratories...  Benzoylecgonine Tetrahydrate...  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Benzoylecgonine Tetrahydrate     Amber Ampoule: 1ml.......      2/16/90
                                          7.5ug, 50ug, 250ug.                                                   
Alltech-Applied Science Laboratories...  Benzphetamine HCL..............  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Boldenone......................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Bromazepam.....................  Vial: 1 ml...............      6/16/89
Alltech-Applied Science Laboratories...  Butabarbital...................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Butethal.......................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Cannabidiol....................  Vial: 1 ml...............      3/30/88
Alltech-Applied Science Laboratories...  Cannabinol.....................  Vial: 1 ml...............      3/30/88
Alltech-Applied Science Laboratories...  Chloral Hydrate................  Vial: 1ml................      4/16/85

[[Page 109]]

                                                                                                                
Alltech-Applied Science Laboratories...  Chlordiazepoxide HCL...........  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Clonazepam.....................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Clorazepate Dipotassium........  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Clostebol......................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Cocaethylene...................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Cocaine........................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Codeine........................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Cyclopentobarbital.............  Vial: 1 ml...............      6/16/89
Alltech-Applied Science Laboratories...  Delta-8-Tetrahydro-cannabinol..  Vial: 1 ml...............      3/30/88
Alltech-Applied Science Laboratories...  Delta-9-Tetrahydrocannabinol...  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Depressants, Mixture 3.........  Vial: 10ml...............     10/04/72
Alltech-Applied Science Laboratories...  Dextropropoxyphene HCL.........  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Diacetylmorphine HCL...........  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Diallybarbituric acid..........  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Diazepam.......................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Diethylpropion HCL.............  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Dihydrocodeine.................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Dimethyltryptamine.............  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Drostanolone...................  Ampule: 2ml..............      9/26/05
Alltech-Applied Science Laboratories...  Drug Mix Four..................  Ampoule: 1 ml............     11/03/86
Alltech-Applied Science Laboratories...  Drug Mix One...................  Ampoule: 1 ml............     10/21/86
Alltech-Applied Science Laboratories...  Drug Mix Three.................  Ampoule: 1 ml............     11/03/86
Alltech-Applied Science Laboratories...  Drug Mix Two...................  Ampoule: 1 ml............     10/21/86
Alltech-Applied Science Laboratories...  Ecgonine HCL...................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Ecgonine Methyl Ester HCl......  Vial: 1 ml...............      3/30/88
Alltech-Applied Science Laboratories...  Ethchlorvynol..................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Ethinamate.....................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Ethylmorphine HCL..............  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Fenfluramine HCL...............  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Fentanyl.......................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Flunitrazepam..................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Fluoxymesterone................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Flurazepam HCL.................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  GC/MS Benzoylecgonine            Kit: 3 vials.............      2/16/90
                                          Calibration Standards Kit.                                            
Alltech-Applied Science Laboratories...  Glutethimide...................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Halazepam......................  Vial: 1ml................      4/16/85

[[Page 110]]

                                                                                                                
Alltech-Applied Science Laboratories...  Hexobarbital...................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Hydrocodone Bitartrate.........  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Hydromorphone HCL..............  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  L-Amphetamine HCl..............  Vial: 1 ml...............      6/16/89
Alltech-Applied Science Laboratories...  L-Methamphetamine HCl..........  Vial: 1 ml...............      6/16/89
Alltech-Applied Science Laboratories...  Levorphanol Tartrate...........  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Lorazepam......................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Lysergic Acid..................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Lysergic Acid Diethylamide.....  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Lysergic Acid N-(methylpropyl)   Vial: 1ml................      4/16/85
                                          amide.                                                                
Alltech-Applied Science Laboratories...  MDA HCl........................  Vial: 1 ml...............      3/30/88
Alltech-Applied Science Laboratories...  MDE HCl........................  Vial: 1 ml...............      6/16/89
Alltech-Applied Science Laboratories...  MDMA HCl.......................  Vial: 1 ml...............      3/30/88
Alltech-Applied Science Laboratories...  Medazepam......................  Vial: 1 ml...............      6/16/89
Alltech-Applied Science Laboratories...  Meperidine HCL.................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Mephobarbital..................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Meprobamate....................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Mescaline......................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Mesterolone....................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Methadone HCL..................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Methamphetamine HCL............  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Methandriol....................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Methandrostenolone.............  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Methaqualone HCL...............  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Metharbital....................  Vial: 1 ml...............      6/16/89
Alltech-Applied Science Laboratories...  Methcathinone..................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Methenolone....................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Methohexital...................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Methylphenidate................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Methyltestosterone.............  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Methyprylon....................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Mixture 1-Opiates..............  Vial: 1ml................     10/04/72
Alltech-Applied Science Laboratories...  Mixture 2-Stimulants...........  Vial: 1ml................     10/04/72
Alltech-Applied Science Laboratories...  Mixture 3-Depressants..........  Vial: 1ml................     10/04/72
Alltech-Applied Science Laboratories...  Mixture 4-Barbiturates.........  Vial: 1ml................     10/04/72
Alltech-Applied Science Laboratories...  Mixture 5-Kit of                 Vial: 1ml................     10/04/72
                                          Representatives.                                                      

[[Page 111]]

                                                                                                                
Alltech-Applied Science Laboratories...  Morphine.......................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  N-Ethylamphetamine.............  Amber Ampoule: 1ml.......      2/16/90
Alltech-Applied Science Laboratories...  N-Hydroxy-MDA..................  Amber Ampoule: 1ml.......      2/16/90
Alltech-Applied Science Laboratories...  Nalorphine.....................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Nandrolone.....................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Nitrazepam.....................  Vial: 1 ml...............      3/30/88
Alltech-Applied Science Laboratories...  Norcocaine.....................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Norcodeine HCL.................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Nordiazepam....................  Vial: 1 ml...............      3/30/88
Alltech-Applied Science Laboratories...  Norethandrolone................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Normeperidine HCL..............  Vial: 1 ml...............      6/16/89
Alltech-Applied Science Laboratories...  Normorphine....................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Opiates Mix #2.................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Opiates, Mixture 1.............  Vial: 10ml...............     10/04/72
Alltech-Applied Science Laboratories...  Oxandrolone....................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Oxazepam.......................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Oxycodone HCL..................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Oxymesterone...................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Oxymetholone...................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Oxymorphone....................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Oxymorphone HCL................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Paraldehyde....................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Pemoline.......................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Pentazocine....................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Pentazocine HBr................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Pentobarbital..................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Phencyclidine HCL..............  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Phendimetrazine Bitartrate.....  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Phenmetrazine HCl..............  Amber Ampoule: 1ml.......      2/16/90
Alltech-Applied Science Laboratories...  Phenobarbital..................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Phentermine....................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Prazepam.......................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Propylbenzoyl-ecgonine.........  Vial: 1 ml...............      3/30/88
Alltech-Applied Science Laboratories...  Psilocybin.....................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Psilocyn.......................  Vial: 1 ml...............     11/06/87
Alltech-Applied Science Laboratories...  Secobarbital...................  Vial: 1ml................      1/24/73

[[Page 112]]

                                                                                                                
Alltech-Applied Science Laboratories...  Spot Chek Test Mix 1-A-PPS.....  Ampule: 2ml..............     12/19/95
Alltech-Applied Science Laboratories...  Spot Chek Test Mix 1A-M........  Ampule: 2ml..............     12/19/95
Alltech-Applied Science Laboratories...  Spot Chek Test Mix 1B-1........  Ampule: 2ml..............     12/19/95
Alltech-Applied Science Laboratories...  Spot Chek Test Mix 1B-2........  Ampule: 2ml..............     12/19/95
Alltech-Applied Science Laboratories...  Spot Chek Test Mix 1B-3........  Ampule: 2ml..............     12/19/95
Alltech-Applied Science Laboratories...  Spot Chek Test Mix 2A-A........  Ampule: 2ml..............     12/19/95
Alltech-Applied Science Laboratories...  Spot Chek Test Mix 2A-N........  Ampule: 2ml..............     12/19/95
Alltech-Applied Science Laboratories...  Spot Chek Test Mix 2B-B........  Ampule: 2ml..............     12/19/95
Alltech-Applied Science Laboratories...  Spot Chek Test Mix 2C-C........  Ampule: 2ml..............     12/19/95
Alltech-Applied Science Laboratories...  Stanolone......................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Stanolone Valerate.............  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Stanolzolol....................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Stimulants, Mixture 2..........  Vial: 10ml...............     10/04/72
Alltech-Applied Science Laboratories...  Talbutal.......................  Vial: 1 ml...............      6/16/89
Alltech-Applied Science Laboratories...  Temazepam......................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  Testosterone...................  Ampule: 2ml..............      9/26/95
Alltech-Applied Science Laboratories...  Thebaine.......................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Thiamylal......................  Vial: 1ml................      1/24/73
Alltech-Applied Science Laboratories...  Thiopental.....................  Vial: 1 ml...............      6/16/89
Alltech-Applied Science Laboratories...  Toxi Clean Test Mix............  Vial: 1 ml...............      3/30/88
Alltech-Applied Science Laboratories...  Triazolam......................  Vial: 1ml................      4/16/85
Alltech-Applied Science Laboratories...  d3-Benzoylecgonine Tetrahydrate  Amber Ampoule: 5ml.......      2/16/90
American Biological Technologies, Inc..  Dade Urine Chemistry Control,    Glass Vial: 15ml.........      4/08/91
                                          Level I & II.                                                         
American Monitor Corporation...........  Qualify I......................  Glass Vial: 10ml.........     10/09/75
American Monitor Corporation...........  Qualify II.....................  Glass Vial: 10ml.........     10/09/75
Amerscham Corporation..................  [N-Methyl-3H]Lysergic Acid       Vial: 5-7ml..............     10/11/95
                                          Diethylamide.                                                         
Amersham Corporation...................  5 Alpha-Dihydro[1, 2, 4, 5, 6,   Vial: 6ml................      4/02/91
                                          7-3H]Testosterone Cat. No.                                            
                                          TRK.443.                                                              
Amersham Corporation...................  5 alpha-Dihydro[1 alpha, 2       Vial: 6ml................      4/02/91
                                          alpha(n)-3H] Testosterone Cat.                                        
                                          No. TRK.395.                                                          
Amersham Corporation...................  5 alpha-dihydro[1, 2, 4, 5, 6,   Vial: 1ml................      4/11/91
                                          7-3H] Testosterone Reagent 4 T/                                       
                                          DHT RIA Kit.                                                          
Amersham Corporation...................  Amerlex T-3 RIA Kit, IM 2000,    Kit: 50 tests, 100 tests,      2/18/80
                                          IM 2001, IM 2004.                400 tests.                           
Amersham Corporation...................  Amerlex T-4 RIA Kit, IM 2010,    Kit: 50 tests, 100 tests,      2/06/80
                                          IM 2011, IM 2014.                400 tests.                           
Amersham Corporation...................  Amerlex-M B-hCG                  Kit: 100 tests, 400 tests      6/19/85
                                          Radioimmunoassay Kit IM 3091,                                         
                                          IM 3094.                                                              
Amersham Corporation...................  Amerlex-M T3 RIA Kit, 1M.3001,   Kit: 100 Tests 400 Tests.      8/27/86
                                          1M.3004.                                                              
Amersham Corporation...................  Amerlex-M T4 RIA Kit, 1M.3011,   Kit: 100 Tests 400 Tests.      8/27/86
                                          1M.3014.                                                              
Amersham Corporation...................  Amerlite FSH Assay, Cat. Code    Glass vial: 5.8ml,             5/30/89
                                          LAN.0077, Cat. Code LAN.2077.    38.1ml, 240 tests, 144               
                                                                           tests.                               
Amersham Corporation...................  Amerlite Rubella Antibody        Glass vial: 5.8ml,             5/30/89
                                          Assay, Cat. Code LAN.0200,       38.1ml, 240 tests, 144               
                                          Cat. Code LAN.2200.              tests.                               
Amersham Corporation...................  Amerlite TSH Assay, Cat. Code    Glass vial: 5.8ml, 240         5/30/89
                                          LAN.0001, Cat. Code LAN.2001.    tests, 144 tests.                    

[[Page 113]]

                                                                                                                
Amersham Corporation...................  Amerlite TT3 Assay: Catalog      Kit: 144 tests, 240           11/24/87
                                          Code Lan. 0003, Lan. 1003, and   tests, 480 tests.                    
                                          Lan.2003.                                                             
Amersham Corporation...................  Amerlite TT4 Assay: Catalog      Kit: 144 tests, 240           11/24/87
                                          Code Lan. 0002, Lan. 1002,       tests, 480 tests.                    
                                          Lan. 2002.                                                            
Amersham Corporation...................  Codeine (N-methyl-C14)           Custom Preparation.......      3/27/72
                                          Hydrochloride.                                                        
Amersham Corporation...................  Dihydrotestosterone Standard     Vial: 5.5ml..............      4/11/91
                                          Reagnet 3 T/DHT RIA Kit.                                              
Amersham Corporation...................  Morphine (N-methyl-C14)          Vial: 0.32 to 1.89mg.....      3/27/72
                                          Hydrocloride No. CFA-363.                                             
Amersham Corporation...................  Pheno [2-14C] barbital Catalog   Vial: 0.39 to 5.85mg.....     11/05/74
                                          No. CFA 537.                                                          
Amersham Corporation...................  Prolactin RIA Kit, IM 1060,      Kit: 50 tests, 100 tests.      3/28/80
                                          1061.                                                                 
Amersham Corporation...................  T-3 Uptake (MAA) Kit-IM 1020,    Kit: 50 tests, 100 tests,      2/05/79
                                          IM 1021, IM 1024.                400 tests.                           
Amersham Corporation...................  Testosterone Standard Reagent 2  Vial: 5.5ml..............      4/11/91
                                          T/DHT RIA Kit.                                                        
Amersham Corporation...................  Testosterone-3-(0-               Vial: 1.2ml..............      4/02/91
                                          carboxymethyl)oximino-(2-                                             
                                          [125I] iodohistamine)10uCi,                                           
                                          25uCi Cat. No. IM.128.                                                
Amersham Corporation...................  Testosterone/                    Kit: 200 assays..........      4/11/91
                                          dihydrotestosterone [3H] assay                                        
                                          system Cat. No. TRK-600.                                              
Amersham Corporation...................  [1(N)-3H] Hydromorphone TRQ      Vial: 47.5-95 micrograms.      7/31/87
                                          4729.                                                                 
Amersham Corporation...................  [1(n)-3H] Codeine, No. TRK 448.  Ampule: 0.002mg to             2/26/74
                                                                           0.015mg.                             
Amersham Corporation...................  [1(n)-3H] Morphine, No. TRK-447  Vial: 0.002 mg to 0.015        2/26/74
                                                                           mg.                                  
Amersham Corporation...................  [1, 2, 6, 7-3H] Testosterone     Vial: 6ml................      4/02/91
                                          Cat. No. TRK.402.                                                     
Amersham Corporation...................  [1, 7, 8(n)-3H]Dihydromorphine,  Vial: 0.0008 mg to 0.008       2/26/74
                                          No. TRK-450.                     mg.                                  
Amersham Corporation...................  [15, 16(n)-3H] Etorphine,        Vial: 3.45 to 6.9             11/19/74
                                          Catalog No. TRK 476.             micrograms.                          
Amersham Corporation...................  [15, 16(n)-3H] Etorphine         Vial: 13.8 to 27.6             2/17/75
                                          Catalog No. TRK 476.             micrograms.                          
Amersham Corporation...................  [17 alpha-methyl-3H] Mibolerone  Vial: 6ml................      4/02/91
                                          Cat. No. TRK.764.                                                     
Amersham Corporation...................  [2(n)-3H] Lysergic Acid          Vial: 0.003mg to 0.04mg..      5/22/74
                                          Diethylamide, No. TRK. 461.                                           
Amersham Corporation...................  [2-14C] Diazepam Catalog No.     Multidose Glass Vial:          9/28/77
                                          CFA.591.                         56mm x 25mm.                         
Amersham Corporation...................  [3H]11-Ketotestosterone Cat.     Vial: 5.7ml..............      6/13/91
                                          No. TRQ.5919.                                                         
Amersham Corporation...................  [4-14C] Testosterone 50uCi,      Vial: 6ml................      4/02/91
                                          250uCi Cat. No. CFA.129.                                              
Amersham Corporation...................  [N-methyl-3H] Diazepam Catalog   Multidose Glass Vial:          9/28/77
                                          Code: TRK.572.                   56mm x 25mm.                         
Amersham Life Science..................  [125I] Iodo-Lysergic Acid        Vial: 1.2ml..............     11/22/95
                                          Diethylamide.                                                         
Analytical Control Systems, Inc........  Benchmark I TDM Control 1L, 2M,  Plastic Vial: 5ml per         10/02/91
                                          3H.                              Vial; 1-120 Vials per                
                                                                           Bag.                                 
Armed Forces Institute of Pathology....  11-nor-9-carboxy-delta 8-THC in  Glass Ampule: 1mg/ml,          1/25/82
                                          Ethanol Ampules.                 1ml, 5ml, 10ml.                      
Astral Medical Systems.................  Barbital Buffer................  Plastic bag: 12.2g/bag...      5/01/85
Astral Medical Systems.................  Barbital Lactate Buffer........  Plastic bag: 18g/bag.....      5/01/85
Astral Medical Systems.................  Isoenzyme Buffer...............  Plastic bag: 14g/bag.....      5/01/85
Astral Medical Systems.................  Tris-Barbital Sodium Barbital    Plastic bag: 18g/bag.....      5/01/85
                                          Buffer.                                                               
Atochem North America, Inc.............  M&T NiproTeq SB Additive.......  Polypropylene Containers:      3/10/88
                                                                           5 gallons, 55 gallons.               
BHP Diagnostix, Inc....................  Kallestad TDM Multi-Calibrator-  Kit: 7-3 ml Vials; 3 ml        8/18/88
                                          Pilot Lot B-G.                   Vial.                                
BHP Diagnostix, Inc....................  Kallestad TDM Multi-Calibrator-  3ml, 6ml, 10ml, 30ml,          8/18/88
                                          Pilot-Lot Phenobarbital.         50ml Vial.                           
BHP Diagnostix, Inc....................  Kodak Ektachem-DT Calibrator...  Bottle: 6ml..............      1/05/85
Baxter Diagnostics Inc.................  Dade Moni-Trol Gold, Level 1X    Kit: 55 Vials............      8/31/94
                                          Chemistry Control and                                                 
                                          Carbonate Diluent 1.                                                  
Baxter Diagnostics Inc.................  Dade Moni-Trol Gold, Level 1X    Bottle: 18ml.............      8/31/94
                                          and Level 2X Chemistry                                                
                                          Controls.                                                             
Baxter Diagnostics Inc.................  Dade Moni-Trol Gold, Level 2X    Kit: 55 Vials............      8/31/94
                                          Chemistry Control and                                                 
                                          Carbonate Diluent 2.                                                  
Baxter Diagnostics Inc.................  EXCEL-QC Level 1 Serum           Bottle: 18ml.............       8/4/93
                                          Chemistry Control.                                                    
Baxter Diagnostics Inc.................  EXCEL-QC Level 1 and Level 2     Kit: 12 Bottles..........       8/4/93
                                          Serum Chemistry Control and                                           
                                          Carbonate Diluent 1 and 2.                                            
Baxter Diagnostics Inc.................  EXCEL-QC Level 2 Serum           Bottle: 18ml.............       8/4/93
                                          Chemistry Control.                                                    
Baxter Diagnostics Inc.................  Paramax Phenobarbital            Kit: 6 Glass Bottles; 6ml       7/7/93
                                          Calibrator I, II, III, Cat. #    each.                                
                                          B-6109-11.                                                            
Baxter Diagnostics Inc.................  Paramax Phenobarbital            Glass Bottle: 6ml........       7/7/93
                                          Calibrator Level II.                                                  
Baxter Diagnostics Inc.................  Paramax Phenobarbital            Glass Bottle: 6ml........      7/07/93
                                          Calibrator Level III.                                                 
Bayer Corporation......................  Estradiol Antibody Conjugate R1  Bulk.....................      8/16/95
Bayer Corporation......................  Technicon Immuno 1 Estradiol     Kit: 1 Cassette..........      8/16/95
                                          Reagents Kit No. T01-3595-51.                                         
Beckman Instruments, Inc...............  ARRAY 360 System: Drug           Bottle: 3ml..............      3/13/95
                                          Calibrator.                                                           
Beckman Instruments, Inc...............  ARRAY 360 System: Drug Control   Bottle: 1ml..............      3/13/95
                                          Kit.                                                                  

[[Page 114]]

                                                                                                                
Beckman Instruments, Inc...............  Beckman Buffer B-2.............  Packet: 18.16 g..........      4/24/71
Beckman Instruments, Inc...............  Beckman ICS Drug Calibrators A,  Vials: 5ml...............     10/29/80
                                          B, C, D, and E.                                                       
Beckman Instruments, Inc...............  Beckman ICS Drug Control Sera..  Kit containing: 6-1ml         11/11/80
                                                                           bottles.                             
Beckman Instruments, Inc...............  Beckman ICS Phenobarbital        Vial: 5ml................     10/29/80
                                          Conjugate.                                                            
Beckman Instruments, Inc...............  Beckman LD Buffer..............  Bottle: 14.3 grams.......      7/31/86
Beckman Instruments, Inc...............  Beckman LD Buffer..............  Bottle: 14.3 grams.......      7/31/86
Beckman Instruments, Inc...............  IFE Gel........................  Foil Packet: 1 Gel; Box:       1/22/96
                                                                           10 Gels.                             
Beckman Instruments, Inc...............  LD Gel.........................  Foil Pack: 1 Gel; Box: 10      1/22/96
                                                                           Gels.                                
Beckman Instruments, Inc...............  Paragon Electrophoresis System:  Plastic Tray: 3.5ml, Box:      5/19/89
                                          Alkaline Phosphatase Isoenzyme   10 trays, Kit: 10 trays.             
                                          Electrophoresis (Isopal) Kit.                                         
Beckman Instruments, Inc...............  Paragon Electrophoresis System:  Plastic Tray: 3.5ml, Box:      5/19/89
                                          High Resolution                  10 trays, Kit: 10 trays.             
                                          Electrophoresis (HRE) Kit.                                            
Beckman Instruments, Inc...............  Paragon Electrophoresis System:  Plastic Tray: 3.5ml, Box:      5/19/89
                                          Immunoelectrophoresis (IEP)      10 trays, Kit: 10 trays.             
                                          Kit.                                                                  
Beckman Instruments, Inc...............  Paragon Electrophoresis System:  Plastic Tray: 3.5ml......      7/31/86
                                          Immunofixation Electrophoresis                                        
                                          (IFE) Kit.                                                            
Beckman Instruments, Inc...............  Paragon Electrophoresis System:  Plastic Tray: 3.5ml......      7/31/86
                                          Lactate Dehydrogenase                                                 
                                          Isoenzyme Electrophoresis (LD)                                        
                                          Kit.                                                                  
Beckman Instruments, Inc...............  Paragon Electrophoresis System:  Plastic Tray: 3.5 ml,          5/19/89
                                          Lipoprotein Electrophoresis      Box: 10 trays, Kit: 10               
                                          (LIPO) Kit.                      trays.                               
Beckman Instruments, Inc...............  Paragon Electrophoresis System:  Plastic Tray: 3.5ml......      7/31/86
                                          Protein Electrophoresis (SPE-                                         
                                          II) Kit.                                                              
Beckman Instruments, Inc...............  Paragon Electrophoresis System:  Plastic Tray: 3.5ml, Box:      5/19/89
                                          Serum Protein Electrophoresis    10 trays, Kit: 10 trays.             
                                          (SPE) Kit.                                                            
Beckman Instruments, Inc...............  SPE Gel........................  Foil Pack: 1 Gel; Box: 10      1/22/96
                                                                           Gels.                                
Beckman Instruments, Inc...............  Synchron CX Systems: CX          Cartridge: 150 Tests.....      3/13/95
                                          Amphetamines Reagent Kit.                                             
Beckman Instruments, Inc...............  Synchron CX Systems: CX          Cartridge: 150 Tests.....      3/13/95
                                          Barbiturates Reagent Kit.                                             
Beckman Instruments, Inc...............  Synchron CX Systems: CX          Cartridge: 150 Tests.....      3/13/95
                                          Benzodiazepine Reagent Kit.                                           
Beckman Instruments, Inc...............  Synchron CX Systems: CX          Cartridge: 150 Tests.....      3/13/95
                                          Cannabinoid 50ng and                                                  
                                          Cannabinoid 100ng Reagent Kits.                                       
Beckman Instruments, Inc...............  Synchron CX Systems: CX DAT      Bottle: 5ml..............      3/13/95
                                          High Urine Calibrator I.                                              
Beckman Instruments, Inc...............  Synchron CX Systems: CX DAT      Bottle: 5ml..............      3/13/95
                                          High Urine Calibrator II.                                             
Beckman Instruments, Inc...............  Synchron CX Systems: CX DAT      Bottle: 5ml..............      3/13/95
                                          High Urine Control I.                                                 
Beckman Instruments, Inc...............  Synchron CX Systems: CX DAT      Bottle: 5ml..............      3/13/95
                                          High Urine Control II.                                                
Beckman Instruments, Inc...............  Synchron CX Systems: CX DAT Low  Bottle: 5ml..............      3/13/95
                                          Urine Calibrator I.                                                   
Beckman Instruments, Inc...............  Synchron CX Systems: CX DAT Low  Bottle: 5ml..............      3/13/95
                                          Urine Calibrator II.                                                  
Beckman Instruments, Inc...............  Synchron CX Systems: CX DAT Low  Bottle: 5ml..............      3/13/95
                                          Urine Control I.                                                      
Beckman Instruments, Inc...............  Synchron CX Systems: CX DAT Low  Bottle: 5ml..............      3/13/95
                                          Urine Control II.                                                     
Beckman Instruments, Inc...............  Synchron CX Systems: CX Opiate   Cartridge: 150 Tests.....      3/13/95
                                          Reagent Kit.                                                          
Beckman Instruments, Inc...............  Synchron CX Systems: CX          Cartridge: 150 Tests.....      3/13/95
                                          Phencyclidine Reagent Kit.                                            
Beckman Instruments, Inc...............  Synchron CX Systems: CX THC      Bottle: 5ml..............      3/13/95
                                          Urine 20ng/ml, 75ng/ml, 125ng/                                        
                                          ml Controls.                                                          
Beckman Instruments, Inc...............  Synchron CX Systems: CX THC      Bottle: 5ml..............      3/13/95
                                          Urine 50ng/ml, 100ng/ml, 200ng/                                       
                                          ml Calibrators.                                                       
Beckman Instruments, Inc...............  Synchron CX Systems: Cocaine     Cartridge: 150 Tests.....      3/13/95
                                          Metabolite Reagent Kit.                                               
Beckman Instruments, Inc...............  Synchron CX Systems: Methadone   Cartridge: 150 Tests.....      3/13/95
                                          Reagent Kit.                                                          
Beckman Instruments, Inc...............  Synchron Control: Multilevel     Plastic Bottle: 20ml;          5/13/91
                                          Comprehensive Chemistry          Kit: 6 bottles.                      
                                          Control Serum Levels I, II,                                           
                                          III.                                                                  
Beckman Instruments, Inc...............  Triad LINK Comprehensive Custom  Plastic Bottle: 20ml;          5/13/91
                                          Unassayed Chemistry Control      Box: 20 Bottles.                     
                                          Serum Levels I, II, III.                                              
Beckman Instruments, Inc...............  Triad NYSPATH Comprehensive      Plastic Bottle: 20ml; Box      5/13/91
                                          Custom Unassayed Chemistry       20 Bottles.                          
                                          Control Serum Levels I, II,                                           
                                          III.                                                                  
Beckman Instruments, Inc...............  Vigil PRx Multilevel Protein/    Plastic Bottle: 10ml;          5/13/91
                                          Drug Control Serum Levels I,     Kit: 6 Bottles.                      
                                          II, III.                                                              
Becton Dickinson & Company.............  IQ Immunochemistry System,       Kit: 25 tests............      6/30/87
                                          Thyroid Stimulating Hormone                                           
                                          Catalog No. 3010.                                                     
Becton Dickinson & Company.............  Neonatal T4 Tracer, Catalog      Bottle: 125ml............      1/15/92
                                          #264015.                                                              
Becton Dickinson & Company.............  T3 Tracer Solution Catalog No.   Bottle: 125ml............      9/27/78
                                          237728.                                                               

[[Page 115]]

                                                                                                                
Becton Dickinson & Company.............  TSH [125I] Tracer, Catalog No.   Clear vial: 10ml.........      9/04/86
                                          259624.                                                               
Behring Diagnostics....................  IEP Buffer, 793001 pH 8.2......  Foil Pouch: 6.5 g........      9/17/79
Behring Diagnostics....................  Immuno-tec II Agarose Plate,     Foil Pouch: ``5.35'' x         9/17/79
                                          839013, 850013.                  ``5.25''.                            
Behring Diagnostics Inc................  Emit 5B3 THC; Calibrators; 0,    Vial: 10ml...............     12/14/95
                                          50, 100, 200ng/ml.                                                    
Behring Diagnostics Inc................  Emit II 5B3 THC Assay..........  Kit: 2 Vials, 500ml each.     12/14/94
Bio-Metric Systems, Incorporated.......  Cocaine-Enzyme Conjugate.......  Vial: 250ml, 100ml, 50ml.      7/07/92
Bio-Metric Systems, Incorporated.......  Cocaine-ImmunoPrime Modified     Vial: 50ml, 10ml.........      7/07/92
                                          Carrier.                                                              
Bio-Metric Systems, Incorporated.......  Morphine-Enzyme Conjugate......  Vial: 250ml, 100ml, 50ml.      7/07/92
Bio-Metric Systems, Incorporated.......  Morphine-ImmunoPrime Modified    Vial: 50ml, 10ml.........      7/07/92
                                          Carrier.                                                              
Bio-Metric Systems, Incorporated.......  Phencyclidine-Enzyme Conjugate.  Vial: 250ml, 100ml, 50ml.      7/07/92
Bio-Metric Systems, Incorporated.......  Phencyclidine-ImmunoPrime        Vial: 50ml, 10ml.........      7/07/92
                                          Modified Carrier.                                                     
Bio-Metric Systems, Incorporated.......  Tetrahydrocannabinol-Enzyme      Vial: 250ml, 100ml, 50ml.      7/07/92
                                          Conjugate.                                                            
Bio-Metric Systems, Incorporated.......  Tetrahydrocannabinol-            Vial: 50ml, 10ml.........      7/07/92
                                          ImmunoPrime Carrier.                                                  
Bio-Rad Laboratories...................  Benzodiazepines/Tricyclic        Kit: 100 tests...........      2/08/90
                                          Antidepressants by HPLC.                                              
Bio-Rad Laboratories...................  CoTube Estradiol Tracer........  Glass Bottle: 125ml......      7/28/93
Bio-Rad Laboratories...................  Dade Urine Chemistry Control     Vial: 20 ml, 50 ml.......      1/05/88
                                          Levels I AND II.                                                      
Bio-Rad Laboratories...................  Dade Urine Toxiology Control...  Vial: 50 ml..............      1/05/88
Bio-Rad Laboratories...................  Internal Standard..............  Amber vial: 30ml Flask:        2/08/90
                                                                           200ml-2000ml.                        
Bio-Rad Laboratories...................  Methadone/Methadone Metabolite   400 tests................      9/17/90
                                          Reagent Kit.                                                          
Bio-Rad Laboratories...................  Quantaphase Thyroxine RIA-125I   Plastic bottle: 60ml,          5/06/81
                                          Tracer/Dissociating Reagent.     260ml.                               
Bio-Rad Laboratories...................  Quantaphase Thyroxine RIA-       Plastic bottle: 60ml,          5/06/81
                                          Thyroxine Immunobeads.           260ml.                               
Bio-Rad Laboratories...................  Quantimune Barbital Buffer.....  Plastic Bottle: 1000ml,        5/31/78
                                                                           250ml, 200ml.                        
Bio-Rad Laboratories...................  Quantimune Radioimmunoassay T-4  Vial: 10 ml..............      7/21/76
                                          Tracer, Iodine-125.                                                   
Bio-Rad Laboratories...................  Quantimune T-3 RIA Barbital      Bottle: 220ml............      9/24/82
                                          Buffer.                                                               
Bio-Rad Laboratories...................  Quantimune T-3 RIA Test Kit....  Kit: 500 tests, 100 tests      5/31/78
Bio-Rad Laboratories...................  Quantimune T-4 RIA Kit.........  Kit: 500 tests...........      7/01/77
Bio-Rad Laboratories...................  Quantimune T-4 RIA Test Kit....  Kit: 5000 tests, 100           5/31/78
                                                                           tests.                               
Bio-Rad Laboratories...................  Quantimune Thyroxine             Plastic Bottle with Screw      7/01/77
                                          Radioimmunoassay Barbital        cap: 1 liter.                        
                                          Buffer.                                                               
Bio-Rad Laboratories...................  Quantimune Thyroxine             Glass Serum Vial: 10 ml..      7/01/77
                                          Radioimmunoassay T-4 125I                                             
                                          Tracer/Dissociating Agent.                                            
Bio-Rad Laboratories...................  REMEDI DPS Check Mix...........  Vial: 20ml, Flask: 1L-10L      9/17/90
Bio-Rad Laboratories...................  REMEDI DPS Internal Standard     Vial: 20ml, Flask: 250ml-      9/17/90
                                          Combination.                     6000ml.                              
Bio-Rad Laboratories...................  REMEDI DPS Internal Standard     Vial: 20ml, Flask: 250ml-      9/17/90
                                          One.                             2500ml.                              
Bio-Rad Laboratories...................  REMEDI DPS Internal Standard     Vial: 20ml, Flask: 250ml-      9/17/90
                                          Two.                             5000ml.                              
Bio-Rad Laboratories...................  REMEDI DPS Urine Calibrator....  Vial: 20ml, Flask: 1L-10L      9/17/90
Bio-Rad Laboratories...................  Serum Calibrator 1.............  Amber vial: 20ml               2/08/90
                                                                           Polypropylene container:             
                                                                           20L.                                 
Bio-Rad Laboratories...................  Serum Calibrator 2.............  Amber vial: 20ml               2/08/90
                                                                           Polypropylene container:             
                                                                           20L.                                 
Bio-Rad Laboratories...................  Serum Calibrator for             Box: 2 vials.............      2/08/90
                                          Benzodiazepines/Tricyclics,                                           
                                          Contains 2.                                                           
Bio-Rad Laboratories...................  T-4 Competitive Binding          Bottle: 385 ml...........      7/21/76
                                          Reagent, Iodine-125.                                                  
Bio-Rad Laboratories, (Chemical          Barbital Buffer................  Vial: 10ml...............      7/21/76
 Division).                                                                                                     
Bio-Rad Laboratories, (Chemical          Barbital Buffer Powder.........  Plastic bottle: 250 ml...      9/09/77
 Division).                                                                                                     
Bio-Rad Laboratories, (Chemical          Barbital Buffer Powder.........  Plastic bottle: 250ml....      7/21/76
 Division).                                                                                                     
Bio-Rad Laboratories, (Chemical          Barbital Buffer-Dry Pack.......  Packages: 9.11 g., 18.21       5/09/74
 Division).                                                                g., 12.14 g.                         
Bio-Rad Laboratories, (Chemical          Bio-Rad Electrophoresis Buffer.  Bottle: 500ml............     12/14/72
 Division).                                                                                                     
Bio-Rad Laboratories, (Chemical          Electrophoresis Buffer, Dry-     Package: 6.15 g..........     12/14/72
 Division).                               Pack.                                                                 

[[Page 116]]

                                                                                                                
Bio-Rad Laboratories, (Chemical          Immunoelectrophoresis Barbital   Dry-pack: 25.6 g.........      8/06/75
 Division).                               Buffer I, pH 8.6.                                                     
Bio-Rad Laboratories, (Chemical          Immunoelectrophoresis Barbital   Dry-pack: 15.61 g........      8/06/75
 Division).                               Buffer II, pH 8.6.                                                    
Bio-Rad Laboratories, (Chemical          Immunoelectrophoresis Barbital   Dry-pack: 6.82 g.........      1/22/76
 Division).                               Buffer III, pH 8.6.                                                   
Bio-Rad Laboratories, (Chemical          Immunoelectrophoresis Barbital   Dry-pack: 15.07 g........      8/06/75
 Division).                               Buffer III-a, pH 8.8.                                                 
Bio-Rad Laboratories, (Chemical          Reagent No. 3..................  Bottle: 165 ml...........     12/14/72
 Division).                                                                                                     
Bio-Rad Laboratories, (Clinical          Benzodiazepines/Tricyclics/      Polypropylene Container:       3/28/91
 Division).                               Plasma Catecholamines (BZ/TCA/   15L - 100L.                          
                                          pCats) Serum Calibrators Bulk                                         
                                          Preparations.                                                         
Bio-Rad Laboratories, (Clinical          Plasma Catecholamines by HPLC,   Kit: 100 Test............      3/28/91
 Division).                               100 Test.                                                             
Bio-Rad Laboratories, (Clinical          Plasma Catecholamines by HPLC,   Vial: 20 ml; Set: 6 vials      3/28/91
 Division).                               Serum Calibrator Set, 1x6                                             
                                          vials.                                                                
Bio-Rad Laboratories, (ECS Division)...  Benzo/TCA Control Levels I & II  Vial: 10ml Box: 6 vials..      3/20/91
Bio-Rad Laboratories, (ECS Division)...  Blind Performance Specimen Set   Kit: 5 bottles...........      9/14/90
                                          Cat. #610.                                                            
Bio-Rad Laboratories, (ECS Division)...  LYPHOCHEK Assayed Chemistry      Vials: 10 ml each........      4/13/88
                                          Control Serum (Human) Levels I                                        
                                          and II.                                                               
Bio-Rad Laboratories, (ECS Division)...  LYPHOCHEK Immunoassay Plus       Vial: 10ml; Kit: 12 vials      9/14/90
                                          Control Serum Levels 1-3.                                             
Bio-Rad Laboratories, (ECS Division)...  LYPHOCHEK Urine Toxicology       Box: 10 vials; Vial: 50ml      9/14/91
                                          Control-Confirm.                                                      
Bio-Rad Laboratories, (ECS Division)...  LYPHOCHEK Urine Toxicology       Vials: 20 ml each........      4/13/88
                                          Control-Law.                                                          
Bio-Rad Laboratories, (ECS Division)...  LYPHOCHEK Urine Toxicology       Box: 10 vials; Vial: 20ml      9/14/90
                                          Control-Screen.                                                       
Bio-Rad Laboratories, (ECS Division)...  Liquichek Therapeutic Drug       Vial: 10ml...............      6/01/94
                                          Monitoring Control (TDM),                                             
                                          Levels 1, 2, 3.                                                       
Bio-Rad Laboratories, (ECS Division)...  Liquichek Unassayed Chemistry    Vial: 20ml...............      6/01/94
                                          Control (Human) Levels 1, 2.                                          
Bio-Rad Laboratories, (ECS Division)...  Lyphochek Immunoassay Control    Vial: 10 ml..............      9/24/87
                                          Levels I, II, III.                                                    
Bio-Rad Laboratories, (ECS Division)...  Lyphochek Quantitative Urine     Vial: 20 ml, 50 ml.......      9/24/87
                                          Control Levels I and II.                                              
Bio-Rad Laboratories, (ECS Division)...  Lyphochek Therapeutic Drug       Vial: 10ml...............      8/20/84
                                          Monitoring Control (TDM),                                             
                                          Levels I, II, III.                                                    
Bio-Rad Laboratories, (ECS Division)...  Lyphochek Unassayed Chemistry    Vial: 20 ml..............      9/24/87
                                          Control (Bovine) Levels I, II.                                        
Bio-Rad Laboratories, (ECS Division)...  Lyphochek Unassayed Chemistry    Vial: 20ml...............      9/24/87
                                          Control (Human) Levels I, II.                                         
Bio-Rad Laboratories, (ECS Division)...  Lyphochek Urine Toxicology       Vial: 20ml...............      6/01/94
                                          Screen-Low Control.                                                   
Bio-Rad Laboratories, (ECS Division)...  Lypochek Fertility Control       Vial: 10ml...............      6/01/94
                                          Serum (Human) Levels 1, 2, 3.                                         
Bio-Rad Laboratories, (ECS Division)...  Positive for Amphetamines......  Bottle: 90ml.............      9/14/90
Bio-Rad Laboratories, (ECS Division)...  Positive for Cocaine...........  Bottle: 90ml.............      9/14/90
Bio-Rad Laboratories, (ECS Division)...  Positive for Marihuana.........  Bottle: 90ml.............      9/14/90
Bio-Rad Laboratories, (ECS Division)...  Positive for Opiates...........  Bottle: 90ml.............      9/14/90
Bio-Rad Laboratories, (ECS Division)...  Positive for Phencyclidine.....  Bottle: 90ml.............      9/14/90
Bio-Rad Laboratories, (ECS Division)...  Urine Toxicology Control No. C-  Amber Vial: 50ml.........      9/19/79
                                          470-25.                                                               
Biochemical Diagnostics, Inc...........  (DL) Methadone.................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  (DL)-9-Carboxy-11-nor-Delta-9-   Vial: 1ml; 200ml (In-         12/22/95
                                          THC.                             house).                              
Biochemical Diagnostics, Inc...........  Alprazolam.....................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Amobarbital....................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Benzoylecgonine................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              

[[Page 117]]

                                                                                                                
Biochemical Diagnostics, Inc...........  Butalbital.....................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Chlordiazepoxide...............  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Codeine........................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  D-Amphetamine..................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  D-Methamphetamine..............  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  D-Propoxyphene.................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Detectabuse GC/MS Liquid         Bottle: 50ml.............     10/31/95
                                          Control Urine.                                                        
Biochemical Diagnostics, Inc...........  Detectabuse Immunoassay Liquid   Bottle: 20ml.............     10/31/95
                                          Control Urine, Series I.                                              
Biochemical Diagnostics, Inc...........  Detectabuse Immunoassay Liquid   Bulk: Up to 100L.........      1/02/96
                                          Control Urine, Series I, II,                                          
                                          II, IV, V.                                                            
Biochemical Diagnostics, Inc...........  Detectabuse Immunoassay Liquid   Bottle: 20ml.............     10/31/95
                                          Control Urine, Series II.                                             
Biochemical Diagnostics, Inc...........  Detectabuse Immunoassay Liquid   Bottle: 20ml.............     10/31/95
                                          Control Urine, Series III.                                            
Biochemical Diagnostics, Inc...........  Detectabuse Immunoassay Liquid   Bottle: 20ml.............     10/31/95
                                          Control Urine, Series IV.                                             
Biochemical Diagnostics, Inc...........  Detectabuse Immunoassay Liquid   Bottle: 20ml.............     10/31/95
                                          Control Urine, Series V.                                              
Biochemical Diagnostics, Inc...........  Diazepam.......................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Hydrocodone Bitartrate.........  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  LSD 25ug/ml....................  Vial: 1ml................     12/22/95
Biochemical Diagnostics, Inc...........  Meperidine.....................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Methaqualone...................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Morphine.......................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Morphine-6-Glucuronide.........  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Nordiazepam....................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Oxazepam.......................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Oxycodone......................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Oxymorphone....................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Pentobarbital..................  Vial: 1ml; 200 ml (In-        12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Phencyclidine..................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Phenobarbital..................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Phentermine....................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Secobarbital...................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biochemical Diagnostics, Inc...........  Triazolam......................  Vial: 1ml; 200ml (In-         12/22/95
                                                                           house).                              
Biodiagnostic International............  Liqui-Ura Toxic Control........  Vial: 5ml................      3/11/85
Biopool International..................  Drugs of Abuse Controls GC/MS L- Kit: 6 Vials.............      1/04/94
                                          2, L-3 and L-4.                                                       
Biopool International..................  Drugs of Abuse Controls GC/MS L- Vial: 12ml...............      1/04/94
                                          2, L-3 and L-4.                                                       
Biopool International..................  Drugs of Abuse Controls L-2, L-  Kit: 6 Vials.............      1/04/94
                                          3 and L-4.                                                            
Biopool International..................  Drugs of Abuse Controls L-2, L-  Vial: 12ml...............      1/04/94
                                          3 and L-4.                                                            
Bioscientific Corp.....................  ECA Buffer, Catalog No. ECA      Plastic Packet: 18.0 g.,       7/14/77
                                          05805.                           10 packets per box.                  
Bioscientific Corp/ECA.................  Agarose Barbital Buffer CSB      Vial: 7 drams............     11/15/90
                                          470182.                                                               
Bioscientific Corp/ECA.................  Agarose Barbital Buffer ECA      Vial: 12 drams; Box: 3        11/15/90
                                          470182.                          vials.                               
Bioscientific Corp/ECA.................  Agarose Barbital-EDTA Buffer     Vial: 12 drams, Box: 3        11/15/90
                                          ECA 470180.                      vials.                               

[[Page 118]]

                                                                                                                
Bioscientific Corp/ECA.................  ECA Buffer ECA 0320024.........  Vial: 12 drams, Box: 12       11/15/90
                                                                           vials.                               
Bioscientific Corp/ECA.................  General Procedure Agarose Film   Plastic Tray 4.5''x5'',        9/10/90
                                          #ECA 470100.                     Kit: 10 trays.                       
Bioscientific Corp/ECA.................  LD Agarose Gel #CSB 102........  Plastic Tray: 3''x5'',         9/10/90
                                                                           Kit: 10 trays.                       
Bioscientific Corp/ECA.................  Protein Agarose Gel #PSB 103...  Plastic Tray 3''x5'',          9/10/90
                                                                           Kit: 10 trays.                       
Biosite Diagnostics....................  Alprazolam Stock Solution,       Vial: 2ml................      5/26/92
                                          31366.                                                                
Biosite Diagnostics....................  Alprazolam Threshold Control     Flask: 250ml.............      5/26/92
                                          Calibrators 2-6; 31446-31450.                                         
Biosite Diagnostics....................  Amphetamine Enzyme Conjugate     Vial: 100ml, 1.5ml.......     10/24/90
                                          31111, Bulk Formulation.                                              
Biosite Diagnostics....................  Amphetamine QC Control.........  Vial: 5ml................     10/29/91
Biosite Diagnostics....................  Amphetamine QC Control (Bulk)..  Bottle: 0.5L-10L.........     10/29/91
Biosite Diagnostics....................  Barbiturate Conjugate..........  Plastic Bottles: 2ml-60       11/30/90
                                                                           ml.                                  
Biosite Diagnostics....................  Barbiturate Conjugate Control..  Vial: 0.5, 1, 2, 5, 15,        3/28/94
                                                                           50ml.                                
Biosite Diagnostics....................  Barbiturate Derivative.........  Vial: 8, 16, 32 ml.......     11/30/90
Biosite Diagnostics....................  Barbiturate Enzyme Conjugate     Vial: 100ml, 1.5ml.......     10/24/90
                                          31110, Bulk Formulation.                                              
Biosite Diagnostics....................  Barbiturate QC Control.........  Vial: 5ml................     10/29/91
Biosite Diagnostics....................  Barbiturate QC Control (Bulk)..  Bottle: 5L-10L...........     10/29/91
Biosite Diagnostics....................  Barbiturate Threshold Control    Flask: 250ml.............      5/26/92
                                          Calibrators 2-6; 31356-31360.                                         
Biosite Diagnostics....................  Benzodiazepine Controls, 1-6     Vial: 50ml, 1.5ml........     10/24/91
                                          31088-31093, 7-11 31098-31102,                                        
                                          Bulk Formulation.                                                     
Biosite Diagnostics....................  Benzodiazepine QC Control 3....  Vial: 5ml................     10/29/91
Biosite Diagnostics....................  Benzodiazepines QC Control 1...  Vial: 5ml................     10/29/91
Biosite Diagnostics....................  Benzodiazepines QC Control 1     Bottle: 0.5L-10L.........     10/29/91
                                          (Bulk).                                                               
Biosite Diagnostics....................  Benzodiazepines QC Control 2...  Vial: 5ml................     10/29/91
Biosite Diagnostics....................  Benzodiazepines QC Control 2     Bottle: 0.5L-10L.........     10/29/91
                                          (Bulk).                                                               
Biosite Diagnostics....................  Benzodiazepines QC Control 3     Bottle: 0.5L-10L.........     10/29/91
                                          (Bulk).                                                               
Biosite Diagnostics....................  Benzoylecgonine Conjugate......  Plastic Bottles: 2ml-60       11/30/90
                                                                           ml.                                  
Biosite Diagnostics....................  Benzoylecgonine Conjugate II,    Vial: 1.5ml..............      3/14/91
                                          III, IV, & V.                                                         
Biosite Diagnostics....................  Benzoylecgonine Conjugate II,    Bottle: 5, 15, 30 & 60 ml      3/14/91
                                          III, IV, & V Bulk.                                                    
Biosite Diagnostics....................  Benzoylecgonine Controls, 1-5    Vial: 50ml, 1.5ml........     10/24/90
                                          31041-31045, Bulk Formulation.                                        
Biosite Diagnostics....................  Benzoylecgonine Enzyme           Vial: 100ml, 1.5ml.......     10/24/90
                                          Conjugate 31105, Bulk                                                 
                                          Formulation.                                                          
Biosite Diagnostics....................  Benzoylecgonine Enzyme           Vial: 1.5ml..............      3/14/91
                                          Conjugate II.                                                         
Biosite Diagnostics....................  Benzoylecgonine Standards, 1-6   Vial: 50ml, 1.5ml........     10/24/90
                                          31035-31040, Bulk Formulation.                                        
Biosite Diagnostics....................  Benzoylecgonine Stock Solution.  Vial: 3ml................      6/01/95
Biosite Diagnostics....................  Benzoylecgonine Stock Solution,  Vial: 2ml................      5/26/92
                                          31322.                                                                
Biosite Diagnostics....................  Benzoylecgonine Stock Solution,  Bottle: 15-100ml.........      6/01/95
                                          Bulk.                                                                 
Biosite Diagnostics....................  Benzoylecgonine Threshold        Flask: 250ml.............      5/26/92
                                          Control Calibrators 2-6; 31341-                                       
                                          31345.                                                                
Biosite Diagnostics....................  Cocaine QC Control.............  Vial: 5ml................     10/29/91
Biosite Diagnostics....................  Cocaine QC Control (Bulk)......  Bottle: 0.5L-10L.........     10/29/91
Biosite Diagnostics....................  Conjugate (Intermediate).......  Vial: 2, 5, 15, 50, 60,        3/28/94
                                                                           100, 250, 500, 1000,                 
                                                                           2000ml.                              
Biosite Diagnostics....................  Conjugate Bead, Intervention...  Bottle: 15, 50, 100, 250,     11/09/93
                                                                           500, 1000, 2000ml.                   
Biosite Diagnostics....................  Conjugate Bead, TCA............  Bottle: 15, 50, 100, 250,     11/09/93
                                                                           500, 1000, 2000ml.                   
Biosite Diagnostics....................  Conjugate Beads (Bulk).........  Bottles: 15, 50, 100,         11/30/90
                                                                           250, 500, 1000, 2000ml.              
Biosite Diagnostics....................  Conjugate Beads Triage MTD.....  Vial: 15, 50, 100, 250,        3/28/94
                                                                           500, 1000, 2000ml.                   
Biosite Diagnostics....................  Conjugate Beads Triage and MTD.  Vial: 15, 50, 100, 250,        3/28/94
                                                                           500, 1000, 2000ml.                   
Biosite Diagnostics....................  D-Amphetamine Stock Solution,    Vial: 2ml................      5/26/92
                                          31323.                                                                
Biosite Diagnostics....................  D-Amphetamine Threshold Control  Flask: 250ml.............      5/26/92
                                          Calibrator, 31376.                                                    
Biosite Diagnostics....................  D-Methamphetamine Stock          Vial: 2ml................      5/26/92
                                          Solution, 31324.                                                      
Biosite Diagnostics....................  D-Methamphetamine Threshold      Flask: 250 ml............      5/26/92
                                          Control Calibrator, 31381.                                            
Biosite Diagnostics....................  Drugs of Abuse Controls-Level    Pack: 6 Vials; 5ml/vial..     12/14/94
                                          2, Positive.                                                          
Biosite Diagnostics....................  Drugs of Abuse Controls-Level    Pack: 6 Vials; 5ml/vial..     12/14/94
                                          3, Hi-Positive.                                                       
Biosite Diagnostics....................  Estazolam TTC Stock Solution...  Vial: 1ml................     11/09/93
Biosite Diagnostics....................  Estazolam Threshold Control      Vial: .25-1ml............     11/09/93
                                          Calibrators 2-6.                                                      
Biosite Diagnostics....................  Estazolam Threshold Control      Vial: 5-20ml.............     11/09/93
                                          Calibrators 2-6 Bulk                                                  
                                          Formulation.                                                          

[[Page 119]]

                                                                                                                
Biosite Diagnostics....................  Flurazepam Enzyme Conjugate      Vial: 100ml, 1.5ml.......     10/24/90
                                          31109, Bulk Formulation.                                              
Biosite Diagnostics....................  Flurazepam Standards, 1-7 31081- Vial: 50ml, 1.5ml........     10/24/90
                                          31087, Bulk Formulation.                                              
Biosite Diagnostics....................  Intervention Bead Solution.....  Vial: 2, 5, 15, 50, 100,       3/28/94
                                                                           250, 500ml.                          
Biosite Diagnostics....................  Intervention Conjugate (Bulk)..  Bottled/Flask: .1L-4L....     11/09/93
Biosite Diagnostics....................  Labeled Benzoylecgonine          Plastic Bottles: 0.5, 1,      11/30/90
                                          Conjugate.                       2 & 5 L.                             
Biosite Diagnostics....................  Labeled Conjugate Mixture 13...  Vial: 2, 5, 15, 50, 100,       3/28/94
                                                                           250, 500ml.                          
Biosite Diagnostics....................  Labeled Conjugate Mixture 2....  Plastic Bottles: 10ml-1L.     11/30/90
Biosite Diagnostics....................  Labeled Conjugate Mixture 5....  Bottles: 2, 5, 15, 50,        10/29/91
                                                                           100, 250, 500ml.                     
Biosite Diagnostics....................  Labeled Conjugate Mixture 7....  Bottle: 20L, 10L, 5L, 1L.     12/22/92
Biosite Diagnostics....................  Labeled Conjugate Mixture 9....  Plastic Bottles: 0.5, 1,      11/30/90
                                                                           2 & 5 L.                             
Biosite Diagnostics....................  Labeled Morphine Conjugate.....  Plastic Bottles: 0.5, 1,      11/30/90
                                                                           2 & 5 L.                             
Biosite Diagnostics....................  Labeled TCA Conjugate..........  Bottled/Flask: 2, 5, 15,      11/09/93
                                                                           50, 60, 100, 250, 260,               
                                                                           500, 1000, 2000ml.                   
Biosite Diagnostics....................  Labeled THC Conjugate..........  Plastic Bottles: 10ml-1L.     11/30/90
Biosite Diagnostics....................  Labeled THC Conjugate (Mixture   Flask: 500, 250, 100, 50,      3/28/94
                                          13).                             15, 5, 2ml.                          
Biosite Diagnostics....................  Labeled THC Conjugate Mixture 4  Bottles: 2, 5, 15, 50,        10/29/91
                                                                           100, 250, 500ml.                     
Biosite Diagnostics....................  Labeled Triage MTD Conjugate     Vial: 2, 5, 15, 50, 60,        3/28/94
                                          (Bulk).                          100, 250, 260, 500ml.                
Biosite Diagnostics....................  Lorazepam Enzyme Conjugate       Vial: 100ml, 1.5ml.......     10/24/90
                                          31108, Bulk Formulation.                                              
Biosite Diagnostics....................  Lorazepam Standards, 1-4 31094-  Vial: 50ml, 1.5ml........     10/24/90
                                          31097, Bulk Formulation.                                              
Biosite Diagnostics....................  Lormetazepam Stock Solution....  Vial: 1ml................     11/09/93
Biosite Diagnostics....................  Methadone Control..............  Vial: 2ml................     12/22/92
Biosite Diagnostics....................  Methadone Standards 1-6........  Vial: 2ml, 50ml..........     12/22/92
Biosite Diagnostics....................  Methadone Stock Solution.......  Vial: 2ml, 50ml..........     12/22/92
Biosite Diagnostics....................  Methamphetamine Enzyme           Vial: 100ml, 1.5ml.......     10/24/90
                                          Conjugate 31104, Bulk                                                 
                                          Formulation.                                                          
Biosite Diagnostics....................  Methamphetamine QC Control.....  Vial: 5ml................     10/29/91
Biosite Diagnostics....................  Methamphetamine QC Control       Bottle: 5L-10L...........     10/29/91
                                          (Bulk).                                                               
Biosite Diagnostics....................  Morphine Conjugate.............  Plastic Bottles: 2ml-60       11/30/90
                                                                           ml.                                  
Biosite Diagnostics....................  Morphine Control 3.............  Vial: 2ml, 50ml..........     12/22/92
Biosite Diagnostics....................  Morphine Controls, 1-5 31076-    Vial: 50ml, 1.5ml........     10/24/90
                                          31080, Bulk Formulation.                                              
Biosite Diagnostics....................  Morphine Enzyme Conjugate        Vial: 100ml, 1.5ml.......     10/24/90
                                          31107, Bulk Formulation.                                              
Biosite Diagnostics....................  Morphine Standard 6, 31220 Bulk  Vial: 1.5ml, 5-20ml;           3/14/91
                                          Formulation.                     Flask: 20-50ml.                      
Biosite Diagnostics....................  Morphine Standards, 1-5 31071-   Vial: 50ml, 1.5ml........     10/24/90
                                          31075, Bulk Formulation.                                              
Biosite Diagnostics....................  Morphine Stock Solution, 31325.  Vial: 2ml................      5/26/92
Biosite Diagnostics....................  Opiate QC Control..............  Vial: 5ml................     10/29/91
Biosite Diagnostics....................  Opiate QC Control (Bulk).......  Bottle: 05.L-10L.........     10/29/91
Biosite Diagnostics....................  Opiate Threshold Control         Flask: 250ml.............      5/26/92
                                          Calibrators 2-6; 31346-31350.                                         
Biosite Diagnostics....................  PCP QC Control.................  Vial: 5ml................     10/29/91
Biosite Diagnostics....................  PCP QC Control (Bulk)..........  Bottle: 0.5L-10L.........     10/29/91
Biosite Diagnostics....................  Phencyclidine Control 7 Bulk     Vial: 5-20ml.............     11/09/93
                                          Formulation.                                                          
Biosite Diagnostics....................  Phencyclidine Controls 5-6,      Vial: 1.5ml, 5-20ml;           3/14/91
                                          31255-31256 Bulk Formulation.    Flask: 20-50ml.                      
Biosite Diagnostics....................  Phencyclidine Controls, 1-4      Vial: 50ml, 1.5ml........     10/24/90
                                          31010-31013, Bulk Formulation.                                        
Biosite Diagnostics....................  Phencyclidine Enzyme Conjugate   Vial: 100ml, 1.5ml.......     10/24/90
                                          31103, Bulk Formulation.                                              
Biosite Diagnostics....................  Phencyclidine Standard 7.......  Vial: .25-1ml............     11/09/93
Biosite Diagnostics....................  Phencyclidine Standards 1-4      Vial: 50ml, 1.5ml........     10/24/90
                                          31006-31009, Bulk Formulation.                                        
Biosite Diagnostics....................  Phencyclidine Standards 5-6,     Vial: 1.5ml, 5-20 ml;          3/14/91
                                          31253-31254 Bulk Formulation.    Flask: 20-50ml.                      
Biosite Diagnostics....................  Phencyclidine Stock Solution,    Vial: 2ml................      5/26/92
                                          31321.                                                                
Biosite Diagnostics....................  Phencyclidine Threshold Control  Flask: 250ml.............      5/26/92
                                          Calibrators 2-6; 31366-31370.                                         

[[Page 120]]

                                                                                                                
Biosite Diagnostics....................  Phenobarbital Controls, 1-8      Vial: 50ml, 1.5ml........     10/24/90
                                          31063-31070, Bulk Formulation.                                        
Biosite Diagnostics....................  Phenobarbital Standards, 1-8     Vial: 50ml, 1.5ml........     10/24/90
                                          31055-31062, Bulk Formulation.                                        
Biosite Diagnostics....................  RT-5 Drugs of Abuse, Positive..  Pack: 6 Vials; 5ml/vial..     12/14/94
Biosite Diagnostics....................  Secobarbital Stock Solution,     Vial: 2ml................      5/26/92
                                          31326.                                                                
Biosite Diagnostics....................  THC Conjugate..................  Plastic Bottles: 2ml-60       11/30/90
                                                                           ml.                                  
Biosite Diagnostics....................  THC Conjugate Control..........  Vial: 0.5, 1, 2, 5, 15,        3/28/94
                                                                           50ml.                                
Biosite Diagnostics....................  THC Controls, 1-3 31052-31054,   Vial: 50ml, 1.5ml........     10/24/90
                                          Bulk Formulation.                                                     
Biosite Diagnostics....................  THC Enzyme Conjugate 31106,      Vial: 100ml, 1.5ml.......     10/24/90
                                          Bulk Formulation.                                                     
Biosite Diagnostics....................  THC QC Control.................  Vial: 5ml................     10/29/91
Biosite Diagnostics....................  THC QC Control (Bulk)..........  Bottle: 0.5L-10L.........     10/29/91
Biosite Diagnostics....................  THC Standards, 1-6 31046-31051,  Vial: 50ml, 1.5ml........     10/24/90
                                          Bulk Formulation.                                                     
Biosite Diagnostics....................  THC Standards, 7-9.............  Vial: .25-1ml............     11/09/93
Biosite Diagnostics....................  THC Standards, 7-9 Bulk          Vial: 5-20ml.............     11/09/93
                                          Formulation.                                                          
Biosite Diagnostics....................  THC Threshold Control            Flask: 250ml.............      5/26/92
                                          Calibrators 2-6 31371-31375.                                          
Biosite Diagnostics....................  Temazepam Stock Solution, 31337  Vial: 2ml................      5/26/92
Biosite Diagnostics....................  Temazepam Threshold Control      Flask: 250ml.............      5/26/92
                                          Calibrators 2-6 31451-31455.                                          
Biosite Diagnostics....................  Threshold Control A & B........  Vial: 5ml................     10/29/91
Biosite Diagnostics....................  Threshold Control A & B (Bulk).  Bottle: 1L-20L...........     10/29/91
Biosite Diagnostics....................  Threshold Control F-1..........  Vial: 3.5-5ml............      6/01/96
Biosite Diagnostics....................  Threshold Control F-1, Bulk      Bottle: .05-5L...........      6/01/95
                                          Solution.                                                             
Biosite Diagnostics....................  Threshold Controls C, D, E, F,   Vial: 3.5-5ml............     11/09/93
                                          G, H.                                                                 
Biosite Diagnostics....................  Thresholds C, D, E, F, G, H      Bottle: 1-5ml............     11/09/93
                                          Bulk Solution.                                                        
Biosite Diagnostics....................  Triage 6 Panel for Drugs of      Box: 10, 25 cassettes....     10/05/92
                                          Abuse.                                                                
Biosite Diagnostics....................  Triage 7 Conjugate.............  Vial: 2, 5, 15, 50, 60,        3/28/94
                                                                           100, 250, 260, 500ml.                
Biosite Diagnostics....................  Triage 8 Panel for Drugs of      Box: 3, 10, 25 Cassettes.      3/23/94
                                          Abuse.                                                                
Biosite Diagnostics....................  Triage 8 Panel for Drugs of      Box: 3, 10, 25 Cassettes.      3/28/94
                                          Abuse.                                                                
Biosite Diagnostics....................  Triage 8 Panel for Drugs of      Pouch: 1 Cassette........      3/28/94
                                          Abuse.                                                                
Biosite Diagnostics....................  Triage DOA Demo Control........  Vial: 5ml................     10/29/91
Biosite Diagnostics....................  Triage DOA Demo Control (Bulk).  Bottle: 0.5L-10L.........     10/29/91
Biosite Diagnostics....................  Triage Drug Screen Control.....  Vial: 5ml................     10/29/91
Biosite Diagnostics....................  Triage Drug Screen Control       Bottle: 0.5-20L..........     10/29/91
                                          (Bulk).                                                               
Biosite Diagnostics....................  Triage Intervention Panel for    Box: 10, 25 Pouches......     11/09/93
                                          Drugs of Abuse.                                                       
Biosite Diagnostics....................  Triage Intervention Test Device  Pouch: 1 each............     11/09/93
Biosite Diagnostics....................  Triage Panel for Drugs of Abuse  Box: 10, 25 cassettes....     11/30/90
Biosite Diagnostics....................  Triage Panel for Drugs of Abuse  Box: 10, 25 Pouches......     11/09/93
                                          Plus Tricyclic Antidepressants.                                       
Biosite Diagnostics....................  Triage Panel for Drugs of Abuse  Box; 3, 10, 25 Cassettes.      3/23/94
                                          Plus Methadone.                                                       
Biosite Diagnostics....................  Triage Panel for Drugs of Abuse  Box: 3, 10, 25 Cassettes.      3/28/94
                                          Plus Methadone.                                                       
Biosite Diagnostics....................  Triage Panel for Drugs of Abuse  Pouch: 1 Cassette........      3/28/94
                                          Plus Methadone Test Device.                                           
Biosite Diagnostics....................  Triage Panel for Drugs of Abuse  Kit: 25 Tests............     11/01/93
                                          Plus Tricyclic                                                        
                                          Antidepressants, Cat #92000.                                          
Biosite Diagnostics....................  Triage Panel for Drugs of Abuse  Kit: 10 Tests............     11/01/93
                                          plus Tricyclic                                                        
                                          Antidepressants, Cat #92010.                                          
Biosite Diagnostics....................  Triage Plus TCA Test Device....  Pouch: 1 each............     11/09/93
Biosite Diagnostics....................  Triage Test Device.............  Metallic Pouch: 1 each...     11/30/90
Biosite Diagnostics....................  Triage and MTD Conjugate (Bulk)  Vial: 2, 5, 15, 50, 60,        3/28/94
                                                                           100, 250, 260, 500ml.                
Biosite Diagnostics....................  Triage-7 Conjugate Beads.......  Bottle: 15, 50, 100, 250,     12/22/92
                                                                           500, 1000, 2000ml.                   
Biosite Diagnostics....................  Triage-7 Device................  Pouch: 1 cassette........     12/22/92
Biosite Diagnostics....................  Triage-7 Panel for Drugs.......  Box: 10, 25 cassettes....     12/22/92
Biosite Diagnostics....................  d-Amphetamine Controls, 1-5      Vial: 50ml, 1.5ml........     10/24/90
                                          31030-31034, Bulk Formulation.                                        
Biosite Diagnostics....................  d-Amphetamine Standards, 1-6     Vial: 50ml, 1.5ml........     10/24/90
                                          31024-31029, Bulk Formulation.                                        
Biosite Diagnostics....................  d-Methamphetamine Controls 5-6,  Vial: 1.5ml, 20-50ml;          3/14/91
                                          31020, 31257 Bulk Formulation.   Flask: 20-50ml.                      
Biosite Diagnostics....................  d-Methamphetamine Controls, 1-4  Vial: 50ml, 1.5ml........     10/24/90
                                          31020-31023, Bulk Formulation.                                        
Biosite Diagnostics....................  d-Methamphetamine Standards, 1-  Vial: 50ml, 1.5ml........     10/24/90
                                          6 31014-31019, Bulk                                                   
                                          Formulation.                                                          
Boehringer Mannheim....................  2a Amph ED Reagent for 500ml;    Vial: 500ml..............      4/13/94
                                          Cat # 1300796.                                                        
Boehringer Mannheim....................  2a Amphetamines ED Reagent for   Vial: 100ml..............      4/13/94
                                          85 ml; Cat # 1404234.                                                 
Boehringer Mannheim....................  Amphetamine System Pack for      Kit: 4 Bottles...........      4/13/94
                                          85ml; Cat # 81-3300.                                                  
Boehringer Mannheim....................  Amphetamines Systems Pack for    Kit: 4 Bottles...........      4/13/94
                                          500ml; Cat # 81-3400.                                                 

[[Page 121]]

                                                                                                                
Boehringer Mannheim....................  Bulk Reference Methadone         Carboy: 5L...............      8/18/95
                                          Manufacturing Calibrators E,                                          
                                          F, G, H, I, J, K, Open.                                               
Boehringer Mannheim....................  CEDIA DAU 4-Drug Cutoff          Bottle: 10, 15ml.........      4/01/94
                                          Calibrator.                                                           
Boehringer Mannheim....................  CEDIA DAU 4-Drug High            Bottle: 10, 15ml.........      4/01/94
                                          Calibrator.                                                           
Boehringer Mannheim....................  CEDIA DAU 4-Drug Intermediate    Bottle: 10, 15ml.........      4/01/94
                                          Calibrator.                                                           
Boehringer Mannheim....................  CEDIA DAU 5-Drug Cutoff          Bottle: 5, 15ml..........      6/30/94
                                          Calibrator.                                                           
Boehringer Mannheim....................  CEDIA DAU Amphetamine Assay-     Kit: 4 Bottles; 18ml each      7/19/94
                                          Cat # 83-3300 and 85-3300.                                            
Boehringer Mannheim....................  CEDIA DAU Barb/Benz 200........  Bottle: 10, 15ml.........      4/01/94
Boehringer Mannheim....................  CEDIA DAU Barb/Benz 300          Bottle: 10, 15ml.........      4/01/94
                                          Calibrator.                                                           
Boehringer Mannheim....................  CEDIA DAU Barb/Benz High         Bottle: 10, 15ml.........      4/01/94
                                          Calibrator.                                                           
Boehringer Mannheim....................  CEDIA DAU Barb/Benz              Bottle: 10, 15ml.........      4/01/94
                                          Intermediate Calibrator.                                              
Boehringer Mannheim....................  CEDIA DAU Cocaine Assay; Cat #   Kit: 4 Bottles; 18ml each      7/19/94
                                          83-2300 and 85-2300.                                                  
Boehringer Mannheim....................  CEDIA DAU Cocaine Assay; Cat #   Kit: 4 Bottles, 85ml.....      1/24/94
                                          81-2300.                                                              
Boehringer Mannheim....................  CEDIA DAU Cocaine Assay; Cat #   Kit: 4 Bottles, 500ml....      1/24/94
                                          81-2400.                                                              
Boehringer Mannheim....................  CEDIA DAU LSD Assay............  Kit: 15, 70ml............     12/01/95
Boehringer Mannheim....................  CEDIA DAU LSD Cutoff Calibrator  Bottle: 10ml.............     12/01/95
Boehringer Mannheim....................  CEDIA DAU LSD High Calibrator..  Vial: 10ml...............     12/01/95
Boehringer Mannheim....................  CEDIA DAU LSD Intermediate       Vial: 10ml...............     12/01/95
                                          Calibrator.                                                           
Boehringer Mannheim....................  CEDIA DAU LSD Reagent..........  Vial: 7, 100ml...........     12/01/95
Boehringer Mannheim....................  CEDIA DAU Methadone Assay......  Kit: 18, 85, 500ml.......      8/18/95
Boehringer Mannheim....................  CEDIA DAU Methadone ED Reagent.  Vial: 7, 100, 190ml......      8/18/95
Boehringer Mannheim....................  CEDIA DAU Multi-Level THC        Kit: 4 Bottles, 85ml.....      1/24/94
                                          Assay; Cat # 81-2700.                                                 
Boehringer Mannheim....................  CEDIA DAU Multi-Level THC        Kit: 4 Bottles, 500ml....      1/24/94
                                          Assay; Cat # 81-2800.                                                 
Boehringer Mannheim....................  CEDIA DAU Opiate Assay- Cat #    Kit: 4 Bottles; 18ml each      7/19/94
                                          83-2900 and 85-2900.                                                  
Boehringer Mannheim....................  CEDIA DAU Opiate Assay; Cat #    Kit: 4 Bottles, 85ml.....      1/24/94
                                          81-2900.                                                              
Boehringer Mannheim....................  CEDIA DAU Opiate Assay; Cat #    Kit: 4 Bottles, 500ml....      1/24/94
                                          81-3000.                                                              
Boehringer Mannheim....................  CEDIA DAU Propoxyphene Assays;   Kit: 4 Bottles...........     11/30/94
                                          18ml, 85ml, 500ml.                                                    
Boehringer Mannheim....................  CEDIA DAU Propoxyphene Cutoff    Vial: 10ml...............     11/30/94
                                          Calibrator.                                                           
Boehringer Mannheim....................  CEDIA DAU Propoxyphene High      Vial: 10ml...............     11/30/94
                                          Calibrator.                                                           
Boehringer Mannheim....................  CEDIA DAU Propoxyphene           Vial: 10ml...............     11/30/94
                                          Intermediate Calibrator.                                              
Boehringer Mannheim....................  CEDIA DAU THC 100ng/ml           Bottle: 15ml.............      4/01/94
                                          Calibrator.                                                           
Boehringer Mannheim....................  CEDIA DAU THC 150ng/ml           Bottle: 15ml.............      4/01/94
                                          Calibrator.                                                           
Boehringer Mannheim....................  CEDIA DAU THC 25ng/ml            Bottle: 15ml.............      4/01/94
                                          Calibrator.                                                           
Boehringer Mannheim....................  CEDIA DAU THC 50ng/ml            Bottle: 15ml.............      4/01/94
                                          Calibrator.                                                           
Boehringer Mannheim....................  CEDIA DAU THC 75 ng/ml           Bottle: 15ml.............      4/01/94
                                          Calibrator.                                                           
Boehringer Mannheim....................  CEDIA Multi-Level THC Assay-Cat  Kit: 4 Bottles; 18ml each      7/19/94
                                          # 83-2700 and 85-2700.                                                
Boehringer Mannheim....................  LSD Conjugate..................  Bottle: 50-200ml.........     12/01/95
Boehringer Mannheim....................  LSD Cutoff Calibrator Bulk.....  Carboy: 4L...............     12/01/95
Boehringer Mannheim....................  LSD ED Bulk Reagent............  Carboy: 25L..............     12/01/95
Boehringer Mannheim....................  LSD High Calibrator Bulk.......  Carboy: 4L...............     12/01/95
Boehringer Mannheim....................  LSD Intermediate Calibrator      Carboy: 4L...............     12/01/95
                                          Bulk.                                                                 
Boehringer Mannheim....................  LSD Spiking Solution...........  Vial: 2L.................     12/01/95
Boehringer Mannheim....................  Methadone Conjugate............  Vial: 25ml...............      8/18/95
Boehringer Mannheim....................  Methadone ED Bulk Reagent......  Carboy: 50L..............      8/18/95
Boehringer Mannheim....................  Methadone Reference              Carboy: 10L..............      8/18/95
                                          Manufacturing Calibrator                                              
                                          Spiking Solution.                                                     
Boehringer Mannheim....................  Multi-Drug Control Set, #946380  2 Vials; 15ml/vial.......      5/10/94
Boehringer Mannheim....................  Multi-Drug Set, #946379........  2 Vials; 5ml/vial........      5/10/94
Boehringer Mannheim....................  Propoxyphene Conjugate.........  Vial: 25ml...............     11/30/94
Boehringer Mannheim....................  Propoxyphene Cutoff Bulk         Carboy: 4L...............     11/30/94
                                          Calibrator.                                                           
Boehringer Mannheim....................  Propoxyphene ED Bulk Reagent...  Carboy: 25L..............     11/30/94
Boehringer Mannheim....................  Propoxyphene ED Reagent........  Vial: 7, 100, 190ml......     11/30/94
Boehringer Mannheim....................  Propoxyphene High Bulk           Carboy: 4L...............     11/30/94
                                          Calibrator.                                                           
Boehringer Mannheim....................  Propoxyphene Intermediate Bulk   Carboy: 4L...............     11/30/94
                                          Calibrator.                                                           
Boehringer Mannheim....................  Propoxyphene Spiking Solution..  Vial: 2L.................     11/30/94
Boehringer Mannheim....................  Reference LSD Manufacturing      Vial: 3 or 5ml...........     12/01/95
                                          Calibrator A, B, C, D, E, F,                                          
                                          G, Open.                                                              
Boehringer Mannheim....................  Reference LSD Manufacturing      Carboy: 5L...............     12/01/95
                                          Calibrator Bulk A, B, C, D, E,                                        
                                          F, G, Open.                                                           
Boehringer Mannheim....................  Reference Methadone              Vial: 3, 5ml.............      8/18/95
                                          Manufacturing Calibrators E,                                          
                                          F, G, H, I, J, K, Open.                                               
Boehringer Mannheim....................  Reference Propoxyphene Bulk      Carboy: 5L...............     11/30/94
                                          Manufacturing Calibrators E,                                          
                                          F, G, H, I, J, K and Open.                                            
Boehringer Mannheim....................  Reference Propoxyphene           Vial: 3, 5ml.............     11/30/94
                                          Manufacturing Calibrators E,                                          
                                          F, G, H, I, J, K and Open.                                            
Boehringer Mannheim....................  Specialty Control Set 1,         2 Vials; 15ml/vial.......      5/10/94
                                          #946381.                                                              
Boehringer Mannheim....................  Specialty Control Set 2,         2 Vials: 15ml/vial.......      5/10/94
                                          #946383.                                                              

[[Page 122]]

                                                                                                                
Boehringer Mannheim....................  THC 100 Control Set............  Box: 2 Bottles; 15ml each      6/30/94
Boehringer Mannheim....................  THC 100 Controls (High & Low)..  Bottle: 15ml.............      6/30/94
Boehringer Mannheim....................  THC 100 Controls (High & Low)    Carboy: 150L.............      6/30/94
                                          Bulk.                                                                 
Boehringer Mannheim....................  THC 25 Control Set.............  Box: 2 Bottles; 15ml each      6/30/94
Boehringer Mannheim....................  THC 25 Controls (High & Low)...  Bottle: 15ml.............      6/30/94
Boehringer Mannheim....................  THC 25 Controls (High & Low)     Carboy: 150L.............      6/30/94
                                          Bulk.                                                                 
Boehringer Mannheim....................  THC 50 Control Set.............  Box: 2 Bottles; 15ml each      6/30/94
Boehringer Mannheim....................  THC 50 Controls (High & Low)...  Bottle: 15ml.............      6/30/94
Boehringer Mannheim Diagnostics........  Amphetamine Spiking............  Carboy: 5-10L............      9/26/95
Boehringer Mannheim Diagnostics........  Barbiturate Spiking Solution...  Carboy: 5-10L............      9/26/95
Boehringer Mannheim Diagnostics........  Benzodiazepine Spiking Solution  Carboy: 5-10L............      9/26/95
Boehringer Mannheim Diagnostics........  Benzodiazepine Spiking Solution  Bottle: 2L...............      9/26/95
                                          ''A''.                                                                
Boehringer Mannheim Diagnostics........  CEDIA DAU Multi-Drug             Vial: 10, 15ml...........      9/26/95
                                          Calibrator, Primary Cutoffs.                                          
Boehringer Mannheim Diagnostics........  CEDIA DAU Multi-Drug             Vial: 10, 15ml...........      9/26/95
                                          Calibrator, Secondary Cutoffs.                                        
Boehringer Mannheim Diagnostics........  CEDIA DAU Multi-Drug High        Vial: 10, 15ml...........      9/26/95
                                          Calibrator.                                                           
Boehringer Mannheim Diagnostics........  CEDIA DAU Multi-Drug             Vial: 10, 15ml...........      9/26/95
                                          Intermediate Calibrator.                                              
Boehringer Mannheim Diagnostics........  Cocaine Spiking Solution.......  Carboy: 5-10L............      9/26/95
Boehringer Mannheim Diagnostics........  Multi-Drug Cutoff, Bulk          Bottle: 20L..............      9/26/95
                                          Calibrator.                                                           
Boehringer Mannheim Diagnostics........  Multi-Drug High Bulk Calibrator  Bottle: 20L..............      9/26/95
Boehringer Mannheim Diagnostics........  Multi-Drug Intermediate Bulk     Bottle: 20L..............      9/26/95
                                          Calibrator.                                                           
Boehringer Mannheim Diagnostics........  Multi-Drug Secondary Cutoffs,    Bottle: 20L..............      9/26/95
                                          Bulk Calibrator.                                                      
Boehringer Mannheim Diagnostics........  Opiate Spiking Solution........  Carboy: 5-10L............      9/26/95
Boehringer Mannheim Diagnostics........  PCP Spiking Solution...........  Carboy: 5-10L............      9/26/95
Boehringere Mannheim Diagnostics.......  Methamphetamine Spiking          Carboy: 5-10L............      9/26/95
                                          Solution.                                                             
California Bionuclear Corporation......  Amobarbital-2-C-14, Catalog No.  Screw Cap Vial: 50             1/08/75
                                          72077.                           microcuries, 0.1, 0.5,               
                                                                           and 1.0 millicuries.                 
California Bionuclear Corporation......  Cocaine (methoxy-C-14) Catalog   Screw Cap Vial: 50             1/08/75
                                          No. 72182.                       microcuries, 0.1, 0.5,               
                                                                           and 1.0 millicuries.                 
California Bionuclear Corporation......  D-Amphetamine (propyl-1-C-14)    Screw Cap Vial: 50             1/08/75
                                          Sulfate, Catalog No. 72078.      microcuries, 0.1, 0.5,               
                                                                           and 1.0 millicuries.                 
California Bionuclear Corporation......  DL-Amphetamine (propyl-1-C-14)   Screw Cap Vial: 50             1/08/75
                                          Sulfate, Catalog No. 72079.      microcuries, 0.1, 0.5,               
                                                                           and 1.0 millicuries.                 
California Bionuclear Corporation......  Meperidine (N-methyl-C-14)       Screw Cap Vial: 50             1/08/75
                                          Hydrochloride, Catalog No.       microcuries, 0.1, 0.5,               
                                          72508.                           1.0 millicuries.                     
California Bionuclear Corporation......  Mescaline (aminomethylene-C-14)  Screw Cap Vial: 50             1/08/75
                                          Hydrochloride, Catalog No.       microcuries, 0.1, 0.5,               
                                          72512.                           1.0 millicuries.                     
California Bionuclear Corporation......  Methadone (heptanone-2-C-14)     Screw Cap Vial: 50             1/08/75
                                          Hydrochloride, Catalog No.       microcuries, 0.1, 0.5,               
                                          72516.                           1.0 millicuries.                     
California Bionuclear Corporation......  Methamphetamine (propyl-1-C-14)  Screw Cap Vial: 50             1/08/75
                                          Sulfate, Catalog No. 72517.      microcuries, 0.1, 0.5,               
                                                                           1.0 millicuries.                     
California Bionuclear Corporation......  Methylphenidate (carbonyl-C-14)  Screw Cap Vial: 50             1/08/75
                                          Hydrochloride, Catalog No.       microcuries, 0.1, 0.5,               
                                          72550.                           1.0 millicuries.                     
California Bionuclear Corporation......  Morphine (n-methyl-C-14)         Screw Cap Vial: 50             1/08/75
                                          Hydrochloride, Catalog No.       microcuries, 0.1, 0.5,               
                                          72560.                           1.0 millicuries.                     

[[Page 123]]

                                                                                                                
California Bionuclear Corporation......  Pentobarbital-2-C-14, Catalog    Screw Cap Vial: 50             1/08/75
                                          No. 72618.                       microcuries, 0.1, 0.5,               
                                                                           1.0 millicuries.                     
California Bionuclear Corporation......  Secobarbital-2-C-14, Catalog     Ampule: 50 microcuries,        1/08/75
                                          No. 72675.                       0.1, 0.5, and 1.0                    
                                                                           millicuries.                         
Cambridge Medical Diagnostics,           125I Human Parathyroid Hormone   Vial: 5ml................      3/29/85
 Incorporated.                            44-68.                                                                
Cambridge Medical Diagnostics,           125I-Tetraiodothyronine........  Vial: 11ml...............      3/29/85
 Incorporated.                                                                                                  
Cambridge Medical Diagnostics,           125I-Triiodothyronine..........  Vial: 11ml...............      3/29/85
 Incorporated.                                                                                                  
Cambridge Medical Diagnostics,           Donkey Anti Goat Gamma Globulin  Vial: 5ml................      3/29/85
 Incorporated.                                                                                                  
Cambridge Medical Diagnostics,           Parathyroid Hormone (Human 1-    6 Vials: 5ml each........      3/29/85
 Incorporated.                            84) Standard.                                                         
Cambridge Medical Diagnostics,           Parathyroid Hormone Assay        Vial: 10ml...............      3/29/85
 Incorporated.                            Buffer.                                                               
Cambridge Medical Diagnostics,           T3 AntiSerum (Rabbit)..........  Vial: 11ml...............      3/29/85
 Incorporated.                                                                                                  
Cambridge Medical Diagnostics,           T3 Standard....................  Vial: 1ml................      3/29/85
 Incorporated.                                                                                                  
Cambridge Medical Diagnostics,           T4 Antiserum (Rabbit)..........  Vial: 11ml...............      3/29/85
 Incorporated.                                                                                                  
Cambridge Medical Diagnostics,           T4 Standard....................  Vial: 1ml................      3/29/85
 Incorporated.                                                                                                  
Casco Standards........................  1-(1-                            Cryo-vial: 1.1ml Box: 25,      3/21/90
                                          Phenylcyclohexyl)pyrrolidine     50, 75 vials Plastic                 
                                          Cross-Reactant.                  Cup: 125ml.                          
Casco Standards........................  1-Phenylcyclohexylamine Cross-   Cryo-vial: 1.1ml Box: 25,      3/23/90
                                          Reactant.                        50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  1-[1-(2-thienyl)-cyclohexyl]-    Cryo-vial: 1.1ml Box: 25,      3/23/90
                                          piperdine Cross-Reactant.        50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  1-[1-2(2-thienyl)-cyclohexyl]-   Cryo-vial: 1.1ml Box: 25,      3/23/90
                                          pyrrolidine Cross-Reactant.      50, 75 Plastic Cup:                  
                                                                           125ml.                               
Casco Standards........................  11-OH-delta-8-THC Cross-         Cryo-vial: 1.1ml Box: 25,      3/21/90
                                          Reactant.                        50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  11-OH-delta-9-THC Cross-         Cryo-vial: 1.1ml Box: 25,      3/21/90
                                          Reactant.                        50, 75 vials Plastic                 
                                                                           cup: 125ml.                          
Casco Standards........................  11-nor-delta-8-THC-9-carboxilic  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                          c acid Cross-Reactant.           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  11-nor-delta-9-THC-9-carboxilic  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                          acid Cross-Reactant.             50, 75 vials.                        
Casco Standards........................  8-B-11-diOH-delta-9-THC Cross-   Cryo-vial: 1.1ml Box: 25,      3/21/90
                                          Reactant.                        50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  8-B-OH-delta-9-THC Cross-        Cryo-vial: 1.1ml Box: 25,      3/21/90
                                          Reactant.                        50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Allobarbital Cross-Reactant....  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Alphenal Cross-Reactant........  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50 75 vials Plastic cup:             
                                                                           125ml.                               
Casco Standards........................  Alprazolam Cross-Reactant......  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Amobarbital Cross-Reactant.....  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Aprobarbital Cross-Reactant....  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          

[[Page 124]]

                                                                                                                
Casco Standards........................  Barbital Cross-Reactant........  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Benzoylecgonine Cross-Reactant.  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Benzphetamine Cross-Reactant...  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Bromazepam Cross-Reactant......  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Butabarbital Cross-Reactant....  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Butalbital Cross-Reactant......  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Butethal Cross-Reactant........  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Cannabidiol Cross-Reactant.....  Cryo-Vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Cannabinol Cross-Reactant......  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           cup: 125ml.                          
Casco Standards........................  Chlordiazepoxide Cross-Reactant  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Clonazepam Cross-Reactant......  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Cocaine Cross-Reactant.........  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Cyclopentobarbital Cross-        Cryo-vial: 1.1ml Box: 25,      3/21/90
                                          Reactant.                        50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Diazepam Cross-Reactant........  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Ecgonine HCl Cross-Reactant....  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Ecgonine-methyl ester HCl        Cryo-vial: 1.1ml Box: 25,      3/21/90
                                          hydrate Cross-Reactant.          50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Fenfluramine Cross-Reactant....  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Flunitrazepam Cross-Reactant...  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Flurazepam Cross-Reactant......  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Halazepam Cross-Reactant.......  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Hexobarbital Cross-Reactant....  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Lorazepam Cross-Reactant.......  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  MDA Cross-Reactant.............  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  MDE Cross-Reactant.............  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          

[[Page 125]]

                                                                                                                
Casco Standards........................  MDMA Cross-Reactant............  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Medazepam Cross-Reactant.......  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Midazolam Cross-Reactant.......  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Nitrazepam Cross-Reactant......  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 03/21/90.                       
Casco Standards........................  Nordiazepam Cross-Reactant.....  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Oxazepam Cross-Reactant........  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Pentobarbital Cross-Reactant...  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Phencyclidine Cross-Reactant...  Cryo-vial: 1.1ml Box: 25,      3/23/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Phenmetrazine Cross-Reactant...  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Phenobarbital Cross-Reactant...  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Phentermine Cross-Reactant.....  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Pinazepam Cross-Reactant.......  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Prazepam Cross-Reactant........  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Propylhexedrine Cross-Reactant.  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Secobarbital Cross-Reactant....  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Talbutal Cross-Reactant........  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Temazepam Cross-Reactant.......  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  Triazolam Cross-Reactant.......  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  d-Amphetamine Cross-Reactant...  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  d-Methamphetamine Cross-         Cryo-vial: 1.1ml Box: 25,      3/21/90
                                          Reactant.                        50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  l-Amphetamine Cross-Reactant...  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Casco Standards........................  p-OH-Amphetamine Cross-Reactant  Cryo-vial: 1.1ml Box: 25,      3/21/90
                                                                           50, 75 vials Plastic                 
                                                                           Cup: 125ml.                          
Cayman Chemical Company................  Testosterone...................  Vial: 3ml................      4/07/93
Ciba Corning Diagnostics Corp..........  Magic Lite HCG Solid Phase.....  Plastic vial: 50ml, Kit:      12/09/88
                                                                           100 tests.                           
Ciba Corning Diagnostics Corp..........  AACC Tox.......................  Glass Vial: 30ml.........      1/20/86

[[Page 126]]

                                                                                                                
Ciba Corning Diagnostics Corp..........  ACS Estradiol Component Sets...  Kits: 3 Vials; 18 vials..      1/31/94
Ciba Corning Diagnostics Corp..........  ACS Estradiol Component Sets     Bottle: 30ml.............      1/31/94
                                          Releasing Reagent.                                                    
Ciba Corning Diagnostics Corp..........  ACS Estradiol-6 Antibody         Bottle: 3ml..............     11/20/95
                                          Reagent.                                                              
Ciba Corning Diagnostics Corp..........  ACS FT4........................  Kit: 50 Test, 300 Test...      3/26/91
Ciba Corning Diagnostics Corp..........  ACS FT4 Lite Reagent...........  Vial: 7ml................      3/26/91
Ciba Corning Diagnostics Corp..........  ACS FT4 Lite Reagent...........  Vial: 7ml................      3/26/91
Ciba Corning Diagnostics Corp..........  ACS FT4 Solid Phase............  Vial: 26ml...............      3/26/91
Ciba Corning Diagnostics Corp..........  ACS Ferritin Lite Reagent......  Vial: 7ml; Kit: 50, 300,       4/15/91
                                                                           3000 Tests.                          
Ciba Corning Diagnostics Corp..........  ACS Ferritin Solid Phase.......  Vial: 26ml; Kit: 50            4/15/91
                                                                           Tests, 300 Tests.                    
Ciba Corning Diagnostics Corp..........  ACS HCG Solid Phase............  Vial: 26ml; Kit: 50            4/18/91
                                                                           Tests, 300 Tests.                    
Ciba Corning Diagnostics Corp..........  ACS Magnetic Check.............  Plastic Vial: 26ml.......      6/18/91
Ciba Corning Diagnostics Corp..........  ACS Magnetic Check II..........  Plastic Vial: 26ml.......      6/18/91
Ciba Corning Diagnostics Corp..........  ACS Multical E Pack (Low & High  Kits: 4 Vials; 2 vials...      1/31/94
                                          Calibrator).                                                          
Ciba Corning Diagnostics Corp..........  ACS Multical High Calibrator...  Vial: 10ml...............      1/31/94
Ciba Corning Diagnostics Corp..........  ACS Multical Low Calibrator....  Vial: 10ml...............      1/31/94
Ciba Corning Diagnostics Corp..........  ACS Performance Verification     Kit: 6 Vials.............      6/18/91
                                          Test Kit.                                                             
Ciba Corning Diagnostics Corp..........  ACS Phenobarbital High           Bottle: 5ml..............      5/08/95
                                          Calibrator.                                                           
Ciba Corning Diagnostics Corp..........  ACS Phenobarbital Lite Reagent.  Bottle: 10ml.............      5/08/95
Ciba Corning Diagnostics Corp..........  ACS Phenobarbital Low            Bottle: 5ml..............      5/08/95
                                          Calibrator.                                                           
Ciba Corning Diagnostics Corp..........  ACS Phenobarbital Master Curve   Bottle: 5ml..............      5/08/95
                                          Material.                                                             
Ciba Corning Diagnostics Corp..........  ACS Phenobarbital Master Curve   Set: 6 Bottles...........      5/08/95
                                          Material Set.                                                         
Ciba Corning Diagnostics Corp..........  ACS T3 Kit.....................  Kit: 50, 300, 3000 Tests.      7/22/91
Ciba Corning Diagnostics Corp..........  ACS T3 Lite Reagent............  Plastic Vial: 7ml........      7/22/91
Ciba Corning Diagnostics Corp..........  ACS T3 Solid Phase.............  Plastic Vial: 26ml.......      7/22/91
Ciba Corning Diagnostics Corp..........  ACS T4.........................  Kit: 50 Test, 300 Test...      3/26/91
Ciba Corning Diagnostics Corp..........  ACS T4 Lite Reagent............  Vial: 7ml................      3/26/91
Ciba Corning Diagnostics Corp..........  ACS T4 Solid Phase.............  Vial: 26ml...............      3/26/91
Ciba Corning Diagnostics Corp..........  ACS Testosterone Component Sets  Set: 2 Bottles...........      3/28/94
                                          (50 Tests).                                                           
Ciba Corning Diagnostics Corp..........  ACS Testosterone Component Sets  Set: 12 Bottles..........      3/28/94
                                          (500 Tests).                                                          
Ciba Corning Diagnostics Corp..........  ACS Testosterone Lite Reagent..  Bottle: 10ml.............      3/28/94
Ciba Corning Diagnostics Corp..........  ACS Testosterone Releasing       Bottle: 30ml.............      7/20/94
                                          Agent.                                                                
Ciba Corning Diagnostics Corp..........  ACS Wash Check Solid Phase.....  Plastic Vial: 26ml.......      6/18/91
Ciba Corning Diagnostics Corp..........  ALP Buffer Concentrate Cat. No.  Plastic Bottle: 175ml....     10/28/91
                                          470244.                                                               
Ciba Corning Diagnostics Corp..........  ALP Gel/12 Cat. No. 470246.....  2 Plates: 24 Tests.......     10/28/91
Ciba Corning Diagnostics Corp..........  ALP Gel/8 Cat. No. 470243......  2 Plates: 16 Tests.......     10/28/91
Ciba Corning Diagnostics Corp..........  ALP Gel/8 and Buffer Cat. No.    Kit: 10 Plates; Plastic       10/28/91
                                          470240.                          Bottle: 175ml.                       

[[Page 127]]

                                                                                                                
Ciba Corning Diagnostics Corp..........  Alkaline Hemoglobin Buffer Cat.  Plastic Vial: 25 Drams...     10/28/91
                                          No. 470580.                                                           
Ciba Corning Diagnostics Corp..........  Alkaline Hemoglobin Kit/8 Cat.   Kit: 10 Plates; Plastic       10/28/91
                                          No. 470678.                      Vial: 25 Drams.                      
Ciba Corning Diagnostics Corp..........  CVM Chemistry (Calibration       Kit: 16 Vials; 5ml/vial..      6/14/94
                                          Verification Material for                                             
                                          Chemistry), Levels 1 thru 8.                                          
Ciba Corning Diagnostics Corp..........  Ciba Corning ANTICONV/ASTH I,    Kit Contains: 10ml vial,      10/22/85
                                          II.                              5 Vials each level.                  
Ciba Corning Diagnostics Corp..........  Ciba Corning Liquid 3..........  Glass Vials: 15; 5ml each      1/31/95
Ciba Corning Diagnostics Corp..........  Ciba Corning Liquid TDM 1......  Glass Vials: 15; 5ml each      1/31/95
Ciba Corning Diagnostics Corp..........  Ciba Corning Liquid TDM 1, 2, 3  Kit: 15 Vials............      1/31/95
Ciba Corning Diagnostics Corp..........  Ciba Corning Liquid TDM 2......  Glass Vials: 15; 5ml each      1/31/95
Ciba Corning Diagnostics Corp..........  Ciba Corning TDM I.............  Vial: 5ml, 10 vials......     10/22/85
Ciba Corning Diagnostics Corp..........  Ciba Corning TDM I, II & III...  Kit Contains: 5 Vials         10/22/85
                                                                           each level.                          
Ciba Corning Diagnostics Corp..........  Ciba Corning TDM II............  Vial: 5ml, 10 vials......     10/22/85
Ciba Corning Diagnostics Corp..........  Ciba Corning TDM III...........  Vial: 5ml, 10 vials......     10/22/85
Ciba Corning Diagnostics Corp..........  Ciba Corning TOX I, II.........  Kit: Contains: 10ml vial,     12/16/85
                                                                           5 Vials each level.                  
Ciba Corning Diagnostics Corp..........  Ciba Corning Urine II..........  Vial: 30ml...............      5/22/85
Ciba Corning Diagnostics Corp..........  DAU I, No. 9076................  Glass vial: 25ml, Box: 10      5/23/89
                                                                           vials.                               
Ciba Corning Diagnostics Corp..........  DAU II No. 9077................  Glass Vial: 25ml, Box: 10      5/23/89
                                                                           vials.                               
Ciba Corning Diagnostics Corp..........  DAU III, No. 9078..............  Glass vial: 25ml, Box: 10      5/23/89
                                                                           Vials.                               
Ciba Corning Diagnostics Corp..........  DAU IV, No. 9079...............  Glass Vial: 25ml, Box: 10      5/23/89
                                                                           Vials.                               
Ciba Corning Diagnostics Corp..........  DAU V, No. 9085................  Glass Vial: 25ml; Box: 10      5/10/91
                                                                           vials.                               
Ciba Corning Diagnostics Corp..........  Double Four-Track Gel Cat. No.   Plate: 8 Tests; Kit: 12       10/28/91
                                          470179.                          Plates.                              
Ciba Corning Diagnostics Corp..........  HDL Cholesterol Gel/8 and        Kit: 10 Plates; Plastic       10/28/91
                                          Buffer Cat. No. 470618.          Vial: 25 Drams.                      
Ciba Corning Diagnostics Corp..........  High Resolution Protein Gel/8    Kit: 12 Plates; 2 Plates:     10/28/91
                                          Cat. NO. 470201.                 16 Tests.                            
Ciba Corning Diagnostics Corp..........  High Resolution Protein Kit/8    Kit: 10 Plates; Plastic       10/28/91
                                          Cat. No. 470682.                 Vial: 25 Drams.                      
Ciba Corning Diagnostics Corp..........  Immophase Ferritin Controls....  Glass Vial: 3 ml.........      1/19/87
Ciba Corning Diagnostics Corp..........  Immophase Ferritin Standards...  Glass Vial: 5 ml.........      9/16/86
Ciba Corning Diagnostics Corp..........  Immunoelectrophoresis Gel/10     Kit: 12 Plates; 2 Plates:     10/28/91
                                          Cat. No. 470090.                 20 Tests.                            
Ciba Corning Diagnostics Corp..........  Immunoelectrophoresis Kit/8      Kit: 10 Plates; Plastic       10/28/91
                                          Cat. No. 470684.                 Vial: 25 Drams.                      
Ciba Corning Diagnostics Corp..........  L-TDM I........................  Glass Vial: 5 ml, Box: 15      5/23/89
                                                                           Vials.                               
Ciba Corning Diagnostics Corp..........  L-TDM I, II, III Kit...........  Kit: 15 Vials............      5/23/89
Ciba Corning Diagnostics Corp..........  L-TDM II.......................  Glass Vial: 5ml, Box: 15       5/23/89
                                                                           Vials.                               
Ciba Corning Diagnostics Corp..........  L-TDM III......................  Glass Vial: 5ml, Box: 15       5/23/89
                                                                           Vials.                               
Ciba Corning Diagnostics Corp..........  LD Isoenzyme Gel/8 and Buffer    Kit: 10 Plates; Plastic       10/28/91
                                          Cat. No. 470620.                 Vial: 25 Drams.                      
Ciba Corning Diagnostics Corp..........  LVM HI-CHEM DIL................  Vial: 10ml...............      6/21/90
Ciba Corning Diagnostics Corp..........  LVM, Product Code--9774........  Carton: 12 vials.........      6/21/90
Ciba Corning Diagnostics Corp..........  Ligand Plus 1, 2, 3............  Kit: 15 Bottles, 5ml/          6/17/94
                                                                           bottle.                              
Ciba Corning Diagnostics Corp..........  Linearity Reference Material     Vial: 10ml; Kit: 2 vials.      2/12/91
                                          LNM-A, LNM-B, LNM-C.                                                  

[[Page 128]]

                                                                                                                
Ciba Corning Diagnostics Corp..........  Linearity Survey LN3-A, LN3-B,   Vial: 10ml; Kit: 2 vials.      2/12/91
                                          LN3-C.                                                                
Ciba Corning Diagnostics Corp..........  Linearity Survey LN4-A, LN4-B,   Vial: 25ml; Kit: 2 vials.      2/12/91
                                          LN4-C.                                                                
Ciba Corning Diagnostics Corp..........  Lipoprotein Kit/8 Cat. No.       Kit: 10 Plates; Plastic       10/28/91
                                          470694.                          Vial: 25 Drams.                      
Ciba Corning Diagnostics Corp..........  MULTIQUAL ABN UNASY............  Vial: 3ml, 10ml, Carton:       4/09/89
                                                                           15 vials, 10 vials.                  
Ciba Corning Diagnostics Corp..........  MULTIQUAL I Assay, Product Code  Kit: 15 vials; 3ml/vial..      8/05/92
                                          9816.                                                                 
Ciba Corning Diagnostics Corp..........  MULTIQUAL II Assay, Product      Kit: 15 vials; 3ml/vial..      8/05/92
                                          Code 9817.                                                            
Ciba Corning Diagnostics Corp..........  MULTIQUAL III Assay, Product     Kit: 15 vials; 3ml/vial..      8/05/92
                                          Code 9818.                                                            
Ciba Corning Diagnostics Corp..........  MULTIQUAL NOR UNASY............  Vial: 3ml, 10ml, Carton:       4/09/89
                                                                           15 vials, 10 vials.                  
Ciba Corning Diagnostics Corp..........  Magic Ferritin 2000 Standard...  Plastic Vial: 1 ml.......      1/19/87
Ciba Corning Diagnostics Corp..........  Magic Ferritin Controls........  Plastic Vial: 5 ml.......      1/19/87
Ciba Corning Diagnostics Corp..........  Magic Ferritin Standards.......  Polypropylene Vial: 3 ml.      9/16/86
Ciba Corning Diagnostics Corp..........  Magic Ferritin Zero Standard...  Plastic Vial: 50 ml......      1/19/87
Ciba Corning Diagnostics Corp..........  Magic Lite FT4 Component Set...  Set: 100, 400 Tests......      7/06/94
Ciba Corning Diagnostics Corp..........  Magic Lite FT4 Kit.............  Kit: 100 Tests...........      7/06/94
Ciba Corning Diagnostics Corp..........  Magic Lite FT4 Lite Reagent....  Bottle: 10ml, 40ml.......      7/06/94
Ciba Corning Diagnostics Corp..........  Magic Lite FT4 Solid Phase.....  Bottle: 50ml, 200ml......      7/06/94
Ciba Corning Diagnostics Corp..........  Magic Lite Ferritin Bulk Lite    Plastic Vial: 50 ml......      2/16/88
                                          Reageant.                                                             
Ciba Corning Diagnostics Corp..........  Magic Lite Ferritin Bulk Solid   Plastic Vial: 200 ml.....      2/16/88
                                          Phase.                                                                
Ciba Corning Diagnostics Corp..........  Magic Lite Ferritin Solid Phase  Plastic Vial: 50 ml......      2/16/88
Ciba Corning Diagnostics Corp..........  Magic Lite T3 Bulk Solid Phase.  Plastic Vial: 200 ml.....      2/16/88
Ciba Corning Diagnostics Corp..........  Magic Lite T3 Kit..............  Kit: 100 Tests...........      6/27/91
Ciba Corning Diagnostics Corp..........  Magic Lite T3 Lite Reagent.....  Plastic Vial: 30ml.......      6/27/91
Ciba Corning Diagnostics Corp..........  Magic Lite T3 Solid Phase......  Plastic Vial: 75ml.......      6/27/91
Ciba Corning Diagnostics Corp..........  Magic Lite T4 Component Set....  Set: 100, 400, 1200 Tests      7/06/94
Ciba Corning Diagnostics Corp..........  Magic Lite T4 Kit..............  Kit: 100 Tests...........      7/06/94
Ciba Corning Diagnostics Corp..........  Magic Lite T4 Solid Phase......  Bottle: 25ml, 100ml......      7/06/94
Ciba Corning Diagnostics Corp..........  Magic T4 Antibody..............  Plastic Vial: 50 ml and        2/16/88
                                                                           200 ml.                              
Ciba Corning Diagnostics Corp..........  Magic T4 Antibody..............  Vial: 50ml, 200ml........     11/01/90
Ciba Corning Diagnostics Corp..........  Multi-LD Gel Cat. No. 470221...  Kit: 12 Plates; 2 Plates:     10/28/91
                                                                           32 Tests.                            
Ciba Corning Diagnostics Corp..........  Multi-SPE Gel Cat. No. 470252..  Kit: 12 Plates; 2 Plates:     10/28/91
                                                                           32 Tests.                            
Ciba Corning Diagnostics Corp..........  Multitrac ALP Gel/12 and Buffer  Kit: 10 Plates; Plastic       10/28/91
                                          Cat. No. 470240.                 Bottle: 175ml.                       
Ciba Corning Diagnostics Corp..........  Multitrac Immunofixation Kit/12  Kit: 10 Plates; Plastic       10/28/91
                                          Cat. No. 470685.                 Vial: 25 Drams.                      
Ciba Corning Diagnostics Corp..........  Multitrac LD Isoenzyme Gel/12    Kit: 10 Plates; Plastic       10/28/91
                                          and Buffer Cat. No. 470622.      vial: 25 Drams.                      
Ciba Corning Diagnostics Corp..........  Multitrac LD Isoenzyme Gel/16    Kit: 10 Plates; Plastic       10/28/91
                                          and Buffer Cat. No. 470625.      Vial: 25 Drams.                      
Ciba Corning Diagnostics Corp..........  Multitrac Lipoprotein Kit/12     Kit: 10 Plates; Plastic       10/28/91
                                          Cat. No. 470695.                 Vial: 25 Drams.                      
Ciba Corning Diagnostics Corp..........  Multitrac Serum Protein Kit/12   Kit: 10 Plates; Plastic       10/28/91
                                          Cat. No. 470697.                 vial: 25 Drams.                      

[[Page 129]]

                                                                                                                
Ciba Corning Diagnostics Corp..........  QCS ABN ASY....................  Vial: 5ml, Kit: 5 vials..      1/21/89
Ciba Corning Diagnostics Corp..........  QCS ABN ASY No. 9705/9705A.....  Box: 10 vials, Vial: 5 ml     12/15/89
Ciba Corning Diagnostics Corp..........  QCS ABN ASY No. 9707/9707A.....  Box: 10 vials, Vial: 5 ml     12/15/89
Ciba Corning Diagnostics Corp..........  QCS ABN UNASY No. 9691/9691A...  Box: 40 vials, Vial: 25       12/15/89
                                                                           ml.                                  
Ciba Corning Diagnostics Corp..........  QCS ABN UNASY No. 9717/9717A...  Box: 10 vials, Vial: 10       12/15/89
                                                                           ml.                                  
Ciba Corning Diagnostics Corp..........  QCS NOR ASY....................  Vial: 5 ml, Kit: 5 vials.      1/21/89
Ciba Corning Diagnostics Corp..........  QCS NOR ASY No. 9702/9702A.....  Box: 10 vials, Vial: 5 ml     12/15/89
Ciba Corning Diagnostics Corp..........  QCS NOR ASY No. 9704/9704A.....  Box: 10 vials, Vial: 5 ml     12/15/89
Ciba Corning Diagnostics Corp..........  QCS Nor UNASY No. 9681/9681A...  Box: 40 vials, Vial: 25       12/15/89
                                                                           ml.                                  
Ciba Corning Diagnostics Corp..........  QCS Nor UNASY No. 9716/9716A...  Box: 10 vials, Vial 10 ml     12/15/89
Ciba Corning Diagnostics Corp..........  Reagent A- Alt 14..............  Vial: 15 ml..............      3/24/79
Ciba Corning Diagnostics Corp..........  Reagent A- Alt 7...............  Vial: 15 ml..............      3/24/79
Ciba Corning Diagnostics Corp..........  Reagent A-Ammonia 10...........  Vial: 10 ml..............      3/24/79
Ciba Corning Diagnostics Corp..........  Serum Protein Kit/8 Cat. No.     Kit: 10 Plates; Plastic       10/28/91
                                          470696.                          Vial: 25 Drams.                      
Ciba Corning Diagnostics Corp..........  Special Barbital Buffer Set,     Vial: 3 per kit..........      4/17/79
                                          Catalog No. 470182.                                                   
Ciba Corning Diagnostics Corp..........  Universal Buffer Cat. No.        Plastic Vial: 25 Drams...     10/28/91
                                          470586.                                                               
Ciba Corning Diagnostics Corp..........  Universal Electrophoresis Film   Plates: 12 per kit.......      4/17/79
                                          Agarose, Catalog No. 470100.                                          
Ciba Corning Diagnostics Corp..........  Universal Gel/12 Cat. No.        Kit: 12 Plates; 2 Plates:     10/28/91
                                          470554.                          24 Tests.                            
Ciba Corning Diagnostics Corp..........  Universal Gel/16 or Multi-SPE    Kit: 12 Plates; 2 Plates:     10/28/91
                                          Gel Cat. No. 470066.             32 Tests.                            
Ciba Corning Diagnostics Corp..........  Universal IEP Gel Cat. No.       Kit: 12 Plates; 2 Plates:     10/28/91
                                          470222.                          16 Tests.                            
Ciba Corning Diagnostics Corp..........  Universal II Gel/12 Cat. No.     Kit: 12 Plates; 2 Plates:     10/28/91
                                          470262.                          24 Tests.                            
Ciba Corning Diagnostics Corp..........  Universal II Gel/12 Cat. No.     Kit: 12 Plates...........      9/22/92
                                          470362.                                                               
Ciba Corning Diagnostics Corp..........  Universal II Gel/16 Cat. No.     Kit: 12 Plates; 2 Plates:     10/28/91
                                          470268.                          32 Tests.                            
Ciba Corning Diagnostics Corp..........  Universal II Gel/8 Cat. No.      Kit: 12 Plates; 2 Plates:     10/28/91
                                          470261.                          16 Tests.                            
Ciba Corning Diagnostics Corp..........  Universal II Gel/8 Cat. No.      Kit: 12 Plates...........      9/22/92
                                          470361.                                                               
Ciba Corning Diagnostics Corp..........  Universal PHAB Buffer Set        Kit: 3 vials per kit.....      9/26/79
                                          Catalog No. 470180.                                                   
Clinical Diagnostic Systems, Inc.......  Gemini TT4 Reagent Assembly....  Kit: 100 Tests...........      1/11/95
Cone Biotech, Inc......................  American Association of          Vial: 20ml Kit: 2 vials..      5/30/90
                                          Bioanalysts, Urine Toxicology                                         
                                          Survey.                                                               
Cone Biotech, Inc......................  CAP/Cocaine Reference Material   Vial: 20 ml..............      3/07/88
                                          Levels II, III, and IV.                                               
Cone Biotech, Inc......................  College of American              Vial: 15ml Kit: 4 vials..      5/30/90
                                          Pathologists (CAP) Reference                                          
                                          Material for Cocaine in Urine.                                        
Cone Biotech, Inc......................  College of American              Vial: 100ml..............      5/30/90
                                          Pathologists Forensic Urine                                           
                                          Drug Testing Survey Material                                          
                                          (AACC/CAP).                                                           
Cone Biotech, Inc......................  College of American              Vial: 50ml...............      5/30/90
                                          Pathologists Toxicology Survey                                        
                                          (CAP).                                                                
Cone Biotech, Inc......................  College of American              Vial: 50ml...............      5/30/90
                                          Pathologists Urine Toxicology                                         
                                          Survey (CAP).                                                         
Cone Biotech, Inc......................  QCM-UTI........................  Vial: 20ml...............      3/07/85
Cone Biotech, Inc......................  RIATRAC-Three Level Ligand       Vials: 8ml...............      2/27/84
                                          Assay Controls.                                                       
Cone Biotech, Inc......................  UDM-CAP/AACC Forensic Urine      Bottle: 60 ml............      8/31/87
                                          Drug Testing Survey (Initial                                          
                                          Phase).                                                               
Cone Biotech, Inc......................  UDS and UDC CAP/AACC Forensic    Vial: 30 ml..............      1/06/88
                                          Urine Drug Testing.                                                   

[[Page 130]]

                                                                                                                
Consolidated Technologies, Inc.........  AAB Urine Drug Screening Survey  Vial: 20ml...............      7/14/94
Consolidated Technologies, Inc.........  AAB Urine Drug Screening Survey  Vial: 20ml...............      9/29/95
                                          Material.                                                             
Consolidated Technologies, Inc.........  AACC/CAP Athletic Drug Testing   Bottle; 125ml............      7/14/94
                                          Survey.                                                               
Consolidated Technologies, Inc.........  AACC/CAP Forensic Urine Drug     Vial: 50ml...............      7/14/94
                                          Testing Confirmatory Survey.                                          
Consolidated Technologies, Inc.........  AACC/CAP Forensic Urine Drug     Vial: 15ml...............      7/14/94
                                          Testing Screening Survey.                                             
Consolidated Technologies, Inc.........  ACA Toxicology Urine Survey....  Bottle: 15-60ml..........      9/29/95
Consolidated Technologies, Inc.........  ADT-1 thru ADT-40..............  Vial: 125ml..............      6/10/92
Consolidated Technologies, Inc.........  CAP Athletic Drug Testing        Bottle: 125ml............      9/29/95
                                          Survey Material.                                                      
Consolidated Technologies, Inc.........  CAP Forensic Pathology Survey..  Vial: 5, 15, 50ml........      7/14/94
Consolidated Technologies, Inc.........  CAP Forensic Pathology Survey    Vial: 5, 15, 50ml........      9/29/95
                                          Material.                                                             
Consolidated Technologies, Inc.........  CAP Forensic Urine Drug Testing  Vial: 50ml...............      9/29/95
                                          Confirmatory Survey Material.                                         
Consolidated Technologies, Inc.........  CAP Toxicology Survey..........  Vial: 30, 50ml...........      7/14/94
Consolidated Technologies, Inc.........  CAP Toxicology Survey Material.  Vial: Vial: 50ml.........      9/29/95
Consolidated Technologies, Inc.........  CAP Urine Toxicology Survey....  Vial: 50ml...............      7/14/94
Consolidated Technologies, Inc.........  CAP Urine Toxicology Survey      Vial: 50ml...............      9/29/95
                                          Material.                                                             
Consolidated Technologies, Inc.........  HIST Multi-Drug Reference        Vial: 15ml...............     10/22/92
                                          Material.                                                             
Consolidated Technologies, Inc.........  Morphine Glucuronide             Kit: 4 Vials.............      9/08/92
                                          Calibration Set.                                                      
Consolidated Technologies, Inc.........  Morphine Glucuronide Reference   Vial: 20ml...............      9/08/92
                                          Levels 1, 2, 3.                                                       
DIagnostics Systems Laboratories Inc...  DHEA Controls I and II, DSL      Vial: 3.5ml..............     10/08/93
                                          8951 & 8952.                                                          
Dade International Inc.................  Absorbed Plasma and Serum        Glass Vial: 5ml                8/16/71
                                          Reagents Kit B4233-2.            (Lyophilized Material).              
Dade International Inc.................  Beckman B-1 Buffer.............  Plastic Vial: 15 g.......      5/22/79
Dade International Inc.................  Bovine Chemistry Control I.X     Bottle: 18ml (Lyophilized      1/29/86
                                          Special Order Request B5107-     Material).                           
                                          55XX.                                                                 
Dade International Inc.................  Bovine Chemistry Control II.X    Bottle: 18 ml                  1/29/86
                                          Special Order Request B5107-     (Lyophilized Material).              
                                          65XX.                                                                 
Dade International Inc.................  Buffered Thrombin (Bovine)       Bottle: 5ml (Lyophilized       1/24/86
                                          Catalog No. B4233-40.            Material).                           
Dade International Inc.................  Dade CA System Buffer, Cat #     Plastic Bottle: 500ml....      7/20/95
                                          B4265-32.                                                             
Dade International Inc.................  Dade CA System Buffer, Cat #     Pack: 4 Bottles, 500ml         7/20/95
                                          B4265-34.                        each.                                
Dade International Inc.................  Dade IAC.X Comprehensive Immuno- Kit: 6 bottles...........      8/27/91
                                          Assay Control, Tri-Level                                              
                                          Unassayed.                                                            
Dade International Inc.................  Dade Immunoassay Control, Level  Bottle: 9ml (Lyophilized       4/25/86
                                          I-Low.                           Material).                           
Dade International Inc.................  Dade Immunoassay Control, Level  Bottle: 9ml (Lyophilized       4/25/86
                                          II-Intermediate.                 Material).                           
Dade International Inc.................  Dade Immunoassay Control, Level  Bottle: 9ml (Lyophilized       4/25/86
                                          III-High.                        Material).                           
Dade International Inc.................  Dade Immunoassay Controls,       Bottles: 18; 9ml each....      3/28/95
                                          Level 1 Cat # B5700-06.                                               
Dade International Inc.................  Dade Immunoassay Controls,       Bottles: 18; 9ml each....      3/28/95
                                          Level 2 Cat # 5700-07.                                                
Dade International Inc.................  Dade Immunoassay Controls, Tri-  Kit: 3 bottles...........      4/25/86
                                          Level.                                                                
Dade International Inc.................  Dade Immunoassay Controls, Tri-  Bottles: 18; 9ml each....      3/28/95
                                          Level Cat # B5700-05.                                                 
Dade International Inc.................  Dade International Inc.........  Bottles: 18; 9ml each....      3/28/95
Dade International Inc.................  Dade Moni-Trol Level 1           Bottle: 9ml..............      8/07/95
                                          Chemistry Control.                                                    
Dade International Inc.................  Dade Moni-Trol Level 2           Bottle: 9ml..............      8/07/95
                                          Chemistry Control.                                                    
Dade International Inc.................  Dade TDM Control Level I-Low     Glass Vial: 9ml                1/21/82
                                          B5700-2.                         (Lyophilized Material).              
Dade International Inc.................  Dade TDM Control Level II-       Glass Vial: 9ml                1/21/82
                                          Intermediate B5700-3.            (Lyophilized Material).              

[[Page 131]]

                                                                                                                
Dade International Inc.................  Dade TDM Control Level III-High  Glass Vial: 9ml                1/21/82
                                          B5700-4.                         (Lyophilized Material).              
Dade International Inc.................  Dade Therapeutic Drug            Kit: 9 Vials.............      3/10/87
                                          Monitoring (TDM) Controls                                             
                                          (Catalog No. B5700-1).                                                
Dade International Inc.................  Dade Urine Chemistry Control     Kit: 10 Bottles; Bottle:       8/02/91
                                          Level I, II.                     18ml.                                
Dade International Inc.................  Data-Fi Fibrin Monomer Control   Glass Vial: 5ml                1/24/86
                                          Catalog Nos. B4233-30 & B4233-   (Lyophilized Material).              
                                          38.                                                                   
Dade International Inc.................  Data-Fi Fibrinogen               Kit: 50 tests............      9/09/86
                                          Determination Reagents Cat.                                           
                                          No. B4233-15.                                                         
Dade International Inc.................  Data-Fi Protamine Sulfate        Kit: 10 Vials............      3/10/87
                                          Reagents Kit (Catalog No.                                             
                                          B4233-30).                                                            
Dade International Inc.................  Immunoassay Control Level I-III  Bottle: 9ml..............      8/27/91
                                          Unassayed.                                                            
Dade International Inc.................  Moni-Trol Level I Chemistry      Bottle: 9ml (Lyophilzed        1/20/84
                                          Control, Assayed, Special        Material).                           
                                          Order Request. B5103-XXX.                                             
Dade International Inc.................  Moni-Trol Level I.X Special      Bottle: 18ml (Lyophilized      6/30/83
                                          Order Request B5106-5X.          Material).                           
Dade International Inc.................  Moni-Trol Level II Chemistry     Bottle: 9ml (Lyophilized       1/20/84
                                          Control, Assayed, Special        Material).                           
                                          Order Request. B5103-XXX,                                             
                                          B5113-XXX.                                                            
Dade International Inc.................  Moni-Trol Level II.X Special     Bottle: 18ml (Lyophilized      6/30/83
                                          Order Request B5106-6X.          Material).                           
Dade International Inc.................  Moni-Trol. ES Level II           Bottles: 9ml, 6.7ml            7/15/83
                                          Chemistry Control, Assayed.      (Lyophilized Material).              
Dade International Inc.................  Moni-Trol. ES Level II.X         Bottle: 18ml, 9ml              6/27/86
                                          Special Order Request Catalog    (Lyophilized Material).              
                                          No. B5106-85AAA Catalog No.                                           
                                          B5106-2XAAA.                                                          
Dade International Inc.................  Owren's Veronal Buffer.........  Bottle: 18ml.............      8/16/71
Dade International Inc.................  Stratus Phenobarbital            Glass Vial: 3ml..........      6/27/83
                                          Calibrators B, C, D, E, & F.                                          
Dade International Inc.................  Stratus Phenobarbital Conjugate  Glass Vial: 6ml..........      1/25/82
Dade International Inc.................  Stratus Phenobarbital            Kit: 120 tests...........      3/10/87
                                          Fluorometric Enzyme                                                   
                                          Immunoassay Kit (Catalog No.                                          
                                          B5700-22).                                                            
Diagnostic  Products  Corporation......  125-I Barbiturate Isotope: Cat.  Vial: 110 ml, 550 ml.....      3/01/88
                                          No. TBA2, TBAY2.                                                      
Diagnostic  Products  Corporation......  125-I Benzolyecgonine Isotope:   Vial: 100 ml, 550 ml.....      3/01/88
                                          Cat. No. TCN2, TCNY2.                                                 
Diagnostic  Products  Corporation......  125-I Benzoylecgonine Isotope    Vial: 10 ml, 100 ml, 675       3/01/88
                                          (DA): Cat. No. CND2, YCND2.      ml.                                  
Diagnostic  Products  Corporation......  125-I Fentanyl Isotope: Cat.     Vial: 500 ml.............      3/01/88
                                          No. TFN2.                                                             
Diagnostic  Products  Corporation......  125-I Methadone Isotope: Cat.    Vial: 100 ml.............      3/01/88
                                          No. TMD2.                                                             
Diagnostic  Products  Corporation......  125-I Methaqualone Isotope:      Vial: 100 ml.............      3/01/88
                                          Cat. No. TMQ2.                                                        
Diagnostic  Products  Corporation......  125-I Morphine Isotope: Cat.     Vial: 110 ml, 550 ml.....      3/01/88
                                          No. TMP2, TMPY2.                                                      
Diagnostic  Products  Corporation......  125-I PCP Isotope: Cat. No.      Vial: 110 ml, 550 ml.....      3/01/88
                                          TPC2, TPCY2.                                                          
Diagnostic  Products  Corporation......  125-I Serum Morphine Isotope:    Vial: 110 ml.............      3/01/88
                                          Cat. No. TSM2.                                                        
Diagnostic  Products  Corporation......  125-I THC Isotope: Cat. No.      Vial: 20 ml, 110 ml, 550       3/01/88
                                          THD2, YTHD2.                     ml.                                  
Diagnostic  Products  Corporation......  Amphetamine Calibrators B-F:     Vial: 3.5 ml.............      3/01/88
                                          Cat. No. APD4-8.                                                      
Diagnostic  Products  Corporation......  Amphetamine Calibrators Cat.     Vial: 5ml................      7/05/90
                                          No. MAP 4-8.                                                          
Diagnostic  Products  Corporation......  Amphetamine Controls, Cat. No.   Vial: 5 ml...............      3/20/89
                                          ACO1, ACO2.                                                           
Diagnostic  Products  Corporation......  Amphetamine Controls: Cat. No.   Vial: 100 ml.............      3/01/88
                                          5AC01, 5ACO2.                                                         
Diagnostic  Products  Corporation......  Amphetamine Isotope: Cat. No.    Vial: 20 ml, 100 ml, 550       3/01/88
                                          APD2, 5APD2, YAPD2.              ml.                                  
Diagnostic  Products  Corporation......  Amphetamine Reference            Vial: 120 ml.............      3/01/88
                                          Preparation: Cat. No. 5YAP7.                                          
Diagnostic  Products  Corporation......  Amphetamine Reference            Vial: 5 ml...............      3/20/89
                                          Preparations, Cat. No. APD5,                                          
                                          APD9.                                                                 
Diagnostic  Products  Corporation......  Barbiturate Calibrators B-G:     Vial: 3.5 ml.............      3/01/88
                                          Cat. No. BAC4-9.                                                      
Diagnostic  Products  Corporation......  Barbiturate Reference            Vial: 120 ml.............      3/01/88
                                          Preparations: Cat. No. 5YBA5.                                         
Diagnostic  Products  Corporation......  Benzoylecgonine Calibrators      Vial: 3.5 ml.............      3/01/88
                                          (CAC) B-F: Cat. No. COC4-8.                                           
Diagnostic  Products  Corporation......  Benzoylecgonine Calibrators      Vial: 3.5 ml.............      3/01/88
                                          (DA) B-F: Cat. No. CND4-8.                                            

[[Page 132]]

                                                                                                                
Diagnostic  Products  Corporation......  Benzoylecgonine Calibrators      Vial: 3.5 ml.............      3/01/88
                                          (DA): Cat. No. CNC4-8.                                                
Diagnostic  Products  Corporation......  Benzoylecgonine Reference        Vial: 120 ml.............      3/01/88
                                          Preparation (DA): Cat. No.                                            
                                          5YCN5.                                                                
Diagnostic  Products  Corporation......  Benzoylecgonine Reference        Vial: 120 ml.............      3/01/88
                                          Preparation: Cat. No. 5YCN5.                                          
Diagnostic  Products  Corporation......  C-Terminal PTH Antiserum: Cat.   Vial: 10 ml..............      3/01/88
                                          No. PCD1.                                                             
Diagnostic  Products  Corporation......  CON6 Immunoassay Tri-level       Kit: 6 vials.............      3/25/91
                                          Control Cat. No. CON6.                                                
Diagnostic  Products  Corporation......  Canine T3 Isotope: Cat. No.      Vial: 120 ml.............      3/01/88
                                          TC32.                                                                 
Diagnostic  Products  Corporation......  Coat-A-Count Barbiturates In     Kit: 100 tests, 500 tests      3/01/88
                                          Urine: Cat. No. TKBA1, TKBA5.                                         
Diagnostic  Products  Corporation......  Coat-A-Count Barbiturates        Kit: 2500 tests..........      3/01/88
                                          Qualitative Determination In                                          
                                          Urine: Cat. No. TKBAY.                                                
Diagnostic  Products  Corporation......  Coat-A-Count Canine T3: Cat.     Kit: 100 tests, 500 tests      3/01/88
                                          No. TKC31, TKC35.                                                     
Diagnostic  Products  Corporation......  Coat-A-Count Cocaine             Kit: 100 tests, 500 tests      3/01/88
                                          Metabolite: Cat. No. TKCN1,                                           
                                          TKCN5.                                                                
Diagnostic  Products  Corporation......  Coat-A-Count Fentanyl: Cat. No.  Kit: 100 tests...........      3/01/88
                                          TKFN1.                                                                
Diagnostic  Products  Corporation......  Coat-A-Count Free Testosterone   Kit: 100, 200 Tests......      3/25/91
                                          Cat. No. TKTF 1, 2.                                                   
Diagnostic  Products  Corporation......  Coat-A-Count LSD 100, 500, Cat.  Kit: 8 vials, 19 vials...      3/20/89
                                          No. TKLS1, TKLS5.                                                     
Diagnostic  Products  Corporation......  Coat-A-Count LSD Qualitative     Kit: 8 vials.............      3/20/89
                                          Determination in Urine, Cat.                                          
                                          No. TKLSY.                                                            
Diagnostic  Products  Corporation......  Coat-A-Count Metabolite          Kit: 2500 tests..........      3/01/88
                                          Qualitative Determinants In                                           
                                          Urine: Cat. No. TKCNY.                                                
Diagnostic  Products  Corporation......  Coat-A-Count Methadone: Cat.     Kit: 100 tests...........      3/01/88
                                          No. TKMD1.                                                            
Diagnostic  Products  Corporation......  Coat-A-Count Methaqualone: Cat.  Kit: 100 tests...........      3/01/88
                                          No. TKMQ1.                                                            
Diagnostic  Products  Corporation......  Coat-A-Count Morphine            Kit: 2500 tests..........      3/01/88
                                          Qualitative Determinations In                                         
                                          Urine: Cat. No. TKMPY.                                                
Diagnostic  Products  Corporation......  Coat-A-Count Morphine: Cat. No.  Kit: 100 tests, 500            3/01/88
                                          TKMP1, TKMP5, TKMPX.             tests, 1000 tests.                   
Diagnostic  Products  Corporation......  Coat-A-Count Opiates Screen      Kit: 2500 tests..........       3/1/88
                                          Qualitative Determinations In                                         
                                          Urine: Cat. No. TKOSY.                                                
Diagnostic  Products  Corporation......  Coat-A-Count Opiates Screen:     Kit: 100 tests, 500 tests       3/1/88
                                          Cat. No. TK0S1, TKOS5.                                                
Diagnostic  Products  Corporation......  Coat-A-Count PCP                 Kit: 100 tests...........       3/1/88
                                          (Phencyclidine) In Urine: Cat.                                        
                                          No. TKCY1.                                                            
Diagnostic  Products  Corporation......  Coat-A-Count PCP                 Kit: 2500 tests..........       3/1/88
                                          (Phencyclidine) Qualitative                                           
                                          Determinations In Urine: Cat.                                         
                                          No. TKPCY.                                                            
Diagnostic  Products  Corporation......  Coat-A-Count Serum Morphine:     Kit: 100 tests...........       3/1/88
                                          Cat. No. TKSM1.                                                       
Diagnostic  Products  Corporation......  Coat-A-Count Total Testosterone  Kit: 100, 200, 500 Tests.      3/25/91
                                          Cat. No. TKTT 1, 2, 5.                                                
Diagnostic  Products  Corporation......  Donkey Anti-Goat Gamma Globulin  Vial: 10 ml..............       3/1/88
                                          (PTH-Ultra): Cat. No. PTDG.                                           
Diagnostic  Products  Corporation......  Double Antibody Amphetamine,     Kit: 6 vials.............      3/20/89
                                          Cat. No. KAPD1, KAPD5.                                                
Diagnostic  Products  Corporation......  Double Antibody Amphetamine,     Kit: 2500 tests..........       3/1/88
                                          Qualitative Determinations In                                         
                                          Urine: Cat. No. KAPDY.                                                
Diagnostic  Products  Corporation......  Double Antibody Amphetamine:     Kit: 100 tests, 500 tests       3/1/88
                                          Cat. No. KAPD1, KAPD5.                                                
Diagnostic  Products  Corporation......  Double Antibody Cannabinoids     Kit: 100 tests, 500 tests       3/1/88
                                          (THC) In Urine: Cat. No.                                              
                                          KTHD1, KTHD5.                                                         
Diagnostic  Products  Corporation......  Double Antibody Cannabinoids     Kit: 2500 tests..........       3/1/88
                                          (THC) Quantitative                                                    
                                          Determinations In Urine: Cat.                                         
                                          No. KTHDY.                                                            
Diagnostic  Products  Corporation......  Double Antibody Cocaine          Kit: 2500 tests..........       3/1/88
                                          Metabolite Qualitive                                                  
                                          Determination In Urine: Cat.                                          
                                          No. KCNDY.                                                            
Diagnostic  Products  Corporation......  Double Antibody Cocaine          Kit: 100 tests, 500 tests       3/1/88
                                          Metabolite: Cat. No. KCND1,                                           
                                          KCND5.                                                                
Diagnostic  Products  Corporation......  Double Antibody PTH-C: KPCD1,    Kit: 70 tests, 140 tests.       3/1/88
                                          KPCD2.                                                                
Diagnostic  Products  Corporation......  Double Antibody PTH-M: Cat. No.  Kit: 70 tests............       3/1/88
                                          KPMD1.                                                                
Diagnostic  Products  Corporation......  Double Antibody Testosterone     Kit: 100, 200 Tests......      3/25/91
                                          Cat. No. KTTD1, 2.                                                    

[[Page 133]]

                                                                                                                
Diagnostic  Products  Corporation......  Double Antibody Ultra-PTH: Cat.  Kit: 70 tests, 140 tests.       3/1/88
                                          No. KPTD1, KPTD2.                                                     
Diagnostic  Products  Corporation......  Enzyme-Labeled Amphetamine Cat.  Vial: 20ml, 60ml.........       7/5/90
                                          No. MEAP2, 5MEAP2.                                                    
Diagnostic  Products  Corporation......  Enzyme-Labeled Cocaine           Glass Vial: 11ml, 60ml...      1/25/91
                                          Metabolite Cat. No. MECC2,                                            
                                          5MECC2.                                                               
Diagnostic  Products  Corporation......  Enzyme-Labeled Methamphetamine   Vial: 11ml, 60ml.........      9/28/90
                                          Cat. No. MEMA2, 5MEMA2.                                               
Diagnostic  Products  Corporation......  Enzyme-Labeled Opiates Cat. No.  Vial: 20ml, 60ml.........       7/5/90
                                          MEOP2, 5MEOP2.                                                        
Diagnostic  Products  Corporation......  Enzyme-Labeled PCP Cat. No.      Vial: 20ml, 60ml.........       7/5/90
                                          MEPC2, 5MEPC2.                                                        
Diagnostic  Products  Corporation......  Enzyme-Labeled THC Cat. No.      Vial: 20ml, 60ml.........       7/5/90
                                          METH 2, 5METH2.                                                       
Diagnostic  Products  Corporation......  EquiCON-DOA Drugs of Abuse       Kit: 2 Vials.............      3/25/91
                                          Equine Urine Controls Cat. No.                                        
                                          EDAC.                                                                 
Diagnostic  Products  Corporation......  EquiCon-DOA Level 2, 3 Cat. No.  Vial: 30ml...............      3/25/91
                                          EDAC 2, 3.                                                            
Diagnostic  Products  Corporation......  Fentanyl Calibrators: Cat. No.   Vial: 3.5 ml.............       3/1/88
                                          FNC4-9.                                                               
Diagnostic  Products  Corporation......  Free Testosterone Calibrators    Vial: 3.5ml..............      3/25/91
                                          Cat. No. TFC4-8.                                                      
Diagnostic  Products  Corporation......  Goat Anti-Rabbit Gamma Globulin/ Vial: 110 ml, 320 ml.....       3/1/88
                                          4% PEG Saline: Cat. No. 5N6.                                          
Diagnostic  Products  Corporation......  LSD Calibrators B-F, Cat. No.    Vial: 5 ml...............      3/20/89
                                          LSCH-8.                                                               
Diagnostic  Products  Corporation......  LSD Controls, Cat. No. 5LCO1,    Vial: 120ml, 5ml.........      3/20/89
                                          5LCO2, LSCO1, LSCO2.                                                  
Diagnostic  Products  Corporation......  LSD Isotope, Cat. No. TLSY2,     Vial: 105 ml, 550 ml.....      3/20/89
                                          TLS2.                                                                 
Diagnostic  Products  Corporation......  LSD Reference Preparation, Cat.  Vial: 120ml..............      3/20/89
                                          No. 5YLS6.                                                            
Diagnostic  Products  Corporation......  Low and High Barbiturate         Vial: 100 ml.............       3/1/88
                                          Urinary Controls: Cat. No.                                            
                                          5BCO1, 5BCO2.                                                         
Diagnostic  Products  Corporation......  Low and High Benzoylecgonine     Vial: 3.5 ml, 100 ml.....       3/1/88
                                          Urinary Controls (DA): Cat.                                           
                                          No. 5COO1, 5COO2, CNC02, CNCO3.                                       
Diagnostic  Products  Corporation......  Low and High Cannabinoid         Vial: 100 ml.............       3/1/88
                                          Urinary Controls: Cat. No.                                            
                                          5TCO1, 5TCO2.                                                         
Diagnostic  Products  Corporation......  Low and High Morphine Urinary    Vial: 100 ml.............       3/1/88
                                          Controls: Cat. No. 5MCO1,                                             
                                          5MCO2.                                                                
Diagnostic  Products  Corporation......  Low and High Opiate Urinary      Vial: 100 ml.............       3/1/88
                                          Controls: Cat. No. 5OCO1,                                             
                                          5OCO2.                                                                
Diagnostic  Products  Corporation......  Low and High PCP Urinary         Vial: 100 ml.............       3/1/88
                                          Controls: Cat. No. 5PCO1,                                             
                                          5PCO2.                                                                
Diagnostic  Products  Corporation......  Methadone Calibrators: Cat. No.  Vial: 3.5 ml.............       3/1/88
                                          MDC4-8.                                                               
Diagnostic  Products  Corporation......  Methamphetamine Calibrators      Vial: 5ml................      9/28/90
                                          Cat. No. MMA-8.                                                       
Diagnostic  Products  Corporation......  Methamphetamine Cartridges Cat.  Cartridge: 5ml...........      1/25/91
                                          No. VMADC.                                                            
Diagnostic  Products  Corporation......  Methamphetamine Positive         Vial: 3ml................      1/25/91
                                          Reference Cat. No. VMAPC.                                             
Diagnostic  Products  Corporation......  Methaqualone Calibrators: Cat.   Vial: 3.5 ml.............       3/1/88
                                          No. MQC4-8.                                                           
Diagnostic  Products  Corporation......  Mid-Molecule PTH Antiserum:      Vial: 10 ml..............       3/1/88
                                          Cat. No. PMD1.                                                        
Diagnostic  Products  Corporation......  Milenia Amphetamine Cat. No.     Kit: 7 vials, 96 tests,         7/5/90
                                          MKAP1, MKAP5.                    480 tests.                           
Diagnostic  Products  Corporation......  Milenia Cannabinoids Cat. No.    Kit: 6 vials, 96 Tests,         7/5/90
                                          MK TH1, MKTH5.                   480 Tests.                           
Diagnostic  Products  Corporation......  Milenia Cocaine Metabolite Cat.  Kit: 96 Tests, 480 Tests.      1/25/91
                                          No. MKCC1, MKCC5.                                                     
Diagnostic  Products  Corporation......  Milenia Cocaine References and   Glass Vial: 5ml..........      1/25/91
                                          Controls Cat. No. MC3, 6;                                             
                                          MCCC1, 2.                                                             
Diagnostic  Products  Corporation......  Milenia Methamphetamine Cat.     Kit: 96 wells, 480 wells.      9/28/90
                                          No. MKMA1, MKMA5.                                                     
Diagnostic  Products  Corporation......  Milenia Opiates Cat. No. MKOP1,  Kit: 6 vials, 96 Tests,         7/5/90
                                          MKOP5.                           480 Tests.                           
Diagnostic  Products  Corporation......  Milenia PCP Cat. No. MKPC1,      Kit: 6 vials, 96 tests,         7/5/90
                                          MKPC5.                           480 tests.                           
Diagnostic  Products  Corporation......  Morphine Calibrators: Cat. No.   Vial: 3.5 ml, 10 ml......       3/1/88
                                          MPC4-8.                                                               

[[Page 134]]

                                                                                                                
Diagnostic  Products  Corporation......  Morphine Reference Preparation:  Vial: 120 ml.............       3/1/88
                                          Cat. No. 5YMPY7.                                                      
Diagnostic  Products  Corporation......  Opiate Calibrators: Cat. No.     Vial: 3.5 ml.............       3/1/88
                                          OSC4-8.                                                               
Diagnostic  Products  Corporation......  Opiate Cartridges Cat. No.       Cartridge: 5ml...........       7/5/90
                                          VOSDC.                                                                
Diagnostic  Products  Corporation......  Opiates Calibrators Cat. No.     Vial: 5ml................       7/5/90
                                          MOP 4-7.                                                              
Diagnostic  Products  Corporation......  Opiates Positive Reference Cat.  Vial: 1ml................       7/5/90
                                          No. VOSPC.                                                            
Diagnostic  Products  Corporation......  Opiates Reference Preparation:   Vial: 120 ml.............       3/1/88
                                          Cat. No. 5YOS7.                                                       
Diagnostic  Products  Corporation......  PCP Calibrators Cat. No. MPC 3-  Vial: 5ml................       7/5/90
                                          7.                                                                    
Diagnostic  Products  Corporation......  PCP Calibrators: Cat. No. PCC4-  Vial: 3.5 ml.............       3/1/88
                                          8.                                                                    
Diagnostic  Products  Corporation......  PCP Reference Preparation: Cat.  Vial: 120 ml.............       3/1/88
                                          No. 5YPC6.                                                            
Diagnostic  Products  Corporation......  PTH (C-Terminal) Isotope: Cat.   Vial: 10 ml..............       3/1/88
                                          No. PCD2.                                                             
Diagnostic  Products  Corporation......  PTH (Ultra) Antiserum: Cat. No.  Vial: 5 ml...............       3/1/88
                                          PTD1.                                                                 
Diagnostic  Products  Corporation......  PTH (Ultra) Isotope: Cat. No.    Vial 5 ml................       3/1/88
                                          PTD2.                                                                 
Diagnostic  Products  Corporation......  PTH-M Isotope: Cat. No. PMD2...  Vial: 10 ml..............       3/1/88
Diagnostic  Products  Corporation......  RIA Controls Level 4, 5, 6 Cat.  Vial: 10ml...............      3/25/91
                                          No. CON4, CON5, CON6.                                                 
Diagnostic  Products  Corporation......  Serum Morphine Calibrators:      Vial: 3.5 ml.............       3/1/88
                                          Cat. No. SMC4-8.                                                      
Diagnostic  Products  Corporation......  Serum Morphine Controls: Cat.    Vail: 3.5 ml.............       3/1/88
                                          No. SMCO2, SMCO3.                                                     
Diagnostic  Products  Corporation......  THC Calibrators B-F: Cat. No.    Vial: 3.5 ml.............       3/1/88
                                          THD4-8.                                                               
Diagnostic  Products  Corporation......  THC Calibrators Cat. No. MTH 4-  Vial: 5ml................       7/5/90
                                          7.                                                                    
Diagnostic  Products  Corporation......  THC Reference Preparation: Cat.  Vial: 120 ml.............       3/1/88
                                          No. 5YTH7.                                                            
Diagnostic  Products  Corporation......  Ten One Methamphetamine Cat.     Kit: 12 Tests, 48 Tests..      1/25/91
                                          No. VKMA1, VKMA4.                                                     
Diagnostic  Products  Corporation......  Ten One Opiates Cat. No. VKSO1,  Kit: 1 vial, 12 & 48 5ml        7/5/90
                                          VKSO4.                           cartridges.                          
Diagnostic  Products  Corporation......  Testosterone Calibrators Cat.    Vial: 3.5ml..............      3/25/91
                                          No. TTD3-8.                                                           
Diagnostic  Products  Corporation......  Total Testosterone Calibrators   Vial: 3.5ml..............      3/25/91
                                          Cat. No. TTC4-8.                                                      
Diagnostic  Products  Corporation......  Triiodothyronine (T3) Isotope:   Vial: 120 ml.............       3/1/88
                                          Cat. No. TT32.                                                        
Diagnostic  Products  Corporation......  [125I] Free Testosterone Cat.    Vial: 105ml..............      3/25/91
                                          No. TTF2.                                                             
Diagnostic  Products  Corporation......  [125I] Testosterone Cat. No.     Vial: 10ml...............      3/25/91
                                          TTD2.                                                                 
Diagnostic  Products  Corporation......  [125I] Total Testosterone Cat.   Vial: 105ml..............      3/25/91
                                          No. TTT 2.                                                            
Diagnostic Systems Laboratories, Inc...  Active DHT DSL 9600............  Kit: 100 Tests...........      1/25/96
Diagnostics Reagents, Inc..............  Amphetamines Enzyme Conjugate    Carboy: 20, 10, 5, 1 L...     10/20/93
                                          Reagent, Bulk.                                                        
Diagnostics Reagents, Inc..............  Amphetamines Enzyme Immunoassay  Kit: 2 Bottles; 100ml         10/20/93
                                          Kit # 0017.                      each.                                
Diagnostics Reagents, Inc..............  Amphetemine Enzyme Immunoassay   Kit: 2 Bottles; 500ml         10/20/93
                                          Kit # 0018.                      each.                                
Diagnostics Reagents, Inc..............  Barbiturate Enzyme Congugate     Carboy: 20, 10, 5, 1 L...     10/20/93
                                          Reagent, Bulk.                                                        
Diagnostics Reagents, Inc..............  Barbiturate Enzyme Immunoassay   Kit: 2 Bottles; 100 ml        10/20/93
                                          Kit # 0225.                      each.                                
Diagnostics Reagents, Inc..............  Barbiturate Enzyme Immunoassay   Kit: 2 Bottles; 500ml         10/20/93
                                          Kit # 0226.                      each.                                
Diagnostics Reagents, Inc..............  Benzodiazepine Enzyme Conjugate  Carboy: 20, 10, 5, 1 L...     10/20/93
                                          Reagent, Bulk.                                                        
Diagnostics Reagents, Inc..............  Benzodiazepine Enzyme            Kit: 2 Bottles; 100ml         10/20/93
                                          Immunoassay Kit # 0039.          each.                                
Diagnostics Reagents, Inc..............  Benzodiazepine Enzyme            Kit: 2 Bottles; 500ml         10/20/93
                                          Immunoassay Kit # 0040.          each.                                
Diagnostics Reagents, Inc..............  Caanbinoid Enzyme Immunoassay    Kit: 2 Bottles; 500ml         10/20/93
                                          Kit # 0186.                      each.                                
Diagnostics Reagents, Inc..............  Cannabinoid Enzyme Conjugate     Carboy: 20, 10, 5, 1 L...     10/20/93
                                          Reagent, Bulk.                                                        
Diagnostics Reagents, Inc..............  Cannabinoid Enzyme Immunoassay   Kit: 2 Bottles; 100ml         10/20/93
                                          Kit # 0185.                      each.                                
Diagnostics Reagents, Inc..............  Cocaine Metabolite Enzyme        Carboy: 20, 10, 5, 1 L...     10/20/93
                                          Conjugate Reagent, Bulk.                                              
Diagnostics Reagents, Inc..............  Cocaine Metabolite Enzyme        Kit: 2 Bottles; 100ml         10/20/93
                                          Immunoassay Kit # 0055.          each.                                
Diagnostics Reagents, Inc..............  Cocaine Metabolite Enzyme        Kit: 2 Bottles; 500ml         10/20/93
                                          Immunoassay Kit # 0056.          each.                                
Diagnostics Reagents, Inc..............  Drugs of Abuse High Calibrator   Bottle: 5L, 1L, 500ml....     10/20/93
                                          A, Bulk.                                                              

[[Page 135]]

                                                                                                                
Diagnostics Reagents, Inc..............  Drugs of Abuse High Calibrator   Bottle: 5ml..............     10/20/93
                                          A, Cat # 0324.                                                        
Diagnostics Reagents, Inc..............  Drugs of Abuse High Calibrator,  Bottle: 5L, 1L, 500ml....     10/20/93
                                          Bulk.                                                                 
Diagnostics Reagents, Inc..............  Drugs of Abuse High Calibrator,  Bottle: 5ml..............     10/20/93
                                          Cat # 0036.                                                           
Diagnostics Reagents, Inc..............  Drugs of Abuse Level 2 Control,  Bottle: 5L, 1L, 500ml....     10/20/93
                                          Bulk.                                                                 
Diagnostics Reagents, Inc..............  Drugs of Abuse Level 2 Control,  Bottle: 5ml..............     10/20/93
                                          Cat # 0208.                                                           
Diagnostics Reagents, Inc..............  Drugs of Abuse Level 2A          Bottle: 5L, 1L, 500ml....     10/20/93
                                          Control, Bulk.                                                        
Diagnostics Reagents, Inc..............  Drugs of Abuse Level 2A          Bottle: 5ml..............     10/20/93
                                          Control, Cat # 0331.                                                  
Diagnostics Reagents, Inc..............  Drugs of Abuse Level I Control,  Bottle: 5L, 1L, 500ml....     10/20/93
                                          Bulk.                                                                 
Diagnostics Reagents, Inc..............  Drugs of Abuse Level I Control,  Bottle: 5ml..............     10/20/93
                                          Cat # 0210.                                                           
Diagnostics Reagents, Inc..............  Drugs of Abuse Level IA          Bottle: 5L, 1L, 500ml....     10/20/93
                                          Control, Bulk.                                                        
Diagnostics Reagents, Inc..............  Drugs of Abuse Level IA          Bottle: 5ml..............     10/20/93
                                          Control, Cat # 0329.                                                  
Diagnostics Reagents, Inc..............  Drugs of Abuse Low Calibrator    Bottle: 5ml..............     10/20/93
                                          A, Cat # 0322.                                                        
Diagnostics Reagents, Inc..............  Drugs of Abuse Low Calibrator,   Bottle: 5L, 1L, 500ml....     10/20/93
                                          Bulk.                                                                 
Diagnostics Reagents, Inc..............  Drugs of Abuse Low Calibrator,   Bottle: 5L, 1L, 500ml....     10/20/93
                                          Bulk.                                                                 
Diagnostics Reagents, Inc..............  Drugs of Abuse Low Calibrator,   Bottle: 5ml..............     10/20/93
                                          Cat # 0034.                                                           
Diagnostics Reagents, Inc..............  Methadone Enzyme Conjugate       Carboy: 20, 10, 5, 1 L...     10/20/93
                                          Reagent, Bulk.                                                        
Diagnostics Reagents, Inc..............  Methadone Enzyme Immunoassay     Kit: 2 Bottles; 100ml         10/20/93
                                          Kit # 0596.                      each.                                
Diagnostics Reagents, Inc..............  Methadone Enzyme Immunoassay     Kit: 2 Bottles; 500ml         10/20/93
                                          Kit # 0597.                      each.                                
Diagnostics Reagents, Inc..............  Methadone Metabolite Enzyme      Carboy: 20, 10, 5, 1 L...     10/20/93
                                          Conjugate Reagent, Bulk.                                              
Diagnostics Reagents, Inc..............  Methadone Metabolite Enzyme      Kit: 2 Bottles; 100ml         10/20/93
                                          Immunoassay Kit # 0200.          each.                                
Diagnostics Reagents, Inc..............  Methadone Metabolite Enzyme      Kit: 2 Bottles; 500ml         10/20/93
                                          Immunoassay Kit # 0201.          each.                                
Diagnostics Reagents, Inc..............  Methaqualone Enzyme Conjugate    Carboy: 20, 10, 5, 1 L...     10/20/93
                                          Reagent, Bulk.                                                        
Diagnostics Reagents, Inc..............  Methaqualone Enzyme Immunoassay  Kit: 2 Bottles; 100ml         10/20/93
                                          Kit # 0514.                      each.                                
Diagnostics Reagents, Inc..............  Methaqualone Enzyme Immunoassay  Kit: 2 Bottles; 500ml         10/20/93
                                          Kit # 0515.                      each.                                
Diagnostics Reagents, Inc..............  Opiate Enzyme Conjugate          Carboy: 20, 10, 5, 1 L...     10/20/93
                                          Reagent, Bulk.                                                        
Diagnostics Reagents, Inc..............  Opiate Enzyme Immunoassay Kit #  Kit: 2 Bottles; 100ml         10/20/93
                                          0135.                            each.                                
Diagnostics Reagents, Inc..............  Opiate Enzyme Immunoassay Kit #  Kit: 2 Bottles; 500ml         10/20/93
                                          0136.                            each.                                
Diagnostics Reagents, Inc..............  Phencyclidine Enzyme Conjugate   Carboy: 20, 10, 5, 1 L...     10/20/93
                                          Reagent, Bulk.                                                        
Diagnostics Reagents, Inc..............  Phencyclidine Enzyme             Kit: 2 Bottles; 100ml         10/20/93
                                          Immunoassay Kit # 0160.          each.                                
Diagnostics Reagents, Inc..............  Phencyclidine Enzyme             Kit: 2 Bottles; 500ml         10/20/93
                                          Immunoassay Kit # 0161.          each.                                
Diagnostics Reagents, Inc..............  Propoxyphene Enzyme Conjugate    Carboy: 20, 10, 5, 1 L...     10/20/93
                                          Reagent, Bulk.                                                        
Diagnostics Reagents, Inc..............  Propoxyphene Enzyme Immunoassay  Kit: 2 Bottles; 100 ml        10/20/93
                                          Kit # 0432.                      each.                                
Diagnostics Reagents, Inc..............  Propoxyphene Enzyme Immunoassay  Kit: 2 Bottles; 500ml         10/20/93
                                          Kit # 0433.                      each.                                
Diagnostics Reagents, Inc..............  THC Urine Calibrator 100ng/ml,   Bottle: 5L, 1L, 500ml....     10/20/93
                                          Bulk.                                                                 
Diagnostics Reagents, Inc..............  THC Urine Calibrator 100ng/ml,   Bottle: 5ml..............     10/20/93
                                          Cat # 0044.                                                           
Diagnostics Reagents, Inc..............  THC Urine Calibrator 200ng/ml    Bottle: 5ml..............     10/20/93
                                          Cat # 0206.                                                           
Diagnostics Reagents, Inc..............  THC Urine Calibrator 200ng/ml,   Bottle: 5L, 1L, 500ml....     10/20/93
                                          Bulk.                                                                 
Diagnostics Reagents, Inc..............  THC Urine Calibrator 50ng/ml...  Bottle: 5ml..............     10/20/93
Diagnostics Reagents, Inc..............  THC Urine Calibrator 50ng/ml,    Bottle: 5L, 1L, 500ml....     10/20/93
                                          Bulk.                                                                 
Diagnostics Reagents, Inc..............  THC Urine Calibrator, 20ng/ml,   Bottle: 5ml..............     10/20/93
                                          Cat # 0235.                                                           
Diagnostics Reagents, Inc..............  THC Urine Control 125ng/ml,      Bottle: 5L, 1L, 500ml....     10/20/93
                                          Bulk.                                                                 
Diagnostics Reagents, Inc..............  THC Urine Control 40ng/ml, Bulk  Bottle: 5L, 1L, 500ml....     10/20/93
Diagnostics Reagents, Inc..............  THC Urine Control 60ng/ml, Bulk  Bottle: 5L, 1L, 500ml....     10/20/93
Diagnostics Reagents, Inc..............  THC Urine Control 75ng/ml, Bulk  Bottle: 5L, 1L, 500ml....     10/20/93
Diagnostics Reagents, Inc..............  THC Urine Control, 125ng/ml,     Bottle: 5ml..............     10/20/93
                                          Cat # 0212.                                                           
Diagnostics Reagents, Inc..............  THC Urine Control, 40ng/ml, Cat  Bottle: 5ml..............     10/20/93
                                          # 0170.                                                               
Diagnostics Reagents, Inc..............  THC Urine Control, 60ng/ml, Cat  Bottle: 5ml..............     10/20/93
                                          # 0168.                                                               
Diagnostics Reagents, Inc..............  THC Urine Control, 75ng/ml, Cat  Bottle: 5ml..............     10/20/93
                                          # 0214.                                                               
Diagnostics Reagents, Inc..............  THC urine Calibrator 20ng/ml,    Bottle: 5L, 1L, 500ml....     10/20/93
                                          Bulk.                                                                 
Diagnostics Systems Laboratories Inc...  DHEA Standards, A-F, DSL 8901-   Vial: 3.5ml..............     10/08/93
                                          8906.                                                                 
Diagnostics Systems Laboratories Inc...  Radioimmunoassay Kit for the     Kit: 100 Tests...........     10/08/93
                                          Measurement of                                                        
                                          Dehydroepiandrosterone (DHEA),                                        
                                          DSL 8900.                                                             
Diagnostics Systems Laboratories Inc...  Radioimmunoassay Kit for the     Kit; 100 Tests...........     10/08/93
                                          Measurement of                                                        
                                          Dehydroepiandrosterone (DHEA),                                        
                                          DSL 9000.                                                             
Diagnostics Systems Laboratories Inc...  Radioimmunoassay Kit for the     Kit: 100 Tests...........     10/08/93
                                          Quantitative Measurement of                                           
                                          Testosterone, DSL 4000.                                               
Diagnostics Systems Laboratories Inc...  Radioimmunoassay Kit for the     Kit: 100 Tests...........     10/08/93
                                          Quantitative Measurement of                                           
                                          Testosterone, DSL 4100.                                               
Diagnostics Systems Laboratories Inc...  Testosterone Controls I and II,  Vial: 3.5ml..............     10/08/93
                                          DSL 4051 & 4052.                                                      
Diagnostics Systems Laboratories Inc...  Testosterone Standards A-F, DSL  Vial: 3.5ml..............     10/08/93
                                          4001-4006.                                                            
Diamedix Corporation...................  Barbital-Acetate Buffer, Powder  Package: 20 envelopes-         7/27/72
                                          709-317.                         10.65 g. per envelope.               
Diamedix Corporation...................  CEP Plate-Amebiasis Testing 40   Plate: 40mm x 80mm x            8/9/73
                                          Test No. 730-274.                2.5mm.                               
Diamedix Corporation...................  CEP VI No. 709-339.............  Plate: 40mm x 80mm x            8/9/73
                                                                           2.5mm.                               

[[Page 136]]

                                                                                                                
Diamedix Corporation...................  Counterelectrophoresis (CEP)     Plastic plates: 40mm x         6/16/75
                                          Plates for Trichinosis Testing.  80mm x 2.5mm.                        
Diamedix Corporation...................  EDTA (0.014M)-GVB Buffer, 753-   Bottle: 5ml..............       8/9/73
                                          034.                                                                  
Diamedix Corporation...................  EDTA (0.01M)-GVB Buffer, 753-    Bottle: 5ml..............       8/9/73
                                          031.                                                                  
Diamedix Corporation...................  GVB(3+) Buffer 753-037.........  Bottle: 50ml.............       8/9/73
Diamedix Corporation...................  Glucose-GVB 1 Buffer, 753-036..  Bottle: 50ml.............       8/9/73
DuPont Medical Products................  DuPont aca Urine Drugs of Abuse  Carton: 10 Vials; 6ml/         5/25/95
                                          Control (Negative/Positive).     vial.                                
Duo Research, Inc......................  Drug Testing Assessment Program  Kit: 25 bottles..........     12/26/86
                                          Quality Control Samples.                                              
Duo Research, Inc......................  Drug Testing Assessment Program- Bottle: 65ml.............      2/27/86
                                          Quality Control Sample.                                               
Duo Research, Inc......................  Drug Testing Assessment Program- Kit: 5-65ml bottles......      2/27/86
                                          Quality Control Sample Kit.                                           
DynaGen, Inc...........................  Benzoylecgonine and delta-8 THC- Plastic Bottle: 100ml....      7/27/93
                                          Carboxylic Acid Cat # 700-111.                                        
DynaGen, Inc...........................  D-Amphetamine and DL-            Plastic Bottle: 100ml....      7/27/93
                                          Methamphetamine Cat # 700-107.                                        
DynaGen, Inc...........................  D-Amphetamine, D-                Plastic Bottle: 100ml....      7/27/93
                                          Methamphetamine and delta-9                                           
                                          THC-Carboxylic Acid Cat # 700-                                        
                                          112.                                                                  
DynaGen, Inc...........................  D-Amphetamine, Pseudoephedrine,  Plastic Bottle: 100ml....      7/27/93
                                          DL-Methamphetamine and                                                
                                          Phenylpropanolamine Cat # 700-                                        
                                          116.                                                                  
DynaGen, Inc...........................  DL-Methamphetamine Cat # 700-    Plastic Bottle: 100ml....      7/27/93
                                          110.                                                                  
DynaGen, Inc...........................  Hydrocodone Cat # 700-106......  Plastic bottle: 100ml....      7/27/93
DynaGen, Inc...........................  Hydromorphone Cat # 700-108....  Plastic Bottle: 100ml....      7/27/93
DynaGen, Inc...........................  Methadone Cat # 700-118........  Plastic Bottle: 100ml....      7/27/93
DynaGen, Inc...........................  Methaqualone Cat # 700-119.....  Plastic Bottle: 100ml....      7/27/93
DynaGen, Inc...........................  Morphine, Codeine and 6-         Plastic Bottle: 100ml....      7/27/93
                                          Monoacetylmorphine Cat # 700-                                         
                                          114.                                                                  
DynaGen, Inc...........................  Oxazepam Cat # 700-120.........  Plastic Bottle: 100ml....      7/27/93
DynaGen, Inc...........................  PeoCheck Blind Performance       Kit: 25 Bottles; 100ml         7/27/93
                                          Specimens Cat # 500-100.         plastic.                             
DynaGen, Inc...........................  Phencyclidine and Hydrocodone    Plastic Bottle: 100ml....      7/27/93
                                          Cat # 700-115.                                                        
DynaGen, Inc...........................  ProCheck Blind Performance       Kit: 5 bottles; 100ml          7/27/93
                                          Specimens Cat # 500-200.         plastic.                             
DynaGen, Inc...........................  Propoxyphene Cat # 700-121.....  Plastic Bottle: 100ml....      7/27/93
DynaGen, Inc...........................  Secobarbital Cat # 700-117.....  Plastic Bottle: 100ml....      7/27/93
DynaGen, Inc...........................  delta 9 THC-Carboxylic Acid and  Plastic Bottle: 100ml....      7/27/93
                                          Phentermine Cat # 700-113.                                            
E.I. duPont de Nemours & Co., Inc......  (1) PREP Sample Preparation and  Kit containing following:      9/25/78
                                          Analysis Kit.                                                         
E.I. duPont de Nemours & Co., Inc......  (2) PREP Buffer/Internal         Box containing following:      9/25/78
                                          Standard and Liquid                                                   
                                          Chromatography Verifier.                                              
E.I. duPont de Nemours & Co., Inc......  (2a) PREP Liquid Chromatography  Vial: 10ml (1 vial/box)..      9/25/78
                                          Verifier.                                                             
E.I. duPont de Nemours & Co., Inc......  (2b) PREP Buffer/Internal        Vial: 100ml (3 vials/box)      9/25/78
                                          Standard.                                                             
E.I. duPont de Nemours & Co., Inc......  (3) PREP Calibrators...........  Box containing following:      9/25/78
E.I. duPont de Nemours & Co., Inc......  (3a) PREP Calibrator-Level 1...  Vial: 10ml (1 vial/box)..      9/25/78
E.I. duPont de Nemours & Co., Inc......  (3b) PREP Calibrator-Level 2...  Vial: 10ml (1 vial/box)..      9/25/78
E.I. duPont de Nemours & Co., Inc......  (3c) PREP Calibrator-Level 3...  Vial: 10ml ( 1 vial/box).      9/25/78
E.I. duPont de Nemours & Co., Inc......  (3d) PREP Calibrator-Level 4...  Vial: 10ml (1 vial/box)..      9/25/78
E.I. duPont de Nemours & Co., Inc......  (4) PREP Controls..............  Box containing following:      9/25/78
E.I. duPont de Nemours & Co., Inc......  (4a) PREP Control-Low Level....  Vial: 10ml (2 vials/box).      9/25/78
E.I. duPont de Nemours & Co., Inc......  (4b) PREP Control-High Level...  Vial: 10ml (2 vials/box).      9/25/78
E.I. duPont de Nemours & Co., Inc......  Cocaine [N-Methyl-3H]..........  Vial: 1 or 5ml...........      10/4/95
E.I. duPont de Nemours & Co., Inc......  DM/TU Saturating Reagent.......  Plastic Bottle: 1L, 10L,       2/22/89
                                                                           20L.                                 
E.I. duPont de Nemours & Co., Inc......  DuPont Drug Calibrator-A         Vial: 6ml, Box: 10 vials.      9/28/90
                                          (levels 1-5).                                                         
E.I. duPont de Nemours & Co., Inc......  DuPont Drug Calibrators- Levels  Vial: 6ml (1 vial and 2         4/4/86
                                          1 through 5.                     vials/box).                          

[[Page 137]]

                                                                                                                
E.I. duPont de Nemours & Co., Inc......  DuPont Phenobarbital Assay.....  Vial: 6 ml...............     10/13/86
E.I. duPont de Nemours & Co., Inc......  DuPont U Amp Enzyme Pack         Bottle: 1 liter..........     10/19/87
                                          Reagent.                                                              
E.I. duPont de Nemours & Co., Inc......  DuPont U Barb Enzyme Pack        Bottle: 1 liter..........     10/19/87
                                          Reagent.                                                              
E.I. duPont de Nemours & Co., Inc......  DuPont U Benz Enzyme Pack        Bottle: 1 liter..........     10/19/87
                                          Reagent.                                                              
E.I. duPont de Nemours & Co., Inc......  DuPont U COC Enzyme Pack         Bottle: 1 liter..........     10/19/87
                                          Reagent.                                                              
E.I. duPont de Nemours & Co., Inc......  DuPont U OPI Enzyme Pack         Bottle: 1 liter..........      8/28/87
                                          Reagent.                                                              
E.I. duPont de Nemours & Co., Inc......  DuPont U THC Enzyme Pack         Bottle: 1 Liter..........       1/4/88
                                          Reagent.                                                              
E.I. duPont de Nemours & Co., Inc......  DuPont Urine Drugs-of-Abuse      Box: 6 Vials, 6ml Vial...      7/27/87
                                          Calibrator (Levels 0, 1, 2).                                          
E.I. duPont de Nemours & Co., Inc......  DuPont Urine Drugs-of-Abuse      Vial: 6ml................       8/3/87
                                          Control.                                                              
E.I. duPont de Nemours & Co., Inc......  DuPont aca Barbiturate Screen    Plastic Packs: 25 tests..     12/23/84
                                          Analytical Test Pack.                                                 
E.I. duPont de Nemours & Co., Inc......  DuPont aca Barbiturate Screen/   6 Vials: 3ml.............      2/23/84
                                          Benzodiazepine Screen                                                 
                                          Calibrator.                                                           
E.I. duPont de Nemours & Co., Inc......  DuPont aca Benzodiazepine        Plastic Packs: 25 tests..      2/23/84
                                          Screen Analytical Test Pack.                                          
E.I. duPont de Nemours & Co., Inc......  Phenobarbital Calibrator-Level   Vial: 6ml (1 vial/box)...       4/2/86
                                          1.                                                                    
E.I. duPont de Nemours & Co., Inc......  Phenobarbital Calibrator-Level   Vial: 6ml (1 vial/box)...       4/2/86
                                          2.                                                                    
E.I. duPont de Nemours & Co., Inc......  Phenobarbital Calibrator-Level   Vial: 6ml (1 vial/box)...       4/2/86
                                          3.                                                                    
E.I. duPont de Nemours & Co., Inc......  Phenobarbital Calibrator-Level   Vial: 6ml (1 vial/box)...       4/2/86
                                          4.                                                                    
E.I. duPont de Nemours & Co., Inc......  Phenobarbital Calibrator-Level   Vial: 6ml (1 vial/box)...       4/2/86
                                          5.                                                                    
E.I. duPont de Nemours & Co., Inc......  Theophylline Calibrator Levels   Vial: 6ml. Box contains 2      9/21/88
                                          1, 2 and 3.                      vials each level.                    
E.I. duPont de Nemours & Co., Inc......  Thyroid Rotor..................  Foil Pouch: 1 Rotor Shelf     10/25/88
                                                                           Carton: 10 Rotors Box: 5             
                                                                           Shelf Cartons (50                    
                                                                           Rotors).                             
E.I. duPont de Nemours & Co., Inc......  Thyronine (TU) Uptake Flex.....  32 Test Cartridge,             3/29/89
                                                                           Carton: 7 cartridges.                
E.I. duPont de Nemours & Co., Inc......  Thyronine (TU) Uptake Flex(tm)   Plastic container: 2.3ml       4/28/86
                                          Reagent Cartridge.               (20 tests).                          
E.I. duPont de Nemours & Co., Inc......  Urine Amphetamine (U Amp) Test   Carton: 50 tests.........      8/27/87
                                          Pack.                                                                 
E.I. duPont de Nemours & Co., Inc......  Urine Barbiturate (U Barb) Test  Carton: 50 tests.........      8/27/87
                                          Pack.                                                                 
E.I. duPont de Nemours & Co., Inc......  Urine Benzodiazepine (U Benz)    Carton: 50 tests.........      8/27/87
                                          Test Pack.                                                            
E.I. duPont de Nemours & Co., Inc......  Urine Cannabinoid (U THC) Test   Carton: 50 tests.........      11/9/87
                                          Pack.                                                                 
E.I. duPont de Nemours & Co., Inc......  Urine Cocaine (U COC) Test Pack  Carton: 50 tests.........      8/27/87
E.I. duPont de Nemours & Co., Inc......  Urine Opiate (U OPI) Test Pack.  Carton: 50 tests.........       7/8/87
E.I. duPont de Nemours & Co., Inc......  aca PHNO Analytical Test Pack..  Carton: 40 tests packs...      8/25/77
E.I. duPont de Nemours & Co., Inc......  aca Thryonine Uptake Analytical  Plastic Pack: 1 test.....      8/25/83
                                          Test Pack.                                                            
E.I. duPont de Nemours & Co., Inc......  aca Urine Methadone Calibrator   Vial: 10ml...............      9/17/93
                                          (Level 1 & 2).                                                        
E.I. duPont de Nemours & Co., Inc......  aca Urine Methadone Control      Vial: 6ml................      9/17/93
                                          (Negative/Positive).                                                  
E.I. duPont de Nemours & Co., Inc.,      5-Cyclohexenyl-3,5,-Dimethyl     Combi-Vial: 250                 1/4/77
 Medical Products.                        barbituric Acid (3H(G)),         microcuries, 1                       
                                          Catalog No. NET-426.             millicurie, and 5                    
                                                                           millicuries.                         
E.I. duPont de Nemours & Co., Inc.,      Acetaldehyde (1, 2-14C) as       Pyrex Glass Breakseal           1/4/77
 Medical Products.                        Paraldehyde, Catalog No. NEC-    Tube: 250 microcuries, 1             
                                          158.                             millicurie.                          

[[Page 138]]

                                                                                                                
E.I. duPont de Nemours & Co., Inc.,      Cocaine, Levo-[Benzoyl] [3.4-    Combi-Vial: 100                 1/4/77
 Medical Products.                        3H(N)] Catalog No. NET-510.      microcuries, 250                     
                                                                           microcuries.                         
E.I. duPont de Nemours & Co., Inc.,      Diazepam [Methyl-3H] Catalog     Combi-Vial: 0.250               9/6/79
 Medical Products.                        No. NET-564.                     millicuries, 1.0                     
                                                                           millicurie.                          
E.I. duPont de Nemours & Co., Inc.,      Dihydromorphine [7, 8-3H(N)]...  Combi-Vial: 250                 1/4/77
 Medical Products.                                                         microcuries, 1                       
                                                                           millicurie.                          
E.I. duPont de Nemours & Co., Inc.,      Dihydromorphine [N-Methyl-3H]    Combi-Vial: 0.250              2/29/80
 Medical Products.                        NET-658.                         millicuries, 1.0                     
                                                                           millicurie.                          
E.I. duPont de Nemours & Co., Inc.,      Dihydrotestosterone, [1, 2, 4,   NENSURE Vial: 0.8ml,           11/1/91
 Medical Products.                        5, 6, 7, 16, 17-3H(N)].          6.2ml.                               
E.I. duPont de Nemours & Co., Inc.,      Dihydrotestosterone, [1, 2, 4,   NENSURE Vial: 0.8ml,           11/1/91
 Medical Products.                        5, 6, 7-3H(N)]-.                 6.2ml.                               
E.I. duPont de Nemours & Co., Inc.,      Dihydrotestosterone, [1, 2-      NENSURE Vial: 0.8ml,           11/1/91
 Medical Products.                        3H(N)].                          6.2ml.                               
E.I. duPont de Nemours & Co., Inc.,      Dihydrotestosterone, [4-14C]-..  NENSURE Vial: 0.8ml,           11/1/91
 Medical Products.                                                         6.2ml.                               
E.I. duPont de Nemours & Co., Inc.,      Drug Discovery Kit, No. NED-     Kit: 100 tests, 500 tests       8/8/89
 Medical Products.                        002, NED-002A.                                                        
E.I. duPont de Nemours & Co., Inc.,      Drugs of Abuse Controls........  Bottle: 5ml..............      1/11/95
 Medical Products.                                                                                              
E.I. duPont de Nemours & Co., Inc.,      Flunitrazepam (Methyl-3H)......  Combi-Vial: 5                   8/8/89
 Medical Products.                                                         microcuries, 14                      
                                                                           microcuries.                         
E.I. duPont de Nemours & Co., Inc.,      Flunitrazepam 2.5 Micro M......  Combi-Vial: 2.0 ml.......       8/8/89
 Medical Products.                                                                                              
E.I. duPont de Nemours & Co., Inc.,      Flunitrazepam [Methyl-3H] NET    Combi-Vial: 0.250              4/29/87
 Medical Products.                        567.                             millicuries, 1.0                     
                                                                           millicurie.                          
E.I. duPont de Nemours & Co., Inc.,      LSD [N-Methyl-3H] NET-638......  Combi-Vial: 0.250              11/6/79
 Medical Products.                                                         millicuries, 1.0                     
                                                                           millicurie.                          
E.I. duPont de Nemours & Co., Inc.,      Mazindol (4'-3H) Catalog No.NET- Combi-Vial: 0.250              5/17/84
 Medical Products.                        816.                             millicuries, 1.0                     
                                                                           millicurie.                          
E.I. duPont de Nemours & Co., Inc.,      Methylenedioxymethamphetamine,   Combi-Vial: 0.0250             8/25/75
 Medical Products.                        (+)3,4-[N-methyl-3H] NET 957.    millicuries, 0.25                    
                                                                           millicuries, 1.0                     
                                                                           millicuries.                         
E.I. duPont de Nemours & Co., Inc.,      Methylphenidate, +/-             Combi-Vial: 0.250              6/11/84
 Medical Products.                        threo[methyl-3H]NET-857.         millicuries, 1.0                     
                                                                           millicurie.                          
E.I. duPont de Nemours & Co., Inc.,      Mibolerone.....................  Glass Vial: 5ml..........      11/1/91
 Medical Products.                                                                                              
E.I. duPont de Nemours & Co., Inc.,      Mibolerone, [17Alpha-methyl-3H]- NENSURE Vial: 0.8ml,           11/1/91
 Medical Products.                        .                                6.2ml.                               
E.I. duPont de Nemours & Co., Inc.,      Morphine [N-methyl-3H] NET-653.  Combi-Vial: 0.250              2/29/80
 Medical Products.                                                         millicuries, 1.0                     
                                                                           millicurie.                          
E.I. duPont de Nemours & Co., Inc.,      N-[1-(2-Thienyl) Cyclohexyl]-3,  Combi-Vial: 0.250              6/11/84
 Medical Products.                        4-Piperidine (Piperidyl-3,4-     millicuries, 1.0                     
                                          3H)NET-886.                      millicurie.                          
E.I. duPont de Nemours & Co., Inc.,      Phencyclidine [Piperidyl-3,4-    Combi-Vial: 0.250               9/6/79
 Medical Products.                        3H(N)], Catalog No.NET-630.      millicurie, 1.0                      
                                                                           millicurie.                          
E.I. duPont de Nemours & Co., Inc.,      Phenobarbital (PHNO) Flex        Cartridge: Plastic.......      5/26/94
 Medical Products.                        Reagent Cartridge.                                                    
E.I. duPont de Nemours & Co., Inc.,      Testosterone, [1,2,6,7,16,17-    NENSURE Vial: 0.8ml,           11/1/91
 Medical Products.                        3H(N)].                          6.2ml.                               

[[Page 139]]

                                                                                                                
E.I. duPont de Nemours & Co., Inc.,      Testosterone, [1,2,6,7-3H(N)]-.  NENSURE Vial: 0.8ml,           11/1/91
 Medical Products.                                                         6.2ml.                               
E.I. duPont de Nemours & Co., Inc.,      Testosterone, [1Alpha, 2Alpha, - NENSURE Vial: 0.8ml,           11/1/91
 Medical Products.                        3H(N)]-.                         6.2ml.                               
E.I. duPont de Nemours & Co., Inc.,      Testosterone, [1Beta, 2Beta,-    NENSURE Vial: 0.8ml,           11/1/91
 Medical Products.                        3H(N)]-.                         6.2ml.                               
E.I. duPont de Nemours & Co., Inc.,      Testosterone, [4-14C]-.........  NENSURE Vial: 0.8ml,           11/1/91
 Medical Products.                                                         6.2ml; Glass Vial: 10ml.             
E.I. duPont de Nemours & Co., Inc.,      Testosterone, [7-3H(N)]-.......  NENSURE Vial: 0.8ml,           11/1/91
 Medical Products.                                                         6.2ml.                               
E.I. duPont de Nemours & Co., Inc.,      Urine Cannabinoids Screen        Cartridge: Plastic.......      4/19/94
 Medical Products.                        (UTHC) Flex Reagent Cartridge.                                        
E.I. duPont de Nemours & Co., Inc.,      Urine Cocaine Metabolites        Cartridge: Plastic.......      4/19/94
 Medical Products.                        Screen (UCOC) Flex Reagent                                            
                                          Cartridge.                                                            
E.I. duPont de Nemours & Co., Inc.,      Urine Opiates Screen (UOPI)      Cartridge: Plastic.......      4/19/94
 Medical Products.                        Flex Reagent Cartridge.                                               
E.I. duPont de Nemours & Co., Inc.,      d-Amphetamine Sulfate (3H(G)),   Combi-Vial: 250                 1/4/77
 Medical Products.                        Catalog No. NET-140.             microcuries, 1                       
                                                                           millicurie, and 5                    
                                                                           millicuries.                         
EDITEK Inc.............................  EZ-SCREEN Amphetamines Bulk      Bottle: 250ml............      8/17/94
                                          Conjugate.                                                            
EDITEK Inc.............................  EZ-SCREEN Amphetamines Bulk      Bottle: 4L...............      8/17/94
                                          Positive Control.                                                     
EDITEK Inc.............................  EZ-SCREEN Amphetamines Positive  Flask: 100ml.............      8/17/94
                                          Control Stock.                                                        
EDITEK Inc.............................  EZ-SCREEN Amphetamines QC        Tube: 50ml...............      8/17/94
                                          Standard.                                                             
EDITEK Inc.............................  EZ-SCREEN Barbiturates Bulk      Tube: 50ml...............      8/17/94
                                          Conjugate.                                                            
EDITEK Inc.............................  EZ-SCREEN Barbiturates Bulk      Bottle: 8L...............      8/17/94
                                          Positive Control.                                                     
EDITEK Inc.............................  EZ-SCREEN Barbiturates Positive  Flask: 100ml.............      8/17/94
                                          Control Stock.                                                        
EDITEK Inc.............................  EZ-SCREEN Barbiturates QC        Tube: 50ml...............      8/17/94
                                          Standard.                                                             
EDITEK Inc.............................  EZ-SCREEN CANNABINOID/COCAINE    Tube: 2.2ml..............      8/17/94
                                          0.5ml Positive Control.                                               

[[Page 140]]

                                                                                                                
EDITEK Inc.............................  EZ-SCREEN CANNABINOID/COCAINE    Bottle: 15ml.............      8/17/94
                                          5.0ml Positive Control.                                               
EDITEK Inc.............................  EZ-SCREEN CANNABINOID/COCAINE/   Bottle: 20L..............      8/17/94
                                          OPIATES Bulk Positive Control.                                        
EDITEK Inc.............................  EZ-SCREEN COCAINE Bulk           Bottle: 250ml............      8/17/94
                                          Conjugate.                                                            
EDITEK Inc.............................  EZ-SCREEN COCAINE Bulk Positive  Bottle: 8L...............      8/17/94
                                          Control.                                                              
EDITEK Inc.............................  EZ-SCREEN COCAINE Positive       Flask: 100ml.............      8/17/94
                                          Control.                                                              
EDITEK Inc.............................  EZ-SCREEN COCAINE QC Standard..  Tube: 50ml...............      8/17/94
EDITEK Inc.............................  EZ-SCREEN OPIATES Bulk           Tube: 50ml...............      8/17/94
                                          Conjugate.                                                            
EDITEK Inc.............................  EZ-SCREEN OPIATES Bulk Positive  Bottle: 4L...............      8/17/94
                                          Control.                                                              
EDITEK Inc.............................  EZ-SCREEN OPIATES Positive       Flask: 100ml.............      8/17/94
                                          Control Stock.                                                        
EDITEK Inc.............................  EZ-SCREEN OPIATES QC Standard..  Tube: 50ml...............      8/17/94
EDITEK Inc.............................  EZ-SCREEN PCP Bulk Conjugate...  Tube: 50ml...............      8/17/94
EDITEK Inc.............................  EZ-SCREEN PCP Bulk Positive      Bottle: 2L...............      8/17/94
                                          Control.                                                              
EDITEK Inc.............................  EZ-SCREEN PCP Positive Control   Flask: 100ml.............      8/17/94
                                          Stock.                                                                
EDITEK Inc.............................  EZ-SCREEN PCP QC Standard......  Tube: 50ml...............      8/17/94
EDITEK Inc.............................  EZ-SCREEN THC Bulk Conjugate...  Tube: 50ml...............      8/17/94
EDITEK Inc.............................  EZ-SCREEN THC Bulk Positive      Bottle: 8L...............      8/17/94
                                          Control.                                                              
EDITEK Inc.............................  EZ-SCREEN THC Positive Control   Flask: 10ml..............      8/17/94
                                          Stock.                                                                
EDITEK Inc.............................  EZ-SCREEN THC QC Standard......  Tube: 50ml...............      8/17/94
EDITEK Inc.............................  EZ-SCREEN: Amphetamines 0.5ml    Tube: 2.2ml..............      8/17/94
                                          Positive Control.                                                     
EDITEK Inc.............................  EZ-SCREEN: Amphetamines 20-Test  Kit: 20 Tests............      8/17/94
                                          Bulk Kit.                                                             
EDITEK Inc.............................  EZ-SCREEN: Amphetamines 20-Test  Kit: 20 Tests............      8/17/94
                                          Pack.                                                                 
EDITEK Inc.............................  EZ-SCREEN: Amphetamines 5.0ml    Bottle: 15ml.............      8/17/94
                                          Positive Control.                                                     
EDITEK Inc.............................  EZ-SCREEN: Amphetamines Enzyme   Ampule: 0.8ml............      8/17/94
                                          Conjugate.                                                            
EDITEK Inc.............................  EZ-SCREEN: Amphetamines Test     Kit: 1 Test..............      8/17/94
                                          Kit.                                                                  
EDITEK Inc.............................  EZ-SCREEN: Barbiturates 0.5ml    Tube: 2.2ml..............      8/17/94
                                          Positive Control.                                                     
EDITEK Inc.............................  EZ-SCREEN: Barbiturates 20-Test  Kit: 20 Tests............      8/17/94
                                          Bulk Kit.                                                             
EDITEK Inc.............................  EZ-SCREEN: Barbiturates 20-Test  Kit: 20 Tests............      8/17/94
                                          Pack.                                                                 
EDITEK Inc.............................  EZ-SCREEN: Barbiturates 5.0ml    Bottle: 15ml.............      8/17/94
                                          Positive Control.                                                     
EDITEK Inc.............................  EZ-SCREEN: Barbiturates Enzyme   Ampule: 0.8ml............      8/17/94
                                          Conjugate.                                                            
EDITEK Inc.............................  EZ-SCREEN: Barbiturates Test     Kit: 1 Test..............      8/17/94
                                          Kit.                                                                  
EDITEK Inc.............................  EZ-SCREEN: CANNABINOID 0.5 ml    Tube: 2.2ml..............      8/17/94
                                          Positive Control.                                                     
EDITEK Inc.............................  EZ-SCREEN: CANNABINOID 20-Test   Kit: 20 Tests............      8/17/94
                                          Bulk Kit.                                                             
EDITEK Inc.............................  EZ-SCREEN: CANNABINOID 20-Test   Kit: 20 Tests............      8/17/94
                                          Pack.                                                                 
EDITEK Inc.............................  EZ-SCREEN: CANNABINOID 5.0ml     Bottle: 15ml.............      8/17/94
                                          Positive Control.                                                     
EDITEK Inc.............................  EZ-SCREEN: CANNABINOID Enzyme    Ampule: 0.8ml............      8/17/94
                                          Conjugate.                                                            
EDITEK Inc.............................  EZ-SCREEN: CANNABINOID Test Kit  Kit: 1 Test..............      8/17/94
EDITEK Inc.............................  EZ-SCREEN: CANNABINOID/COCAINE   Kit: 20 Tests............      8/17/94
                                          20-Test Bulk Kit.                                                     
EDITEK Inc.............................  EZ-SCREEN: CANNABINOID/COCAINE   Kit: 20 Tests............      8/17/94
                                          20-Test Pack.                                                         
EDITEK Inc.............................  EZ-SCREEN: CANNABINOID/COCAINE   Ampule: 0.8ml............      8/17/94
                                          Enzyme Conjugate.                                                     
EDITEK Inc.............................  EZ-SCREEN: CANNABINOID/COCAINE   Kit: 1 Test..............      8/17/94
                                          Test Kit.                                                             
EDITEK Inc.............................  EZ-SCREEN: CANNABINOID/COCAINE/  Tube: 2.2ml..............      8/17/94
                                          OPIATES 0.5ml Positive Control.                                       
EDITEK Inc.............................  EZ-SCREEN: CANNABINOID/COCAINE/  Kit: 10 Tests............      8/17/94
                                          OPIATES 10-Test Bulk Kit.                                             
EDITEK Inc.............................  EZ-SCREEN: CANNABINOID/COCAINE/  Kit: 20 Tests............      8/17/94
                                          OPIATES 20-Test Kit Pack.                                             
EDITEK Inc.............................  EZ-SCREEN: CANNABINOID/COCAINE/  Bottle: 15ml.............      8/17/94
                                          OPIATES 5.0ml Positive Control.                                       
EDITEK Inc.............................  EZ-SCREEN: CANNABINOID/COCAINE/  Ampule: 0.8ml............      8/17/94
                                          OPIATES Enzyme Conjugate.                                             
EDITEK Inc.............................  EZ-SCREEN: CANNABINOID/COCAINE/  Kit: 1 Test..............      8/17/94
                                          OPIATES Test Kit.                                                     
EDITEK Inc.............................  EZ-SCREEN: COCAINE 0.5ml         Tube: 2.2ml..............      8/17/94
                                          Positive Control.                                                     
EDITEK Inc.............................  EZ-SCREEN: COCAINE 20 Test Bulk  Kit: 20 Tests............      8/17/94
                                          Kit.                                                                  
EDITEK Inc.............................  EZ-SCREEN: COCAINE 20-Test Pack  Kit: 20 Tests............      8/17/94
EDITEK Inc.............................  EZ-SCREEN: COCAINE 5.0ml         Bottle: 15ml.............      8/17/94
                                          Positive Control.                                                     
EDITEK Inc.............................  EZ-SCREEN: COCAINE Enzyme        Ampule: 0.8ml............      8/17/94
                                          Conjugate.                                                            
EDITEK Inc.............................  EZ-SCREEN: COCAINE Test Kit....  Kit: 1 Test..............      8/17/94
EDITEK Inc.............................  EZ-SCREEN: OPIATES 0.5ml         Tube: 2.2ml..............      8/17/94
                                          Positive Control.                                                     
EDITEK Inc.............................  EZ-SCREEN: OPIATES 20 Test Pack  Kit: 20 Tests............      8/17/94
EDITEK Inc.............................  EZ-SCREEN: OPIATES 20-Test Bulk  Kit: 20 Tests............      8/17/94
                                          Kit.                                                                  
EDITEK Inc.............................  EZ-SCREEN: OPIATES 5.0ml         Bottle: 15ml.............      8/17/94
                                          Positive Control.                                                     
EDITEK Inc.............................  EZ-SCREEN: OPIATES Enzyme        Ampule: 0.8ml............      8/17/94
                                          Conjugate.                                                            
EDITEK Inc.............................  EZ-SCREEN: OPIATES Test Kit....  Kit: 1 Test..............      8/17/94
EDITEK Inc.............................  EZ-SCREEN: PCP 0.5ml Positive    Ampule: 0.8ml............      8/17/94
                                          Control.                                                              
EDITEK Inc.............................  EZ-SCREEN: PCP 20-Test Bulk Kit  Kit: 20 Tests............      8/17/94
EDITEK Inc.............................  EZ-SCREEN: PCP 20-Test Kit.....  Kit: 20 Tests............      8/17/94
EDITEK Inc.............................  EZ-SCREEN: PCP 5.0ml Positive    Bottle: 15ml.............      8/17/94
                                          Control.                                                              
EDITEK Inc.............................  EZ-SCREEN: PCP Enzyme Conjugate  Ampule: 0.8ml............      8/17/94
EDITEK Inc.............................  EZ-SCREEN: PCP Test Kit........  Kit: 1 Test..............      8/17/94
EDITEK Inc.............................  VERDICT COCAINE One-Step Drug    Pouch: 1 each; Box: 50          8/2/94
                                          Test; Product # 600230.          Pouches.                             
EDITEK Inc.............................  VERDICT Cocaine Bulk Conjugate.  Vial: 2ml................      8/14/94
EDITEK Inc.............................  VERDICT Cocaine Bulk Conjugate.  Vial: 2ml................      8/14/94
EDITEK Inc.............................  VERDICT Cocaine QC Standard....  Tube: 50ml...............      8/14/94
EDITEK Inc.............................  VERDICT OPIATES One-Step Drug    Pouch: 1 each; Box: 50          8/2/94
                                          Test; Product # 600233.          Pouches.                             
EDITEK Inc.............................  VERDICT Opiates Bulk Conjugate.  Vial: 2ml................      8/14/94
EDITEK Inc.............................  VERDICT Opiates Bulk Conjugate.  Vial: 5ml................      8/14/94
EDITEK Inc.............................  VERDICT Opiates QC Standard....  Tube: 15ml...............      8/14/94
EDITEK Inc.............................  VERDICT PCP 50-Test Kit, Cat #   Kit: 50 Tests............      1/11/96
                                          600226.                                                               
EDITEK Inc.............................  VERDICT PCP Bulk Conjugate       Vial: 2ml................      1/11/96
                                          0.5ml, 2.0ml.                                                         
EDITEK Inc.............................  VERDICT PCP QC Standard........  Tube: 50ml...............      1/11/96
EDITEK Inc.............................  VERDICT THC Bulk Conjugate.....  Vial: 2ml................      8/14/94
EDITEK Inc.............................  VERDICT THC Bulk Conjugate.....  Vial: 5ml................      8/14/94
EDITEK Inc.............................  VERDICT THC One-Step Drug Test;  Pouch: 1 each; Box: 50          8/2/94
                                          Product # 600212.                Pouches.                             
EDITEK Inc.............................  VERDICT THC QC Standard........  Tube: 50ml...............      8/14/94
EDITEK Inc.............................  VERDICT THC/COCAINE One-Step     Pouch: 2 Kits............      8/14/94
                                          Drug Test.                                                            
EM Diagnostic Systems, Inc.............  EMDS Antiepileptic Drug          Box: 3 Vials, 5 ml each..      6/11/86
                                          Calibrator Item No. 67630/95.                                         
EM Diagnostic Systems, Inc.............  EMDS Test Packs, Phenobarbital   Carton: 48 Test Packs....       9/9/86
                                          (PHENO) Item No. 67677/95.                                            
EM Diagnostic Systems, Inc.............  Easytest Phenobarbital Assay     Cuvette: 1.8ml (40             6/11/86
                                          Item No. 67534/93.               cuvettes /carton).                   
Eastman Kodak Company..................  KODATROL Control I Control and   1 Set: 2 amber glass           7/21/88
                                          Diluent Set.                     vials ea. 6 ml 1 Box: 12             
                                                                           sets.                                
Eastman Kodak Company..................  KODATROL Control II Control and  1 Set: 2 amber glass           7/21/88
                                          Diluent Set.                     vials ea. 6 ml 1 Box: 12             
                                                                           sets.                                
Eastman Kodak Company..................  Kodak EKTACHEM Specialty         Vial: 3ml................      9/13/85
                                          Calibrator.                                                           
Eastman Kodak Company..................  Kodak EKTACHEM Specialty         Vial: 3ml................      9/13/85
                                          Control I.                                                            
Eastman Kodak Company..................  Kodak Ektachem Specialty         Glass Vial: 6 ml.........     11/10/87
                                          Control II.                                                           

[[Page 141]]

                                                                                                                
Electro-Nucleonics Laboratories,         VIRGO IPA Immuno-Precipitation   Kit......................     11/30/82
 Incorporated.                            Assay for Phenobarbital.                                              
Eli Lilly and Company..................  Propoxyphene Industrial Hygiene  Cassette: Plastic........      7/13/94
                                          Air Monitoring Sample Cassette.                                       
Elsohly Laboratories, Inc..............  (-)-11 Nor-delta-9-THC-COOH      Vial: 1ml................      3/26/95
                                          100ug/ml.                                                             
Elsohly Laboratories, Inc..............  11-Hydroxy-delta-9-THC, 100ug/   Vial: 1ml................      3/26/95
                                          ml.                                                                   
Elsohly Laboratories, Inc..............  8-Beta, 11-dihydroxy-delta-9-    Vial: 1ml................      3/26/95
                                          THC, 100ug/ml.                                                        
Elsohly Laboratories, Inc..............  8-Beta-hydroxy-delta-9-THC,      Vial: 1ml................      3/26/95
                                          100ug/ml.                                                             
Elsohly Laboratories, Inc..............  Difluorobenzoylecgonine, 100ug/  Vial: 1ml................      3/26/95
                                          ml.                                                                   
Elsohly Laboratories, Inc..............  Difluorococaine, 100ug/ml......  Vial: 1ml................      3/26/95
Elsohly Laboratories, Inc..............  Difluorophencyclidine, 100ug/ml  Vial: 1ml................      3/26/95
Elsohly Laboratories, Inc..............  Urine Controls.................  Bottles: 15ml-40L........      3/26/95
Elsohly Laboratories, Inc..............  d2-Dihydrocodeine, 100ug/ml....  Vial: 1ml................      3/26/95
Elsohly Laboratories, Inc..............  d2-Dihydromorphine, 100ug/ml...  Vial: 1ml................      3/26/95
Elsohly Laboratories, Inc..............  d3-Codeine, 100ug/ml...........  Vial: 1ml................      3/26/95
Elsohly Laboratories, Inc..............  d3-Hydrocodone, 100ug/ml.......  Vial: 1ml................      3/26/95
Elsohly Laboratories, Inc..............  d3-Hydromorphone, 100ug/ml.....  Vial: 1ml................      3/26/95
Elsohly Laboratories, Inc..............  d3-Morphine, 100ug/ml..........  Vial: 1ml................      3/26/95
Elsohly Laboratories, Inc..............  d3-Oxycodone, 100ug/ml.........  Vial: 1ml................      3/26/95
Elsohly Laboratories, Inc..............  d6-11-Nor-delta-8-THC-9-COOH,    Vial: 1ml................      3/26/95
                                          100ug/ml.                                                             
Elsohly Laboratories, Inc..............  d6-11-Nor-delta-9-THC-9-COOH,    Vial: 1ml................      3/26/95
                                          100ug/ml.                                                             
Elsohly Laboratories, Inc..............  d6-Amphetamine, 100ug/ml.......  Vial: 1ml................      3/26/95
Elsohly Laboratories, Inc..............  d6-Delta-8-THC, 100ug/ml.......  Vial: 1ml................      3/26/95
Elsohly Laboratories, Inc..............  d9-Delta-9-THC, 100ug/ml.......  Vial: 1ml................      3/26/95
Elsohly Laboratories, Inc..............  d9-Methamphetamine, 100ug/ml...  Vial: 1ml................      3/26/95
Endocrine Metabolic Center.............  0.1% Lysozyme-Barbital Buffer,   Glass Bottle: 2 liter....      5/28/87
                                          0.05M.                                                                
Endocrine Metabolic Center.............  1% Lysozyme-Barbital Buffer,     Glass Bottle: 2 liter....      5/28/87
                                          0.05M.                                                                
Endocrine Metabolic Center.............  Barbital Buffer, 0.05M.........  Plastic Bottle: 3000 ml..      5/28/87
Endocrine Metabolic Center.............  Barbital Buffer, 0.1M..........  Plastic Bottle: 3000 ml..      5/28/87
Endocrine Metabolic Center.............  Tracer Diluent.................  Glass Bottle: 1 or 2           5/28/87
                                                                           liter.                               
Environmental Diagnostics, Inc.........  EZ-Screen: Cannabinoid Enzyme    Ampule: 1 ml.............       2/3/87
                                          Conjugate.                                                            
Environmental Diagnostics, Inc.........  EZ-Screen: Cannabinoid Kit       Kit: 1 test..............       2/3/87
                                          Catalog No. 216-2BP.                                                  
Environmental Diagnostics, Inc.........  EZ-Screen: Cannabinoid Positive  Ampule: 1 ml.............       2/3/87
                                          Control.                                                              
Environmental Diagnostics, Inc.........  EZ-Screen: Cannabinoid/Cocaine-  Polyethylene Tube:            12/20/88
                                          Enzyme Conjugate.                containing ampule with 1             
                                                                           tablet, Kit: 1 test.                 
Environmental Diagnostics, Inc.........  EZ-Screen: Cannabinoid/Cocaine-  Polyethylene Tube: 2.2ml,     12/20/89
                                          Positive Control.                Kit: 1 test.                         
Fisher Diagnostics.....................  TheraChem Anticonvulsants/       Kit: 9 vials, vial: 5ml..       3/3/81
                                          Theophylline, Level I, II.                                            
Fisher Scientific......................  Electrophoretic Buffer No. 1 pH  Packet: 12.14 g..........     10/27/72
                                          8.60, Ionic Strength 0.05,                                            
                                          Catalog No. E-1.                                                      
Fisher Scientific......................  Electrophoretic Buffer No. 2,    Packet: 18.16 g..........     10/27/72
                                          pH 8.60, Ionic Strength 0.075,                                        
                                          Catalog No. E-2.                                                      
Fisher Scientific......................  IL-Test Phenobarbital..........  Kit: contains 2 plastic        3/15/88
                                                                           containers of reagent 2.             
Fisher Scientific......................  IL-Test Phenobarbital            Plastic Container: 16 ml.      3/15/88
                                          Conjugate, Reagent 2.                                                 
Fisher Scientific......................  Owren's Veronal Buffer, CS1094-  Vial: 10 ml..............      8/18/86
                                          34.                                                                   
Fisher Scientific......................  Owren's Veronal Buffer, CS1094-  Vial: 25 ml..............      8/18/86
                                          38.                                                                   
Fisher Scientific......................  SeraChem Abnormal Clinical       Vial: 5ml, 10ml..........      4/16/82
                                          Chemistry Control Serum                                               
                                          (Human) Unassayed No. 2906.                                           
Fisher Scientific......................  SeraChem Abnormal Clinical       Vial: 5ml................      4/16/82
                                          Chemistry Control Serum                                               
                                          (Human), Assayed No. 2905.                                            
Fisher Scientific......................  SeraChem Normal Clinical         Vial: 5ml................      4/16/82
                                          Chemistry Control Serum                                               
                                          (Human), Assayed No. 2907.                                            
Fisher Scientific......................  SeraChem Plus Clinical           Vial: 10ml, Box: 50            7/25/89
                                          Chemistry Control Sera           vials, Carton: 4 boxes.              
                                          Unassayed (Bovine) Level I.                                           
Fisher Scientific......................  SeraChem Plus Clinical           Vial: 10 ml, Box: 50           7/25/89
                                          Chemistry Control Sera           vials, Carton: 4 boxes.              
                                          Unassayed (Bovine) Level II.                                          
Fisher Scientific......................  SeraChem Normal Clinical         Vial: 5ml, 10ml..........      4/16/82
                                          Chemistry Control Serum                                               
                                          (Human), Unassayed No. 2908.                                          
Fisher Scientific......................  TDM Cal........................  Kit: 7 Vials.............     11/26/86
Fisher Scientific......................  TDM Cal (B-F)..................  Vials: 5 ml..............     11/26/86
Fisher Scientific......................  Thera Chem TDC Therapeutic Drug  Kit: 6 vials.............      1/12/84
                                          Controls, Low and High Levels,                                        
                                          2840-58.                                                              
Fisher Scientific......................  TheraChem-Plus TDC Therapeutic   Kit: 9 vials.............      3/19/86
                                          Drug Controls, Tri-Level, No.                                         
                                          2845-94.                                                              
Fisher Scientific......................  Therapeutic Drug Control, High   Vial: 5ml................      3/19/86
                                          Level III, No. 2848-31.                                               
Fisher Scientific......................  Therapeutic Drug Control, High   Vial: 5ml................      1/12/84
                                          Level, 2842-31.                                                       
Fisher Scientific......................  Therapeutic Drug Control, Low    Vial: 5ml................      3/19/86
                                          Level I, No. 2846-31.                                                 

[[Page 142]]

                                                                                                                
Fisher Scientific......................  Therapeutic Drug Control, Low    Vial: 5ml................      1/12/84
                                          Level, 2841-31.                                                       
Fisher Scientific......................  Therapeutic Drug Control, Mid-   Vial: 5ml................      3/19/86
                                          Range Level II, No. 2847-31.                                          
Fisher Scientific......................  Urine Chemistry Control (Human)  Vial: 25ml...............       4/6/78
                                          Level II, No. 2935-80.                                                
Fisher Scientific......................  Urine Toxicology Control No.     Vial: 25ml...............       4/6/78
                                          2950-61.                                                              
Flow Laboratories......................  DGV No. 28-010.................  Bottle: 125 ml...........      4/16/73
Flow Laboratories......................  Human ``O'' DGV (Dextrose        Glass Vial: 100 ml.......     10/14/76
                                          Gelatin Veronal Buffer) No. 28-                                       
                                          080.                                                                  
GIBCO Laboratories.....................  Complement Fixation Buffer       Bottle: 1 liter..........      1/28/74
                                          Solution, pH 7.3-7.4, NDC                                             
                                          0118115-0247-1.                                                       
GIBCO Laboratories.....................  Complement Fixation Buffer       Bottle: 500 ml...........       4/5/77
                                          Solution, pH 7.3-7.4, NDC                                             
                                          011815-0247-2.                                                        
GIBCO Laboratories.....................  Dextrose-Gelatin-Veronal Buffer  Bottle: 100 and 500 ml...       7/5/73
                                          Solution NDC No. 815-0566-1                                           
                                          and No. 815-0566-2.                                                   
GIBCO Laboratories.....................  Electrophoresis Buffer           Bottle: 1 liter..........      1/28/74
                                          Solution, pH 8.6, NDC 011815-                                         
                                          0245-1.                                                               
GIBCO Laboratories.....................  I.E.P. Buffer Solution pH 8.2    Bottle: 1 liter..........      1/28/74
                                          NDC 011815-0246-1.                                                    
Gelman Sciences, Inc...................  Drug Control Set No. 51911.....  Set: 3 vials of 50 ml           4/6/72
                                                                           each.                                
Gelman Sciences, Inc...................  Drug Standard Set, No. 51910...  Set: 3 vials of 2 ml each       4/6/72
Gelman Sciences, Inc...................  Hi-Phore Buffer................  Glass Vial: 15 g.........      2/11/82
Gelman Sciences, Inc...................  High Resolution Buffer-Tris      Vial: 10 dr..............     12/22/71
                                          Barbital Buffer No. 51104.                                            
Gumm Chem. Co..........................  Niflow Initial Additive........  Drums: 5 Gallons.........      9/30/85
Gumm Chem. Co..........................  Niflow Maintenace Additive.....  Drums: 5 Gallons.........      9/30/85
Hach Chemical Co.......................  pH 8.3 Buffer Powder Pillows.    Pillow: 1 g. each........     11/30/71
                                          No. 898-98.                                                           
Helena Laboratories....................  Cardio REP CK Isoenzymes Gel...  Plate: 4.6'' x 2.4''.....      9/24/93
Helena Laboratories....................  CK-LD Buffer Catalog No. 5808..  Packet: 18.332 g. , 10         3/26/86
                                                                           packets/box.                         
Helena Laboratories....................  Cardio REP CK Isoenzymes Kit,    Kit: 10 Plates...........      9/24/93
                                          Cat. # 3310.                                                          
Helena Laboratories....................  Cardio REP CK Isoforms Gel.....  Plate: 4.6'' x 2.4''.....      9/24/93
Helena Laboratories....................  Cardio REP CK Isoforms Kit,      Kit: 10 Plates...........      9/24/93
                                          Cat. # 3305.                                                          
Helena Laboratories....................  Electra B1 Buffer, Catalog No.   Packet: 13.1g. 10 packets/    12/28/73
                                          5016.                             box.                                
Helena Laboratories....................  Electra B2 Buffer, Catalog No.   Packet: 18.2 g. 10            12/28/73
                                          5017.                            packets/ box.                        
Helena Laboratories....................  Electra HR Buffer, Catalog No.   Packet: 18.1 g. 10            12/28/73
                                          5805.                            packets/ box.                        
Helena Laboratories....................  HDL Electrophoresis Buffer.....  Packet: 36 g.............     12/18/85
Helena Laboratories....................  Isoamylase Cathode Buffer......  Packet: 9.7 g............     12/18/85
Helena Laboratories....................  Isoamylase Kit Catalog No. 5925  Kit: 2 Packets Cathode         1/24/86
                                                                           Buffer.                              
Helena Laboratories....................  Owren's Veronal Buffer Cat. No.  Plastic Bottle: 125 ml...      9/15/88
                                          5375.                                                                 
Helena Laboratories....................  REP ALP-15 Gel.................  Plate: 5.8'' x 5.5''.....      8/26/93
Helena Laboratories....................  REP Alkaline Phosphatase Cat. #  Kit: 10 Plates...........      8/26/93
                                          3152.                                                                 
Helena Laboratories....................  REP CK Isoforms-15.............  Plate: 5.8'' x 5.5''.....       3/9/88
Helena Laboratories....................  REP CK Isoforms-15 Kit: Cat.     Kit: 10 plates...........       3/9/88
                                          No. 3081.                                                             
Helena Laboratories....................  REP CK Isoforms-4 Cat. # 3083..  Kit: 10 Plates...........      8/26/93
Helena Laboratories....................  REP CK Isoforms-4 Gel..........  PLate: 5.8'' x 1.25''....      8/26/93
Helena Laboratories....................  REP CK Isoforms-8 Cat. # 3082..  Kit: 10 Plates...........      8/26/93
Helena Laboratories....................  REP CK Isoforms-8 Gel..........  Plate: 5.8'' x 2.18''....      8/26/93
Helena Laboratories....................  REP CK-12......................  Plate: 5.8'' x 2.18''....       3/9/88
Helena Laboratories....................  REP CK-12 Isoenzyme Kit: Cat.    Kit: 10 plates...........       3/9/88
                                          No. 3071.                                                             
Helena Laboratories....................  REP CK-2 STAT Kit, Cat. No.      Kit: 10 plates (5.8'' x        3/30/89
                                          3074.                            0.6'').                              
Helena Laboratories....................  REP CK-30......................  Plate: 5.8'' x 5.5''.....       3/9/88
Helena Laboratories....................  REP CK-30 Isoenzyme Kit........  Kit: 10 plates...........       3/9/88
Helena Laboratories....................  REP CK-6.......................  Plate: 5.8'' x 1.25''....       3/9/88
Helena Laboratories....................  REP CK-6 Isoenzyme Kit: Cat.     Kit: 10 plates...........       3/9/88
                                          No. 3072.                                                             
Helena Laboratories....................  REP ImmunoFix Kit # 3150.......  Kit: 10 plates...........       3/9/93
Helena Laboratories....................  REP LD.........................  Plates: 5.8'' x 5.5'',          3/9/88
                                                                           5.8'' x 2.18'', 5.8'' x              
                                                                           1.25''.                              
Helena Laboratories....................  REP SPE Hi Res-15 Kit, Cat. No.  Kit: 10 plates (5.8'' x        3/30/89
                                          3176.                            5.5'').                              
Helena Laboratories....................  REP SPE-16 Template (Acid Blue)  Kit: 10 Plates...........      9/14/93
                                          Kit, Cat. # 3171.                                                     
Helena Laboratories....................  REP SPE-16 Template (Ponceau S)  Kit: 10 Plates...........      9/14/93
                                          Kit, Cat. # 3161.                                                     
Helena Laboratories....................  REP SPE-16 Template Gel........  Plate: 5.8'' 2.18''......      9/14/93
Helena Laboratories....................  REP SPE-30 Template (Acid Blue)  Kit: 10 Plates...........      9/14/93
                                          Kit, Cat. # 3170.                                                     
Helena Laboratories....................  REP SPE-30 Template (Ponceau S)  Kit: 10 Plates...........      9/14/93
                                          Kit, Cat. # 3160.                                                     
Helena Laboratories....................  REP SPE-30 Template Gel........  Plate: 5.8'' x 5.5''.....      9/14/93
Helena Laboratories....................  REP SPE-8 Template (Acid Blue)   Kit: 10 Plates...........      9/14/93
                                          Kit, Cat. # 3172.                                                     
Helena Laboratories....................  REP SPE-8 Template (Ponceau S)   Kit: 10 Plates...........      9/14/93
                                          Kit, Cat. # 3162.                                                     
Helena Laboratories....................  REP SPE-8 Template Gel.........  Plate: 5.8'' x 1.25''....      9/14/93
Helena Laboratories....................  REP Ultra-30 HDL, VLDL/LDL Gel.  Plate: 5.8'' x 5.5''.....      9/24/93
Helena Laboratories....................  REP Ultra-30 HDL, VLDL/LDL Kit,  Kit: 10 Plates...........      9/24/93
                                          Cat. # 3183.                                                          

[[Page 143]]

                                                                                                                
Helena Laboratories....................  REP Ultra-8 HDL, VLDL/LDL Gel..  Plate: 5.8'' x 1.25''....      9/24/93
Helena Laboratories....................  REP Ultra-8 HDL, VLDL/LDL Kit,   Kit: 10 Plates...........      9/24/93
                                          Cat. # 3185.                                                          
Helena Laboratories....................  REP-HDL-12 Isoenzyme Kit Cat.    Kit: 10 Plates (5.8'' x        9/15/88
                                          No. 3187.                        2.18'').                             
Helena Laboratories....................  REP-HDL-30 Isoenzyme Kit Cat.    Kit: 10 Plates (5.8'' x        9/15/88
                                          No. 3186.                        5.5'').                              
Helena Laboratories....................  REP-HDL-6 Isoenzyme Kit Cat.     Kit: 10 Plates (5.8'' x        9/15/88
                                          No. 3188.                        1.25'').                             
Helena Laboratories....................  REP-Lipo-12 Kit Cat. No. 3181..  Kit: 10 Plates (5.8'' x        9/15/88
                                                                           2.18'').                             
Helena Laboratories....................  REP-Lipo-30 Kit Cat. No. 3180..  Kit: 10 Plates (5.8'' x        9/15/88
                                                                           5.5'').                              
Helena Laboratories....................  REP-Lipo-6 Kit Cat. No. 3182...  Kit: 10 Plates (5.8'' x        9/15/88
                                                                           1.25'').                             
Helena Laboratories....................  REP-SP-12 Isoenzyme Kit Cat.     Kit: 10 Plates (5.8'' x        9/15/88
                                          No. 3171.                        2.18'').                             
Helena Laboratories....................  REP-SP-30 Isoenzyme Kit Cat.     Kit: 10 Plates (5.8'' x        9/15/88
                                          No. 3170.                        5.5'').                              
Helena Laboratories....................  REP-SP-6 Isoenzyme Kit Cat. No.  Kit: 10 Plates (5.8'' x        9/15/88
                                          3172.                            1.25'').                             
Helena Laboratories....................  Super Z-12XHDL Cholesterol       Kit: 3 Packages buffer 36      1/24/86
                                          Supply Kit Catalog No. 5470).    g.                                   
Helena Laboratories....................  TITAN GEL Alkaline Phosphatase   Kit: 10 Plates...........      8/26/93
                                          (HR) Cat. No. 3058.                                                   
Helena Laboratories....................  TITAN GEL Alkaline Phosphatase   Kit: 1 bag...............      6/19/89
                                          (HR) Kit, Cat. No. 3058.                                              
Helena Laboratories....................  TITAN GEL Alkaline Phosphatase   Plastic Bag: 13.1g.......      6/19/89
                                          Buffer.                                                               
Helena Laboratories....................  TITAN GEL Alkaline Phosphatase   Plate: 3.5'' x 2.9''.....      8/26/93
                                          Gel.                                                                  
Helena Laboratories....................  Titan Gel High Resolution        Packet: 25.9 g...........      4/12/83
                                          Protein Buffer.                                                       
Helena Laboratories....................  Titan Gel High Resolution        Kit: 10 Plates (90mm x          3/3/86
                                          Protein Kit Catalog No. 3040.    75mm), 2 Packages Buffer.            
Helena Laboratories....................  Titan Gel High Resolution        Plate: (90mm x 75mm).....       3/3/86
                                          Protein Plate.                                                        
Helena Laboratories....................  Titan Gel IFE Buffer...........  Packet: 25.9 g...........     12/18/85
Helena Laboratories....................  Titan Gel IFE Plate............  Plate: (90mm x 75mm).....       3/5/86
Helena Laboratories....................  Titan Gel Immuno Fix Kit         Kit: 10 Plates (90mm x         1/24/86
                                          Catalog No. 3046.                75mm), 2 Packets IFE                 
                                                                           Buffer.                              
Helena Laboratories....................  Titan Gel ImmunoFix Plus Kit #   Kit: 10 plates, 1 pkg IFE       3/9/93
                                          3067.                            buffer.                              
Helena Laboratories....................  Titan Gel ImmunoFix-9 Kit #      Kit: 10 plates, 1 pkg IFE       3/9/93
                                          3051.                            buffer.                              
Helena Laboratories....................  Titan Gel Iso Dot LDH Buffer...  Packet: 19.6 g...........       1/7/86
Helena Laboratories....................  Titan Gel Iso Dot LDH Isoenzyme  Plate: (90mm x 75mm).....     12/18/85
                                          Plate.                                                                
Helena Laboratories....................  Titan Gel Iso Dot LDH Kit        Kit: 10 Plates (90mm x         1/24/86
                                          Catalog No. 3062.                75mm), 1 Packet Iso Dot              
                                                                           LDH Buffer.                          
Helena Laboratories....................  Titan Gel LD Buffer............  Packet: 21.5 g...........     11/26/86
Helena Laboratories....................  Titan Gel LD Isoenzyme Diluent.  Bottle: 10 ml............     11/26/86
Helena Laboratories....................  Titan Gel LDH Isoenzyme Buffer.  Packet: 22.7 g...........       3/7/83
Helena Laboratories....................  Titan Gel LDH Isoenzyme Plate..  Plate: (90mm x 75mm).....     12/18/85
Helena Laboratories....................  Titan Gel LDH Isoenzyme Reagent  Vial: 2ml, 10 vials/box..       1/7/86
Helena Laboratories....................  Titan Gel Lipoprotein Buffer...  Packet: 17.3 g...........     12/18/85
Helena Laboratories....................  Titan Gel Lipoprotein Kit        Kit: 1 Packet Buffer.....      1/24/86
                                          Catalog No. 3045.                                                     
Helena Laboratories....................  Titan Gel Lipoprotein Plate....  Plate: (90 x 75 mm)......       1/9/87
Helena Laboratories....................  Titan Gel Multi-Slot Lipo-17     Kit: 10 plates (81 x 143        1/9/87
                                          Kit Catalog No. 3095.            mm) 1 packet buffer                  
                                                                           (21.6 g).                            
Helena Laboratories....................  Titan Gel Multi-Slot Lipo-17     Plate: (81 x 143 mm).....       1/9/87
                                          Plate.                                                                
Helena Laboratories....................  Titan Gel Multi-Slot SP-17 Kit   Kit: 10 plates (81 x 143        1/9/87
                                          Catalog No. 3091.                mm) 1 packet buffer                  
                                                                           (29.1 g).                            
Helena Laboratories....................  Titan Gel Multi-Slot SP-17       Plate: 81 x 143 mm.......       1/9/87
                                          Plate.                                                                
Helena Laboratories....................  Titan Gel Serum Protein Buffer.  Packet: 29.1 g...........      4/12/83
Helena Laboratories....................  Titan Gel Serum Protein Kit      Kit: 10 Plates (90mm x         1/24/86
                                          Catalog No. 3041.                75mm), 1 Packet Buffer.              
Helena Laboratories....................  Titan Gel Serum Protein Plate..  Plate: (90mm x 75mm).....     12/18/85
Helena Laboratories....................  Titan Gel Silver Stain Buffer..  Packet: 25.9g............     12/18/85
Helena Laboratories....................  Titan Gel Silver Stain Kit       Kit: 10 Plates (90mm x         1/24/86
                                          Catalog No. 3035.                75mm), 2 Packets Buffer.             
Helena Laboratories....................  Titan Gel Silver Stain Plate...  Plate: (90mm x 75mm).....       3/3/86
Helena Laboratories....................  Titan Gel-PC LDH Isoenzyme Kit   Kit: 10 Plates (90mm x         1/24/86
                                          Catalog No. 3053.                75mm), 1 Packet LDH                  
                                                                           Buffer, 1 Box LDH                    
                                                                           Reagent.                             
Helena Laboratories....................  Titan Gel-PC LDH Isoenzyme       Plate: (90mm x 75mm).....     12/18/85
                                          Plate.                                                                
Helena Laboratories....................  Titan III Agar Catalog No. 5023  Packet: 5 g. (5 Packets/      12/28/73
                                                                           box).                                
Helena Laboratories....................  Titan IV IE Plate (large)......  Package: plates, 3 by 4       12/28/73
                                                                           in.                                  
Helena Laboratories....................  Titan IV IE Plate (small)......  Package: plates, 1 by 3       12/28/73
                                                                           in.                                  

[[Page 144]]

                                                                                                                
Helena Laboratories....................  Titan IV IE Plate Kit..........  Kit: 12 small (1 by 3         12/28/73
                                                                           in.) IE plates, 1 box B1             
                                                                           Buffer.                              
Helena Laboratories....................  Titan IV IE Plate Kit..........  Kit: 10 large (3 by 4         12/28/73
                                                                           in.) IE Plates, 1 box B1             
                                                                           Buffer.                              
High Standard Products.................  (DL) Methamphetamine 1.0mg/ml..  Ampule: 2ml..............      5/11/93
High Standard Products.................  (DL) Methamphetamine-d10         Ampule: 2ml..............      5/11/93
                                          100g/ml.                                                     
High Standard Products.................  (DL) Methamphetamine-d5          Ampule: 2ml..............      5/11/93
                                          100g/ml.                                                     
High Standard Products.................  11-Nor-Delta-8-Carboxy-          Ampule: 2ml..............      5/11/93
                                          Tetrahydrocannabinol 100g/ml.                                                               
High Standard Products.................  11-Nor-Delta-9-Carboxy-          Ampule: 2ml..............      5/11/93
                                          Tetrahydrocannabinol 100ug/ml.                                        
High Standard Products.................  11-Nor-Delta-9-Carboxy-          Ampule: 2ml..............      5/11/93
                                          Tetrahydrocannabinol-d10 100ug/                                       
                                          ml.                                                                   
High Standard Products.................  11-Nor-Delta-9-Carboxy-          Ampule: 2ml..............      5/11/93
                                          Tetrahydrocannabinol-d3 100ug/                                        
                                          ml.                                                                   
High Standard Products.................  11-Nor-Delta8 carboxy THC;       Ampule: 2ml..............      4/15/94
                                          1.0mg/ml.                                                             
High Standard Products.................  11-Nor-Delta9 carboxy THC        Ampules: 10; 5 of 2ml, 5       4/15/94
                                          Screening/Confirmation           of 20ml.                             
                                          Calibrators; 10, 25, 50, 100,                                         
                                          250, ng/ml.                                                           
High Standard Products.................  11-Nor-Delta9 carboxy THC-d10;   Ampule: 2ml..............      4/15/94
                                          0.1mg/ml.                                                             
High Standard Products.................  11-Nor-Delta9 carboxy THC;       Ampule: 2ml..............      4/15/94
                                          1.0mg/ml.                                                             
High Standard Products.................  11-nor-Delta9 carboxy THC        Ampules: 6; 3 of 2ml, 3        4/15/94
                                          Controls; 10, 20, 100 ng/ml.     of 20ml.                             
High Standard Products.................  3, 4-                            Ampule: 2ml..............      5/11/93
                                          Methylenedioxymethamphetamine                                         
                                          (MDMA) 100ug/ml.                                                      
High Standard Products.................  3, 4-                            Ampule: 2ml..............      5/11/93
                                          Methylenedioxymethamphetamine-                                        
                                          d5 (MDMA) 100ug/ml.                                                   
High Standard Products.................  3-Methylfentanyl 100ug/ml......  Ampule: 2ml..............      5/11/93
High Standard Products.................  3-Methylfentanyl-d3 100ug/ml...  Ampule: 2ml..............      5/11/93
High Standard Products.................  4-Hydroxyamphetamine; 1.0mg/ml.  Ampule: 2ml..............      4/15/94
High Standard Products.................  4-Hydroxymethamphetamine; 1.0mg/ Ampule: 2ml..............      4/15/94
                                          ml.                                                                   
High Standard Products.................  4-Methoxyamphetamine 1.0mg/ml..  Ampule: 2ml..............      5/11/93
High Standard Products.................  4-Methoxyamphetamine-d5 100ug/   Ampule: 2ml..............      5/11/93
                                          ml.                                                                   
High Standard Products.................  6-Acetylmorphine 100ug/ml......  Ampule: 2ml..............      5/11/93
High Standard Products.................  6-Acetylmorphine-d3 100ug/ml...  Ampule: 2ml..............      5/11/93
High Standard Products.................  6-Acetylmorphine; 0.1mg/ml,      Ampule: 2ml..............      4/15/94
                                          1.0mg/ml.                                                             
High Standard Products.................  Amphetamine Cut-Off Controls;    Ampules: 3; 20ml each....      4/15/94
                                          375, 625, 1500 ng/ml.                                                 
High Standard Products.................  Amphetamine Screening            Ampules: 4; 20ml each....      4/15/94
                                          Confirmation Calibrators; 500,                                        
                                          1000, 1500, 2000 ng/ml.                                               
High Standard Products.................  Benzoylecgonine 1.0mg/ml.......  Ampule: 2ml..............      5/11/93
High Standard Products.................  Benzoylecgonine Cut-Off          Ampules: 3; 20ml each....      4/15/94
                                          Controls; 100, 200, 300, ng/ml.                                       
High Standard Products.................  Benzoylecgonine Propyl Ester     Ampule: 2ml..............      5/11/93
                                          1.0mg/ml.                                                             
High Standard Products.................  Benzoylecgonine Screening        Ampules: 4; 20ml each....      4/15/94
                                          Confirmation Calibrators; 150,                                        
                                          300, 450, 600 ng/ml.                                                  
High Standard Products.................  Benzoylecgonine-d3 100ug/ml....  Ampule: 2ml..............      5/11/93
High Standard Products.................  Benzoylecgonine-d3; 0.1mg/ml...  Ampule: 2ml..............      4/15/94
High Standard Products.................  Benzoylecgonine-d8 100ug/ml....  Ampule: 2ml..............      5/11/93
High Standard Products.................  Benzoylecgonine-d8; 0.1mg/ml...  Ampule; 2ml..............      4/15/94
High Standard Products.................  Cocaethylene 1.0mg/ml..........  Ampule: 2ml..............      5/11/93
High Standard Products.................  Cocaethylene-d3 100ug/ml.......  Ampule: 2ml..............      5/11/93
High Standard Products.................  Cocaethylene-d3; 0.1mg/ml......  Ampule: 2ml..............      4/15/94
High Standard Products.................  Cocaethylene-d8 100ug/ml.......  Ampule: 2ml..............      5/11/93
High Standard Products.................  Cocaethylene-d8; 0.1mg/ml......  Ampule: 2ml..............      4/15/94
High Standard Products.................  Cocaine 1.0mg/ml...............  Ampule: 2ml..............      5/11/93
High Standard Products.................  Cocaine-d3 100ug/ml............  Ampule: 2ml..............      5/11/93
High Standard Products.................  Cocaine-d8 1.0mg/ml............  Ampule: 2ml..............      5/11/93
High Standard Products.................  Codeine 100ug/ml...............  Ampule: 2ml..............      5/11/93
High Standard Products.................  Codeine Cut-Off Controls; 225,   Ampules: 3; 20ml each....      4/15/94
                                          375, 900 ng/ml.                                                       
High Standard Products.................  Codeine Screening Confirmation   Ampules: 4; 20ml each....      4/15/94
                                          Calibrators; 300, 600, 900,                                           
                                          1200 ng/ml.                                                           
High Standard Products.................  Codeine-d3 100ug/ml............  Ampule: 2ml..............      5/11/93
High Standard Products.................  Codeine-d3; 0.1mg/ml...........  Ampule: 2ml..............      4/15/94
High Standard Products.................  Codeine-d6 100ug/ml............  Ampule: 2ml..............      5/11/93
High Standard Products.................  Codeine-d6; 0.1mg/ml...........  Ampule: 2ml..............      4/15/94
High Standard Products.................  D-Amphetamine; 1.0mg/ml........  Ampule: 2ml..............      4/15/94
High Standard Products.................  DL Amphetamine 1.0mg/ml........  Ampule: 2ml..............      5/11/93
High Standard Products.................  DL Amphetamine-d10 100ug/ml....  Ampule: 2ml..............      5/11/93
High Standard Products.................  DL Amphetamine-d5 100ug/ml.....  Ampule: 2ml..............      5/11/93
High Standard Products.................  DL-Amphetamine-d11; 0.1mg/ml...  Ampule: 2ml, 20ml........      4/15/94
High Standard Products.................  DL-Amphetamine-d5; 0.1mg/ml....  Ampule; 2ml..............      4/15/94
High Standard Products.................  DL-Amphetamine-d6; 0.1mg/ml....  Ampule: 2ml, 20ml........      4/15/94
High Standard Products.................  Delta-8-Tetrahydrocannabinol     Ampule: 2ml..............      5/11/93
                                          100ug/ml.                                                             

[[Page 145]]

                                                                                                                
High Standard Products.................  Delta-9-Tetrahydrocannabinol     Ampule: 2ml..............      5/11/93
                                          100ug/ml.                                                             
High Standard Products.................  Delta-9-Tetrahydrocannabinol     Ampule: 2ml..............      5/11/93
                                          100ug/ml.                                                             
High Standard Products.................  Delta-9-Tetrahydrocannabinol-    Ampule: 2ml..............      5/11/93
                                          d10 100ug/ml.                                                         
High Standard Products.................  Delta-9-Tetrahydrocannabinol-d6  Ampule: 2ml..............      5/11/93
                                          100ug/ml.                                                             
High Standard Products.................  Delta-9-THC; 1.0mg/ml..........  Ampule: 2ml..............      4/15/94
High Standard Products.................  Diazepam 1.0mg/ml..............  Ampule: 2ml..............      5/11/93
High Standard Products.................  Diazepam-d5 100ug/ml...........  Ampule: 2ml..............      5/11/93
High Standard Products.................  Diphenoxylate 1.0 mg/ml........  Ampule: 2ml..............      5/11/93
High Standard Products.................  Ecgonine 1.0mg/ml..............  Ampule: 2ml..............      5/11/93
High Standard Products.................  Ecgonine Methyl Ester 1.0mg/ml.  Ampule: 2ml..............      5/11/93
High Standard Products.................  Ecgonine Methyl Ester-d3 100ug/  Ampule: 2ml..............      5/11/93
                                          ml.                                                                   
High Standard Products.................  Ecgonine-d3 100ug/ml...........  Ampule: 2ml..............      5/11/93
High Standard Products.................  Fentanyl 1.0mg/ml..............  Ampule: 2ml..............      5/11/93
High Standard Products.................  Fentanyl-d5 100ug/ml...........  Ampule: 2ml..............      5/11/93
High Standard Products.................  Fentanyl-d5; 0.1mg/ml..........  Ampule: 2ml..............      4/15/94
High Standard Products.................  Heroin, 1.0mg/ml...............  Ampule: 2ml..............      3/21/95
High Standard Products.................  Heroin-D9, 0.1mg/ml............  Ampule: 2ml..............      3/21/95
High Standard Products.................  Hydrocodone 1.0mg/ml...........  Ampule: 2ml..............      5/11/93
High Standard Products.................  Hydrocodone-d3 100ug/ml........  Ampule: 2ml..............      5/11/93
High Standard Products.................  Hydromorphone 1.0mg/ml.........  Ampule: 2ml..............      5/11/93
High Standard Products.................  Hydromorphone-d3 100ug/ml......  Ampule: 2ml..............      5/11/93
High Standard Products.................  Lysergic Acid Diethylamide 25    Ampule: 2ml..............      5/11/93
                                          ug/ml.                                                                
High Standard Products.................  Lysergic Acid Diethylamide-d3    Ampule: 2ml..............      5/11/93
                                          25 ug/ml.                                                             
High Standard Products.................  Lysergic Acid Diethylamide-dl    Ampule: 2ml..............      5/11/93
                                          25ug/ml.                                                              
High Standard Products.................  Lysergic Acid N-Methyl-          Ampule: 2ml..............      5/11/93
                                          Propylamide (LAMPA) 25ug/ml.                                          
High Standard Products.................  Lysergic acid diethylamide-d7;   Ampule: 2ml..............      4/15/94
                                          0.025mg/ml.                                                           
High Standard Products.................  Methadone 1.0mg/ml.............  Ampule: 2ml..............      5/11/93
High Standard Products.................  Methadone-D6, 0.1mg/ml.........  Ampule: 2ml..............      3/21/95
High Standard Products.................  Methadone-d3 100ug/ml..........  Ampule: 2ml..............      5/11/93
High Standard Products.................  Methamphetamine Cut-Off          Ampules: 3; 20ml each....      4/15/94
                                          Controls; 225, 375, 900 ng/ml.                                        
High Standard Products.................  Methamphetamine Screening        Ampules: 4; 20ml each....      4/15/94
                                          Confirmation Calibrators; 500,                                        
                                          1000, 1500, 2000 ng/ml.                                               
High Standard Products.................  Methamphetamine-d14; 0.1mg/ml..  Ampule: 2ml, 20ml........      4/15/94
High Standard Products.................  Methamphetamine-d5; 0.1mg/ml...  Ampule: 2ml..............      4/15/94
High Standard Products.................  Methamphetamine-d9; 0.1mg/ml...  Ampule: 2ml, 20ml........      4/15/94
High Standard Products.................  Methaqualone 1.0 mg/ml.........  Ampule: 2ml..............      5/11/93
High Standard Products.................  Methaqualone-d3 100ug/ml.......  Ampule: 2ml..............      5/11/93
High Standard Products.................  Methylenedioxyamphetamine (MDA)  Ampule: 2ml..............      5/11/93
                                          1.0mg/ml.                                                             
High Standard Products.................  Methylenedioxyamphetamine (MDA)  Ampule: 2ml..............      5/11/93
                                          d-5 100ug/ml.                                                         
High Standard Products.................  Methylenedioxyethylamphetamine,  Ampule: 2ml..............      3/21/95
                                          1.0mg/ml.                                                             
High Standard Products.................  Methylenedioxyethylamphetamine-  Ampule: 2ml..............      3/21/95
                                          D7, 0.1mg/ml.                                                         
High Standard Products.................  Morphine 1.0mg/ml..............  Ampule: 2ml..............      5/11/93
High Standard Products.................  Morphine Cut-Off Controls; 225,  Ampules: 3; 20ml each....      4/15/94
                                          375, 900 ng/ml.                                                       
High Standard Products.................  Morphine Screening Confirmation  Ampule: 4; 20ml each.....      4/15/94
                                          Calibrators; 300, 600, 900,                                           
                                          1200 ng/ml.                                                           
High Standard Products.................  Morphine-d3 100ug/ml...........  Ampule: 2ml..............      5/11/93
High Standard Products.................  Morphine-d3; 0.1mg/ml..........  Ampule: 2ml..............      4/15/94
High Standard Products.................  Morphine-d4; 0.1mg/ml..........  Ampule: 2ml, 20ml........      4/15/94
High Standard Products.................  NIDA Cut-Off Controls; Levels    Ampules: 6; 3 of 2ml, 3        4/15/94
                                          1, 2, 3.                         of 20ml.                             
High Standard Products.................  Norcocaine 1.0mg/ml............  Ampule: 2ml..............      5/11/93
High Standard Products.................  Norcodeine 1.0mg/ml............  Ampule: 2ml..............      5/11/93
High Standard Products.................  Nordiazepam 1.0mg/ml...........  Ampule: 2ml..............      5/11/93
High Standard Products.................  Nordiazepam-d5 100ug/ml........  Ampule: 2ml..............      5/11/93
High Standard Products.................  Normorphine 1.0mg/ml...........  Ampule: 2ml..............      5/11/93
High Standard Products.................  Oxazepam 1.0mg/ml..............  Ampule: 2ml..............      5/11/93
High Standard Products.................  Oxazepam-d5 100ug/ml...........  Ampule: 2ml..............      5/11/93
High Standard Products.................  Phencyclidine 1.0mg/ml.........  Ampule: 2ml..............      5/11/93
High Standard Products.................  Phencyclidine Cut-Off Controls;  Ampules: 3; 20ml each....      4/15/94
                                          18, 32, 75 ng/ml.                                                     
High Standard Products.................  Phencyclidine Screening          Ampule: 4; 20ml each.....      4/15/94
                                          Confirmation Calibrators; 25,                                         
                                          50, 75, 100 ng/ml.                                                    
High Standard Products.................  Phencyclidine-d10 100ug/ml.....  Ampule: 2ml..............      5/11/93
High Standard Products.................  Phencyclidine-d10; 0.1mg/ml....  Ampule: 2ml..............      4/15/94
High Standard Products.................  Phencyclidine-d5 100ug/ml......  Ampule: 2ml..............      5/11/93
High Standard Products.................  Phencyclidine-d5; 0.1mg/ml.....  Ampule: 2ml..............      4/15/94
High Standard Products.................  Phenobarbital, 1.0mg/ml........  Ampule: 2ml..............      3/21/95
High Standard Products.................  Phenobarbital-D5...............  Ampule: 2ml..............      3/21/95
High Standard Products.................  Propoxyphene, 1.0mg/ml.........  Ampule: 2ml..............      3/21/95
High Standard Products.................  Propoxyphene-D5, 0.1mg/ml......  Ampule: 2ml..............      3/21/95
High Standard Products.................  Secobarbital, 1.0mg/ml.........  Ampule: 2ml..............      3/21/95

[[Page 146]]

                                                                                                                
High Standard Products.................  Secobarbital-D5, 0.1mg/ml......  Ampule: 2ml..............      3/21/95
High Standard Products.................  Temazepam 1.0mg/ml.............  Ampule: 2ml..............      5/11/93
High Standard Products.................  Temazepam-d5 100ug/ml..........  Ampule: 2ml..............      5/11/93
High Standard Products.................  Urine Confirm (+25%)...........  Ampule: 20ml.............      3/20/95
High Standard Products.................  Urine Confirm (-25%)...........  Ampule: 20ml.............      3/20/95
High Standard Products.................  Urine Confirm (-40%) Retest....  Ampule: 20ml.............      3/20/95
High Standard Products.................  Urine Confirm 3X Cutoff........  Ampule: 20ml.............      3/20/95
High Standard Products.................  Urine Confirm Cutoff...........  Ampule: 20ml.............      3/20/95
High Standard Products.................  Urine Screen (+25%)............  Ampule: 20ml.............      3/20/95
High Standard Products.................  Urine Screen (-25%)............  Ampule: 20ml.............      3/20/95
High Standard Products.................  Urine Screen 3X Cutoff.........  Ampule: 20ml.............      3/20/95
High Standard Products.................  Urine Screen Cutoff............  Ampule: 20ml.............      3/20/95
HyClone Laboratories, Inc..............  HyQ-CCM1.......................  Bottle: 50-1000ml; Lined        2/9/95
                                                                           container: 10-1000L.                 
HyClone Laboratories, Inc..............  HyQ-CCM1 w/o Phenol Red........  Bottle: 50-1000ml; Lined        2/9/95
                                                                           Container: 10-1000L.                 
HyClone Laboratories, Inc..............  Medium 925 w/o L-Glutamine, w/o  Bottle: 50-1000ml; Lined        2/9/95
                                          Phenol Red.                      Container: 10-1000L.                 
HyClone Laboratories, Inc..............  Medium 925 with IGF, w/o Phenol  Bottle: 50-1000ml; Lined        2/9/95
                                          Red.                             Container: 10-1000L.                 
HyClone Laboratories, Inc..............  Medium 925 with L-Glutamine, w/  Bottle: 50-1000ml; Lined        2/9/95
                                          o Phenol Red.                    Container: 10-1000L.                 
HyClone Laboratories, Inc..............  Medium TLF with L-Glutamine....  Bottle: 50-1000ml; Lined        2/9/95
                                                                           Container: 10-1000L.                 
Hycor Biomedical, Inc..................  Hycor AccuPINCH Cocaine Test...  Bottle: 3ml Kit: 50 tests      8/21/90
Hycor Biomedical, Inc..................  Hycor AccuPINCH Morphine Test..  Bottle: 3ml Kit: 50 tests      8/21/90
Hycor Biomedical, Inc..................  Hycor AccuPINCH Phencyclidine    Bottle: 3ml Kit: 50 tests      8/21/90
                                          Test.                                                                 
Hycor Biomedical, Inc..................  Hycor AccuPinch Methamphetamine  Bottle: 3ml; Kit: 50          10/29/91
                                          Test.                            Tests.                               
Hycor Biomedical, Inc..................  Hycor AccuPinch THC Test.......  Bottle: 3ml; Kit: 50          10/29/91
                                                                           Tests.                               
Hycor Biomedical, Inc..................  Sentry Drugs of Abuse Urine      Bottle: 10ml Kit: 4            8/24/90
                                          Calibrator BARBITURATES Urine    bottles, 12 bottles.                 
                                          Calibrator- 4 levels.                                                 
Hycor Biomedical, Inc..................  Sentry Drugs of Abuse Urine      Bottle: 10ml Kit: 4            8/24/90
                                          Calibrator DELTA-9-THC Urine     bottles, 12 bottles.                 
                                          Calibrator - 4 levels.                                                
Hycor Biomedical, Inc..................  Sentry Drugs of Abuse Urine      Bottle: 10ml Kit: 4            8/24/90
                                          Calibrator NORDIAZEPAM Urine     bottles, 12 bottles.                 
                                          Calibrator - 3 levels.                                                
Hycor Biomedical, Inc..................  Sentry Drugs of Abuse Urine      Bottle: 10ml Kit: 4            8/24/90
                                          Calibrator OPIATES Urine         bottles, 12 bottles.                 
                                          Calibrator - 4 levels.                                                
Hycor Biomedical, Inc..................  Sentry Drugs of Abuse Urine      Bottle: 10ml Kit: 4            8/24/90
                                          Calibrator PHENCYCLIDINE Urine   bottles, 12 bottles.                 
                                          Calibrator - 4 levels.                                                
Hycor Biomedical, Inc..................  Sentry Drugs of Abuse Urine      Vial: 10ml, Kit: 12            3/29/89
                                          Calibrator, Amphetamine Urine    vials, Kit: 4 vials.                 
                                          Calibrator - 4 level.                                                 
Hycor Biomedical, Inc..................  Sentry Drugs of Abuse Urine      Vial: 10ml, Kit: 12            3/29/89
                                          Calibrator, Benzoylecgonine      vials, Kit: 4 vials.                 
                                          Urine Calibrator - 4 level.                                           
Hycor Biomedical, Inc..................  Sentry Ligand/Combo Control      Vial: 10ml Box: 15 vials.       3/1/90
                                          High Level.                                                           
Hycor Biomedical, Inc..................  Sentry Ligand/Combo Control Low  Vial: 10ml Box: 15 vials.       3/1/90
                                          Level.                                                                
Hycor Biomedical, Inc..................  Sentry Ligand/Combo Control Mid  Vial: 10ml Box: 15 vials.       3/1/90
                                          Level.                                                                
Hycor Biomedical, Inc..................  Sentry Ligand/Combo Control      Kit: 15 vials............       3/1/90
                                          Multi-Pack.                                                           
Hycor/ICL Scientific...................  Drugs of Abuse Comprehensive     Bottle: 30ml.............      2/24/89
                                          Urine Control, HIGH POSITIVE.                                         
Hycor/ICL Scientific...................  Drugs of Abuse Comprehensive     Bottle: 30ml.............      2/24/89
                                          Urine Control, LOWER THRESHOLD.                                       
Hycor/ICL Scientific...................  Drugs of Abuse Comprehensive     Bottle: 30ml.............      2/24/89
                                          Urine Control, UPPER THRESHOLD.                                       
Hycor/ICL Scientific...................  Drugs of Abuse Urine Control,    Box: 4-100 ml Bottles....     10/21/88
                                          CONFIRMATION.                                                         
Hycor/ICL Scientific...................  Drugs of Abuse Urine Control,    Box: 4-30 ml Bottles.....     10/21/88
                                          SCREEN.                                                               
ICL Scientific.........................  Therapeutic Drug Control I ,     Glass Vial: 10ml.........      8/14/85
                                          TDC I (High Level).                                                   
ICL Scientific.........................  Therapeutic Drug Control I, II,  Glass Vials (12): 10ml...      8/14/85
                                          III, Tri-Level TDC Multipack.                                         
ICL Scientific.........................  Therapeutic Drug Control II,     Glass Vial: 10ml.........      8/14/85
                                          TDC II (Mid-Level).                                                   
ICL Scientific.........................  Therapeutic Drug Control III,    Glass Vial: 10ml.........      8/14/85
                                          TDC III (Low Level).                                                  
ICN Micromedic Systems, Inc............  Immunogen: BZ-A................  Plastic Vial: 1.5 ml.....      2/29/88
ICN Micromedic Systems, Inc............  Immunogen: BZ-B................  Plastic Vial: 1.5 ml.....      2/29/88
ICN Micromedic Systems, Inc............  Immunogen: CD-A................  Plastic Vial: 1.5 ml.....      2/29/88
ICN Micromedic Systems, Inc............  Immunogen: M-A.................  Plastic Vial: 1.5 ml.....      2/29/88
ICN Micromedic Systems, Inc............  Immunogen: M-B.................  Plastic Vial: 1.5 ml.....      2/29/88
ICN Micromedic Systems, Inc............  Immunogen: TF-A................  Plastic Vial: 1.5 ml.....      2/29/88

[[Page 147]]

                                                                                                                
ICN Micromedic Systems, Inc............  Micromedic Combostat THC/        Amber Glass Vial: 2 ml         2/24/88
                                          Cocaine STANDARDS-2, 3, and 4.   Plastic Bottle: 100 ml.              
ICN Micromedic Systems, Inc............  Micromedic CrackPot 57Co/125I    Plastic Bottle: 25 ml,         2/24/88
                                          Tracer Solution.                 1000 ml.                             
ICN Micromedic Systems, Inc............  Micromedic Morphine 125I Tracer  Bottle: 50 ml, 1000 ml...      2/29/88
                                          Solution.                                                             
ICN Micromedic Systems, Inc............  Micromedic Morphine Standards    Bottle: 5 ml, 100 ml.....      2/29/88
                                          2, 3 and 4.                                                           
INCSTAR Corporation....................  (125I) Human TSH Tracer Cat.     Vial: 15ml...............      3/08/91
                                          No. CA-2623.                                                          
INCSTAR Corporation....................  Anticonvulsant Drug Controls     Vial: 3.5ml..............      3/08/91
                                          Levels I and II Cat. Nos. CA-                                         
                                          2419, CA-2420.                                                        
INCSTAR Corporation....................  Assay Buffer Cat. No. CA-2742..  Bottle: 150ml............      3/08/91
INCSTAR Corporation....................  Clinical Assays Gamma Coat       Kit: 50, 500 assays......      3/08/91
                                          (125I) Phenobarbital                                                  
                                          Radioimmunoassay Kits Cat.                                            
                                          Nos. CA-2545, CA-2565.                                                
INCSTAR Corporation....................  Clinical Assays Gamma Coat       Kit: 50, 500 assays......      3/08/91
                                          (125I) Phenytoin                                                      
                                          Radioimmunoassay Kits Cat.                                            
                                          Nos. CA-2537, CA-2557.                                                
INCSTAR Corporation....................  Clinical Assays Gamma Coat       Kit: 100, 500 assays.....      3/08/91
                                          (125I) T3 Uptake                                                      
                                          Radioimmunoassay Kit Catalog                                          
                                          Nos. CA-2539, CA-2539J, CA-                                           
                                          2559, CA-2559J.                                                       
INCSTAR Corporation....................  Clinical Assays Gamma Dab        Kit: 125 assays; Vial:         3/08/91
                                          (125I) hTSH Radioimmunoassay     15ml.                                
                                          Kit Cat. No. CA-1591.                                                 
INCSTAR Corporation....................  HTSH Non-Specific Binding        Vial: 3.5ml..............      3/08/91
                                          Reagent Cat. No. CA-2752.                                             
INCSTAR Corporation....................  Human TSH Controls Levels I &    Vial: 3.5ml..............      3/08/91
                                          II Cat. Nos. CA-2452, CA-2453.                                        
INCSTAR Corporation....................  Human hTSH Blank Cat. No. CA-    Vial: 15ml...............      3/08/91
                                          2885.                                                                 
INCSTAR Corporation....................  Phenobarbital Standards: 1, 3,   Bottle: 3.5ml............      3/08/91
                                          10, 30, 100 ug/ml Cat. Nos. CA-                                       
                                          2380-2384.                                                            
INCSTAR Corporation....................  Rabbit Anti-Human TSH Serum      Vial: 15ml...............      3/08/91
                                          Cat. No. CA-2145.                                                     
INCSTAR Corporation....................  htsH Standards: 2, 5, 10, 20,    Bottle: 3.5ml............      3/08/91
                                          50 uIU/ml Cat. Nos. CA-2886-                                          
                                          2890.                                                                 
ISOTEC, Inc............................  (-) 11 Nor-9-Carboxy-Delta-9-    Ampule: 2ml..............      6/19/95
                                          THC-D3, 100ug/ml.                                                     
ISOTEC, Inc............................  (-) 11-Nor-9-Carboxy-Delta-9-    Ampule: 2ml..............      6/19/95
                                          THC, 100ug/ml.                                                        
ISOTEC, Inc............................  6-Acetylmorphine, 1 mg/ml......  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  6-Acetylmorphine-D3, 100ug/ml,   Ampule: 2ml..............      6/19/95
                                          1mg/ml.                                                               
ISOTEC, Inc............................  6-Acetylmorphine-D6, 100ug/ml,   Ampule; 2ml..............      6/19/95
                                          1mg/ml.                                                               
ISOTEC, Inc............................  Benzoylecgonine, 1mg/ml........  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  Benzoylecgonine-D3, 100ug/ml,    Ampule: 2ml..............      6/19/95
                                          1mg/ml.                                                               
ISOTEC, Inc............................  Cocaethylene, 1mg/ml...........  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  Cocaethylene-D3, 100ug/ml, 1mg/  Ampule: 2ml..............      6/19/95
                                          ml.                                                                   
ISOTEC, Inc............................  Cocaine, 1mg/ml................  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  Cocaine-D3, 100ug/ml, 1mg/ml...  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  Codeine, 1mg/ml................  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  Codeine-D3, 100ug/ml, 1mg/ml...  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  DL-3, 4-                         Ampule: 2ml..............      9/18/95
                                          Methylenedioxyamphetamine, 1mg/                                       
                                          ml.                                                                   
ISOTEC, Inc............................  DL-3, 4-                         Ampule: 2ml..............      9/18/95
                                          Methylenedioxyamphetamine-D5,                                         
                                          100ug/ml, 1mg/ml.                                                     
ISOTEC, Inc............................  DL-3, 4-                         Ampule: 2ml..............      9/18/95
                                          Methylenedioxymethamphetamine,                                        
                                          1mg/ml.                                                               
ISOTEC, Inc............................  DL-3, 4-                         Ampule: 2ml..............      9/18/95
                                          Methylenedioxymethamphetamine-                                        
                                          D8, 100ug/ml, 1mg/ml.                                                 
ISOTEC, Inc............................  DL-Amphetamine-D6, 100ug/ml,     Ampule: 2ml..............      6/19/95
                                          1mg/ml.                                                               
ISOTEC, Inc............................  DL-Amphetamine, 1mg/ml.........  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  DL-Methamphetamine, 1mg/ml.....  Ampule: 2ml..............      9/18/95
ISOTEC, Inc............................  DL-Methamphetamine-D9, 100ug/    Ampule: 2ml..............      9/18/95
                                          ml, 1mg/ml.                                                           
ISOTEC, Inc............................  DL-Methylphenidate, 1mg/ml.....  Ampule: 2ml..............      9/18/95
ISOTEC, Inc............................  Delta-9-THC, 1mg/ml............  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  Delta-9-THC-D3, 100ug/ml.......  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  Ecgonine Methyl Ester, 1mg/ml..  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  Ecgonine Methyl Ester-D3, 100ug/ Ampule: 2ml..............      6/19/95
                                          ml, 1mg/ml.                                                           
ISOTEC, Inc............................  Ecgonine, 1mg/ml...............  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  Fentanyl, 100ug/ml, 1mg/ml.....  Ampule: 2ml..............      9/18/95
ISOTEC, Inc............................  Fentanyl-D5, 100ug/ml, 1mg/ml..  Ampule: 2ml..............      9/18/95
ISOTEC, Inc............................  Hydrocodone, 1mg/ml............  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  Hydrocodone-D3, 100ug/ml, 1mg/   Ampule: 2ml..............      6/19/95
                                          ml.                                                                   
ISOTEC, Inc............................  Hydromorphone, 1mg/ml..........  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  Hydromorphone-D3, 100ug/ml, 1mg/ Ampule: 2ml..............      6/19/95
                                          ml.                                                                   
ISOTEC, Inc............................  Lysergic Acid Diethylamide,      Ampule: 2ml..............      6/19/95
                                          25ug/ml.                                                              
ISOTEC, Inc............................  Lysergic Acid Diethylamide-D3,   Ampule: 2ml..............      6/19/95
                                          25ug/ml.                                                              
ISOTEC, Inc............................  Lysergic Acid N-Methyl           Ampule: 2ml..............      6/19/95
                                          Propylamide, 25ug/ml.                                                 
ISOTEC, Inc............................  Methadone, 1mg/ml..............  Ampule: 2ml..............      9/18/95

[[Page 148]]

                                                                                                                
ISOTEC, Inc............................  Methadone-D3, 100ug/ml, 1mg/ml.  Ampule: 2ml..............      9/18/95
ISOTEC, Inc............................  Morphine, 1mg/ml...............  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  Morphine-3-beta-D-Glucuronide,   Ampule: 2ml..............      9/18/95
                                          100ug/ml, 1mg/ml.                                                     
ISOTEC, Inc............................  Morphine-D3, 100ug/ml, 1mg/ml..  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  Norcocaine, 1mg/ml.............  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  Pentobarbital, 1mg/ml..........  Ampule: 2ml..............      9/18/95
ISOTEC, Inc............................  Pentobarbital-D5, 100ug/ml, 1mg/ Ampule: 2ml..............      9/18/95
                                          ml.                                                                   
ISOTEC, Inc............................  Phencyclidine, 1mg/ml..........  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  Phencyclidine-D5, 100ug/ml.....  Ampule: 2ml..............      6/19/95
ISOTEC, Inc............................  Secobarbital, 1mg/ml...........  Ampule: 2ml..............      9/18/95
ISOTEC, Inc............................  Secobarbital-D5, 100ug/ml, 1mg/  Ampule: 2ml..............      9/18/95
                                          ml.                                                                   
Immunotech Corp........................  Amphetamine Enzyme Conjugate...  Bottle: 10.5ml...........      9/28/89
Immunotech Corp........................  Amphetamine Positive Urine       Bottle: 1ml..............      9/28/89
                                          Calibrator.                                                           
Immunotech Corp........................  Amphetamine-ALK Phos Cat. No.    Bottle: 10ml.............      3/12/90
                                          612; 50 units, 300 units.                                             
Immunotech Corp........................  Amphetamine-HRP Cat. No. 613;    Bottle: 10ml.............      3/12/90
                                          50 units.                                                             
Immunotech Corp........................  Benzoylecgonine-Alk Phos Cat. #  Bottle: 10ml.............      3/12/90
                                          602; 50 units, 300 units.                                             
Immunotech Corp........................  Benzoylecgonine-HRP Cat. No.     Bottle: 10ml.............      3/12/90
                                          604; 50 units, 300 units.                                             
Immunotech Corp........................  Cocaine Conjugate No. 0364-SIG.  Bottle: 75ml.............      6/13/91
Immunotech Corp........................  Cocaine Metabolite Enzyme        Vial: 10.5ml.............      9/28/89
                                          Conjugate.                                                            
Immunotech Corp........................  Cocaine Metabolite Positive      Vial: 2ml................      9/28/90
                                          Urine Calibrator.                                                     
Immunotech Corp........................  Delta-8-tetrahydrocannabinol-    Bottle: 10 ml............      3/12/90
                                          ALK Phos Cat. No. 616; 50                                             
                                          units, 300 units.                                                     
Immunotech Corp........................  Delta-8-tetrahydrocannabinol-    Bottle: 10ml.............      3/12/90
                                          HRP Cat. No. 618; 50 units.                                           
Immunotech Corp........................  ENDAB Phenobarbital Kit, Cat.    Kit: 100 tests, 4              9/28/89
                                          No. 119.                         Bottles: 1 ml ea.                    
Immunotech Corp........................  Methamphetamine-ALK Phos Cat.    Bottle: 10ml.............      3/12/90
                                          No. 614; 50 units.                                                    
Immunotech Corp........................  Methamphetamine-HRP Cat. No.     Bottle: 10 ml............      3/12/90
                                          615; 50 units.                                                        
Immunotech Corp........................  Micro Dau Amphetamine Enzyme     Kit: 96 tests, Bottle:         9/28/89
                                          Immunoassay Test Kit.            10.5 ml, 2 ml.                       
Immunotech Corp........................  Micro Dau Benzodiazepine Enzyme  Kit: 96 tests, Bottle:         9/28/89
                                          Immunoassay Test Kit.            10.5 ml, 2 ml.                       
Immunotech Corp........................  Micro Dau Cocaine Metabolite     Kit: 96 tests, Bottle:         9/28/89
                                          Enzyme Immunoassay Test Kit.     10.5 ml, 2 ml.                       
Immunotech Corp........................  Micro Dau Opiates Enzyme         Kit: 96 tests............     12/19/89
                                          Immunoassay Test Kit.                                                 
Immunotech Corp........................  Micro Dau PCP Enzyme             Kit: 96 tests............      7/11/90
                                          Immunoassay Kit Cat. No. 175.                                         
Immunotech Corp........................  Micro Dau THC Enzyme             Kit: 96 tests............      7/11/90
                                          Immunoassay Test Kit Cat. No.                                         
                                          173.                                                                  
Immunotech Corp........................  Morphine Positive Urine          Vial: 3.5 ml.............     12/19/89
                                          Calibrator.                                                           
Immunotech Corp........................  Morphine-ALK Phos Cat. No. 610;  Bottle: 10ml.............      3/12/90
                                          50 units, 300 units.                                                  
Immunotech Corp........................  Morphine-HRP Cat. No. 611; 50    Bottle: 10ml.............      3/12/90
                                          units, 300 units.                                                     
Immunotech Corp........................  Opiates Enzyme Conjugate.......  Vial: 10 ml..............     12/19/89
Immunotech Corp........................  Oxazepam Enzyme Conjugate......  Bottle: 10.5ml...........      9/28/89
Immunotech Corp........................  Oxazepam Positive Urine          Bottle: 2ml..............      9/28/89
                                          Calibrator.                                                           
Immunotech Corp........................  Oxazepam-ALK Phos Cat. No. 606;  Bottle: 10ml.............      3/12/90
                                          50 units.                                                             
Immunotech Corp........................  Oxazepam-HRP Cat No. 608; 50     Bottle: 10ml.............      3/12/90
                                          units.                                                                
Immunotech Corp........................  PCP Enzyme Conjugate Cat. No.    Vial: 20ml...............      7/11/90
                                          375.                                                                  
Immunotech Corp........................  PCP Positive Urine Calibrator    Vial: 3ml................      7/11/90
                                          Cat. No. 418.                                                         
Immunotech Corp........................  Phenobarbital Enzyme Conjugate.  Bottle: 10.0ml...........      9/28/89
Immunotech Corp........................  Phenobarbital Serum Standard:    4 Bottles: 1ml each......      9/28/89
                                          3ug/ml, 10ug/ml, 30ug/ml, 80ug/                                       
                                          ml.                                                                   
Immunotech Corp........................  THC Enzyme Conjugate Cat. No.    Vial: 20ml...............      7/11/90
                                          373.                                                                  
Immunotech Corp........................  THC Positive Urine Calibrator    Vial: 3ml................      7/11/90
                                          Cat No. 416 50ng/ml, 417 100ng/                                       
                                          ml.                                                                   
Industrial Analytical Laboratory, Inc..  11-Nor-Carboxy-Delta-9-          Ampule: 1ml..............      9/04/85
                                          Tetrahydrocannabinol.                                                 
Industrial Analytical Laboratory, Inc..  11-hydroxy-delta-9-              Ampule: 1 ml.............      2/18/87
                                          tetrahydrocannabinol.                                                 
Industrial Optical.....................  Opti-Kleen.....................  Bottle: 5 gallon.........      6/24/81
International BioClinical, Inc.........  Innofluor Phenobarbital          Bottle: 3 ml.............       7/9/87
                                          Calibrators 0.0, 3.0, 8.0,                                            
                                          20.0, 40.0, and 80.0 mcg/ml.                                          
International BioClinical, Inc.........  Phenobarbital Stock Tracer.....  Vial: 5 ml...............      9/23/87
International Technidyne Corp..........  Hemochron Control Plasma         Kit: 18 Tests; Test tube:      3/11/91
                                          Quality Control Test Kit.        9ml; Vial: 5ml.                      
JRH Biosciences........................  HH4 Cell Culture Media.........  Bulk Plastic Bag: 20, 10,      5/11/95
                                                                           1L.                                  
Janssen Pharmaceutica, Inc.............  3H Alfentanil..................  Vial: 0.5 ml.............       2/1/87

[[Page 149]]

                                                                                                                
Janssen Pharmaceutica, Inc.............  3H Fentanyl....................  Vial: 0.5 ml.............       2/1/87
Janssen Pharmaceutica, Inc.............  3H Sufentanil..................  Vial: 0.5 ml.............       2/1/87
Janssen Pharmaceutica, Inc.............  Alfentanil Radioimmunoassay Kit  Kit: 200 tests...........      5/13/85
Janssen Pharmaceutica, Inc.............  Fentanyl Radioimmunoassay Kit..  Kit: 200 tests...........      5/13/85
Janssen Pharmaceutica, Inc.............  Sufentanil Radioimmunoassay Kit  Kit: 500 tests...........      5/13/85
Kallestad Diagnostics..................  Barbital Buffer 901............  Vial.....................      5/19/81
Kallestad Diagnostics..................  IEP Buffer No. 900.............  Vial: 7 Dram.............     12/26/78
Kallestad Diagnostics..................  Immunoelectrofilm Catalog No.    1 Film Sealed in               3/11/80
                                          910.                             Cardboard Container.                 
Kallestad Diagnostics..................  Immunoelectrofilms, Catalog No.  Styrofoam Container: 25        6/22/87
                                          1013.                            film.                                
Kallestad Diagnostics..................  Immunoelectrophoresis Reagent    Kit: 3 Vials.............      6/22/87
                                          Kit, Catalog No. 1012.                                                
Kallestad Diagnostics..................  Quanticoat 125I-T3 Uptake Kit    Kit: 400 Determinations..     12/16/85
                                          Catalog No. 823.                                                      
Kallestad Diagnostics..................  Quanticoat 125I-T3 Uptake Kit,   Kit: 100 tests...........      6/24/81
                                          Catalog No. 833.                                                      
Kallestad Diagnostics..................  Quanticoat 125I-T3 Uptake        Bottle: 500ml............     12/16/85
                                          Reagent Catalog No. 785.                                              
Kallestad Diagnostics..................  Quanticoat 125I-T3 Uptake        2 Glass Bottles: 110ml...      6/24/81
                                          Reagent No. 834.                                                      
LIfe Technologies, Inc.................  AmnioMax-C100 Second Dilution..  Bottle: 1L...............      2/17/94
LKB Instruments, Inc...................  Tris-barbiturate Buffer pH 8.6.  Packet: each 6.788 g. 20       5/15/78
                                                                           packets/box.                         
Lemmon Company.........................  Etorphine Standard Solution....  Plastic Carboy: 1 Liter..     10/31/83
Life Technologies, Inc.................  AmnioMax-C100 First Dilution...  Bottle: 1L...............      2/17/94
Life Technologies, Inc.................  AmnioMax-C100 Stock Solution...  Bottle: 1L...............      2/17/94
Life Technologies, Inc.................  AmnioMax-C100 Supplement.......  Bottle: 15ml, 60ml, 75ml,      2/17/94
                                                                           100ml.                               
Life Technologies, Inc.................  Testosterone Stock Solution....  Bottle: 1L...............      10/4/94
MCI Biomedical.........................  IEP Buffer, pH 8.2, 0.04 Ionic   Package: 6.510 grams.....      8/28/72
                                          Strength.                                                             
Mallinckrodt Chemical, Inc.............  Naloxone/6-Beta Naltrexol......  Bottle: 60ml.............      10/6/94
Mallinckrodt Chemical, Inc.............  Naltrexone/6-beta Naltrexol      Bottle: 60ml.............      10/4/94
                                          Standard Solution.                                                    
Materials & Technology Systems.........  5-Ethyl-5-(1 -Carboxy-N-Propyl)  Screw Cap Vial: 8ml......       5/3/73
                                          Barbituric Acid.                                                      
Materials & Technology Systems.........  5-Ethyl-5-(1-Carboxy-N-          Vaccine Vial: 8ml........       5/3/73
                                          Propyl)Barbituric Acid Bovine                                         
                                          Serum Albumin or Rabbit Serum                                         
                                          Albumin.                                                              
Materials & Technology Systems.........  5-Ethyl-5-(1-Carboxy-N-          Vaccine Vial: 8ml........       5/3/73
                                          Propyl)Barbituric Acid                                                
                                          Sensitized RBC.                                                       
Materials & Technology Systems.........  Barbiturate Standard...........  Screwcap Vial: 10ml......      9/17/76
Materials & Technology Systems.........  Benzoylecgonine................  Screw Cap Vial: 25mg and       4/18/74
                                                                           100 mg.                              
Materials & Technology Systems.........  Benzoylecgonine Standard.......  Screwcap Vial: 10ml......      9/17/76
Materials & Technology Systems.........  Carboxymethylmorphine..........  Screw Cap Vial: 8ml......       5/3/73
Materials & Technology Systems.........  Carboxymethylmorphine Bovine     Vaccine Vial: 8ml........       5/3/73
                                          Serum Albumin or Rabbit Serum                                         
                                          Albumin.                                                              
Materials & Technology Systems.........  Carboxymethylmorphine            Vaccine Vial: 50ml.......       5/3/73
                                          Sensitized RBC.                                                       
Materials & Technology Systems.........  Ecgonine Bovine Serum Albumin    Vaccine Vial: 8ml........       5/3/73
                                          or Rabbit Serum Albumin.                                              
Materials & Technology Systems.........  Ecgonine Sensitized RBC........  Vaccine Vial: 50ml.......       5/3/73
Materials & Technology Systems.........  Methadone Standard.............  Screwcap Vial: 10ml......      9/17/76
Materials & Technology Systems.........  Morphine Standard..............  Screw Cap Vial: 10ml.....      7/17/73
Materials & Technology Systems.........  Tropinecarboxylic Acid.........  Screw Cap Vial: 8ml, 10ml       5/3/73
McGean-Rocho, Inc......................  Chloral Solution Denatured.....  Plastic container; 1, 5,       1/11/91
                                                                           55 Gallons.                          
McGean-Rocho, Inc......................  Reflexion Semi-Bright B........  Plastic container; 1, 5,       1/11/91
                                                                           55 Gallons.                          
McGean-Rocho, Inc......................  Reflexion Semi-Bright S........  Plastic container; 1, 5,       1/11/91
                                                                           55 Gallons.                          
Medi-Chem, Inc.........................  Barbiturate Test Set (Sodium     Bottle: 120ml............      2/22/74
                                          Secobarbital Standard 10mg % w/                                       
                                          v) Catalog No.250.                                                    
Medical Analysis Systems, Inc..........  ACE II Calibrator for the        Glass Vial: 2238mm, 5ml..       8/7/86
                                          DuPont aca Level 1.                                                   

[[Page 150]]

                                                                                                                
Medical Analysis Systems, Inc..........  ACE II Calibrator for the        Glass Vial: 2238mm, 5ml..       8/7/86
                                          DuPont aca Level 2.                                                   
Medical Analysis Systems, Inc..........  ACE II Calibrator for the        Glass Vial: 2238mm, 5ml..       8/7/86
                                          DuPont aca Level 3.                                                   
Medical Analysis Systems, Inc..........  Amobarbital, #117 Intermediate   Bottle: 10-100ml.........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  Benzoylecgonine, #432            Bottle: 10-250ml.........     10/22/93
                                          Intermediate Solution.                                                
Medical Analysis Systems, Inc..........  Benzoylecgonine, #483            Bottle: 10-100ml.........     10/22/93
                                          Intermediate Solution.                                                
Medical Analysis Systems, Inc..........  Benzoylecgonine, #719            Bottle: 10-1800ml........     10/22/93
                                          Intermediate Solution.                                                
Medical Analysis Systems, Inc..........  Butalbital, #429 Intermediate    Bottle: 10-100ml.........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  CHALLENGE Liquid Therapeutic     Kit: 10 Bottles..........      1/24/91
                                          Drug Linearity Controls.                                              
Medical Analysis Systems, Inc..........  CHALLENGE Liquid Therapeutic     Glass Bottles: 5ml; 1          1/24/91
                                          Drug Linearity Controls TD1 A-   Set: 5 Bottles.                      
                                          E; TD2 A-E.                                                           
Medical Analysis Systems, Inc..........  Chemistry Control Assayed,       Vial: 15ml...............      4/30/85
                                          Level 1, 2, & 3.                                                      
Medical Analysis Systems, Inc..........  Chemistry Control, Level 1, 2,   Vial: 15ml...............      4/30/85
                                          & 3.                                                                  
Medical Analysis Systems, Inc..........  Clonazepam, #473 Intermediate    Bottle: 50-500ml.........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  Codeine, #435 Intermediate       Bottle: 10-100ml.........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  D-Amphetamine, #423              Bottle: 10-250ml.........     10/22/93
                                          Intermediate Solution.                                                
Medical Analysis Systems, Inc..........  D-Methamphetamine, #422          Bottle: 10-250ml.........     10/22/93
                                          Intermediate Solution.                                                
Medical Analysis Systems, Inc..........  DOA Calibrator 1, #1921 Bulk     Bottle: 10-100L..........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  DOA Calibrator 2, #1922 Bulk     Bottle: 10-100L..........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  DOA Calibrator 2, #C38979 Bulk   Bottle: 10-100L..........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  DOA Calibrator 3, #C38978 Bulk   Bottle: 10-100L..........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  DOA Calibrator 4, #C38980 Bulk   Bottle: 10-100L..........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  DOA Calibrator 4, #C38980P       Bottle: 20-300L..........     10/22/93
                                          Pilot Solution.                                                       
Medical Analysis Systems, Inc..........  DOA Control 2, #1912 Bulk        Bottle: 20-200L..........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  DOA Control 3, #1943 Bulk        Bottle: 20-100L..........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  DOA Control 3, #1913 Bulk        Bottle: 20-300L..........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  DOA Control 4, #1914 Bulk        Bottle: 20-300L..........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  DOA Control 4, #1914P Pilot      Bottle: .1-1L............     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  DOA Control 4, #1944 Bulk        Bottle: 20-100L..........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  DOA Control 4, #1944P Pilot      Bottle: .1-1L............     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  DOA Control G2, #1915 Bulk       Bottle: 20-200L..........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  DOA Control G3, #1916 Bulk       Bottle: 20-300L..........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  DOA Control G4, #1917 Bulk       Bottle: 20-300L..........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  DOA Control G4, #1917P Pilot     Bottle: .1-1L............     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  DOA Cutoff Control, #1946 Bulk   Bottle: 1-10L............     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  DOA Cutoff Control, #1946P       Bottle: .1-1L............     10/22/93
                                          Pilot Solution.                                                       
Medical Analysis Systems, Inc..........  DOA High Control, #1945 Bulk     Bottle: 1-10L............     10/22/93
                                          Solution.                                                             

[[Page 151]]

                                                                                                                
Medical Analysis Systems, Inc..........  DOA Liquid Drugs of Abuse        Vial: 5ml, 18ml; Box: 6-      10/12/90
                                          Controls Level 2, 3, 4.          8ml vials; Box: 8-5ml                
                                                                           vials.                               
Medical Analysis Systems, Inc..........  DOA Low Cointrol, #1947 Bulk     Bottle: 1-10L............     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  DOA Positive Control, #1924      Bottle: 10-100L..........     10/22/93
                                          Bulk Solution.                                                        
Medical Analysis Systems, Inc..........  DOA Positive Control, #1924P     Bottle: .1-1L............     10/22/93
                                          Pilot Solution.                                                       
Medical Analysis Systems, Inc..........  DOA Positive Control, #C38981    Bottle: 10-100L..........     10/22/93
                                          Bulk Solution.                                                        
Medical Analysis Systems, Inc..........  Diazepam, #430 Intermediate      Bottle: 10-100ml.........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  Liquid Urine Control Level 1...  Vial: 5 ml...............      4/03/87
Medical Analysis Systems, Inc..........  Liquimmune Immunoassay Control   Bottle: 40-100L..........     10/22/93
                                          1, #2300 Bulk Solution.                                               
Medical Analysis Systems, Inc..........  Liquimmune Immunoassay Control   Bottle: .1-1L............     10/22/93
                                          1, #2300P Pilot Solution.                                             
Medical Analysis Systems, Inc..........  Liquimmune Immunoassay Control   Bottle: 20-300L..........     10/22/93
                                          2, #2301 Bulk Solution.                                               
Medical Analysis Systems, Inc..........  Liquimmune Immunoassay Control   Bottle: 20-300L..........     10/22/93
                                          3, #2302 Bulk Solution.                                               
Medical Analysis Systems, Inc..........  Liquimmune Immunoassay Control   Bottle: .1-1L............     10/22/93
                                          3, #2302P Pilot Solution.                                             
Medical Analysis Systems, Inc..........  Methadone, #438 Intermediate     Bottle: 10-250ml.........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  Methaqualone, #439 Intermediate  Bottle: 10-250ml.........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  Morphine Glucuronide, #433       Bottle: 10-100ml.........     10/22/93
                                          Intermediate Solution.                                                
Medical Analysis Systems, Inc..........  Morphine, #434 Intermediate      Bottle: 10-250ml.........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  Nordiazepam, #431 Intermediate   Bottle: 10-250ml.........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  Pentobarbital, #426              Bottle: 10-100ml.........     10/22/93
                                          Intermediate Solution.                                                
Medical Analysis Systems, Inc..........  Phencyclidine, #437              Bottle: 10-100ml.........     10/22/93
                                          Intermediate Solution.                                                
Medical Analysis Systems, Inc..........  Phenobarbital, #418              Bottle: 50-700ml.........     10/22/93
                                          Intermediate Solution.                                                
Medical Analysis Systems, Inc..........  Phenobarbital, #425              Bottle: 10-100ml.........     10/22/93
                                          Intermediate Solution.                                                
Medical Analysis Systems, Inc..........  Phenobarbital, #745              Bottle: 50-200ml.........     10/22/93
                                          Intermediate Solution.                                                
Medical Analysis Systems, Inc..........  Propoxyphene, #440 Intermediate  Bottle: 10-250ml.........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  Secobarbital, #427 Intermediate  Bottle: 10-250ml.........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  TDM Plus.XL Level I, II or III   Bottle: 5ml, Box: 6             9/5/90
                                          Unassayed Enhanced Liquid Drug   bottles.                             
                                          Control.                                                              
Medical Analysis Systems, Inc..........  Testosterone, #748 Intermediate  Bottle: 50-200ml.........     10/22/93
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  Therapeutic Drug Monitoring      Bottle: 20-300L..........     10/22/93
                                          Control 1, #1581 Bulk Solution.                                       
Medical Analysis Systems, Inc..........  Therapeutic Drug Monitoring      Bottle: 20-300L..........     10/22/93
                                          Control 2, #1582 Bulk Solution.                                       
Medical Analysis Systems, Inc..........  Therapeutic Drug Monitoring      Bottle: 20-300L..........     10/22/93
                                          Control 3, #1583 Bulk Solution.                                       
Medical Analysis Systems, Inc..........  Therapeutic Drug Monitoring      Bottle: .1-1L............     10/22/93
                                          Control 3, #1583P Pilot                                               
                                          Solution.                                                             
Medical Analysis Systems, Inc..........  Transfer Pilot Material          Glass vial: 3-5ml........      7/29/94
                                          Calibrators; Levels 2, 3, 4, 5.                                       
Medical Analysis Systems, Inc..........  Transfer Pilot Material          Glass vial: 3-5ml........      7/29/94
                                          Controls; Negative QC and                                             
                                          Positive QC.                                                          
Medical Analysis Systems, Inc..........  Tri-Point LiquImmune Ligand      Glass Bottle: 5ml; Kit: 6     10/23/91
                                          Control, Levels 1, 2 and 3.      Bottles.                             
Medical Analysis Systems, Inc..........  Tri-Point LiquImmune Ligand      Glass Bottle: 5ml; Kit: 6     10/23/91
                                          Control, Levels 1, 2 and 3.      bottles.                             
Medical Analysis Systems, Inc..........  chemTRAK Liquid Unassayed        Kit: 65ml Vials..........      10/8/86
                                          Therapeuitic Drug Control                                             
                                          Level 2.                                                              

[[Page 152]]

                                                                                                                
Medical Analysis Systems, Inc..........  chemTRAK Liquid Unassayed        Kit: 65ml Vials..........      10/8/86
                                          Therapeutic Drug Control Level                                        
                                          3.                                                                    
Medical Analysis Systems, Inc..........  chemTRAK Liquid Unassayed        Kit: 65ml Vials..........      10/8/86
                                          Therapeutic Drug Control Level                                        
                                          I.                                                                    
Medical Analysis Systems, Inc..........  chemTrak Liquid Unassayed......  Vial: 15ml...............      4/30/85
Meloy Labs, Inc........................  Counterelectrophoresis Plates,   Plates: 10 determinations       9/5/73
                                          G-301.                                                                
Meloy Labs, Inc........................  Immunoelectrophoresis Plates, G- Plates: 6 / unit.........       9/5/73
                                          201.                                                                  
Merck and Co., Inc.....................  Amphetamine - d6 HCl, Cat. No.   Ampule: 2 or 5ml.........      8/30/89
                                          MD-3892.                                                              
Merck and Co., Inc.....................  Cocaine-d3 HCl Catalog # MD-     Ampule: 2 or 5ml.........      6/13/88
                                          3677.                                                                 
Merck and Co., Inc.....................  Codeine - d3 H2O (N-methyl-d3)   2ml, 5ml ampule Carton: 5       9/6/88
                                          No. MD-3776.                     ampules.                             
Merck and Co., Inc.....................  Codeine-d3 Catalog # MD-3678...  Ampule: 2 or 5ml.........      6/13/88
Merck and Co., Inc.....................  DL-1 Phenyl-2-aminopropane 1,    Ampule: 2 or 5ml.........      6/13/88
                                          1, 2, 3, 3, 3, -d6                                                    
                                          (Amphetamine-d6) Catalog # MD-                                        
                                          3682.                                                                 
Merck and Co., Inc.....................  DL-1 Phenyl-2-                   Ampule: 2 or 5ml.........      6/13/88
                                          methylaminopropane-1, 1, 2, 3,                                        
                                          3, 3-d6 HCl (Methamphetamine                                          
                                          d6) Catalog # MD-3683.                                                
Merck and Co., Inc.....................  DL-1-Phenyl-2-aminopropane-1,    2ml, 5ml amber ampule           9/6/88
                                          1, 2, 3, 3, 3-d6 HCL No. MD-     Carton: 5 ampules.                   
                                          3778.                                                                 
Merck and Co., Inc.....................  Ecgonine - d3 Methyl Ester HCl   Ampule: 2 or 5ml.........      6/13/88
                                          Catalog # MD- 3679.                                                   
Merck and Co., Inc.....................  Methamphetamine - d9 HCl, Cat.   Ampule: 2 or 5ml.........      8/30/89
                                          No. MD-3853.                                                          
Merck and Co., Inc.....................  Morphine - d3 HCl 3H20 (N-       2ml, 5ml ampule Carton: 5       9/6/88
                                          methyl-d3) No. MD-3777.          ampules.                             
Merck and Co., Inc.....................  Morphine - d3 HCl Catalog # MD-  Ampule: 2 or 5 ml........      6/13/88
                                          3680.                                                                 
Merck and Co., Inc.....................  O-Benzoylecgonine-d3 Catalog #   Ampule: 2 or 5 ml........      6/13/88
                                          MD-3676.                                                              
Merck and Co., Inc.....................  Phen-d5-cyclidine HCl Catalog #  Ampule: 2 or 5 ml........      6/13/88
                                          MD-3681.                                                              
Microdiagnostics, Inc..................  Amphetamine Bulk Tracer........  Tube: 1ml; Bottle: 10ml,       1/17/96
                                                                           100ml, 500ml.                        
Microdiagnostics, Inc..................  Amphetamine Enzyme Conjugate...  Bottle: 10ml.............     12/24/92
Microdiagnostics, Inc..................  Benzoylecgonine Bulk Tracer....  Tube: 1ml; Bottle: 10ml,       1/17/96
                                                                           100ml, 500ml.                        
Microdiagnostics, Inc..................  Cocaine Enzyme Conjugate.......  Bottle: 10ml.............     12/24/92
Microdiagnostics, Inc..................  EIA for Amphetamine Metabolites  Kit: 2 bottles...........     12/24/92
Microdiagnostics, Inc..................  EIA for Cocaine Metabolites....  Kit: 2 bottles...........     12/24/92
Microdiagnostics, Inc..................  EIA for Marijuana Metabolites..  Kit: 2 bottles...........     12/24/92
Microdiagnostics, Inc..................  EIA for Opiate Metabolites.....  Kit: 2 bottles...........     12/24/92
Microdiagnostics, Inc..................  EIA for PCP Metabolites........  Kit: 2 bottles...........     12/24/92
Microdiagnostics, Inc..................  Morphine Bulk Tracer...........  Tube: 1ml; Bottle: 10ml,       1/17/96
                                                                           100ml, 500ml.                        
Microdiagnostics, Inc..................  Opiate Enzyme Conjugate........  Bottle: 10ml.............     12/24/92
Microdiagnostics, Inc..................  PCP Enzyme Conjugate...........  Bottle: 10ml.............     12/24/92
Microdiagnostics, Inc..................  Phencyclidine Bulk Tracer......  Tube: 1ml; Bottle: 10ml,       1/17/96
                                                                           100ml, 500ml.                        
Microdiagnostics, Inc..................  Positive Amphetamine Standard..  Bottle: 2ml..............     12/24/92
Microdiagnostics, Inc..................  Positive Cocaine Standard......  Bottle: 2ml..............     12/24/92
Microdiagnostics, Inc..................  Positive Opiate Standard.......  Bottle: 2ml..............     12/24/92
Microdiagnostics, Inc..................  Positive PCP Standard..........  Bottle: 2ml..............     12/24/92
Microdiagnostics, Inc..................  Positive THC Standard..........  Bottle: 2ml..............     12/24/92
Microdiagnostics, Inc..................  THC Enzyme Conjugate...........  Bottle: 10ml.............     12/24/92
Microdiagnostics, Inc..................  Tetrahydrocannabinol Bulk        Tube: 1ml; Bottle: 10ml,       1/17/96
                                          Tracer.                          100ml, 500ml.                        
Microgenics Corporation................  4-Drug Barbiturate Spiking       Carboy: 2L...............      12/1/93
                                          Solution.                                                             
Microgenics Corporation................  4-Drug Cutoff Bulk Calibrator..  Carboy: 6L...............      12/1/93
Microgenics Corporation................  4-Drug High Bulk Calibrator....  Carboy: 4L...............      12/1/93
Microgenics Corporation................  4-Drug Intermediate Bulk         Carboy: 4L...............      12/1/93
                                          Calibrator.                                                           
Microgenics Corporation................  5-Drug Cutoff Bulk Calibrator..  Carboy: 4L...............      12/1/93
Microgenics Corporation................  Amphetamine ED Bulk Reagent....  Carboy: 25L..............      4/13/94
Microgenics Corporation................  Amphetamine Manufacturing Bulk   Carboy or Beaker: 4L.....      4/20/94
                                          Calibrators B, C, D, E, F, G,                                         
                                          H, I, J, K, Open.                                                     
Microgenics Corporation................  Amphetamine Manufacturing        Vial: 3.5 or 5.0ml.......      4/20/94
                                          Calibrators B, C, D, E, F, G,                                         
                                          H, I, J, K, Open.                                                     
Microgenics Corporation................  Amphetamine/Methamphetamine      Carboy or Beaker: 4L.....      4/20/94
                                          Bulk Manufacturing Calibrator                                         
                                          Open.                                                                 
Microgenics Corporation................  Amphetamine/Methamphetamine      Vial: 3.5 or 5.0ml.......      4/20/94
                                          Manufacturing Calibrator Open.                                        
Microgenics Corporation................  Amphetamines Spiking Solution..  Carboy: 2L...............      12/1/93
Microgenics Corporation................  Barbiturate Manufacturing Bulk   Carboy or Beaker: 4L.....      4/20/94
                                          Calibrators B, C, D, E, F, G,                                         
                                          H, I, J, K, Open.                                                     
Microgenics Corporation................  Barbiturate Spiking Solution...  Carboy: 2L...............      12/1/93
Microgenics Corporation................  Barbiturate/Benzodiazepine 200   Carboy: 4L...............      12/1/93
                                          Cutoff Calibrator.                                                    
Microgenics Corporation................  Barbiturate/Benzodiazepine 300   Carboy: 2L...............      12/1/93
                                          Cutoff Calibrator.                                                    
Microgenics Corporation................  Barbiturate/Benzodiazepine High  Carboy: 2L...............      12/1/93
                                          Bulk Calibrator.                                                      

[[Page 153]]

                                                                                                                
Microgenics Corporation................  Barbiturate/Benzodiazepine       Carboy: 2L...............      12/1/93
                                          Intermediate Bulk Calibrator.                                         
Microgenics Corporation................  Barbiturates Manufacturing       Vial: 3.5 or 5.0ml.......      4/20/94
                                          Calibrators B, C, D, E, F, G,                                         
                                          H, I, J, K, Open.                                                     
Microgenics Corporation................  Benzodiazepine Ethanol Stock...  Vial: 25ml...............      12/1/93
Microgenics Corporation................  Benzodiazepine Manufacturing     Carboy or Beaker: 4L.....      4/20/94
                                          Bulk Calibrators B, C, D, E,                                          
                                          F, G, H, I, J, K, Open.                                               
Microgenics Corporation................  Benzodiazepine Manufacturing     Vial: 3.5 or 5.0ml.......      4/20/94
                                          Calibrators B, C, D, E, F, G,                                         
                                          H, I, J, K, Open.                                                     
Microgenics Corporation................  Benzodiazepine Spiking Solution  Carboy: 2L...............      12/1/93
Microgenics Corporation................  Bulk Calibrator Solution 80ug/   Carboy: 10L..............     11/13/90
                                          ml, 40ug/ml.                                                          
Microgenics Corporation................  CEDAI DAU Opiate Assay Cat # 80- Kit: 4 Bottles, 500ml....      12/1/93
                                          3000.                                                                 
Microgenics Corporation................  CEDIA DAU 4-Drug Cutoff          Bottle: 10, 15ml.........      12/1/93
                                          Calibrator.                                                           
Microgenics Corporation................  CEDIA DAU 4-Drug High            Bottle: 10, 15ml.........      12/1/93
                                          Calibrator.                                                           
Microgenics Corporation................  CEDIA DAU 4-Drug Intermediate    Bottle: 10, 15ml.........      12/1/93
                                          Calibrator.                                                           
Microgenics Corporation................  CEDIA DAU 5-Drug Cutoff          Bottle: 5, 15ml..........      12/1/93
                                          Calibrator.                                                           
Microgenics Corporation................  CEDIA DAU Amphetamine Assay      Kit: 4 Bottles...........      4/13/94
                                          (For 85ml, 500ml).                                                    
Microgenics Corporation................  CEDIA DAU Amphetamine ED         Vial: 100ml, 500ml.......      4/13/94
                                          Reagent.                                                              
Microgenics Corporation................  CEDIA DAU Barb/Benz 200          Bottle: 10, 15ml.........      12/1/93
                                          Calibrator.                                                           
Microgenics Corporation................  CEDIA DAU Barb/Benz 300          Bottle: 10, 15ml.........      12/1/93
                                          Calibrator.                                                           
Microgenics Corporation................  CEDIA DAU Barb/Benz High         Bottle: 10, 15ml.........      12/1/93
                                          Calibrator.                                                           
Microgenics Corporation................  CEDIA DAU Barb/Benz              Bottle: 10, 15ml.........      12/1/93
                                          Intermediate Calibrator.                                              
Microgenics Corporation................  CEDIA DAU Cocaine Assay Cat #    Kit: 4 Bottles, 85ml.....      12/1/93
                                          80-2300.                                                              
Microgenics Corporation................  CEDIA DAU Cocaine Assay Cat #    Kit: 4 Bottles, 500ml....      12/1/93
                                          80-2400.                                                              
Microgenics Corporation................  CEDIA DAU Cocaine ED Reagent,    Vial: 100ml..............      12/1/93
                                          Cat # 80-2300.                                                        
Microgenics Corporation................  CEDIA DAU Cocaine ED Reagent,    Vial: 500ml..............      12/1/93
                                          Cat # 80-2400.                                                        
Microgenics Corporation................  CEDIA DAU Multi-Drug Control     2 Vials; 5ml/vial........      5/10/94
                                          Set, #80-0120.                                                        
Microgenics Corporation................  CEDIA DAU Multi-Level THC Assay  Kit: 4 Bottles, 85ml.....      12/1/93
                                          Cat # 80-2700.                                                        
Microgenics Corporation................  CEDIA DAU Multi-Level THC Assay  Kit: 4 Bottles, 500ml....      12/1/93
                                          Cat # 80-2800.                                                        
Microgenics Corporation................  CEDIA DAU Multi-Level THC ED     Vial: 100ml..............      12/1/93
                                          Reagent, Cat # 80-2700.                                               
Microgenics Corporation................  CEDIA DAU Multi-Level THC ED     Vial: 500ml..............      12/1/93
                                          Reagent, Cat # 80-2800.                                               
Microgenics Corporation................  CEDIA DAU Multi-grug Control     2 Vials; 15ml/vial.......      5/10/94
                                          Set, #80-0124.                                                        
Microgenics Corporation................  CEDIA DAU Opiate Assay Cat # 80- Kit: 4 Bottles, 85ml.....      12/1/93
                                          2900.                                                                 
Microgenics Corporation................  CEDIA DAU Opiate ED Reagent,     Vial: 100ml..............      12/1/93
                                          Cat # 80-2900.                                                        
Microgenics Corporation................  CEDIA DAU Opiates ED Reagent,    Vial: 500ml..............      12/1/93
                                          Cat # 80-3000.                                                        
Microgenics Corporation................  CEDIA DAU PPX/METD Cutoff        Vial: 10ml...............       3/2/95
                                          Calibrator.                                                           
Microgenics Corporation................  CEDIA DAU PPX/METD High          Vial: 10ml...............       3/2/95
                                          Calibrator.                                                           
Microgenics Corporation................  CEDIA DAU PPX/METD Intermediate  Vial: 10ml...............       3/2/95
                                          Calibrator.                                                           
Microgenics Corporation................  CEDIA DAU Specialty Control Set  2 Vials; 15ml/vial.......      5/10/94
                                          1, #80-0121.                                                          
Microgenics Corporation................  CEDIA DAU Specialty Control Set  2 Vials; 15ml/vial.......      5/10/94
                                          2, #80-0122.                                                          
Microgenics Corporation................  CEDIA DAU THC 100ng/ml           Bottle: 15ml.............      12/1/93
                                          Calibrator.                                                           
Microgenics Corporation................  CEDIA DAU THC 150ng/ml           Bottle: 15ml.............      12/1/93
                                          Calibrator.                                                           
Microgenics Corporation................  CEDIA DAU THC 25ng/ml            Bottle: 15ml.............      12/1/93
                                          Calibrator.                                                           
Microgenics Corporation................  CEDIA DAU THC 50ng/ml            Bottle: 15ml.............      12/1/93
                                          Calibrator.                                                           
Microgenics Corporation................  CEDIA DAU THC 75ng/ml            Bottle: 15ml.............      12/1/93
                                          Calibrator.                                                           
Microgenics Corporation................  Cocaine Conjugate..............  Vial: 25ml...............      12/1/93
Microgenics Corporation................  Cocaine ED Bulk Reagent........  Carboy: 25L..............      12/1/93
Microgenics Corporation................  Cocaine Manufacturing Bulk       Carboy or Beaker: 4L.....      4/20/94
                                          Calibrators B, C, D, E, F, G,                                         
                                          H, I, J, K, Open.                                                     
Microgenics Corporation................  Cocaine Manufacturing            Vial: 3.5 or 5.0ml.......      4/20/94
                                          Calibrators B, C, D, E, F, G,                                         
                                          H, I, J, K, Open.                                                     
Microgenics Corporation................  Cocaine Spiking Solution.......  Carboy: 2L...............      12/1/93
Microgenics Corporation................  In-house Phenobarbital Bulk      Bottle: 2L...............     11/13/90
                                          Primary Standard 40ug/ml, 80ug/                                       
                                          ml.                                                                   
Microgenics Corporation................  In-house Phenobarbital Primary   Micro tube: 1.5ml; Box:       11/13/90
                                          Standard 40ug/ml, 80ug/ml.       100 tubes.                           
Microgenics Corporation................  In-house manufacturing Bulk      Bottle: 2L...............     11/13/90
                                          Calibrator 10ug/ml, 20ug/ml,                                          
                                          40 ug/ml, 60ug/ml, 80ug/ml,                                           
                                          90ug/ml Phenobarbital.                                                
Microgenics Corporation................  In-house manufacturing           Vial: 3.5ml..............     11/13/90
                                          Calibrator 10ug/ml, 20ug/ml,                                          
                                          40ug/ml, 60ug/ml80ug/ml, 90ug/                                        
                                          ml Phenobarbital.                                                     
Microgenics Corporation................  Methadone Spiking Solution.....  Vial: 2L.................       3/2/95
Microgenics Corporation................  Methamphetamine Conjugate......  Vial: 25ml...............      4/13/94
Microgenics Corporation................  Methamphetamine Manufacturing    Carboy or Beaker: 4L.....      4/20/94
                                          Bulk Calibrators B, C, D,                                             
                                          E.F.G.H, I, J, K, Open.                                               
Microgenics Corporation................  Methamphetamine Manufacturing    Vial: 3.5ml or 5.0ml.....      4/20/94
                                          Calibrators B, C, D, E, F, G,                                         
                                          H, I, J, K, Open.                                                     
Microgenics Corporation................  Microgenics CEDIA Phenobarbital  Vial: 3.5ml; Kit: 2 vials     11/13/90
                                          Assay 40ug/ml, 80ug/ml.                                               
Microgenics Corporation................  Morphine Conjugate.............  Vial: 25ml...............      12/1/93

[[Page 154]]

                                                                                                                
Microgenics Corporation................  Opiate ED Bulk Reagent.........  Carboy: 25L..............      12/1/93
Microgenics Corporation................  Opiate Manufacturing Bulk        Carboy or Beaker: 4L.....      4/20/94
                                          Calibrators E, F, G, H, I, J,                                         
                                          K, Open.                                                              
Microgenics Corporation................  Opiate Manufacturing             Vial: 3.5 or 5.0ml.......      4/20/94
                                          Calibrators E, F, G, H, I, J,                                         
                                          K, Open.                                                              
Microgenics Corporation................  Opiate Spiking Solution........  Carboy: 2L...............      12/1/93
Microgenics Corporation................  PCP Spiking Solution...........  Carboy: 2L...............      12/1/93
Microgenics Corporation................  PCP Stock Concentrate..........  Vial: 10ml...............      12/1/93
Microgenics Corporation................  Phencyclidine Manufacturing      Carboy or Beaker: 4L.....      4/20/94
                                          Bulk Calibrators E, F, G, H,                                          
                                          I, J, K, Open.                                                        
Microgenics Corporation................  Phencyclidine Manufacturing      Vial: 3.5 or 5.0ml.......      4/20/94
                                          Calibrators E, F, G, H, I, J,                                         
                                          K, Open.                                                              
Microgenics Corporation................  Phenobarbital Stock Solution...  Flask: 100ml.............     11/13/90
Microgenics Corporation................  Propoxyphene/Methadone Cutoff    Bulk: 4L.................       3/2/95
                                          Calibrator.                                                           
Microgenics Corporation................  Propoxyphene/Methadone High      Bulk: 4L.................       3/2/95
                                          Calibrator.                                                           
Microgenics Corporation................  Propoxyphene/Methadone           Bulk: 4L.................       3/2/95
                                          Intermediate Calibrator.                                              
Microgenics Corporation................  THC 100 Control Set............  Box: 2 Bottles; 15ml each      6/30/94
Microgenics Corporation................  THC 100 Controls (High & Low)..  Bottle: 15ml.............      6/30/94
Microgenics Corporation................  THC 100 Controls (High & Low)    Carboy: 150L.............      6/30/94
                                          Bulk.                                                                 
Microgenics Corporation................  THC 100ng/ml Bulk Calibrator...  Carboy: 4L...............      12/1/93
Microgenics Corporation................  THC 150ng/ml Bulk Calibrator...  Carboy: 4L...............      12/1/93
Microgenics Corporation................  THC 25 Control Set.............  Box: 2 Bottles; 15ml each      6/30/94
Microgenics Corporation................  THC 25 Controls (High & Low)...  Bottle: 15ml.............      6/30/94
Microgenics Corporation................  THC 25 Controls (High & Low)     Carboy: 150L.............      6/30/94
                                          Bulk.                                                                 
Microgenics Corporation................  THC 25ng/ml Bulk Calibrator....  Carboy: 2L...............      12/1/93
Microgenics Corporation................  THC 50 Control Set.............  Box: 2 Bottles; 15ml each      6/30/94
Microgenics Corporation................  THC 50 Controls (High & Low)...  Bottle: 15ml.............      6/30/94
Microgenics Corporation................  THC 50 Controls (High & Low)     Carboy: 150L.............      6/30/94
                                          Bulk.                                                                 
Microgenics Corporation................  THC 50ng/ml Bulk Calibrator....  Carboy: 4L...............      12/1/93
Microgenics Corporation................  THC 75ng/ml Bulk Calibrator....  Carboy: 1L...............      12/1/93
Microgenics Corporation................  THC Conjugate..................  Vial: 25ml...............      12/1/93
Microgenics Corporation................  THC ED Bulk Reagent............  Carboy: 25L..............      12/1/93
Microgenics Corporation................  THC Manufacturing Bulk           Carboy or Beaker: 4L.....      4/20/94
                                          Calibrators B, C, D, E, F, G,                                         
                                          H, I, J, K, L, Open.                                                  
Microgenics Corporation................  THC Manufacturing Calibrators    Vial: 3.5 or 5.0ml.......      4/20/94
                                          B, C, D, E, F, G, H, I, J, K,                                         
                                          L, Open.                                                              
Micromedic Systems.....................  Micromedic Neonatal T4 125I      Nalgene Bottle: 4 oz.....      6/25/87
                                          Tracer Solution.                                                      
Micromedic Systems.....................  Micromedic Neonatal T4 Elution   Nalgene Bottle: 2 oz.....      6/25/87
                                          Solution.                                                             
Micromedic Systems.....................  Neonatal T4 125I Tracer          Vial: 30ml...............      5/21/80
                                          Solution.                                                             
Micromedic Systems.....................  Neonatal T4 Buffer Solution....  Bottle: 8ounce...........      5/21/80
Micromedic Systems.....................  T3 RIA 125I Tracer Solution....  Vial: 30ml...............     12/14/76
Micromedic Systems.....................  T3 RIA Buffer Solution.........  High Density Polyethylene     12/14/76
                                                                           Bottle: 8 ounce.                     
Micromedic Systems.....................  T3 Uptake 125I Tracer Solution.  Vial: 30ml...............     12/14/76
Micromedic Systems.....................  T3 Uptake Buffer Solution......  High Density Polyethylene     12/14/76
                                                                           Bottle: 8 ounce.                     
Micromedic Systems.....................  T4 RIA 125I Tracer Solution....  Vial: 30ml...............     12/14/76
Micromedic Systems.....................  T4 RIA Buffer Solution.........  High Density Polyethylene     12/14/76
                                                                           Bottle: 8 ounce.                     
Miles Inc..............................  Immuno-1 Setpoint TDM            Glass Bottles: 5ml; Kit:        1/3/91
                                          Calibrators Kit No. T03-2864     5 Bottles.                           
                                          Component No. T13-2864(02-06).                                        
Miles Inc..............................  Technicon Immuno 1 TESTpoint     Glass vial; 5ml; Kit: 6        3/16/92
                                          Ligand Controls, Kit No. T03-    vials.                               
                                          3393-01; Level I T13-3394-01;                                         
                                          Level II T13-3395-01; Level                                           
                                          III T13-3396-01.                                                      
Miles Inc..............................  Technicon RA Systems Set Point.  Vial: 5ml Kit: 5 vials...      7/20/90
Miles Laboratories, Inc................  SERALYZER ARIS Phenobarbital     Kit: 2 vials; 1ml/vial...      4/29/93
                                          Calibrator Kit, # 6453.                                               
Miles Laboratories, Inc................  SERALYZER ARIS Phenobarbital     Kit: 4 vials; 1ml/vial...      4/29/93
                                          Calibrator and Control Kit, #                                         
                                          6455T.                                                                
Miles Laboratories, Inc................  SERALYZER ARIS Phenobarbital     Kit: 2 vials; 1ml/vial...      4/29/93
                                          Control Kit, # 6454T.                                                 
Miles Laboratories, Inc................  SERALYZER ARIS Phenytoin Bulk    Bulk.....................      6/15/94
                                          Reagent Paper.                                                        
Miles Laboratories, Inc................  Seralyzer ARIS Drug Assay        Vial: 1ml................      1/17/84
                                          Control.                                                              
Miles Laboratories, Inc................  Seralyzer ARIS Drug Assay High   Vial: 0.5ml..............      1/17/84
                                          Calibrator.                                                           
Miles Laboratories, Inc................  Seralyzer ARIS Drug Assay Low    Vial: 0.5ml..............      1/17/84
                                          Calibrator.                                                           
Miles Laboratories, Inc................  Seralyzer ARIS Phenytoin         Bottle Containing 25 and       5/28/86
                                          Reagent Strips.                  50 Strips.                           
Miles Laboratories, Inc................  T-4 Buffer.....................  Glass Screwtop Vial: \3/       3/28/77
                                                                           4\ ounce.                            
Monobind, Inc..........................  Monobind T3 Antibody Reagent...  Test Tube w/Cap: 70ml....      11/8/77
Monobind, Inc..........................  Monobind T3 Tracer Reagent.....  Wheaton Glass Container:       11/8/77
                                                                           55ml.                                

[[Page 155]]

                                                                                                                
Monobind, Inc..........................  Monobind T4 Antibody Reagent...  Test Tube w/Cap: 70ml....      11/8/77
Monobind, Inc..........................  Monobind T4 Tracer Reagent.....  Wheaton Glass Container        11/8/77
                                                                           55ml.                                
Monobind, Inc..........................  Monobind TSH Antibody Reagent..  Test Tube w/Cap: 10.5ml..      11/8/77
Monobind, Inc..........................  Monobind TSH Non-Specific        Wheaton Glass: 1.05ml....      11/8/77
                                          Buffer.                                                               
Monobind, Inc..........................  Monobind TSH Precipitating       Plastic Container w/Cap :      11/8/77
                                          Reagent.                         105ml.                               
Monobind, Inc..........................  Monobind TSH Tracer Reagent....  Wheaton Glass Container        11/8/77
                                                                           10.5ml.                              
Monobind, Inc..........................  T3 Adsorbent Reagent...........  Glass Bottle: 110ml, 50ml      5/15/78
                                                                           Plastic Bottle: 260ml.               
Monobind, Inc..........................  T3 Uptake Tracer Reagent.......  Glass Bottle: 55ml, 30ml       5/15/78
                                                                           Plastic Bottle: 125ml.               
Monobind, Inc..........................  TSH Radioimmunoassay Test        Kit: 100 Tests...........      11/8/77
                                          System.                                                               
Monobind, Inc..........................  Thyroxine Radioimmunoassay Test  Kit: 100 Tests...........      11/8/77
                                          System.                                                               
Monobind, Inc..........................  Triiodothyronine                 Kit: 100 tests...........      11/8/77
                                          Radioimmunoassay Test System.                                         
Monoclonal Antibodies, Inc.............  Test Kit for Cocaine             Kit: 50 tests............     10/17/86
                                          Metabolites in Urine.                                                 
Monoclonal Antibodies, Inc.............  Test Kit for Opiates in Urine..  Kit: 50 tests............     10/17/86
Monoclonal Antibodies, Inc.............  Test Kit for                     Kit: 50 tests............     10/17/86
                                          Tetrahydrocannabinol (THC) in                                         
                                          Urine.                                                                
NSI Technology Services Corp...........  Alpha, alpha-dimethyl-           Amber Ampoule: 2ml.......      3/02/89
                                          phenethylamine.                                                       
Nuclear Diagnostics, Inc...............  MAAT T3 Uptake Reagent.........  Bottle: 105ml, 210ml;         11/16/90
                                                                           Kit: 1 bottle 210ml.                 
Nuclear Diagnostics, Inc...............  SPINSEP-TBG Reagent Catalog No.  Polypropylene Bottle:         12/15/77
                                          17100.                           105ml.                               
Nuclear Diagnostics, Inc...............  TETRIA P.E.G. Antiserum Catalog  Polypropylene Bottle:          3/10/78
                                          No. 16100A.                      55ml.                                
Nuclear Diagnostics, Inc...............  TETRIA P.E.G. Reagent Catalog    Polypropylene Bottle:           7/8/77
                                          No. 16100.                       105ml.                               
Nuclear Diagnostics, Inc...............  TETRIA P.E.G. Reagent Catalog    Polypropylene Bottle:          3/10/78
                                          No. 16100R.                      55ml.                                
Nuclear Diagnostics, Inc...............  TRIA-P.E.G. Antiserum Catalog    Polypropylene Bottle:          3/10/78
                                          No. 12100A.                      55ml.                                
Nuclear Diagnostics, Inc...............  TRIA-P.E.G. Reagent Catalog      Polypropylene Bottle:          3/10/78
                                          No.12100R.                       55ml.                                
OMI International Corporation..........  Compound N Solution............  Steel Drum: 55 gallon....      10/1/75
Organon Teknika Corp...................  Barbital Buffered Saline with    Plastic Bottle: 1L.......       1/5/90
                                          Azide.                                                                
Organon Teknika Corp...................  Modified Barbital Buffer.......  Plastic Bottle: 1L.......       1/5/90
Organon Teknika Corp...................  Owren's Veronal Buffer for       Bottle: 37 ml............       5/7/80
                                          FIBRIQUIK.                                                            
Organon Teknika Corp...................  Platelin.......................  Vial: 7.3ml..............      3/13/72
Organon Teknika Corp...................  Simplastin.....................  Vial: 4.7ml, 7.3ml, and        3/13/72
                                                                           16.5ml.                              
Organon Teknika Corp...................  Simplastin-A...................  Vial: 7.3ml..............      3/13/72
Organon Teknika Corp...................  TRIS/Barbital Buffer...........  Plastic Bottle: 1L.......       1/5/90
Ortho Diagnostic Systems, Inc..........  Activated ThromboFAX No.721000.  Bottle: 3.2ml............      9/21/71
Ortho Diagnostic Systems, Inc..........  ORTHO Owren's Buffer...........  Kit: 6-20 ml vials.......      8/26/88
Ortho Diagnostic Systems, Inc..........  Ortho Activated PTT Reagent....  Glass Vial: 30                 5/23/83
                                                                           determination size, 100.             
Ortho Diagnostic Systems, Inc..........  Ortho Plasma Coagulation         Glass Vial: 5ml..........     10/25/83
                                          Control Level I.                                                      
Ortho Diagnostic Systems, Inc..........  Ortho Plasma Coagulation         Glass Vial: 5ml..........     10/25/83
                                          Control Level II.                                                     
Ortho-McNeil Pharmaceutical............  Codeine-N-Oxide................  Bottle: 2ml..............     10/11/95
PB Diagnostic Systems, Inc.............  Estradiol Reagent..............  6 Vials; 1ml/vial........     10/28/93
PB Diagnostic Systems, Inc.............  Estradiol Test Module..........  Plastic plate: 1.7''x         10/28/93
                                                                           .7''x 3.5''.                         
PB Diagnostic Systems, Inc.............  OPUS Estradiol Kit.............  Kit: 50 Tests............     10/28/93
PB Diagnostic Systems, Inc.............  OPUS Phenobarbital Calibrators:  Vial: 2.5ml Carton: 5           8/7/90
                                          5, 10, 20, 40, 80g/ml.  vials.                               
PB Diagnostic Systems, Inc.............  OPUS Phenobarbital Test Modules  Plastic Test Module,            8/7/90
                                                                           Tray: 5 modules, Carton:             
                                                                           50 modules.                          
Pacific Hemostasis.....................  Barbital Buffered Saline.......  Vial: 100ml..............      5/24/84
Pacific Hemostasis.....................  Barbital Buffered Saline (Bulk)  Carboy: 100L.............      10/5/94
Pacific Hemostasis.....................  Barbital Buffered Saline with    Vial: 90ml...............      5/24/84
                                          Heparin.                                                              
Pacific Hemostasis.....................  Barbital Buffered Saline with    Carboy: 100L.............      10/5/94
                                          Heparin (Bulk).                                                       
Pacific Hemostasis.....................  Barbital Buffered with Heparin.  Bulk in Process..........      1/24/95
Pacific Hemostasis.....................  Diluting Fluid.................  Bulk in Process..........      1/24/95
Pacific Hemostasis.....................  Diluting Fluid.................  Vial: 20ml...............      5/24/84
Pacific Hemostasis.....................  Diluting Fluid (Bulk)..........  Carboy: 100L.............      10/5/94
Pacific Hemostasis.....................  Kontact........................  Bulk in Process..........      1/24/95
Pacific Hemostasis.....................  Kontact........................  Vial: 4ml, 10ml..........      3/22/94

[[Page 156]]

                                                                                                                
Pacific Hemostasis.....................  Kontact (Bulk).................  Carboy: 200L.............      10/5/94
Pacific Hemostasis.....................  Kontact Kit (10ml) Cat # 224-    Kit: 10 Vials............      3/22/94
                                          006.                                                                  
Pacific Hemostasis.....................  Kontact Kit (4ml) Cat # 257-324  Kit: 10 Vials............      3/22/94
Pantex.................................  Immuno T3 Kit: (1)L-             Kit Containing Bottles:         1/4/79
                                          Triiodothyronine 125I (2)1st     (1)10ml (2)10ml (3)50ml              
                                          Antiserum (3)2nd Antiserum       (4)5ml (5)3ml.                       
                                          (4)Diluent (5)Standards.                                              
Pantex.................................  Immuno-Digoxin Kit Containing:   Kit Containing Bottles:         1/4/79
                                          (1)Digoxin 125I (2)1st           (1)10ml (2)20ml (3)50ml              
                                          Antiserum (3) 2nd Antiserum      (4)5ml.                              
                                          (4)Diluent.                                                           
Pantex.................................  Immuno-Estriol 125I Kit: 2nd     Bottle: 50ml.............       1/4/79
                                          Antiserum.                                                            
Pantex.................................  Immuno-Estriol Kit: (1)Estriol   Kit Containing Bottles:         1/4/79
                                          3H RIA (2)Estriol 3H Recovery    (1)10ml (2)5ml (3)10ml               
                                          (3)1st Antiserum (4)2nd          (4)20ml (5)100ml (6)50ml             
                                          Antiserum (5)Diluent (6)Buffer   (7)5ml.                              
                                          (7)Standards.                                                         
Pantex.................................  Immuno-T4 Kit: (1)Thyroxine      Kit Containing Bottles:         1/4/79
                                          125I (2)1st Antiserum (3)2nd     (1)100ml, 1000ml (2)50ml             
                                          Antiserum (4)Diluent             (3)100ml (4)5ml (5)3ml.              
                                          (5)Standards.                                                         
Pantex.................................  Immuno-Testosterone 125I Kit:    Kit Containing Bottles:         1/4/79
                                          (1)Testosterone 125I (2)1st      (1)10ml (2)10ml (3)50ml              
                                          Antiserum (3)2nd Antiserum       (4)100ml (5)5ml.                     
                                          (4)Diluent (5)Standards.                                              
Pantex.................................  T3 Uptake Kit: L-                Bottle: 100ml, 1000ml....       1/4/79
                                          Triiodothyronine 125I.                                                
Perkin-Elmer Corporation...............  Amphetamine Polarization         Kit: 100 tests...........     12/18/86
                                          Fluoroimmunoassay Kit.                                                
Perkin-Elmer Corporation...............  Barbiturates Polarization        Kit: 100 tests...........     12/18/86
                                          Fluoroimmunoassay Kit.                                                
Perkin-Elmer Corporation...............  Cocaine Polarization             Kit: 100 tests...........     12/18/86
                                          Fluoroimmunoassay Kit.                                                
Perkin-Elmer Corporation...............  Methadone Polarization           Kit: 100 tests...........     12/18/86
                                          Fluoroimmunoassay Kit.                                                
Perkin-Elmer Corporation...............  Morphine Polarization            Kit: 100 tests...........     12/18/86
                                          Fluoroimmunoassay Kit.                                                
Perkin-Elmer Corporation...............  Opiates Polarization             Kit: 100 tests...........     12/18/86
                                          Fluoroimmunoassay Kit.                                                
Princeton Separations, Inc.............  Panagel 16.....................  Pouch: 1 slide...........      6/29/87
Princeton Separations, Inc.............  Panagel 8......................  Pouch: 1 slide...........      6/29/87
Princeton Separations, Inc.............  Panagel Electrobuffer..........  Fiber Drum: 25 kg........      6/29/87
Princeton Separations, Inc.............  Panagel Electrode Buffer.......  Pouch: 18.3 gms..........      6/29/87
Princeton Separations, Inc.............  Panagel LD Isoenzyme Electrode   Pouch: 11.85 gms.........      6/29/87
                                          Buffer.                                                               
Princeton Separations, Inc.............  Panagel LD Isoenzyme Slide.....  Pouch: 1 slide...........      6/29/87
Quality Assurance Service Corp.........  Q.A. Toxicology Blood Controls.  Vial: 6ml, 12ml Plastic        1/23/90
                                                                           Bottle: 60ml, 90ml,                  
                                                                           250ml, 625ml Glass                   
                                                                           Bottle: 6ml-100ml.                   
Quality Assurance Service Corp.........  Q.A. Toxicology Serum Controls.  Vial: 6ml, 12ml Plastic        1/23/90
                                                                           Bottle: 60ml, 90ml,                  
                                                                           250ml, 625ml Glass                   
                                                                           Bottle: 6ml-100ml.                   
Quality Assurance Service Corp.........  Q.A. Toxicology Urine Controls.  Vial: 6ml, 12ml Plastic        1/23/90
                                                                           Bottle: 60ml, 90ml,                  
                                                                           250ml, 625ml Glass                   
                                                                           Bottle: 6ml-100ml.                   
Quantimetrix...........................  Quantimetrix Anticonvulsant      Polyethylene Dropper           4/16/86
                                          Serum Drug Control, Liquid       Bottle: 15ml.                        
                                          Level II Control No. 17-0303-2.                                       
Quantimetrix...........................  Quantimetrix Antidepressant      Polyethylene Dropper           4/16/86
                                          Serum Drug Control, Liquid       Bottle: 15ml.                        
                                          Level I Control No. 17-0303-1.                                        
Quantimetrix...........................  Quantimetrix Antidepressant      Polyethylene Dropper           4/16/86
                                          Serum Drug Control, Liquid       Bottle: 15ml.                        
                                          Level I Control No. 17-0305-1.                                        
Quantimetrix...........................  Quantimetrix Antidepressant      Polyethylene Dropper           4/16/86
                                          Serum Drug Control, Liquid       Bottle: 15ml.                        
                                          Level II Control No. 17-0305-2.                                       
Quantimetrix...........................  Urine Drugs of Abuse Control     Dropper Bottle: 15 ml....      2/23/87
                                          Catalog No. 12-2411-1.                                                
Quin-Tec, Inc..........................  Additive SB-1..................  Drum: 55 gals............      5/11/87
Quin-Tec, Inc..........................  Quin-Tec Brightener 402........  Plastic Pail: 5 gallons,      10/13/81
                                                                           Plastic Drum: 55 gallons.            
Quin-Tec, Inc..........................  Quin-Tec Brightener 404........  Plastic Pail: 5 gallons,      10/13/81
                                                                           Plastic Drum: 55 gallons.            
Radian Corporation.....................  (+/-) 11-Nor-9-Carboxy-delta 9-  Vial: 2ml................      6/12/91
                                          THC-D9 0.01mg/ml, 0.1mg/ml,                                           
                                          1.0mg/ml.                                                             
Radian Corporation.....................  (-)-11-Nor-9-carboxy-delta-9     Vial: 2ml................      1/25/95
                                          THC; 1.0mg/ml, 100g/                                         
                                          ml.                                                                   
Radian Corporation.....................  17alpha-Methyl-5alpha-           Ampule: 2ml..............      7/07/95
                                          androstane-3alpha, 17beta-                                            
                                          diol, 100g/ml, 1mg/ml.                                       
Radian Corporation.....................  17alpha-Methyl-5beta-androstane- Ampule: 2ml..............      7/07/95
                                          3alpha, 17beta-diol, 100g/ml, 1mg/ml.                                                       
Radian Corporation.....................  2-S Methcathinone-D5 HCl         Ampule: 2ml..............     12/22/93
                                          100g/ml, 1.0mg/ml.                                           
Radian Corporation.....................  2R-Cathinone HCL 100g/  Ampule: 2ml..............     12/22/93
                                          ml, 1.0mg/ml.                                                         
Radian Corporation.....................  2R-Cathinone-D5 HCL 100g/ml, 1.0mg/ml.                                                     
Radian Corporation.....................  2R-Methcathinone HCL 100g/ml, 1.0mg/ml.                                                     

[[Page 157]]

                                                                                                                
Radian Corporation.....................  2R-Methcathinone-D5 HCL          Ampule: 2ml..............     12/22/93
                                          100g/ml, 1.0mg/ml.                                           
Radian Corporation.....................  2S-Cathinone HCL 100g/  Ampule: 2ml..............     12/22/93
                                          ml, 1.0mg/ml.                                                         
Radian Corporation.....................  2S-Cathinone-D5 HCL 100g/ml, 1.0mg/ml.                                                     
Radian Corporation.....................  2S-Methcathinone HCL 100g/ml, 1.0mg/ml.                                                     
Radian Corporation.....................  3'-Hydroxystanozolol-D3;         Ampule: 2ml..............      6/06/94
                                          100g/ml, 1.0mg/ml.                                           
Radian Corporation.....................  3'-Hydroxystanozolol; 100g/ml, 1.0mg/ml.                                                     
Radian Corporation.....................  3, 4-Methylenedioxy-amphetamine- 2 ml amber ampule........     10/19/88
                                          D5 0.1 mg/ml.                                                         
Radian Corporation.....................  3, 4-Methylenedioxy-amphetamine- 2 ml amber ampule........     10/19/88
                                          D5 1.0 mg/ml.                                                         
Radian Corporation.....................  3, 4-Methylenedioxy-             2 ml amber ampule........     10/19/88
                                          methamphetamine-D5 0.1 mg/ml.                                         
Radian Corporation.....................  3, 4-Methylenedioxy-             2 ml amber ampule........     10/19/88
                                          methamphetamine-D5 1.0 mg/ml.                                         
Radian Corporation.....................  3, 4-Methylenedioxyamphetamine   Amber glass ampule: 2ml..      1/12/89
                                          0.1, 1.0 mg/ml.                                                       
Radian Corporation.....................  3, 4-                            Amber glass ampule: 2ml..      1/12/89
                                          Methylenedioxymethamphetamine                                         
                                          0.1, 1.0 mg/ml.                                                       
Radian Corporation.....................  4-Methylaminorex 100g/  Ampule: 2ml..............      1/29/93
                                          ml, 1.0mg/ml.                                                         
Radian Corporation.....................  4-Methylaminorex-D5 100g/ml, 1.0mg/ml.                                                     
Radian Corporation.....................  6-Acetylmorphine...............  Ampule: 2 ml.............      12/4/87
Radian Corporation.....................  6-Acetylmorphine-D3............  Ampule: 2 ml.............      12/4/87
Radian Corporation.....................  6-Acetylmorphine-D6; 100g/ml, 1.0mg/ml.                                                     
Radian Corporation.....................  6beta-Hydroxyfluoxymesterone,    Ampule: 2ml..............       7/7/95
                                          100g/ml, 1mg/ml.                                             
Radian Corporation.....................  6beta-Hydroxymethandienone,      Ampule: 2ml..............       7/7/95
                                          100g/ml, 1mg/ml.                                             
Radian Corporation.....................  9-Carboxy-11-nor-Delta-9-        Ampule: 2 ml.............      12/4/87
                                          Tetrahydrocannabinol-D3.                                              
Radian Corporation.....................  9-Carboxy-11-nor-delta-9-THC     Amber glass ampule: 2ml..      1/12/89
                                          0.1, 1.0 mg/ml.                                                       
Radian Corporation.....................  Alpha-Hydroxyalprazolam 0.1 mg/  Vial: 2ml................      6/12/91
                                          ml, 1.0 mg/ml.                                                        
Radian Corporation.....................  Alpha-Hydroxyalprazolam-D5 0.1   Vial: 2ml................      6/12/91
                                          mg/ml, 1.0 mg/ml.                                                     
Radian Corporation.....................  Alpha-Hydroxytriazolam 0.1mg/    Ampule: 2ml..............      4/27/92
                                          ml, 1.0mg/ml.                                                         
Radian Corporation.....................  Alpha-Hydroxytriazolam-D4,       Ampule: 2ml..............      4/27/92
                                          0.1mg/ml, 1.0mg/ml.                                                   
Radian Corporation.....................  Alprazolam 0.1mg/ml, 1.0mg/ml..  Ampule: 2ml..............      11/5/90
Radian Corporation.....................  Alprazolam-D5 0.1mg/ml, 1.0mg/   Ampule: 2ml..............      11/5/90
                                          ml.                                                                   
Radian Corporation.....................  Amobarbital 0.1mg/ml, 1.0mg/ml.  Ampule: 2ml..............      4/27/92
Radian Corporation.....................  Amphetamine-D3 0.1 mg/ml.......  Ampule: 2 ml.............      12/4/87
Radian Corporation.....................  Anhydroecgonine 100g/   Ampule: 2ml..............      1/29/93
                                          ml, 1.0mg/ml.                                                         
Radian Corporation.....................  Anhydroecgonine HCL, 100g/ml, 1mg/ml.                                                       
Radian Corporation.....................  Anhydroecgonine methyl ester,    Ampule: 2ml..............       7/7/95
                                          100g/ml, 1mg/ml.                                             
Radian Corporation.....................  Anhydroecgonine-D3 100g/ml, 1.0mg/ml.                                                     
Radian Corporation.....................  Benzoylecgonine................  Ampule: 2ml..............      12/4/87
Radian Corporation.....................  Benzoylecgonine isopropyl        Ampule: 2ml..............       7/7/95
                                          ester, 100g/ml, 1mg/                                         
                                          ml.                                                                   
Radian Corporation.....................  Benzoylecgonine-D3.............  Ampule: 2ml..............      12/4/87
Radian Corporation.....................  Bromazepam; 1.0mg/ml, 100g/ml.                                                               
Radian Corporation.....................  Buprenorphine 0.1..............  Ampule: 2ml..............       2/1/91
Radian Corporation.....................  Buprenorphine-D4 0.1 mg/ml.....  Ampule: 2ml..............       2/1/91
Radian Corporation.....................  Chlordiazepoxide 100g/  Ampule: 2ml..............     12/22/93
                                          ml, 1.0mg/ml.                                                         
Radian Corporation.....................  Clobazam, 100g/ml, 1mg/ Ampule: 2ml..............       7/7/95
                                          ml.                                                                   
Radian Corporation.....................  Clonazepam-D4; 1.0mg/ml,         Vial: 2ml................      1/25/95
                                          100g/ml.                                                     
Radian Corporation.....................  Cocaethylene 0.1mg/ml, 1.0mg/ml  Ampule: 2ml..............     12/13/90
Radian Corporation.....................  Cocaethylene-D3................  Ampule: 2ml..............     12/13/90
Radian Corporation.....................  Cocaethylene-D8 100g/   Ampule: 2ml..............     12/22/93
                                          ml, 1.0mg/ml.                                                         
Radian Corporation.....................  Cocaine 0.1, 1.0 mg/ml.........  Amber glass ampule: 2ml..      1/12/89
Radian Corporation.....................  Cocaine-D3.....................  Ampule: 2 ml.............      12/4/87
Radian Corporation.....................  Codeine........................  Ampule: 2 ml.............       3/9/88
Radian Corporation.....................  Codeine-D3.....................  Ampule: 2 ml.............      12/4/87
Radian Corporation.....................  D-Amphetamine 0.1, 1.0 mg/ml...  Amber glass ampule: 2ml..      1/12/89
Radian Corporation.....................  D-Methamphetamine 0.1 mg/ml,     Vial: 2ml................      6/12/91
                                          1.0 mg/ml.                                                            
Radian Corporation.....................  D-Propoxyphene 0.1, 1.0 mg/ml..  Amber glass ampule: 2ml..      4/27/92
Radian Corporation.....................  D-Propoxyphene 0.1mg/ml, 1.0mg/  Ampule: 2ml..............      4/27/92
                                          ml.                                                                   
Radian Corporation.....................  DL-3, 4-MDEA 100g/ml,   Ampule: 2ml..............     12/22/93
                                          1.0mg/ml.                                                             
Radian Corporation.....................  DL-3, 4-MDEA-D5 100g/   Ampule: 2ml..............     12/22/93
                                          ml, 1.0mg/ml.                                                         
Radian Corporation.....................  DL-Amphetamine 0.1, 1.0 mg/ml..  Ampule: 2ml..............      12/4/87
Radian Corporation.....................  DL-Amphetamine-D11, 0.1mg/ml,    Ampule: 2ml..............      4/27/92
                                          1.0mg/ml.                                                             
Radian Corporation.....................  DL-Amphetamine-D3 0.1, 1.0 mg/   Ampule: 2ml..............      12/4/87
                                          ml.                                                                   
Radian Corporation.....................  DL-Amphetamine-D5 (SC) 0.1, 1.0  Ampule: 2ml..............      12/4/87
                                          mg/ml.                                                                
Radian Corporation.....................  DL-Amphetamine-D5 0.1, 1.0 mg/   Ampule: 2 ml.............      12/4/87
                                          ml.                                                                   
Radian Corporation.....................  DL-Amphetamine-D5 0.1, 1.0 mg/   Ampule: 2ml..............      12/4/87
                                          ml.                                                                   
Radian Corporation.....................  DL-Amphetamine-D8, 0.1mg/ml,     Ampule: 2ml..............      4/27/92
                                          1.0mg/ml.                                                             
Radian Corporation.....................  DL-MDEA-D6; 1.0mg/ml, 100g/ml.                                                               
Radian Corporation.....................  DL-Methamphetamine 0.1, 1.0 mg/  Amber glass ampule: 2ml..      1/12/89
                                          ml.                                                                   
Radian Corporation.....................  DL-Methamphetamine-D11 0.1mg/    Ampule: 2ml..............      6/16/93
                                          ml, 1.0mg/ml.                                                         
Radian Corporation.....................  DL-Methamphetamine-D5 0.1, 1.0   Ampule: 2 ml.............      12/4/87
                                          mg/ml.                                                                
Radian Corporation.....................  DL-Methamphetamine-D8 (Phenyl-   Ampule: 2ml..............       4/6/93
                                          D5 & N-Methyl-D3) 100g/ml, 1.0mg/ml.                                                     
Radian Corporation.....................  DL-Methamphetamine-D8 0.1 mg/ml  Ampule: 2ml..............      12/4/87
Radian Corporation.....................  DL-Methamphetamine-D8, 0.1mg/    Ampule: 2ml..............      4/27/92
                                          ml, 1.0mg/ml.                                                         
Radian Corporation.....................  DL-Propoxyphene-D5 0.1, 1.0 mg/  2 ml amber ampule........     10/19/88
                                          ml.                                                                   
Radian Corporation.....................  Delta-9-Tetrahydrocannabinol     Amber glass ampule: 2ml..      1/12/89
                                          0.1, 1.0 mg/ml.                                                       

[[Page 158]]

                                                                                                                
Radian Corporation.....................  Delta-9-Tetrahydrocannabinol-D3  Ampule: 2 ml.............      12/4/87
Radian Corporation.....................  Diazepam 0.1, 1.0 mg/ml........  Amber glass ampule: 2ml..      1/12/89
Radian Corporation.....................  Diazepam-D5 0.1 mg/ml..........  2 ml amber ampule........     10/19/88
Radian Corporation.....................  Diazepam-D5 1.0 mg/ml..........  2 ml amber ampule........     10/19/88
Radian Corporation.....................  Ecgonine 0.1 mg/ml, 1.0 mg/ml..  Vial: 2ml................      6/12/91
Radian Corporation.....................  Ecgonine Methyl Ester 0.1, 1.0   Amber glass ampule: 2ml..      1/12/89
                                          mg/ml.                                                                
Radian Corporation.....................  Ecgonine Methyl Ester-D3 0.1 mg/ 2 ml amber ampule........     10/19/88
                                          ml.                                                                   
Radian Corporation.....................  Ecgonine Methyl Ester-D3 1.0 mg/ 2 ml amber ampule........     10/19/88
                                          ml.                                                                   
Radian Corporation.....................  Ecgonine ethyl ester, 100ug/ml,  Ampule: 2ml..............       7/7/95
                                          1mg/ml.                                                               
Radian Corporation.....................  Ecgonine-D3 0.1 mg/ml, 1.0 mg/   Vial: 2ml................      6/12/91
                                          ml.                                                                   
Radian Corporation.....................  Estazolam; 1.0mg/ml, 100ug/ml..  Vial: 2ml................      1/25/95
Radian Corporation.....................  Fentanyl.......................  Ampule: 2ml..............       1/2/91
Radian Corporation.....................  Fentanyl-D5....................  Ampule: 2ml..............       1/2/91
Radian Corporation.....................  Flunitrazepam; 1.0mg/ml, 100ug/  Vial: 2ml................      1/25/95
                                          ml.                                                                   
Radian Corporation.....................  Fluoxymesterone, 100ug/ml, 1mg/  Ampule: 2ml..............       7/7/95
                                          ml.                                                                   
Radian Corporation.....................  Flurazepam 0.1mg/ml, 1.0mg/ml..  Ampule: 2ml..............      4/27/92
Radian Corporation.....................  Heroin-D3; 1.0mg/ml, 100ug/ml..  Vial: 2ml................      1/25/95
Radian Corporation.....................  Heroin-D6; 1.0mg/ml, 100ug/ml..  Vial: 2ml................      1/25/95
Radian Corporation.....................  Heroin-D9; 1.0mg/ml, 100ug/ml..  Vial: 2ml................      1/25/95
Radian Corporation.....................  Heroin; 1.0mg/ml, 100ug/ml.....  Ampule: 2ml..............      8/23/94
Radian Corporation.....................  Hexobarbital; 1.0mg/ml, 100ug/   Ampule: 2ml..............      8/23/94
                                          ml.                                                                   
Radian Corporation.....................  Hydrocodone-D3 0.1 mg/ml.......  2 ml amber ampule........     10/19/88
Radian Corporation.....................  Hydrocodone-D3 1.0 mg/ml.......  2 ml amber ampule........     10/19/88
Radian Corporation.....................  Hydrocodone 0.1, 1.0 mg/ml.....  Amber glass ampule: 2ml..      1/12/89
Radian Corporation.....................  Hydromorphone-D3 0.1 mg/ml.....  2 ml amber ampule........     10/19/88
Radian Corporation.....................  Hydromorphone-D3 1.0 mg/ml.....  2 ml amber ampule........     10/19/88
Radian Corporation.....................  Hydromorphone 0.1, 1.0 mg/ml...  Amber glass ampule: 2ml..      1/12/89
Radian Corporation.....................  Ibogaine 100ug/ml, 1.0mg/ml....  Ampule: 2ml..............     12/22/93
Radian Corporation.....................  Ibogaine-D3 100ug/ml, 1.0mg/ml.  Ampule: 2ml..............     12/22/93
Radian Corporation.....................  Lorazepam 0.1mg/ml, 1.0mg/ml...  Ampule: 2ml..............      4/27/92
Radian Corporation.....................  Lorazepam glucuronide, 50ug/ml,  Ampule: 2ml..............       7/7/95
                                          100ug/ml, 1mg/ml.                                                     
Radian Corporation.....................  Lorazepam-D4, 0.1mg/ml, 1.0mg/   Ampule: 2ml..............      4/27/92
                                          ml.                                                                   
Radian Corporation.....................  Lormetazepam, 100ug/ml, 1mg/ml.  Ampule: 2ml..............       7/7/95
Radian Corporation.....................  Meperidine 0.1mg/ml, 1.0mg/ml..  Ampule: 2ml..............      4/27/92
Radian Corporation.....................  Meperidine 0.1mg/ml, 1.0mg/ml..  Ampule: 2ml..............      4/27/92
Radian Corporation.....................  Meprobamate 0.1mg/ml, 1.0mg/ml.  Ampule: 2ml..............      4/27/92
Radian Corporation.....................  Mescaline 100ug/ml, 1.0mg/ml...  Ampule: 2ml..............      1/29/93
Radian Corporation.....................  Mescaline-D9 100ug/ml, 1.0mg/ml  Ampule: 2ml..............      1/29/93
Radian Corporation.....................  Methadone-D5 0.1 mg/ml.........  2 ml amber ampule........     10/19/88
Radian Corporation.....................  Methadone-D5 1.0 mg/ml.........  2 ml amber ampule........     10/19/88
Radian Corporation.....................  Methadone 0.1, 1.0 mg/ml.......  Amber glass ampule: 2ml..      1/12/89
Radian Corporation.....................  Methandienone, 100ug/ml, 1mg/ml  Ampule: 2ml..............       7/7/95
Radian Corporation.....................  Methaqualone-D4 0.1 mg/ml......  2 ml amber ampule........     10/19/88
Radian Corporation.....................  Methaqualone-D4 1.0 mg/ml......  2 ml amber ampule........     10/19/88
Radian Corporation.....................  Methaqualone 0.1, 1.0 mg/ml....  Amber glass ampule: 2ml..      1/12/89
Radian Corporation.....................  Methcathinone 100ug/ml, 1.0mg/   Ampule: 2ml..............      1/29/93
                                          ml.                                                                   
Radian Corporation.....................  Methcathinone-D5 100ug/ml,       Ampule: 2ml..............      1/29/93
                                          1.0mg/ml.                                                             
Radian Corporation.....................  Methenolone, 100ug/ml, 1mg/ml..  Ampule: 2ml..............       7/7/95
Radian Corporation.....................  Method 8270 Supplemental Stock   Vial: 2ml................      1/25/95
                                          Standard--2000ug/ml.                                                  
Radian Corporation.....................  Methohexital 0.1mg/ml, 1.0mg/ml  Ampule: 2ml..............      4/27/92
Radian Corporation.....................  Methohexital-D5; 1.0mg/ml,       Ampule: 2ml..............      8/23/94
                                          100ug/ml.                                                             
Radian Corporation.....................  Methylphenidate 0.1mg/ml, 1.0mg/ Ampule: 2ml..............      4/27/92
                                          ml.                                                                   
Radian Corporation.....................  Methylphenidate HCL, 100ug/ml,   Ampule: 2ml..............       7/7/95
                                          1mg/ml.                                                               
Radian Corporation.....................  Methyltestosterone; 1.0mg/ml,    Vial: 2ml................      1/25/95
                                          100ug/ml.                                                             
Radian Corporation.....................  Midazolam; 1.0mg/ml, 100ug/ml..  Vial: 2ml................      1/25/95
Radian Corporation.....................  Morphine.......................  Ampule: 2 ml.............       3/9/88
Radian Corporation.....................  Morphine-3-Beta-D-glucuronide    Ampule: 2ml..............       2/1/91
                                          0.1, 1.0mg/ml.                                                        
Radian Corporation.....................  Morphine-3-Beta-D-glucuronide-   Ampule: 2ml..............       2/1/91
                                          D3 0.1, 1.0mg/ml.                                                     
Radian Corporation.....................  Morphine-D3....................  Ampule: 2 ml.............      12/4/87
Radian Corporation.....................  N-Ethylamphetamine; 1.0mg/ml,    Vial: 2ml................      1/25/95
                                          100ug/ml.                                                             
Radian Corporation.....................  Nitrazepam 0.1 mg/ml, 1.0 mg/ml  Ampule: 2ml..............      9/17/90
Radian Corporation.....................  Nitrazepam-D5 0.1 mg/ml, 1.0 mg/ Ampule: 2ml..............      9/17/90
                                          ml.                                                                   
Radian Corporation.....................  Norbenzoylecgonine, 100ug/ml,    Ampule: 2ml..............       7/7/95
                                          1mg/ml.                                                               
Radian Corporation.....................  Norcocaethylene, 100ug/ml, 1mg/  Ampule: 2ml..............       7/7/95
                                          ml.                                                                   
Radian Corporation.....................  Norcocaine 0.1 mg/ml, 1.0 mg/ml  Vial: 2ml................      6/12/91
Radian Corporation.....................  Norcocaine-D8 100ug/ml, 1.0mg/   Ampule: 2ml..............     12/22/93
                                          ml.                                                                   
Radian Corporation.....................  Nordiazepam-D5 0.1 mg/ml.......  2 ml amber ampule........     10/19/88
Radian Corporation.....................  Nordiazepam-D5 1.0 mg/ml.......  2 ml amber ampule........     10/19/88
Radian Corporation.....................  Nordiazepam 0.1, 1.0 mg/ml.....  Amber glass ampule: 2ml..      1/12/89
Radian Corporation.....................  Norethandrolone, 100ug/ml, 1mg/  Ampule: 2ml..............       7/7/95
                                          ml.                                                                   
Radian Corporation.....................  Noroxycodone 0.1mg/ml, 1.0mg/ml  Ampule: 2ml..............      6/16/93

[[Page 159]]

                                                                                                                
Radian Corporation.....................  Noroxymorphone 100ug/ml, 1.0mg/  Ampule: 2ml..............      6/16/93
                                          ml.                                                                   
Radian Corporation.....................  Oxazepam-D5 0.1 mg/ml..........  2 ml amber ampule........     10/19/88
Radian Corporation.....................  Oxazepam-D5 1.0 mg/ml..........  2 ml amber ampule........     10/19/88
Radian Corporation.....................  Oxazepam-3-Beta-D-Glucuronide-   Ampule: 2ml..............      4/25/94
                                          D5; 100ug/ml, 1.0mg/ml.                                               
Radian Corporation.....................  Oxazepam 0.1, 1.0 mg/ml........  Amber glass ampule: 2ml..      1/12/89
Radian Corporation.....................  Oxazepam-3-Beta-D-Glucuronide;   Ampule: 2ml..............      4/25/94
                                          100ug/ml, 1.0mg/ml.                                                   
Radian Corporation.....................  Oxycodone-D6 0.1mg/ml, 1.0mg/ml  Ampule: 2ml..............      6/16/93
Radian Corporation.....................  Pentobarbital 0.1 mg/ml, 1.0 mg/ Ampule: 2ml..............      9/24/90
                                          ml.                                                                   
Radian Corporation.....................  Pentobarbital-D5 0.1 mg/ml, 1.0  Ampule: 2ml..............      9/24/90
                                          mg/ml.                                                                
Radian Corporation.....................  Phencyclidine 0.1 mg/ml, 1.0 mg/ Amber glass ampule: 2ml..      1/12/89
                                          ml.                                                                   
Radian Corporation.....................  Phencyclidine-D5...............  Ampule: 2 ml.............      12/4/87
Radian Corporation.....................  Phenobarbital 0.1 mg/ml, 1.0 mg/ Amber glass ampule: 2ml..      1/12/89
                                          ml.                                                                   
Radian Corporation.....................  Phenobarbital-D5 0.1 mg/ml, 1.0  Ampule: 2 ml.............      12/4/87
                                          mg/ml.                                                                
Radian Corporation.....................  Phentermine-D3; 1.0mg/ml, 100ug/ Vial: 2ml................      1/25/95
                                          ml.                                                                   
Radian Corporation.....................  Phentermine; 1.0mg/ml, 100ug/ml  Vial: 2ml................      1/25/95
Radian Corporation.....................  Prazepam 100ug/ml, 1.0mg/ml....  Ampule: 2ml..............      1/29/93
Radian Corporation.....................  Prazepam-D5 100ug/ml, 1.0mg/ml.  Ampule: 2ml..............      1/29/93
Radian Corporation.....................  Quazepam; 1.0mg/ml, 100ug/ml...  Vial: 2ml................      1/25/95
Radian Corporation.....................  Stanozolol-D3; 100ug/ml, 1.omg/  Ampule: 2ml..............       6/6/94
                                          ml.                                                                   
Radian Corporation.....................  Stanozolol; 100ug/ml, 1.omg/ml.  Ampule: 2ml..............       6/6/94
Radian Corporation.....................  Temazepam 0.1 mg/ml, 1.0 mg/ml.  Ampule: 2ml..............      9/17/90
Radian Corporation.....................  Temazepam-D5 0.1 mg/ml, 1.0 mg/  Ampule: 2ml..............      9/17/90
                                          ml.                                                                   
Radian Corporation.....................  Triazolam 0.1mg/ml, 1.0mg/ml...  Ampule: 2ml..............      4/27/92
Radian Corporation.....................  Triazolam-D4 0.1mg/ml, 1.0mg/ml  Ampule: 2ml..............      4/27/92
Radian Corporation.....................  alpha-Hydroxyalprazolam          Ampule: 2ml..............       7/7/95
                                          glucuronide, 50ug/ml, 100ug/                                          
                                          ml, 1mg/ml.                                                           
Radian Corporation.....................  alpha-Hydroxymidazolam, 100ug/   Ampule: 2ml..............       7/7/95
                                          ml, 1mg/ml.                                                           
Radian Corporation.....................  alpha-Hydroxytriazolam           Ampule: 2ml..............       7/7/95
                                          glucuronide, 50ug/ml, 100ug/                                          
                                          ml, 1mg/ml.                                                           
Radian Corporation.....................  m-Hydroxybenzoylecgonine; 1.0mg/ Vial: 2ml................      1/25/95
                                          ml, 100ug/ml.                                                         
Research Diagnostics...................  3H Alfentanil..................  Vial: 0.5ml..............      6/15/89
Research Diagnostics...................  3H Fentanyl....................  Vial: 0.5ml..............      6/15/89
Research Diagnostics...................  3H Sufentanil..................  Vial: 0.5ml..............      6/15/89
Research Diagnostics...................  Alfentanil Radioimmunoassay....  Kit: 200 tests...........      6/15/89
Research Diagnostics...................  Alfentanil Radioimmunoassay....  Kit: 200 tests...........      6/15/89
Research Diagnostics...................  Fentanyl Analogs Reference       Amber Ampule: 1 ml,           10/17/89
                                          Standards for Drug Analysis.     Plastic Shell: 5                     
                                                                           ampules, Kit: 2 shells               
                                                                           (10 ampules).                        
Research Diagnostics...................  Fentanyl Radioimmunoassay......  Kit: 200 tests...........      6/15/89
Research Diagnostics...................  Sufentanil Radioimmunoassay....  Kit: 200 tests...........      6/15/89
Research Triangle Institute............  11-Nor-9-carboxy-delta-9 THC     Kit Containing: 18-21ml       10/26/81
                                          Blood Standards Kit.             Ampuls; 1-5ml Ampul.                 
Research Triangle Institute............  11-Nor-9-carboxy-delta-9 THC     Kit Containing: 18-21ml       10/26/81
                                          Plasma Standards Kit.            Ampuls; 1-5ml Ampul.                 
Research Triangle Institute............  Delta-9 THC Blood Standards Kit  Kit Containing: 16-2ml        10/26/81
                                                                           Ampuls; 1-5ml Ampul.                 
Research Triangle Institute............  Delta-9 THC Plasma Standards     Kit Containing: 16-2ml         11/2/81
                                          Kit.                             Ampuls; 1-5ml Ampul.                 
Research Triangle Institute............  Iodine Kit for Radioimmunoassay  Kit Containing: 26-1ml        10/26/81
                                          of 11-Nor-9-carboxy-delta-9      Ampuls; 2-20ml Vials; 2-             
                                          THC in Blood.                    250ml Bottles.                       
Research Triangle Institute............  Iodine Kit for Radioimmunoassay  Kit Containing: 24-1ml        10/26/81
                                          of 11-Nor-9-carboxy-delta-9      Ampuls; 2-20ml Vials; 2-             
                                          THC in Plasma.                   250ml Bottles.                       
Research Triangle Institute............  Iodine Kit for Radioimmunoassay  Kit Containing: 20-1ml        10/20/80
                                          of Delta-9 THC.                  Ampules; 2-20ml Vials; 2-            
                                                                           250ml Bottles.                       
Research Triangle Institute............  Iodine Kit for Radioimmunoassay  Kit Containing: 22-1ml         7/10/81
                                          of Delta-9 THC in Blood.         Ampules; 2-20ml Vials; 2-            
                                                                           250ml Bottles.                       
Research Triangle Institute............  Tritium Kit for                  Kit Containing: 20-1ml         6/27/80
                                          Radioimmunoassay of Delta-9      Ampules; 2- 20ml Vials;              
                                          THC.                             2- 250ml Bottles.                    
Restek Corp............................  Alprazolam.....................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Amobarbital....................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Amphetamine....................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Aprobarbital...................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Barbital.......................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Benzoylecgonine................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Benzphetamine..................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Bromazepam.....................  Ampule: 2ml..............       1/8/93

[[Page 160]]

                                                                                                                
Restek Corp............................  Butabarbital...................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Butalbital.....................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Cannabidiol delta-8............  Ampule: 2ml..............       1/8/93
Restek Corp............................  Cannabinol.....................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Chlordiazepoxide...............  Ampule: 2ml..............       1/8/93
Restek Corp............................  Clobazam.......................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Clonazepam.....................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Cocaethylene...................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Cocaine........................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Codeine........................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Desmethyl Diazepam.............  Ampule: 2ml..............       1/8/93
Restek Corp............................  Diacetylmorphine...............  Ampule: 2ml..............       1/8/93
Restek Corp............................  Diazepam.......................  Ampule: 2ml..............       1/8/93
Restek Corp............................  EPA Exempt Mix #1..............  Ampule: 1.25ml...........      3/18/94
Restek Corp............................  EPA Exempt Mix #2..............  Ampule: 1.25ml...........      3/18/94
Restek Corp............................  EPA Exempt Mix #3..............  Ampule: 1.25ml...........      3/18/94
Restek Corp............................  Ecgonine.......................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Ecgonine methyl ester..........  Ampule: 2ml..............       1/8/93
Restek Corp............................  Fenfluramine...................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Fentanyl.......................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Flunitrazepam..................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Flurazepam.....................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Glutethimide...................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Hexobarbital...................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Hydrocodone....................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Levorphanol....................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Lorazepam......................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Medazepam......................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Meperidine.....................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Mephobarbital..................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Meprobamate....................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Methadone......................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Methamphetamine................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Methohexital...................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Methyprylon....................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Morphine.......................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Nitrazepam.....................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Oxazepam.......................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Oxycodone......................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Pentazocine....................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Pentobarbital..................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Phencyclidine..................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Phendimetrazine................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Phenmetrazine..................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Phenobarbital..................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Phentermine....................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Prazepam.......................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Propoxyphene...................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Secobarbital...................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Talbutal.......................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Temazepam......................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Tetrahydrocannabinol 11-nor      Ampule: 2ml..............       1/8/93
                                          delta-9-THC-carboxylic acid.                                          
Restek Corp............................  Tetrahydrocannabinol delta-9...  Ampule: 2ml..............       1/8/93
Restek Corp............................  Thebaine.......................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Thiamylal......................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Thiopental.....................  Ampule: 2ml..............       1/8/93
Restek Corp............................  Triazolam......................  Ampule: 2ml..............       1/8/93
Roche Diagnostic Systems, Inc..........  Abuscreen Calibration Standard   Kit: 2 Vials.............     10/12/87
                                          for Amphetamine.                                                      
Roche Diagnostic Systems, Inc..........  Abuscreen Calibration Standard   Kit: 2 Vials.............     10/12/87
                                          for Barbiturate.                                                      
Roche Diagnostic Systems, Inc..........  Abuscreen Calibration Standard   Kit: 2 Vials.............     10/12/87
                                          for Cannabinoids.                                                     
Roche Diagnostic Systems, Inc..........  Abuscreen Calibration Standard   Kit: 2 Vials.............     10/12/87
                                          for Cocaine Metabolite.                                               
Roche Diagnostic Systems, Inc..........  Abuscreen Calibration Standard   Kit: 2 Vials.............     10/12/87
                                          for LSD (Lysergic Acid                                                
                                          Diethylamide).                                                        
Roche Diagnostic Systems, Inc..........  Abuscreen Calibration Standard   Kit: 2 vials.............      5/27/92
                                          for Methamphetamine (High                                             
                                          Specificity).                                                         
Roche Diagnostic Systems, Inc..........  Abuscreen Calibration Standard   Kit: 2 Vials.............     10/12/87
                                          for Morphine.                                                         

[[Page 161]]

                                                                                                                
Roche Diagnostic Systems, Inc..........  Abuscreen Calibration Standard   Kit: 2 Vials.............     10/12/87
                                          for Phencyclidine (PCP).                                              
Roche Diagnostic Systems, Inc..........  Abuscreen ONLINE                 Bottle: 4.5L.............      3/31/94
                                          Benzoylecgonine Microparticle                                         
                                          Reagent.                                                              
Roche Diagnostic Systems, Inc..........  Abuscreen ONLINE Calibration     Kit: 8 vials.............      5/18/92
                                          Pack.                                                                 
Roche Diagnostic Systems, Inc..........  Abuscreen ONLINE Calibrator      Pack: 6 vials............      5/18/92
                                          Level 3.                                                              
Roche Diagnostic Systems, Inc..........  Abuscreen ONLINE Cannabinoids    Bottle: 4.5L.............      3/31/94
                                          Microparticle Reagent.                                                
Roche Diagnostic Systems, Inc..........  Abuscreen ONLINE Opiates         Bottle: 4.5L.............      3/31/94
                                          Microparticle Reagent.                                                
Roche Diagnostic Systems, Inc..........  Abuscreen ONLINE Positive        Pack: 6 vials............      5/18/92
                                          Control.                                                              
Roche Diagnostic Systems, Inc..........  Abuscreen ONLINE THC Positive    Kit: 6 vials; 4ml/vial...      3/22/93
                                          Control.                                                              
Roche Diagnostic Systems, Inc..........  Abuscreen ONLINE for Cocaine     Kit: 100, 1000, 8000           3/19/91
                                          Metabolite.                      Tests.                               
Roche Diagnostic Systems, Inc..........  Abuscreen ONLINE for Opiates...  Kit: 100, 1000, 8000           3/19/91
                                                                           Tests.                               
Roche Diagnostic Systems, Inc..........  Abuscreen ONLINE for THC.......  Vial: 100, 1000, 8000          3/19/91
                                                                           Tests.                               
Roche Diagnostic Systems, Inc..........  Abuscreen ONTRAK Amphetamine...  Kit: 50 tests, 100 tests.      3/14/88
Roche Diagnostic Systems, Inc..........  Abuscreen ONTRAK Amphetamine     Vial: 4 ml...............      3/14/88
                                          Positive Control.                                                     
Roche Diagnostic Systems, Inc..........  Abuscreen ONTRAK Barbiturate...  Kit: 50 tests, 100 tests.      3/14/88
Roche Diagnostic Systems, Inc..........  Abuscreen ONTRAK Barbiturates    Vial: 4 ml...............      3/14/88
                                          Positive Control.                                                     
Roche Diagnostic Systems, Inc..........  Abuscreen ONTRAK                 Kit: 50 Tests, 100 Tests.       5/3/91
                                          Benzodiazepines.                                                      
Roche Diagnostic Systems, Inc..........  Abuscreen ONTRAK Cocaine         Kit: 50 tests, 100 tests.      3/14/88
                                          Metabolite.                                                           
Roche Diagnostic Systems, Inc..........  Abuscreen ONTRAK Cocaine         Vial: 4 ml...............      3/14/88
                                          Metabolite Positive Control.                                          
Roche Diagnostic Systems, Inc..........  Abuscreen ONTRAK Methadone.....  Kits: 50, 100 Tests......       9/8/93
Roche Diagnostic Systems, Inc..........  Abuscreen ONTRAK Morphine......  Kits: 50 tests, 100 tests      3/14/88
Roche Diagnostic Systems, Inc..........  Abuscreen ONTRAK Morphine        Vial: 4 ml...............      3/14/88
                                          Positive Control.                                                     
Roche Diagnostic Systems, Inc..........  Abuscreen ONTRAK Multianalyte    Kit: 1 Vial, 8ml.........      9/18/95
                                          Positive Control.                                                     
Roche Diagnostic Systems, Inc..........  Abuscreen ONTRAK Phencyclidine   Kit: 50 tests, 100 tests.     11/22/89
                                          (PCP).                                                                
Roche Diagnostic Systems, Inc..........  Abuscreen ONTRAK Phencyclidine   Vial: 4 ml...............     11/22/89
                                          (PCP) Positive Control.                                               
Roche Diagnostic Systems, Inc..........  Abuscreen ONTRAK THC (100ng/ml)  Kit: 50 tests, 100 tests.      3/14/88
Roche Diagnostic Systems, Inc..........  Abuscreen ONTRAK THC (50ng/ml).  Kit: 50 Tests, 100 Tests.       5/3/91
Roche Diagnostic Systems, Inc..........  Abuscreen ONTRAK THC Positive    Vial: 4 ML...............      3/14/88
                                          Control.                                                              
Roche Diagnostic Systems, Inc..........  Abuscreen ONTRAK for             Vial: 4ml................      3/22/93
                                          Benzodiazepines Positive                                              
                                          Control.                                                              
Roche Diagnostic Systems, Inc..........  Abuscreen Radioimmunoassay for   Kit: 100 tests, 2500           9/13/85
                                          Amphetamine High Specificity.    tests.                               
Roche Diagnostic Systems, Inc..........  Abuscreen Radioimmunoassay for   Kit: 100 tests, 2500           2/15/83
                                          Barbiturates.                    tests.                               
Roche Diagnostic Systems, Inc..........  Abuscreen Radioimmunoassay for   Kit: 100 tests, 2500            3/6/87
                                          Benzodiazepines.                 tests.                               
Roche Diagnostic Systems, Inc..........  Abuscreen Radioimmunoassay for   Kit: 100 Tests 2, 500          8/14/81
                                          Cannabinoids.                    Tests.                               
Roche Diagnostic Systems, Inc..........  Abuscreen Radioimmunoassay for   Kit: 100 Tests, 2500           2/15/83
                                          Cocaine Metabolite.              Tests.                               
Roche Diagnostic Systems, Inc..........  Abuscreen Radioimmunoassay for   Kit: 100 tests, 2500           1/28/86
                                          LSD (Lysergic Acid               tests.                               
                                          Diethylamide).                                                        
Roche Diagnostic Systems, Inc..........  Abuscreen Radioimmunoassay for   Kit: 100 tests, 2500            3/1/89
                                          Methamphetamine High             tests.                               
                                          Specificity.                                                          
Roche Diagnostic Systems, Inc..........  Abuscreen Radioimmunoassay for   Kit: 100 tests, 2500           2/15/83
                                          Methaqualone.                    tests.                               

[[Page 162]]

                                                                                                                
Roche Diagnostic Systems, Inc..........  Abuscreen Radioimmunoassay for   Kit: 100 tests, 2500           2/15/83
                                          Morphine.                        tests.                               
Roche Diagnostic Systems, Inc..........  Abuscreen Radioimmunoassay for   Kit: 100 tests, 2500           2/15/83
                                          Phencyclidine (PCP).             tests.                               
Roche Diagnostic Systems, Inc..........  Abuscreen Reference Controls     Kit: 3 Vials, 100ml each.     10/12/87
                                          and Calibrator for Amphetamine.                                       
Roche Diagnostic Systems, Inc..........  Abuscreen Reference Controls     Kit: 3 Vials, 100ml each.     10/12/87
                                          and Calibrator for Barbiturate.                                       
Roche Diagnostic Systems, Inc..........  Abuscreen Reference Controls     Kit: 3 Vials, 100ml each.     10/12/87
                                          and Calibrator for                                                    
                                          Cannabinoids.                                                         
Roche Diagnostic Systems, Inc..........  Abuscreen Reference Controls     Kit: 3 Vials, 100ml each.     10/12/87
                                          and Calibrator for Cocaine                                            
                                          Metabolite.                                                           
Roche Diagnostic Systems, Inc..........  Abuscreen Reference Controls     Kit: 3 Vials, 100ml each.     10/12/87
                                          and Calibrator for LSD                                                
                                          (Lysergic Acid Diethylamide).                                         
Roche Diagnostic Systems, Inc..........  Abuscreen Reference Controls     Kit: 3 vials, 100ml each.      5/27/92
                                          and Calibrator for                                                    
                                          Methamphetamine (High                                                 
                                          Specificity).                                                         
Roche Diagnostic Systems, Inc..........  Abuscreen Reference Controls     Kit: 3 Vials, 100ml each.     10/12/87
                                          and Calibrator for Morphine.                                          
Roche Diagnostic Systems, Inc..........  Abuscreen Reference Controls     Kit: 3 Vials, 100ml each.     10/12/87
                                          and Calibrator for                                                    
                                          Phencyclidine (PCP).                                                  
Roche Diagnostic Systems, Inc..........  Abuscreenm ONTRAK Methadone      Vial: 4ml................      9/08/93
                                          Positive Reference Control.                                           
Roche Diagnostic Systems, Inc..........  CAL PACK Abuscreen ONLINE THC    Kit: 4 vials.............      9/11/91
                                          Calibration Pack.                                                     
Roche Diagnostic Systems, Inc..........  COBAS FP Phenobarbital           Kit: 6 Vials.............     11/13/84
                                          Calibrators.                                                          
Roche Diagnostic Systems, Inc..........  COBAS FP Reagents for            Kit: 100 tests...........     11/13/84
                                          Phenobarbital.                                                        
Roche Diagnostic Systems, Inc..........  COBAS FP TDM Controls..........  Kit: 6 Vials.............     11/13/84
Roche Diagnostic Systems, Inc..........  COBAS INTEGRA Cassette for       Kit: 3 Vials.............      9/27/95
                                          Cannabinoids.                                                         
Roche Diagnostic Systems, Inc..........  COBAS INTEGRA Cassette for       Kit: 3 Vials.............      9/27/95
                                          Cocaine Metabolite.                                                   
Roche Diagnostic Systems, Inc..........  COBAS INTEGRA Cassette for       Kit: 3 Vials.............      9/27/95
                                          Opiates.                                                              
Roche Diagnostic Systems, Inc..........  Immunizing Preparation No. 1,    Vial: 10, 20, 50, or           1/25/83
                                          2, 3, 4, 5, 6, 7, or 8.          100ml.                               
Roche Diagnostic Systems, Inc..........  Immunizing Preparation No. 9...  Vial: 10ml, 20ml, 50ml,        7/24/84
                                                                           or 100ml.                            
Roche Diagnostic Systems, Inc..........  Immunizing Preparation No. 9A..  Vial: 10ml, 20ml, 50ml,        7/24/84
                                                                           or 100ml.                            
Roche Diagnostic Systems, Inc..........  Immunizing Preparation No.10...  Vial: 10ml, 20ml, 50ml,         4/2/86
                                                                           or 100ml.                            
Roche Diagnostic Systems, Inc..........  Immunizing Preparation No.10A..  Vial: 10ml, 20ml, 50ml,         4/2/86
                                                                           or 100ml.                            
Roche Diagnostic Systems, Inc..........  Immunizing Preparations No. 1A,  Vial: 10ml, 20ml, 50ml,        7/12/83
                                          2A, 3A, 4A, 5A, 6A, 7A, or 8A.   or 100ml.                            
Roche Diagnostic Systems, Inc..........  OnTrak TesTcup Positive Control  Box: 6 Vials.............      9/25/95
Rowley Biochemical Institute, Inc......  Aldehyde Fuchsin Solution......  Bottle: Pint, Quart,            2/2/84
                                                                           Gallon.                              
Rowley Biochemical Institute, Inc......  Aldehyde Thionin Solution......  Bottle: Pint, Quart,            2/2/84
                                                                           Gallon.                              
Rowley Biochemical Institute, Inc......  Mayer's Hematoxylin Solution...  Bottle: Pint, Quart,            2/2/84
                                                                           Gallon.                              
Schering Corp..........................  Hepaquik.......................  Vial: 9 Dram and Plate...      7/16/72
Serex Inc..............................  Benzoylecgonine Positive         Bottle: 1 ml.............     12/16/89
                                          Control.                                                              
Serex Inc..............................  Benzoylecgonine Standards......  Bottle: 1 ml.............     12/16/89
Serex Inc..............................  CoMA EIA for Cocaine Metabolite  Kit: 96 tests, 2 Bottles:     10/17/89
                                                                           5 ml ea., Assay Plate:               
                                                                           96 wells.                            
Serex Inc..............................  Cocaine Metabolite Standards     Kit: 3 bottles--100           12/16/89
                                          and Controls Kit.                Assays.                              
Serex, Inc.............................  Automates CoMA Cocaine           Kit: 3 Bottles; 50, 1000       7/22/92
                                          Metabolite Assay.                Tests.                               
Serex, Inc.............................  Automates CoMA Cocaine           Bottle: 12.5ml, 50ml.....      7/22/92
                                          Metabolite Assay Reagent B.                                           
Serex, Inc.............................  Automates CoMA High Calibrator.  Vial: 5ml................      7/22/92
Serex, Inc.............................  Automates CoMA Plus Cocaine      Kit: 3 Bottles; 50, 1000       7/22/92
                                          Metabolite Assay.                Tests.                               
Serex. Inc.............................  Automates CoMA Low Calibrator..  Vial: 5ml................      7/22/92

[[Page 163]]

                                                                                                                
Serex. Inc.............................  Automates CoMA Plus Cocaine      Bottle: 12, 5ml, 50ml....      7/22/92
                                          Metabolite Assay Reagent B.                                           
Serono Diagnostics, Inc................  rT3 Barbital Buffer............  Glass Vial: 120ml........     10/26/84
Serono Diagnostics, Inc................  rT3-125I.......................  Glass Vial: 13ml.........     10/26/84
Serono Diagnostics, Inc................  rT3-Antiserum..................  Glass Vial: 13ml.........     10/26/84
Sherwood Medical Company...............  Lancer Fibrinogen                Kit......................      4/17/75
                                          Determination, Reagent Kit                                            
                                          Catalog No. 8889-007608.                                              
Sigma Chemical Co......................  (+)Deoxyephedrine-d5 HCl #D-     Ampule: 2ml..............      8/28/90
                                          5914.                                                                 
Sigma Chemical Co......................  (+/-)-(2                         Ampule: 1ml..............      7/30/92
                                          Methylamino)propiophenone                                             
                                          Hydrochloride.                                                        
Sigma Chemical Co......................  (+/-) 2, 5-Dimethoxy-4-bromo-    Ampule: 2ml..............      9/25/91
                                          amphetamine Hydrobromide, D-                                          
                                          7633.                                                                 
Sigma Chemical Co......................  (+/-) 2, 5-Dimethoxy-4-methyl-   Ampule: 2ml..............      9/25/91
                                          amphetamine HCl, D-7883.                                              
Sigma Chemical Co......................  (+/-) Deoxyephedrine HCl, D-     Ampule: 2ml..............      9/25/91
                                          7508.                                                                 
Sigma Chemical Co......................  (-) Deoxyephedrine, D-7258.....  Ampule: 2ml..............      9/25/91
Sigma Chemical Co......................  1-Dehydrotestosterone, Product   Ampule: 2ml..............      1/30/92
                                          #D5791.                                                               
Sigma Chemical Co......................  1-Tetrahydrocannabinol, Product  Vial: 1ml................      5/11/81
                                          No. T4764.                                                            
Sigma Chemical Co......................  11-Hydroxy-delta 9               Ampule: 2ml..............      11/6/91
                                          Tetrahydrocannabinol Cat. No.                                         
                                          H3879.                                                                
Sigma Chemical Co......................  11-nor-delta-9-                  Glass Ampule: 2 ml.......      6/29/89
                                          Tetrahyrocannabinol, 9-                                               
                                          carboxylic .05 mg/ml acid, No.                                        
                                          N-5642.                                                               
Sigma Chemical Co......................  11-nor-delta-9THC-9-Carboxylic   Ampule: 2ml..............      8/28/90
                                          Acid #N-6893.                                                         
Sigma Chemical Co......................  11Beta-Hydroxytestosterone, H-   Vial: 2ml................      2/04/94
                                          4646.                                                                 
Sigma Chemical Co......................  17alpha-Methyltestosterone,      Ampule: 2ml..............      1/30/92
                                          Product #M8783.                                                       
Sigma Chemical Co......................  19-Nortesterone 17-              Ampule: 1ml..............      7/30/92
                                          Phenylpropionate, N 2771.                                             
Sigma Chemical Co......................  19-Nortesterone 17-Propionate,   Ampule: 1ml..............      7/30/92
                                          N 2896.                                                               
Sigma Chemical Co......................  19-Nortestosterone 17-           Ampule: 1ml..............      7/30/92
                                          Decanoate, N 3021.                                                    
Sigma Chemical Co......................  19-Nortestosterone, Product      Ampule: 2ml..............      1/30/92
                                          #N1269.                                                               
Sigma Chemical Co......................  3,4                              Glass Ampule: 2 ml.......      6/29/89
                                          Methylenedioxymethamphetamine                                         
                                          1 mg/ml, No. M-5029.                                                  
Sigma Chemical Co......................  3,4-Methylenedioxyamphetamine,   Glass Ampule: 2ml........       6/6/89
                                          No. M-3272.                                                           
Sigma Chemical Co......................  3-Methylfentanyl HCl, M-6255...  Ampule: 2ml..............      9/25/91
Sigma Chemical Co......................  5,5-Diallylbarbituric Acid,      Sealed Ampule: 1ml.......      6/30/77
                                          Product No. D-6013.                                                   
Sigma Chemical Co......................  5-Alpha-Androstan-17beta-ol-3-   Ampule: 1ml..............      7/30/92
                                          one Benzoate, A 9768.                                                 
Sigma Chemical Co......................  5-Androstene-3Beta, 17Beta-      Ampule: 2ml..............      1/30/92
                                          Diol, Product #A0684.                                                 
Sigma Chemical Co......................  6-Tetrahydrocannabinol, Product  Vial: 1ml................      5/11/81
                                          No. T-4889.                                                           
Sigma Chemical Co......................  AST Reagent A, Stock No. 56-2..  Vial: 10ml...............      6/27/79
Sigma Chemical Co......................  Acid Hematoxylin Solution, No.   Bulk: 1000L..............      5/04/93
                                          285-2.                                                                
Sigma Chemical Co......................  Acid Hematoxylin Solution,       Bottle: 25ml, 100ml......       8/6/73
                                          No.285-2.                                                             
Sigma Chemical Co......................  Adenosine Phosphate Substrate,   Bottle: 4 ounce..........      7/25/83
                                          Product No. 675-1.                                                    
Sigma Chemical Co......................  Allylcyclopentylbarbituric Acid  Sealed Ampule: 1ml.......      4/10/85
                                          (A-7787).                                                             
Sigma Chemical Co......................  Allylisobutylbarbituric Acid (A- Sealed Ampule: 1ml.......      4/10/85
                                          1038).                                                                
Sigma Chemical Co......................  Alpha-Ethyltryptamine Acetate,   Vial: 2ml................       2/4/94
                                          Product #E1392.                                                       
Sigma Chemical Co......................  Alphaprodine Hydrochloride (A-   Ampule: 1ml..............      8/27/84
                                          1537).                                                                
Sigma Chemical Co......................  Alphenal (A-1163)..............  Ampule: 1ml..............      4/10/85
Sigma Chemical Co......................  Alprazolam .25 mg/ml, No. A-     Glass Ampule: 2 ml.......      6/29/89
                                          5052.                                                                 
Sigma Chemical Co......................  Alprazolam-d5 #A-7055..........  Ampule: 2ml..............      8/28/90
Sigma Chemical Co......................  Ammonia Reagent , Stock No. 170- Vial: 10ml...............      2/17/77
                                          10.                                                                   
Sigma Chemical Co......................  Ammonia Reagent Kit: Stock No.   Kit: 10 Vials............      2/17/77
                                          170-10.                                                               
Sigma Chemical Co......................  Ammonia Reagent Stock No. 170-   Vial: 30ml...............     12/13/77
                                          10.                                                                   
Sigma Chemical Co......................  Ammonia in Plasma Kit..........  Kit: 100 tests, 30 tests.     12/13/77
Sigma Chemical Co......................  Amobarbital , Product No. A-     Sealed Ampule: 1ml.......      6/30/77
                                          5142.                                                                 
Sigma Chemical Co......................  Amobarbital Sodium Salt,         Ampule: 1ml..............      5/13/93
                                          Product No. A-7441.                                                   
Sigma Chemical Co......................  Antibody Sensitized Sheep        Vials: 2ml and 5X 2ml....       4/2/86
                                          Erythrocytes (EA7S).                                                  
Sigma Chemical Co......................  Aprobarbital, Product No. A-     Sealed Ampule: 1ml.......      6/30/77
                                          7023.                                                                 
Sigma Chemical Co......................  Barbital Buffer, Product No. B-  Polyethylene Vial: 30ml..      5/11/77
                                          6632.                                                                 
Sigma Chemical Co......................  Barbital Buffer 5X Concentrate   Bottle: 200ml............     11/14/91
                                          Electrophoresis Reagent Cat.                                          
                                          No. B-3506.                                                           
Sigma Chemical Co......................  Barbital Buffer with Albumin     Vial: 20ml...............      7/11/80
                                          Stock No. 880-3.                                                      
Sigma Chemical Co......................  Barbital, Product No. B-8632...  Sealed Ampule: 1ml.......      6/30/77
Sigma Chemical Co......................  Benzoylecgonine 1 mg/ml, No. B-  Glass Ampule: 2 ml.......      6/29/89
                                          8900.                                                                 
Sigma Chemical Co......................  Benzoylecgonine-d3 #B-3277.....  Ampule: 2ml..............      8/28/90
Sigma Chemical Co......................  Benzphetamine Hydrochloride,     Sealed Ampule: 1ml.......       6/8/84
                                          Product No. B-8765.                                                   
Sigma Chemical Co......................  Bolasterone, Product #B3404....  Ampule: 1ml..............      1/30/92
Sigma Chemical Co......................  Bromazepam #B-5402.............  Ampule: 2ml..............      8/28/90
Sigma Chemical Co......................  Bufotenine Monooxalate, Product  Sealed Ampule: 1ml.......      6/30/77
                                          No. B-8757.                                                           
Sigma Chemical Co......................  Buprenorphine Hydrochloride....  Vial: 2ml................      9/12/94
Sigma Chemical Co......................  Butabarbital , Product No. B-    Sealed Ampule: 1ml.......      6/30/77
                                          8882.                                                                 
Sigma Chemical Co......................  Butalbital, Product No. B-5514.  Sealed Ampule: 1ml.......      9/19/83
Sigma Chemical Co......................  Butethal (B-7516)..............  Ampule: 1ml..............       9/5/85
Sigma Chemical Co......................  Cannabidiol, Product No. C-6395  Vial: 1ml................      5/11/81
Sigma Chemical Co......................  Cannabinol, Product No. C-6520.  Vial: 1ml................      5/11/81

[[Page 164]]

                                                                                                                
Sigma Chemical Co......................  Chloral Hydrate , Product No. C- Sealed Ampule: 1ml.......      6/30/77
                                          6516.                                                                 
Sigma Chemical Co......................  Chloral Hydrate, Product #C9954  Ampule: 1ml..............      5/10/95
Sigma Chemical Co......................  Chlorazepam Dipotassium Salt,    Ampule: 1ml..............      5/24/85
                                          (C-9531).                                                             
Sigma Chemical Co......................  Chlordiazepoxide (C-4782)......  Ampule: 1ml..............       9/5/85
Sigma Chemical Co......................  Chlordiazepoxide Hydrochloride   Ampule: 2ml..............      6/26/90
                                          Acetonitrile Drug Standard #C-                                        
                                          9547.                                                                 
Sigma Chemical Co......................  Chlordiazepoxide-d5 #C-5047....  Ampule: 2ml..............      8/28/90
Sigma Chemical Co......................  Clobazam, No. C-6667...........  Glass Ampule: 2ml........       6/6/89
Sigma Chemical Co......................  Clonazepam, Product No. C-4404.  Sealed Ampule: 1ml.......       6/8/84
Sigma Chemical Co......................  Cocaethylene, #C-8205..........  Ampule: 1ml..............      10/9/95
Sigma Chemical Co......................  Cocaethylene, C-7313...........  Vial: 2ml................       2/4/94
Sigma Chemical Co......................  Cocaethylene-D5, #C-7073.......  Ampule: 1ml..............      10/9/95
Sigma Chemical Co......................  Cocaine Hydrochloride Product    Sealed Ampule: 1ml.......      9/19/83
                                          No. C-1528.                                                           
Sigma Chemical Co......................  Cocaine-d3 #C-3547.............  Ampule: 2ml..............      8/28/90
Sigma Chemical Co......................  Codeine-d3 HCl #C-3672.........  Ampule: 2ml..............      8/28/90
Sigma Chemical Co......................  Codeine, Product No. C-1653....  Sealed Ampule: 1ml.......      9/19/83
Sigma Chemical Co......................  D-Amphetamine Sulfate, Product   Vial: 1ml................      5/11/81
                                          No. A-3278.                                                           
Sigma Chemical Co......................  D-Propoxyphene Hydrochloride, P- Ampule: 1ml..............      9/27/84
                                          1550.                                                                 
Sigma Chemical Co......................  DL-Amphetamine HCL , Product     Sealed Ampule: 1ml.......      6/30/77
                                          No. A-5017.                                                           
Sigma Chemical Co......................  Delorazepam #D-5789............  Ampule: 2ml..............      8/28/90
Sigma Chemical Co......................  Desmethyldiazepam 1 mg/ml, No.   Glass Ampule: 2 ml.......      6/29/89
                                          D-3162.                                                               
Sigma Chemical Co......................  Desmethyldiazepam-d5 #D-6039...  Ampule: 2ml..............      8/28/90
Sigma Chemical Co......................  Diazepam, Product No. D-9900...  Sealed Ampule: 1ml.......       6/8/84
Sigma Chemical Co......................  Diazepam-d5 #D-5664............  Ampule: 2ml..............      8/28/90
Sigma Chemical Co......................  Diethylpropion Hydrochloride,    Sealed Ampule: 1ml.......      9/19/83
                                          Product No. D-7274.                                                   
Sigma Chemical Co......................  Diphenoxylate HCL, Product       Ampule: 1ml..............       9/5/85
                                          #D0780.                                                               
Sigma Chemical Co......................  Drug Standard Mix 1, D-3155....  Ampule: 2ml..............      4/18/86
Sigma Chemical Co......................  Drug Standard Mix 2, D-3030....  Ampule: 2ml..............      4/18/86
Sigma Chemical Co......................  Ecgonine Hydrochloride 1 mg/ml,  Glass Ampule: 2 ml.......      6/29/89
                                          No. E-9762.                                                           
Sigma Chemical Co......................  Ecgonine-d3 HCl #E-2014........  Ampule: 2ml..............      8/28/90
Sigma Chemical Co......................  Ecgonine-d3 Methyl Ester HCl #E- Ampule: 2ml..............      8/28/90
                                          2139.                                                                 
Sigma Chemical Co......................  Estazolam #E-1139..............  Ampule: 2ml..............      8/28/90
Sigma Chemical Co......................  Ethinamate (E-8508)............  Ampule: 1ml..............      4/10/85
Sigma Chemical Co......................  Ethylmorphine, E-3377..........  Ampule: 2ml..............      9/25/91
Sigma Chemical Co......................  Fencamfamine Hydrochloride.....  Vial: 2ml................      9/12/94
Sigma Chemical Co......................  Fenfluramine Hydrochloride,      Sealed Ampule: 1ml.......      9/19/83
                                          Product No. F-1884.                                                   
Sigma Chemical Co......................  Fenproporex Hydrochloride, No.   Glass Ampule: 2ml........       6/6/89
                                          F-7261.                                                               
Sigma Chemical Co......................  Fentanyl Citrate, No. F-5886...  Glass Ampule: 2 ml.......       6/6/89
Sigma Chemical Co......................  Fentanyl-d5 Citrate #F-2520....  Ampule: 2ml..............      8/28/90
Sigma Chemical Co......................  Flunitrazepam No. F-8763.......  Vial: 1 ml...............      6/30/87
Sigma Chemical Co......................  Fluoxymesterone, Product #F6891  Ampule: 2ml..............      1/30/92
Sigma Chemical Co......................  Flurazepam Dihydrochloride       Vial: 1 ml...............     10/20/89
                                          Product #F9134.                                                       
Sigma Chemical Co......................  Gelatin Veronal Buffer (GVB2+)   Vial: 50 ml, 250ml.......      9/15/86
                                          No. G-6514.                                                           
Sigma Chemical Co......................  Glutethimide, Product No. G-     Sealed Ampule: 1 ml......      6/30/77
                                          3134.                                                                 
Sigma Chemical Co......................  Glycerophosphate Substrate,      Bottle: 4 ounce..........      7/25/83
                                          Product No. 675-2.                                                    
Sigma Chemical Co......................  Heroin Hydrochloride .1 mg/ml,   Glass Ampule: 2 ml.......      6/29/89
                                          No. H-5144.                                                           
Sigma Chemical Co......................  Hexobarbital, Product No. H-     Sealed Ampule: 1 ml......      6/30/77
                                          2007.                                                                 
Sigma Chemical Co......................  Hydrocodone Bitartrate, No. H-   Glass Ampule: 2 ml.......       6/6/89
                                          2269.                                                                 
Sigma Chemical Co......................  Hydromorphone Hydrochloride No.  Vial: 1 ml...............      6/30/87
                                          H-7141.                                                               
Sigma Chemical Co......................  Hydroxytestosterone, Product     Vial: 0.5 ml.............      5/10/95
                                          #H9901.                                                               
Sigma Chemical Co......................  Ibogaine HCL, Product No. I-     Sealed Ampule: 1 ml......      6/30/77
                                          4630.                                                                 
Sigma Chemical Co......................  LDH Electrophoresis Buffer,      Bottle: 30 ml............       1/4/77
                                          Stock No. 705-1.                                                      
Sigma Chemical Co......................  LDH-P Reagent No. 125-100......  Vial: 100 ml.............      5/29/73
Sigma Chemical Co......................  Levorphanol Tartrate 1 mg/ml,    Glass Ampule: 2 ml.......      6/29/89
                                          No. L-0896.                                                           
Sigma Chemical Co......................  Lorazepam (L-0140).............  Ampule: 1 ml.............      5/24/85
Sigma Chemical Co......................  Lormetazepam, No. 8145.........  Glass Ampule: 2 ml.......       6/6/89
Sigma Chemical Co......................  Lysergic Acid , Product No. L-   Sealed Ampule: 1 ml......      6/30/77
                                          5881.                                                                 
Sigma Chemical Co......................  Lysergic Acid Diethylamide #L-   Ampule: 2 ml.............      8/28/90
                                          8147.                                                                 
Sigma Chemical Co......................  Lysergic Acid Diethylamide,      Ampule: 1 ml.............      8/17/94
                                          Drug Standard No. L-5406.                                             
Sigma Chemical Co......................  Mayer's Hematoxylin Solution,    Bottle: 3 ml, 6 ml, 25          8/6/73
                                          MHS-1, MHS-16, MHS-32, MHS-80,   ml, 100 ml, 225 ml, 500              
                                          MHS-128.                         ml, 1.0L, 2.5L, 4.0L.                
Sigma Chemical Co......................  Mayer's Hematoxylin Solution,    Bulk: 1000L..............       5/4/93
                                          No. MHS-1.                                                            
Sigma Chemical Co......................  Mebutamate (M-3772)............  Ampule: 1 ml.............       9/5/85
Sigma Chemical Co......................  Medazepam (M-7646).............  Ampule: 1 ml.............      5/24/85
Sigma Chemical Co......................  Meperidine Hydrochloride (M-     Ampule: 1 ml.............      8/27/84
                                          1020).                                                                
Sigma Chemical Co......................  Mephobarbital, Product No. M-    Vial: 1 ml...............      5/11/81
                                          3514.                                                                 
Sigma Chemical Co......................  Meprobamate (M-0271)...........  Ampule: 1 ml.............      5/24/85
Sigma Chemical Co......................  Mescaline HC1 , Product No. M-   Sealed Ampule: 1 ml......      6/30/77
                                          5153.                                                                 
Sigma Chemical Co......................  Mesterolone, Product #M8283....  Ampule: 2 ml.............      1/30/92
Sigma Chemical Co......................  Methadone Hydrochloride,         Sealed Ampule: 1 ml......      9/19/83
                                          Product No. M-3268.                                                   

[[Page 165]]

                                                                                                                
Sigma Chemical Co......................  Methadone-d3 #M-4781...........  Ampule: 2 ml.............      8/28/90
Sigma Chemical Co......................  Methamphetamine HC1 , Product    Sealed Ampule: 1 ml......      6/30/77
                                          No. M-5260.                                                           
Sigma Chemical Co......................  Methandrostenolone, Product      Ampule: 2 ml.............      1/30/92
                                          #M6910.                                                               
Sigma Chemical Co......................  Methaqualone Hydrochloride,      Sealed Ampule: 1 ml......      9/19/83
                                          Product No. M-3393.                                                   
Sigma Chemical Co......................  Methaqualone-d4 #M-5406........  Ampule: 2 ml.............      8/28/90
Sigma Chemical Co......................  Methylphenidate Hydrochloride    Ampule: 1 ml.............     10/31/84
                                          (M-1145).                                                             
Sigma Chemical Co......................  Methyprylon, Product No. M-1769  Sealed Ampule: 1 ml......       6/8/84
Sigma Chemical Co......................  Morphine Sulfate, No. M-9524...  Glass Ampule: 2 ml.......       6/6/89
Sigma Chemical Co......................  Morphine-3-B-D Glucuronide,      Ampule: 1 ml.............     10/21/82
                                          Product No. M-4266.                                                   
Sigma Chemical Co......................  Morphine-d3 HCl, M-6380........  Ampule: 2 ml.............      9/25/91
Sigma Chemical Co......................  N, N-Diethyltryptamine, Product  Vial: 1 ml...............      5/11/81
                                          No. D-0392.                                                           
Sigma Chemical Co......................  N, N-Dimethyltryptamine,         Sealed Ampule: 1 ml......      6/30/77
                                          Product No. D-6263.                                                   
Sigma Chemical Co......................  Nalorphine Hydrochloride.......  Ampule: 1 ml.............      8/27/84
Sigma Chemical Co......................  Nitrazepam, N-3397.............  Ampule: 1 ml.............       9/8/93
Sigma Chemical Co......................  Norcodeine Hydrochloride, No. N- Glass Ampule: 2 ml.......       6/6/89
                                          3017.                                                                 
Sigma Chemical Co......................  Normorphine HCl #N-7393........  Ampule: 2 ml.............      8/28/90
Sigma Chemical Co......................  Noroxymorphone #N-7018.........  Ampule: 2 ml.............      8/28/90
Sigma Chemical Co......................  Owren's Buffer, No. 05880......  Bottle: 500 ml; Vial: 20        4/5/89
                                                                           ml; Box: 5vials.                     
Sigma Chemical Co......................  Oxazepam, No. O-1755...........  Vial: 1 ml...............      6/30/87
Sigma Chemical Co......................  Oxazepam-d5 #O-1381............  Ampule: 2 ml.............      8/28/90
Sigma Chemical Co......................  Oxazolam, No. O-8005...........  Glass Ampule: 2 ml.......       6/6/89
Sigma Chemical Co......................  Oxycodone Hydrochloride,         Sealed Ampule: 1 ml......      9/19/83
                                          Product No. O-2628.                                                   
Sigma Chemical Co......................  Oxymetholone, Product #O4006...  Ampule: 2 ml.............      1/30/92
Sigma Chemical Co......................  Paraldehyde, Product No. P-3778  Ampule: 1 ml.............     10/21/82
Sigma Chemical Co......................  Pemoline, Product No. P-3518...  Sealed Ampule: 1 ml......      6/30/77
Sigma Chemical Co......................  Pentazocine Hydrochloride,       Sealed Ampule: 1 ml......      9/19/83
                                          Product No. P-7530.                                                   
Sigma Chemical Co......................  Pentobarbital, Product No. P-    Sealed Ampule: 1ml.......      6/30/77
                                          3393.                                                                 
Sigma Chemical Co......................  Phencyclidine HCL, Product       Vial: 1 ml...............      6/30/87
                                          #P7043.                                                               
Sigma Chemical Co......................  Phencyclidine-d5 HCl #P-6054...  Ampule: 2ml..............      8/28/90
Sigma Chemical Co......................  Phendimetrazine Bitartrate,      Vial: 1ml................      5/11/81
                                          Product #P3524.                                                       
Sigma Chemical Co......................  Phenobarbital FPIA Calibrator    Kit: 6 vials.............     11/21/89
                                          Set Cat. No. P9051.                                                   
Sigma Chemical Co......................  Phenobarbital FPIA Calibrator:   Vial: 2.5 ml.............     11/21/89
                                          A-No.P8301, B-No.P8426, C-                                            
                                          No.P8551, D-No.P8676, E-                                              
                                          No.P8801, F-No.P8926.                                                 
Sigma Chemical Co......................  Phenobarbital Primary Stock      Bottle: 10, 5, 1L, 500,         2/1/91
                                          Solution No. Z-5419.             100ml.                               
Sigma Chemical Co......................  Phenobarbital Prod. No.P-3643..  Sealed Ampule: 1ml.......      6/30/77
Sigma Chemical Co......................  Phentermine Hydrochloride,       Sealed Ampule: 1ml.......      9/19/83
                                          Product No. P-7655.                                                   
Sigma Chemical Co......................  Phenylacetone, Product #P3958..  Ampule: 1ml..............      5/10/95
Sigma Chemical Co......................  Phenylacetone, Product No. P-    Vial: 1ml................      5/11/81
                                          2024.                                                                 
Sigma Chemical Co......................  Prazepam, No. P-7168...........  Vial: 1 ml...............      6/30/87
Sigma Chemical Co......................  Psilocin #P-4054...............  Ampule: 2ml..............      8/28/90
Sigma Chemical Co......................  SIA Cocaine Metabolites........  Kit: 96 Tests............      7/11/91
Sigma Chemical Co......................  SIA Conjugate Cocaine            Bottle: 75ml.............      7/11/91
                                          Metabolites.                                                          
Sigma Chemical Co......................  SIA Positive Reference Cocaine   Vial: 1ml................      7/11/91
                                          Metabolites.                                                          
Sigma Chemical Co......................  Secobarbital, Product No. S-     Sealed Ampule: 1ml.......      6/30/77
                                          4006.                                                                 
Sigma Chemical Co......................  Secobarbital-d5, S-4628........  Ampule: 2ml..............      9/25/91
Sigma Chemical Co......................  Stanozolol, Product #S7649.....  Ampule: 2ml..............      1/30/92
Sigma Chemical Co......................  Stanozolol-d3, Product #S7774..  Ampule: 2ml..............      1/30/92
Sigma Chemical Co......................  Temazepam, No. T-4903..........  Vial: 1 ml...............      6/30/87
Sigma Chemical Co......................  Tenocyclidine HCl, T-3507......  Ampule: 2ml..............      9/25/91
Sigma Chemical Co......................  Testosterone 17beta-Cypionate,   Ampule: 1ml..............      7/30/92
                                          T 3415.                                                               
Sigma Chemical Co......................  Testosterone Acetate, Product    Ampule: 2ml..............      1/30/92
                                          #T5661.                                                               
Sigma Chemical Co......................  Testosterone Benzoate, Product   Ampule: 2ml..............      1/30/92
                                          #T1913.                                                               
Sigma Chemical Co......................  Testosterone Enanthate, T 3540.  Ampule: 1ml..............      7/30/92
Sigma Chemical Co......................  Testosterone Propionate, T 3665  Ampule: 1ml..............      7/30/92
Sigma Chemical Co......................  Testosterone, Product #T5411...  Ampule: 2ml..............      1/30/92
Sigma Chemical Co......................  Testosterone-d3, Product #T5536  Ampule: 2ml..............      1/30/92
Sigma Chemical Co......................  Thebaine, Product No. T-5270...  Sealed Ampule: 1ml.......      9/19/83
Sigma Chemical Co......................  Thiamylal Sodium, Product No. T- Sealed Ampule: 1ml.......       6/8/84
                                          6896.                                                                 
Sigma Chemical Co......................  Thiopental (T-1022)............  Ampule: 1ml..............      8/27/84
Sigma Chemical Co......................  Triazolam #T-7658..............  Ampule: 2ml..............      8/28/90
Sigma Chemical Co......................  Trizma-Barbital Buffer, Stock    Bottle: 30ml.............       1/4/77
                                          No. 710-1.                                                            
Sigma Chemical Co......................  Tropacocaine HCL, Product        Vial: 1ml................      5/11/81
                                          #T4576.                                                               
Sigma Chemical Co......................  Z9999, Field Test Sample         Vial: 400ml..............      3/14/91
                                          PSEUDOnarcotics Marihuana                                             
                                          Formulation.                                                          
Sigma Chemical Co......................  d-Amphetamine-d3 Sulfate #A-     Ampule: 2ml..............      8/28/90
                                          7180.                                                                 
Sigma Chemical Co......................  d-Lysergic Acid Cat. No. L-9752  Ampule: 2ml..............      11/6/91
Sigma Chemical Co......................  d-Propoxyphene-d7 HCl #P-4179..  Ampule: 2ml..............      8/28/90
Sigma Chemical Co......................  delta-9-tetrahydrocannabinol-d3  Ampule: 2ml..............      8/28/90
                                          #T-8783.                                                              
Sigma Chemical Co......................  dl-Amphetamine, A-2262.........  Ampule: 2ml..............      9/25/91

[[Page 166]]

                                                                                                                
Sigma Chemical Co......................  l-Amphetamine, A-9136..........  Ampule: 2ml..............      9/25/91
Sigma Chemical Co......................  p-Methoxyamphetamine HCl #M-     Ampule: 2ml..............      8/28/90
                                          4656.                                                                 
Sigma Diagnostics......................  Amelung Systems Buffer.........  Box: 6 Vials; Bottle:           2/8/96
                                                                           25ml.                                
Sigma Diagnostics......................  CA System Buffer...............  Bottle: 500ml............       9/9/93
Smart Chemical Co......................  Regal 180XL....................  Plastic Drum: 55 gallon..      6/12/86
SmithKline Beecham.....................  Benzo/PCP QC...................  Bottle: 10ml.............      7/31/95
SmithKline Beecham.....................  GC/MS 1........................  Bottle: 50ml.............      7/31/95
SmithKline Beecham.....................  NIDA LODQC.....................  Bottle: 50ml.............      7/31/95
SmithKline Beecham.....................  SAP LODQC......................  Bottle: 50ml.............      7/31/95
SmithKline Beecham.....................  SB50N..........................  Bottle: 10, 25, 50ml.....      7/31/95
SmithKline Beecham.....................  SB50P..........................  Bottle: 10, 25, 50ml.....      7/31/95
SmithKline Beecham.....................  Urine Drug Standards Pool A, B,  Bottle: 25ml.............      7/31/95
                                          C, D, E, F, G.                                                        
SolarCare Technology Corporation.......  Benzoylecgonine Cutoff           Vial: 4ml................       6/5/90
                                          Calibrator.                                                           
SolarCare Technology Corporation.......  Benzoylecgonine Negative         Vial: 4ml................       6/5/90
                                          Control.                                                              
SolarCare Technology Corporation.......  Benzoylecgonine Positive         Vial: 4ml................       6/5/90
                                          Control.                                                              
SolarCare Technology Corporation.......  Cocaine Cutoff Calibrator......  Vial: 4ml................       6/5/90
SolarCare Technology Corporation.......  Cocaine EIA....................  Kit: 3 vials.............       6/5/90
SolarCare Technology Corporation.......  Cocaine Metabolite EIA.........  Kit: 30 vials............       6/5/90
SolarCare Technology Corporation.......  Cocaine Negative Control.......  Vial: 4ml................       6/5/90
SolarCare Technology Corporation.......  Cocaine Positive Control.......  Vial: 4ml................       6/5/90
SolarCare Technology Corporation.......  LSD Cutoff Calibrator..........  Vial: 4ml................       6/5/90
SolarCare Technology Corporation.......  LSD EIA........................  Kit: 3 vials.............       6/5/90
SolarCare Technology Corporation.......  LSD Negative Control...........  Vial: 4ml................       6/5/90
SolarCare Technology Corporation.......  LSD Positive Control...........  Vial: 4ml................       6/5/90
SolarCare Technology Corporation.......  Low Level Benzodiazepine         Kit: 3 vials.............       6/5/90
                                          (Triazolam) EIA.                                                      
SolarCare Technology Corporation.......  Triazolam Cutoff Control.......  Vial: 4ml................       6/5/90
SolarCare Technology Corporation.......  Triazolam Negative Control.....  Vial: 4ml................       6/5/90
SolarCare Technology Corporation.......  Triazolam Positive Control.....  Vial: 4ml................       6/5/90
Supelco, Inc...........................  Gamma-DEX Programmed Column      Ampule: 1ml..............      9/15/95
                                          Test Mix.                                                             
Supelco, Inc...........................  Alk Mix No. 04-9210............  Vial: 1ml................      8/28/73
Supelco, Inc...........................  Amobarbital, No. 04-9170.......  Ampule: 1ml..............     12/22/72
Supelco, Inc...........................  Amph. Mix Catalog No. 4-9205...  Glass Ampule: 2ml........       6/9/86
Supelco, Inc...........................  Amphetamine No. 04-9165........  Ampule: 1ml..............     12/22/72
Supelco, Inc...........................  Anticonvulsant Mixture No. 1;    Glass Serum Bottle: 50ml.      6/16/77
                                          No. 04-9202.                                                          
Supelco, Inc...........................  Antiepileptic Calibration        Kit: 3 Ampules...........      5/21/80
                                          Standard Kit, No. 4-9259.                                             
Supelco, Inc...........................  Antiepileptic Calibration        Glass Ampule: 5ml........      5/21/80
                                          Standards, Nos. 4-9256, 4-                                            
                                          9257, 4-9258.                                                         
Supelco, Inc...........................  Appendix IX Contract Mix 3.....  Ampule: 2ml..............     12/22/94
Supelco, Inc...........................  Aprobarbital No. 04-9171.......  Ampule: 1ml..............     12/22/72
Supelco, Inc...........................  Barb. Mix 1, Catalog No. 4-9200  Glass Ampule: 2ml........       6/9/86
Supelco, Inc...........................  Barb. Mix 2, Catalog No. 4-9201  Glass Ampule: 2ml........       6/9/86
Supelco, Inc...........................  Barbital, Catalog No. 4-9279...  Glass Ampule: 10ml.......       6/9/86
Supelco, Inc...........................  Barbiturates Test Mix Catalog    Ampule: 2 ml.............      2/25/87
                                          No. 4-9295.                                                           
Supelco, Inc...........................  Cannabidiol, No. 04-9221.......  Ampule: 1ml..............     11/27/74
Supelco, Inc...........................  Cannabinol, No. 04-9235........  Ampule: 1ml..............     11/27/74
Supelco, Inc...........................  Chloral Hydrate Kit, Product #   Kit: 19 Vials; 2ml each..       9/6/94
                                          4-8112.                                                               
Supelco, Inc...........................  Chloral Hydrate, Product # 4-    Ampule: 2ml..............      9/15/95
                                          7335.                                                                 
Supelco, Inc...........................  Cocaine, No. 04-9188...........  1000 mcg /Glass Ampule...       6/5/75
Supelco, Inc...........................  Codeine No. 04-9161............  Ampule: 1ml..............     12/22/72
Supelco, Inc...........................  Custom Appendix IX Mix-3,        Ampule: 10ml.............       4/6/95
                                          Product # 86-8043.                                                    
Supelco, Inc...........................  Cyclobarbital No. 04-9175......  Ampule: 1ml..............     12/22/72
Supelco, Inc...........................  Delta-1 THC, No. 04-9237.......  Ampule: 1ml..............     11/27/74
Supelco, Inc...........................  Delta-6 THC, No. 04-9238.......  Ampule: 1ml..............     11/27/74
Supelco, Inc...........................  Dextroamphetamine, No. 4-9185..  Glass Ampule: 1ml........      5/21/80
Supelco, Inc...........................  EPA 8270 Base/Neutrals Mix B,    Vial: 2ml................      8/31/94
                                          Product # 4-8195.                                                     
Supelco, Inc...........................  Glutethimide No. 04-9173.......  Ampule: 1ml..............     12/22/72

[[Page 167]]

                                                                                                                
Supelco, Inc...........................  Heroin No. 04-9162.............  Ampule: 1ml..............     12/22/72
Supelco, Inc...........................  Hexobarbital No. 04-9177.......  Ampule: 1ml..............     12/22/72
Supelco, Inc...........................  Mephobarbital No. 04-9178......  Ampule: 1ml..............     12/22/72
Supelco, Inc...........................  Meprobamate, No. 4-9184........  Glass Ampule: 1ml........      5/21/80
Supelco, Inc...........................  Methadone No. 04-9163..........  Ampule: 1ml..............     12/22/72
Supelco, Inc...........................  Methamphetamine No. 04-9168....  Ampule: 1ml..............     12/22/72
Supelco, Inc...........................  Methaqualone, No. 04-9183......  1000 mcg /Glass Ampule...       6/5/75
Supelco, Inc...........................  Morphine No. 04-9160...........  Glass Ampule: 1000mcg....       3/8/78
Supelco, Inc...........................  NET Appendix IX Mix-3, Product   Ampule: 2ml..............       5/3/95
                                          # 86-8-58.                                                            
Supelco, Inc...........................  Pentobarbital No. 04-9179......  Glass Ampule: 1000mcg....       3/8/78
Supelco, Inc...........................  Phenobarbital No. 04-9181......  Glass Ampule: 1000mcg....       3/8/78
Supelco, Inc...........................  Psilocybin, No. 04-9191........  1000 mcg /Glass Ampule...       6/5/75
Supelco, Inc...........................  Secobarbital No. 04-9180.......  Glass Ampule: 1000mcg....       3/8/78
Supelco, Inc...........................  alpha, alpha-                    Ampule: 2ml..............       2/7/95
                                          Dimethylphenethylamine.                                               
Supelco, Inc...........................  alpha, alpha-                    Vial: 2ml................      8/31/94
                                          Dimethylphenethylamine,                                               
                                          Product # 4-8377.                                                     
Sure-Tech Diagnostic Associates, Inc...  3, 4-Methylenedioxyamphetamine   Vial: 20ml...............      4/24/92
                                          in Urine Matrix; Prod 928.                                            
Sure-Tech Diagnostic Associates, Inc...  3, 4-                            Vial: 20ml...............      4/24/92
                                          Methylenedioxymethylamphetamin                                        
                                          e in Urine Matrix; Prod 929.                                          
Sure-Tech Diagnostic Associates, Inc...  Alprazolam in Urine Matrix;      Vial: 20ml...............      4/24/92
                                          Prod. 920.                                                            
Sure-Tech Diagnostic Associates, Inc...  Codeine in Urine Matrix; Prod    Vial: 20ml...............      4/24/92
                                          924.                                                                  
Sure-Tech Diagnostic Associates, Inc...  D-Methamphetamine/D-Amphetamine  Vial: 20ml...............      4/24/92
                                          in Urine Matrix; Prod 926.                                            
Sure-Tech Diagnostic Associates, Inc...  D-Propoxyphene in Urine Matrix;  Vial: 20ml...............      4/24/92
                                          Prod 936.                                                             
Sure-Tech Diagnostic Associates, Inc...  Drugs of Abuse Urine Control     Vial: 4ml Kit: 1 vial....      5/11/90
                                          (Blind Sample) Positive                                               
                                          Amphetamine Kit No. ST 904,                                           
                                          Vial No. 904-P.                                                       
Sure-Tech Diagnostic Associates, Inc...  Drugs of Abuse Urine Control     Kit: 2 vials.............      5/11/90
                                          (Blind Sample) Positive                                               
                                          Cocaine & Marijuana Kit No. ST                                        
                                          903.                                                                  
Sure-Tech Diagnostic Associates, Inc...  Drugs of Abuse Urine Control     Vial: 4ml Kit: 1 vial....      5/11/90
                                          (Blind Sample) Positive                                               
                                          Cocaine, Kit No. ST 901, Vial                                         
                                          No. 901-P.                                                            
Sure-Tech Diagnostic Associates, Inc...  Drugs of Abuse Urine Control     Vial: 4ml Kit: 1 vial....      5/11/90
                                          (Blind Sample) Positive                                               
                                          Marijuana, Kit No. ST 902,                                            
                                          Vial No. 902-P.                                                       
Sure-Tech Diagnostic Associates, Inc...  Drugs of Abuse Urine Control     Vial: 4ml Kit: 1 vial....      5/11/90
                                          (Blind Sample) Positive                                               
                                          Opiates Kit No. ST 905, Vial                                          
                                          No. 905-P.                                                            
Sure-Tech Diagnostic Associates, Inc...  Drugs of Abuse Urine Control     Vial: 4ml Kit: 1 vial....      5/11/90
                                          (Blind Sample) Positive                                               
                                          Phencyclidine Kit No. ST 906,                                         
                                          Vial No. 906-P.                                                       
Sure-Tech Diagnostic Associates, Inc...  Drugs of Abuse: Urine Controls   Vial: 20ml; Box: 1 vial..      9/13/90
                                          (Blind Samples) positive                                              
                                          Codeine No. 907-P.                                                    
Sure-Tech Diagnostic Associates, Inc...  Drugs of Abuse: Urine Controls   Vial: 20ml; Box: 1 vial..      9/13/90
                                          (Blind Samples) positive                                              
                                          Methadone No. 908-P.                                                  
Sure-Tech Diagnostic Associates, Inc...  Drugs of Abuse: Urine Controls   Vial: 20ml; Box: 1 vial..      9/13/90
                                          (Blind Samples) positive                                              
                                          Methamphetamine No. 909-P.                                            
Sure-Tech Diagnostic Associates, Inc...  Drugs of Abuse: Urine Controls   Vial: 20ml, Box: 1 vial..      9/13/90
                                          (Blind Samples) positive                                              
                                          Methaqualone No. 913-P.                                               
Sure-Tech Diagnostic Associates, Inc...  Drugs of Abuse: Urine Controls   Vial: 20ml, Box: 1 vial..      9/13/90
                                          (Blind Samples) positive                                              
                                          Oxazepam No. 910-P.                                                   
Sure-Tech Diagnostic Associates, Inc...  Drugs of Abuse: Urine Controls   Vial: 20ml, Box: 1 vial..      9/13/90
                                          (Blind Samples) positive                                              
                                          Propoxyphene No. 911-P.                                               
Sure-Tech Diagnostic Associates, Inc...  Drugs of Abuse: Urine Controls   Vial: 20ml, Box: 1 vial..      9/13/90
                                          (Blind Samples) positive                                              
                                          Secobarbital No. 912-P.                                               
Sure-Tech Diagnostic Associates, Inc...  Meperidine in Urine Matrix;      Vial: 20ml...............      4/24/92
                                          Prod 930.                                                             
Sure-Tech Diagnostic Associates, Inc...  Methadone in Urine Matrix; Prod  Vial: 20ml...............      4/24/92
                                          925.                                                                  
Sure-Tech Diagnostic Associates, Inc...  Methaqualone in Urine Matrix;    Vial: 20ml...............      4/24/92
                                          Prod 927.                                                             
Sure-Tech Diagnostic Associates, Inc...  Morphine-3-Glucuronide in Urine  Vial: 20ml...............      4/24/92
                                          Matrix; Prod 931.                                                     
Sure-Tech Diagnostic Associates, Inc...  Nordiazepam in Urine Matrix;     Vial: 20ml...............      4/24/92
                                          Prod 932.                                                             
Sure-Tech Diagnostic Associates, Inc...  Normeperidine in Urine Matrix;   Vial: 20ml...............      4/24/92
                                          Prod 933.                                                             
Sure-Tech Diagnostic Associates, Inc...  Oxazepam in Urine Matrix; Prod   Vial: 20ml...............      4/24/92
                                          934.                                                                  
Sure-Tech Diagnostic Associates, Inc...  Phencyclidine in Urine Matrix;   Vial: 20 ml..............      4/24/92
                                          Prod 935.                                                             
Sure-Tech Diagnostic Associates, Inc...  Secobarbital in Urine Matrix;    Vial: 20ml...............      4/24/92
                                          Prod 937.                                                             

[[Page 168]]

                                                                                                                
Sure-Tech Diagnostic Associates, Inc...  Temazepam in Urine Matrix; Prod  Vial: 20ml...............      4/24/92
                                          938.                                                                  
Sure-Tech Diagnostic Associates, Inc...  Triazolam in Urine Matrix; Prod  Vial: 20ml...............      4/24/92
                                          939.                                                                  
Sure-Tech Diagnostics Associates, Inc..  9-Carboxyl-11 Nor-A-9-THC in     Vial: 20ml...............      4/24/92
                                          Urine Matrix; Prod 923.                                               
Sure-Tech Diagnostics Associates, Inc..  Benzoylecgonine in Urine         Vial: 20ml...............      4/24/92
                                          Matrix; Prod 922.                                                     
Sure-Tech Diagnostics Associates, Inc..  D-Amphetamine in Urine Matrix;   Vial: 20ml...............      4/24/92
                                          Prod. 921.                                                            
Syva Co................................  AccuLevel Phenobarbital Test     Flask: 50ml..............     10/31/85
                                          Control Stock Solution.                                               
Syva Co................................  AccuLevel Phenobarbital Test     (1) Glass Vial: 6ml; (2)       1/24/86
                                          Kit (Catalog No. 10C019)         Glass Vial: 9ml, 12                  
                                          Contains: (1) AccuLevel          Vials per test kit.                  
                                          Phenobarbital Control (2)                                             
                                          AccuLevel Reagent I.                                                  
Syva Co................................  Advance T-3 Uptake Assay.......  Kit: 100 tests...........      5/11/82
Syva Co................................  Advance Thyroxin Assay.........  Kit: 100 tests...........      5/11/82
Syva Co................................  Antiepileptic Drug Control.....  Vial: 10ml , Lyophilized.      8/27/74
Syva Co................................  EMIT 2000 Phenobarbital Bulk     Bottle: 1000ml...........      7/14/94
                                          Reagent 1.                                                            
Syva Co................................  EMIT 2000 Phenobarbital Bulk     Bottle: 200ml............      2/22/93
                                          Reagent B.                                                            
Syva Co................................  EMIT 2000 Phenobarbital          Bottle: 3ml..............      7/14/94
                                          Calibrators 5, 10, 20, 40 and                                         
                                          80.                                                                   
Syva Co................................  EMIT IIC Cannabinoid Assay       Bottle: 500ml............     12/15/93
                                          Reagent 2.                                                            
Syva Co................................  EMIT IIC Cannabinoid Assay.....  Kit: 2 Bottles...........     12/15/93
Syva Co................................  EMIT IIC Phencyclidine Assay...  Kit: 2 Bottles...........     12/15/93
Syva Co................................  EMIT IIC Phencyclidine Assay     Bottle: 500ml............     12/15/93
                                          Reagent 2.                                                            
Syva Co................................  EMIT Thyroxine Assay, Cat. No.   Glass Bottle: 4oz., Kit:       1/23/89
                                          6J909.                           500 Assays.                          
Syva Co................................  Emit 2000 Phenobarbital Assay    Kit: 1 cassette;                8/5/91
                                          (Convenience Pack).              Cassette: 11ml.                      
Syva Co................................  Emit 2000 Phenobarbital Assay;   Kit: 1 bottle; Bottle:          8/5/91
                                          Enzyme Reagent 2.                15ml.                                
Syva Co................................  Emit 2000 Phenobarbital Bulk     Bottle: 200ml............       6/9/93
                                          Reagent.                                                              
Syva Co................................  Emit 2000 Phenobarbital          Kit: 5 vials.............       8/5/91
                                          Calibrators (5, 10, 20, 40,                                           
                                          80).                                                                  
Syva Co................................  Emit 700 Amphetamine Assay       Bottle: 180ml............     10/12/84
                                          Catalog No. 3C919.                                                    
Syva Co................................  Emit 700 Barbiturate Assay       Bottle: 180ml............     10/12/84
                                          Catalog No.3D919.                                                     
Syva Co................................  Emit 700 Benzodiazepine Assay    Glass Bottle: 180ml, Kit:      2/21/89
                                          Reagent 2.                       2 bottles.                           
Syva Co................................  Emit 700 Calibrator A Catalog    Bottle: 3ml..............      10/5/84
                                          No. 3A919.                                                            
Syva Co................................  Emit 700 Calibrator B Catalog    Bottle: 3ml..............      10/5/84
                                          No. 3A969.                                                            
Syva Co................................  Emit 700 Cannabinoid (100)       Bottle: 180ml............     10/12/84
                                          Assay Catalog No. 3M919.                                              
Syva Co................................  Emit 700 Cannabinoid (100)       Bottle: 3ml..............      10/9/84
                                          Calibrator Catalog No. 3M969.                                         
Syva Co................................  Emit 700 Cannabinoid (20)        Plastic Bottle: 180ml....      9/15/86
                                          Assay, Catalog No. 3M959.                                             
Syva Co................................  Emit 700 Cannabinoid 100ng       Bottle: 3ml..............      7/31/89
                                          Assay, Positive Control.                                              
Syva Co................................  Emit 700 Cannabinoid 20ng Assay  Glass Bottle: 5ml, Kit: 2      2/21/89
                                          Calibrator.                      bottles.                             
Syva Co................................  Emit 700 Cannabinoid 20ng Assay  Glass Bottle: 5ml, Kit: 2      2/21/89
                                          Control Set-Positive Control.    bottles.                             
Syva Co................................  Emit 700 Cannabinoid Control     2 Bottles: 3ml...........      10/9/84
                                          Set Catalog No. 3M989.                                                
Syva Co................................  Emit 700 Cocaine Metabolite      Bottle: 180ml............     10/12/84
                                          Assay Catalog No. 3H919.                                              
Syva Co................................  Emit 700 Control Set A Catalog   2 Bottles: 3ml...........      10/9/84
                                          No. 3A939.                                                            
Syva Co................................  Emit 700 Control Set B Catalog   2 Bottles: 3ml...........      10/9/84
                                          No. 3A989.                                                            
Syva Co................................  Emit 700 Methaqualone Assay      Bottle: 180ml............     10/19/84
                                          Catalog No. 3Q919.                                                    
Syva Co................................  Emit 700 Opiate Assay Catalog    Bottle: 180ml............     10/12/84
                                          No.3B919.                                                             
Syva Co................................  Emit 700 Phencyclidine Assay     Bottle: 180ml............     10/12/84
                                          Catalog No. 3J919.                                                    
Syva Co................................  Emit AED-No. 1 Calibrator......  Vial: 3ml , Lyophilized..      8/27/74
Syva Co................................  Emit AED-No. 2 Calibrator......  Vial: 3ml , Lyophilized..      8/27/74
Syva Co................................  Emit AED-No. 3 Calibrator......  Vial: 3ml , Lyophilized..      8/27/74
Syva Co................................  Emit AED-No. 4 Calibrator......  Vial: 3ml , Lyophilized..      8/27/74
Syva Co................................  Emit AED-No. 5 Calibrator......  Vial: 3ml , Lyophilized..      8/27/74
Syva Co................................  Emit Amphetamine Bulk Powder     Bottle: 1000ml...........      10/4/89
                                          Reagent 2.                                                            
Syva Co................................  Emit Amphetamine Bulk Powder     Bottle: 4 oz.............      4/20/90
                                          Reagent 2 Satellite.                                                  
Syva Co................................  Emit Amphetamine Bulk Reagent B  Glass bottle: 1000ml.....      12/5/90
Syva Co................................  Emit Barbiturate Bulk Powder     Bottle: 1000ml...........      10/4/89
                                          Reagent 2.                                                            
Syva Co................................  Emit Barbiturate Bulk Powder     Bottle: 4 oz.............      4/20/90
                                          Reagent 2 Satellite.                                                  

[[Page 169]]

                                                                                                                
Syva Co................................  Emit Barbiturate Bulk Reagent B  Glass Bottle: 1000ml.....      12/5/90
Syva Co................................  Emit Benzodiazepine Bulk Powder  Bottle: 1000ml...........      10/4/89
                                          Reagent 2.                                                            
Syva Co................................  Emit Benzodiazepine Bulk Powder  Bottle: 4 oz.............      4/20/90
                                          Reagent 2 Satellite.                                                  
Syva Co................................  Emit Benzodiazepine Bulk         Glass Bottle: 1000ml.....      12/5/90
                                          Reagent B.                                                            
Syva Co................................  Emit Calibrator B Level 1        Vial: 5ml, 25ml..........      6/19/91
                                          (cutoff).                                                             
Syva Co................................  Emit Calibrator B Level 2        Vial: 5ml, 25ml..........      6/19/91
                                          (high).                                                               
Syva Co................................  Emit Cannabinoid (100) Bulk      Bottle: 1000ml...........      10/4/89
                                          Powder Reagent 2.                                                     
Syva Co................................  Emit Cannabinoid (100) Bulk      Bottle: 4 oz.............      4/20/90
                                          Powder Reagent 2 Satellite.                                           
Syva Co................................  Emit Cannabinoid Bulk Reagent B  Glass bottle: 1000ml.....      12/5/90
Syva Co................................  Emit Cocaine Metabolite Bulk     Bottle: 1000ml...........      10/4/89
                                          Powder Reagent 2.                                                     
Syva Co................................  Emit Cocaine Metabolite Bulk     Bottle: 4 oz.............      4/20/90
                                          Powder Reagent 2 Satellite.                                           
Syva Co................................  Emit Cocaine Metabolite Bulk     Glass Bottle: 1000ml.....      12/5/90
                                          Reagent B.                                                            
Syva Co................................  Emit Convenience Pack            Plastic Cassette: 100         11/23/87
                                          Phenobarbital Assay: Catalog     tests.                               
                                          No. 5D009.                                                            
Syva Co................................  Emit Convenience Pack: T-Uptake  Kit: 100 Tests Ea. Kit-         5/9/88
                                          Assay (Thyroid Hormone Binding   Plastic Cassette: 16 ml.             
                                          Ratio).                                                               
Syva Co................................  Emit Convenience Pack:           Plastic Cassette: 8ml,         2/22/89
                                          Thyroxine Assay Enzyme Reagent   Kit: 100 Assays.                     
                                          B.                                                                    
Syva Co................................  Emit Delta 9 Cannabinoid 100 ng/ Vial: 3ml................      8/22/89
                                          ml Calibrator/Control.                                                
Syva Co................................  Emit Delta 9 Cannabinoid 20 ng/  Vial: 3ml................      8/22/89
                                          ml Calibrator/Control.                                                
Syva Co................................  Emit Delta 9 Cannabinoid 400 ng/ Vial: 3ml................      8/22/89
                                          ml Calibrator/Control.                                                
Syva Co................................  Emit Delta 9 Cannabinoid 50 ng/  Vial: 3ml................      8/22/89
                                          ml Calibrator/Control.                                                
Syva Co................................  Emit HVA Amphetamine Assay       Kit: 2500 Assays.........      6/30/88
                                          Catalog No. 3C619.                                                    
Syva Co................................  Emit HVA Barbiturate Assay       Kit: 2500 Assays.........      6/30/88
                                          Catalog No. 3D619.                                                    
Syva Co................................  Emit HVA Calibrator Kit Catalog  Kit: 500 Tests Each Kit -      5/10/88
                                          No. 3A619.                       2 Glass Bottles 100 ml.              
Syva Co................................  Emit HVA Cannabinoid 100 ng      Kit: 2 Bottles, 50 ml ea.      7/15/88
                                          Assay Control Kit, Catalog No.                                        
                                          3M739.                                                                
Syva Co................................  Emit HVA Cannabinoid 100 ng.     Kit: 3 Bottles 50 ml ea..      7/15/88
                                          Assay Calibrator Kit, Catalog                                         
                                          No. 3M729.                                                            
Syva Co................................  Emit HVA Cannabinoid 100 ng.     Kit: 2500 Assays.........      7/15/88
                                          Assay Kit, Catalog No. 3M719.                                         
Syva Co................................  Emit HVA Cocaine Metabolite      Bottle: 125 ml...........      5/10/88
                                          Assay Catalog No. 3H619.                                              
Syva Co................................  Emit HVA Control Kit Catalog     Kit: 500 Tests Each Kit-2      5/10/88
                                          No. 3A629.                       Glass Bottles--100ml.                
Syva Co................................  Emit HVA Opiate Assay Catalog    Bottle: 125ml............      5/10/88
                                          No. 3B619.                                                            
Syva Co................................  Emit HVA Phencyclidine Assay     Bottle: 125ml............      5/19/88
                                          Catalog No. 3J619.                                                    
Syva Co................................  Emit II Barbiturate Assay......  Kit: 100ml, 500ml Bottle:      6/29/90
                                                                           4oz, 500ml.                          
Syva Co................................  Emit II Calibrator A Level 1     Vial: 10ml, 50ml.........      6/29/90
                                          (Cutoff).                                                             
Syva Co................................  Emit II Calibrator A Level 2     Vial: 10ml, 50ml.........      6/29/90
                                          (high).                                                               
Syva Co................................  Emit II Cannabinoid 20ng, 50ng,  Bottle: 4oz, 500ml; Kit:      10/12/90
                                          100ng Assay.                     100ml, 500ml.                        
Syva Co................................  Emit II Cocaine Metabolite       Kit: 100ml, 500ml Bottle:      6/29/90
                                          Assay.                           4oz, 500ml.                          
Syva Co................................  Emit II Delta 9 Cannabinoid      Vial: 10ml, 50ml.........     10/12/90
                                          20ng/ml, 50ng/ml, 100ng/ml,                                           
                                          200ng/ml, Calibrator/Control.                                         
Syva Co................................  Emit II Methadone Assay........  Kit: 2 vials.............      1/26/93
Syva Co................................  Emit II Methadone Assay Reagent  Bottle: 100ml, 500ml.....      1/26/93
                                          2.                                                                    
Syva Co................................  Emit II Methaqualone Assay.....  Kit: 2 vials.............      1/26/93
Syva Co................................  Emit II Methaqualone Assay       Bottle: 100ml, 500ml.....      1/26/93
                                          Reagent 2.                                                            
Syva Co................................  Emit II Monoclonal Amphetamine/  Kit: 2 vials.............      1/26/93
                                          Methamphetamine Assay.                                                
Syva Co................................  Emit II Monoclonal Amphetamine/  Vial: 100ml, 500ml.......      1/26/93
                                          Methamphetamine Assay Enzyme                                          
                                          Reagent 2.                                                            
Syva Co................................  Emit II Opiate Assay...........  Kit: 100ml, 500ml Bottle:      6/29/90
                                                                           4oz, 500ml.                          
Syva Co................................  Emit II Phencyclidine Assay....  Bottle: 4oz, 500ml; Kit:      10/26/90
                                                                           100ml, 500ml.                        
Syva Co................................  Emit IIC Barbiturate Assay.....  Kit: 2 Vials.............       1/6/94
Syva Co................................  Emit IIC Barbiturate Enzyme      Vial: 500ml..............       1/6/94
                                          Reagent 2.                                                            
Syva Co................................  Emit IIC Calibrators 0, 1, 2,    Vial: 10ml...............       1/6/94
                                          3, 4, 5.                                                              
Syva Co................................  Emit IIC Opiate Assay..........  Kit: 2 Vials.............       1/6/94
Syva Co................................  Emit IIC Opiate Enzyme Reagent   Vial: 500ml..............       1/6/94
                                          2.                                                                    
Syva Co................................  Emit Methadone Bulk Powder       Bottle: 1000 ml..........      10/4/89
                                          Reagent 2.                                                            
Syva Co................................  Emit Methadone Bulk Powder       Bottle: 4 oz.............      4/20/90
                                          Reagent 2 Satellite.                                                  
Syva Co................................  Emit Methadone Bulk Reagent....  Bottle: 1000ml...........       6/7/93
Syva Co................................  Emit Methaqualone Bulk Powder    Bottle: 1000 ml..........      10/4/89
                                          Reagent 2.                                                            
Syva Co................................  Emit Methaqualone Bulk Powder    Bottle: 4 oz.............      4/20/90
                                          Reagent 2 Satellite.                                                  
Syva Co................................  Emit Opiate Bulk Powder Reagent  Bottle: 1000 ml..........      10/4/89
                                          2.                                                                    

[[Page 170]]

                                                                                                                
Syva Co................................  Emit Opiate Bulk Powder Reagent  Bottle: 4 oz.............      4/20/90
                                          2 Satellite.                                                          
Syva Co................................  Emit Opiate Bulk Reagent B.....  Glass bottle: 1000ml.....      12/5/90
Syva Co................................  Emit Phencyclidine Bulk Powder   Bottle: 1000 ml..........      10/4/89
                                          Reagent 2.                                                            
Syva Co................................  Emit Phencyclidine Bulk Powder   Bottle: 4 oz.............      4/20/90
                                          Reagent 2 Satellite.                                                  
Syva Co................................  Emit Phencyclidine Bulk Reagent  Glass Bottle: 1000ml.....      12/5/90
                                          B.                                                                    
Syva Co................................  Emit Phenobarbital Bulk Powder   Bottle: 1000 ml..........      10/4/89
                                          Reagent B.                                                            
Syva Co................................  Emit Phenobarbital Bulk Powder   Bottle: 4 oz.............      4/20/90
                                          Reagent B Satellite.                                                  
Syva Co................................  Emit Phenobarbital Enzyme        Vial: 6 ml , Lyophilized.      8/27/74
                                          Reagent B.                                                            
Syva Co................................  Emit Qst Phenobarbital Bulk      Steel Drum: 7 gallon.....       6/5/86
                                          Powder Reagent.                                                       
Syva Co................................  Emit Qst Primidone Assay         Glass Vial: 6ml, 50 Vials/    11/12/85
                                          Catalog No. 60819.               Kit.                                 
Syva Co................................  Emit Serum Barbiturate-Enzyme    Bottle: 3ml..............      5/22/79
                                          Reagent B.                                                            
Syva Co................................  Emit T-Uptake Assay............  Bottle: 4 oz., 1L, Kit:        5/25/89
                                                                           500 tests, 5000 tests.               
Syva Co................................  Emit T-Uptake Assay (Thyroid     Polyethylene Bottle: 4 oz      2/29/88
                                          Hormone Binding Ratio) Catalog                                        
                                          No. 6J519.                                                            
Syva Co................................  Emit T-Uptake Bulk Powder        Bottle: 1000 ml..........      10/4/89
                                          Reagent A.                                                            
Syva Co................................  Emit T-Uptake Bulk Powder        Bottle: 4 oz.............      4/20/90
                                          Reagent A Satellite.                                                  
Syva Co................................  Emit THC 50/100ng Assay........  Kit; 2vials, 500ml each..     10/11/93
Syva Co................................  Emit THC Calibrators; 0ng/mlk,   Vial: 10ml...............     10/11/93
                                          50ng/ml, 100ng/ml, 200ng/ml.                                          
Syva Co................................  Emit THC Controls; Levels I,     Vial: 10ml...............     10/11/93
                                          II, III, IV.                                                          
Syva Co................................  Emit Thyroxine Assay...........  Glass Bottle: 8 oz., 1L,       5/25/89
                                                                           Kit: 1300 tests, 5000                
                                                                           tests.                               
Syva Co................................  Emit Thyroxine Bulk Powder       Bottle: 1000 ml..........      10/4/89
                                          Reagent B.                                                            
Syva Co................................  Emit Thyroxine Bulk Powder       Bottle: 4 oz.............      4/20/90
                                          Reagent B Satellite.                                                  
Syva Co................................  Emit Tox Serum Benzodiazepine    Bottle: 3ml..............       2/1/79
                                          Assay Kit Containing: Emit                                            
                                          Enzyme Reagent B.                                                     
Syva Co................................  Emit d.a.u. Amphetamine Assay    Kit: 100 tests, 1000           9/27/84
                                          Catalog Nos. 3C019, 3C119.       tests.                               
Syva Co................................  Emit d.a.u. Amphetamine Class    Glass Vial: 5ml..........      1/30/89
                                          Low Calibrator, Cat. No. 3C179.                                       
Syva Co................................  Emit d.a.u. Amphetamine Class    Glass Vial: 5ml..........      1/30/89
                                          Medium Calibrator, Cat. No.                                           
                                          3C189.                                                                
Syva Co................................  Emit d.a.u. Barbiturate Assay    Kit: 100 tests, 1000           9/27/84
                                          Catalog Nos. 3D019, 3D119.       tests.                               
Syva Co................................  Emit d.a.u. Benzodiazepine       Kit: 100 tests, 1000           9/27/84
                                          Assay Catalog Nos. 3F019,        tests.                               
                                          3F119.                                                                
Syva Co................................  Emit d.a.u. Cannabinoid 100 ng   Kit: 1000 tests..........      9/12/86
                                          Assay, Catalog No. 3M119.                                             
Syva Co................................  Emit d.a.u. Cannabinoid 100ng    Kit: 3 vials.............      7/31/89
                                          Assay Calibrator.                                                     
Syva Co................................  Emit d.a.u. Cannabinoid 100ng    Vial: 3ml................      7/31/89
                                          Assay Low Calibrator.                                                 
Syva Co................................  Emit d.a.u. Cannabinoid 100ng    Vial: 3ml................      7/31/89
                                          Assay Medium Calibrator.                                              
Syva Co................................  Emit d.a.u. Cannabinoid 20ng     Kit: 100 tests...........      2/10/86
                                          Assay Catalog No. 3M619.                                              
Syva Co................................  Emit d.a.u. Cannabinoid 20ng     Vial: 10ml Lyophilized         2/10/86
                                          Enzyme Reagent B.                Powder.                              
Syva Co................................  Emit d.a.u. Cannabinoid 50 ng    Vial: 5 ml...............       6/1/88
                                          Assay Calibrators, Low And                                            
                                          Medium: Cat. No. 3M509.                                               
Syva Co................................  Emit d.a.u. Cannabinoid 50 ng    Kit: 100 tests...........       6/1/88
                                          Assay: Cat. No. 3M519.                                                
Syva Co................................  Emit d.a.u. Cannabinoid Assay    Kit: 100 tests...........      9/24/84
                                          Catalog No. 3M019.                                                    
Syva Co................................  Emit d.a.u. Cannabinoid Urine    Kit: 3 Vials, 3ml Each...       1/3/80
                                          Calibrator Set.                                                       
Syva Co................................  Emit d.a.u. Cocaine Metabolite   Kit: 100 tests, 1000           9/27/84
                                          Assay Catalog Nos. 3H019,        tests.                               
                                          3H119.                                                                
Syva Co................................  Emit d.a.u. Low Calibrator A...  Bottle: 5ml..............      7/20/84
Syva Co................................  Emit d.a.u. Low Calibrator A...  Vial: 5 ml...............      6/30/89
Syva Co................................  Emit d.a.u. Low Calibrator A,    5 ml vial................      10/6/88
                                          Catalog No. 3C579.                                                    
Syva Co................................  Emit d.a.u. Low Calibrator B...  Bottle: 5ml..............       8/3/84
Syva Co................................  Emit d.a.u. Medium Calibrator A  Bottle: 5ml..............      7/20/84
Syva Co................................  Emit d.a.u. Medium Calibrator A  Vial: 5 ml...............      6/30/89
Syva Co................................  Emit d.a.u. Medium Calibrator    5 ml vial................      10/6/88
                                          A, Catalog No. 3C569.                                                 
Syva Co................................  Emit d.a.u. Medium Calibrator B  Bottle: 5ml..............       8/3/84
Syva Co................................  Emit d.a.u. Methadone Assay      Kit: 100 tests, 1000           10/5/84
                                          Catalog Nos. 3E019, 3E119.       tests.                               
Syva Co................................  Emit d.a.u. Monoclonal           Kit: 100 tests, 1000           10/6/88
                                          Amphetamine/Methamphetamine      tests.                               
                                          Assay, Catalog No3C549 100                                            
                                          tests, 3C559 1000 tests.                                              
Syva Co................................  Emit d.a.u. Opiate Assay         Kit: 100 tests, 1000           9/27/84
                                          Catalog Nos. 3B019, 3B119.       tests.                               
Syva Co................................  Emit d.a.u. Phencyclidine Assay  Bottle: 6ml..............       2/1/79
                                          Kit Containing: (1)Emit                                               
                                          Phencyclidine Enzyme Reagent B.                                       

[[Page 171]]

                                                                                                                
Syva Co................................  Emit-Qst Phenobarbital Assay,    Kit: 50 Vials............      1/18/84
                                          Catalog Number 6D819.                                                 
Syva Co................................  Emit-Tox Serum Barbiturate       Kit: 50 tests............      5/22/79
                                          Assay.                                                                
Syva Co................................  Emit-Tox Serum Calibrators; Low  Bottle: 3ml..............       2/1/79
                                          and Medium.                                                           
Syva Co................................  Emit-d.a.u. Methaqualone Assay.  Kit: 100 tests...........      4/27/82
Syva Co................................  Emit-st Amphetamine Assay......  Vial: 3ml, 80 vials/kit..      10/3/80
Syva Co................................  Emit-st Barbiturate Assay......  Vial: 3ml, 80 vials/kit..      10/3/80
Syva Co................................  Emit-st Benzodiazepine Assay...  Vial: 3ml, 80 vials/kit..      10/3/80
Syva Co................................  Emit-st Cannabinoid Assay        Vial: 6ml, 80 Vials/Kit..      9/27/84
                                          Catalog No. 3M319.                                                    
Syva Co................................  Emit-st Cannabinoid Calibrator.  Vial: 3ml, 2 vials/kit...      7/10/81
Syva Co................................  Emit-st Cannabinoid Controls...  Vial: 3ml, 2 vials/kit...      7/10/81
Syva Co................................  Emit-st Opiate Assay...........  Kit: 3ml, 80 vials/kit...      10/3/80
Syva Co................................  Emit-st Phencyclidine Assay....  Vial: 3ml, 80 vials/kit..       1/7/81
Syva Co................................  Emit-st Serum Barbiturate Assay  Vial: 3ml, 80 vials/kit..      2/16/81
Syva Co................................  Emit-st Serum Benzodiazepine     Vial: 3ml, 80 vials/kit..      2/16/81
                                          Assay.                                                                
Syva Co................................  Emit-st Serum Calibrator.......  Vial: 3ml................      2/16/81
Syva Co................................  Emit-st Serum Controls.........  Vial: 3ml, 2 vials/kit...      2/16/81
Syva Co................................  Emit-st Serum Phencyclidine      Vial: 3ml, 80 vials/kit..      2/16/81
                                          Assay.                                                                
Syva Co................................  Emit-st Urine Calibrator A.....  Vial: 1ml, 3 vials/kit...      10/3/80
Syva Co................................  Emit-st Urine Cocaine            Vial: 3 ml, 80 Vials/Kit.      3/16/82
                                          Metabolite Assay.                                                     
Syva Co................................  Emit-st Urine Controls A.......  Vial: 1ml, 6 vials/kit...      10/3/80
Syva Co................................  Emit-st Urine Methadone Assay..  Vial: 3ml , 80 vials/kit.      3/22/82
Syva Co................................  Emit-st Urine Methaqualone       Kit: 80 Vials............      4/27/82
                                          Assay.                                                                
Syva Co................................  Emit-st Urine Methaqualone       Vial: 3ml................      4/27/82
                                          Calibrator.                                                           
Syva Co................................  Emit-st Urine Methaqualone       Vial: 3ml................      4/27/82
                                          Controls.                                                             
Syva Co................................  IL test AED Calibrator 1.......  Vial: 5 ml...............       4/6/90
Syva Co................................  IL test AED Calibrator 2.......  Vial: 5ml................       4/6/90
Syva Co................................  IL test AED Calibrator 3.......  Vial: 5ml................       4/6/90
Syva Co................................  IL test AED Calibrator 4.......  Vial: 5ml................       4/6/90
Syva Co................................  IL test AED Calibrator 5.......  Vial: 5ml................       4/6/90
Syva Co................................  IL test Cannabinoid 100ng,       Vial: 5ml................       4/6/90
                                          400ng calibrator.                                                     
Syva Co................................  IL test set A calibrator.......  Vial: 5ml................       4/6/90
Syva Co................................  IL test set A control..........  Vial: 5ml................       4/6/90
Syva Co................................  IL test set B calibrator.......  Vial: 5ml................       4/6/90
Syva Co................................  IL test set B control..........  Vial: 5ml................       4/6/90
Syva Co................................  Vista Thyroxine Uptake Reagent   Cartridge: 4ml...........      1/22/93
                                          Cartridge.                                                            
Syva Co................................  Vista Triiodothyronine (T3)      Cartridge: 2.02 ml.......      9/11/92
                                          Reagent Cartridge.                                                    
Tempil Division. Big Three Industries,   Tempilaq Striped Mylar.........  Plastic Sheet: 6 by 12         9/22/76
 Inc.                                                                      in. 50 sheets per                    
                                                                           envelope.                            
The Binding Site, Inc..................  I.F.E. Buffer..................  Plastic Bottle: 125ml....      12/5/91
The Binding Site, Inc..................  Immunofixation Kit.............  Kit: 125ml Plastic Bottle      12/5/91
The Theta Corp.........................  Allobarbital No.FP305..........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Amobarbital No. FP313..........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Amphetamine No. FP604..........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Anileridine No. FP203..........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Aprobarbital No. FP306.........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Barbital No.FP314..............  Vial: 2ml................      4/10/73
The Theta Corp.........................  Benzoylecgonine FP-1001........  Vial: 2 ml...............      1/24/87
The Theta Corp.........................  Butabarbital No. FP315.........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Butalbital No. FP307...........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Chloral Betaine No. FP502......  Vial: 2ml................      4/10/73
The Theta Corp.........................  Chloral Hydrate No. FP501......  Vial: 2ml................      4/10/73
The Theta Corp.........................  Cocaine No. FP601..............  Vial: 2ml................      4/10/73
The Theta Corp.........................  Codeine No. FP102..............  Vial: 2ml................      4/10/73
The Theta Corp.........................  Cyclobarbital No. FP308........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Dihydrocodeine No. FP108.......  Vial: 2ml................      4/10/73
The Theta Corp.........................  Diphenoxylate No. FP205........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Ethchlorvynol No. FP508........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Ethylmorphine No. FP106........  Vial: 2ml................      4/10/73
The Theta Corp.........................  FP207..........................  Vial: 2ml................       9/4/80
The Theta Corp.........................  FP210..........................  Vial: 2ml................      5/15/84
The Theta Corp.........................  FP214..........................  Vial: 2ml................      4/10/84
The Theta Corp.........................  FP327..........................  Vial: 2ml................      4/10/84
The Theta Corp.........................  FP405..........................  Vial: 2ml................       3/8/79
The Theta Corp.........................  FP411..........................  Vial: 2ml................      5/15/84
The Theta Corp.........................  FP412..........................  Vial: 2ml................      5/15/84
The Theta Corp.........................  FP416..........................  Vial: 2ml................      5/15/84
The Theta Corp.........................  FP512..........................  Vial: 2ml................       3/8/79
The Theta Corp.........................  FP513..........................  Vial: 2ml................       3/8/79
The Theta Corp.........................  FP514..........................  Vial: 2ml................      5/15/84
The Theta Corp.........................  FP515..........................  Vial: 2ml................       3/8/79
The Theta Corp.........................  FP556..........................  Vial: 2ml................      4/10/84

[[Page 172]]

                                                                                                                
The Theta Corp.........................  FP601A.........................  Vial: 2ml................      5/15/84
The Theta Corp.........................  FP607..........................  Vial: 2ml................      5/15/84
The Theta Corp.........................  FP609..........................  Vial: 2ml................      5/15/84
The Theta Corp.........................  Fentanyl No. FP211.............  Vial: 2ml................      4/10/73
The Theta Corp.........................  Glutethimide No. FP404.........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Heptabarbital No. FP309........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Hexabarbital No. FP303.........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Hydrocodone No. FP107..........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Hydromorphone No. FP103........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Levorphanol No. FP208..........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Marker Mixture No. FPM-104.....  Vial: 2ml................      4/10/73
The Theta Corp.........................  Marker Mixture No. FPM-201.....  Vial: 2ml................      4/10/73
The Theta Corp.........................  Meperidine No.FP201............  Vial: 2ml................      4/10/73
The Theta Corp.........................  Mephobarbital No. FP301........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Meprobamate No. FP402..........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Methadone No. FP206............  Vial: 2ml................      4/10/73
The Theta Corp.........................  Methamphetamine No. FP603......  Vial: 2ml................      4/10/73
The Theta Corp.........................  Metharbital No. FP302..........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Methohexital No. FP304.........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Methylphenidate No. FP605......  Vial: 2ml................      4/10/73
The Theta Corp.........................  Monthly Urine Test No. FPM-103.  Vial: 2ml................      4/10/73
The Theta Corp.........................  Morphine No. FP101.............  Vial: 2ml................      4/10/73
The Theta Corp.........................  Oxycodone No. FP109............  Vial: 2ml................      4/10/73
The Theta Corp.........................  Oxymorphone No. FP104..........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Paraldehyde No.FP506...........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Pentobarbital No. FP318........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Phenazocine No. FP213..........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Phenmetrazine No. FP606........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Phenobarbital No. FP320........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Piminodine No. FP202...........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Probarbital No. FP319..........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Secobarbital No. FP310.........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Talbutal No. FP311.............  Vial: 2ml................      4/10/73
The Theta Corp.........................  Test Mixture SM No. 1..........  Vial: 2ml................      6/19/74
The Theta Corp.........................  Test Mixture SM No. 2..........  Vial: 2ml................      6/19/74
The Theta Corp.........................  Test Mixture SM No. 3..........  Vial: 2ml................      6/19/74
The Theta Corp.........................  Test Mixture SM No. 4..........  Vial: 2ml................      6/19/74
The Theta Corp.........................  Test Mixture SP No. 1..........  Vial: 2ml................      6/19/74
The Theta Corp.........................  Test Mixture SP No. 2..........  Vial: 2ml................      6/19/74
The Theta Corp.........................  Test Mixture SP No. 3..........  Vial: 2ml................      6/19/74
The Theta Corp.........................  Test Mixture SP No. 4..........  Vial: 2ml................      6/19/74
The Theta Corp.........................  Test Mixture TM No. 1..........  Vial: 2ml................      6/19/74
The Theta Corp.........................  Test Mixture TM No. 2..........  Vial: 2ml................      6/19/74
The Theta Corp.........................  Thiamylal No. FP322............  Vial: 2ml................      4/10/73
The Theta Corp.........................  Thiopental No. FP321...........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Vinbarbital No. FP312..........  Vial: 2ml................      4/10/73
The Theta Corp.........................  Weekly Urine Test (FDA) No. FPM- Vial: 2ml................      4/10/73
                                          101.                                                                  
The Theta Corp.........................  Weekly Urine Test (States) No.   Vial: 2ml................      4/10/73
                                          FPM-102.                                                              
The Upjohn Company.....................  DDHQ Spent Oxidant.............  Fiber Drum: 30 Gallons...     12/19/94
Toxi-Lab, Inc..........................  Proficiency Sample.............  Plastic bottle containing      6/22/82
                                                                           40 ml.                               
Toxi-Lab, Inc..........................  Special Toxi-Discs.............  Plastic vial or bottle         3/30/77
                                                                           containing 50 Standard               
                                                                           Discs.                               
Toxi-Lab, Inc..........................  Supplemental Standard Toxi-      Plastic vial containing        6/15/88
                                          Discs No. SD-4 Catalog No. 234.  50 Standard Discs.                   
Toxi-Lab, Inc..........................  Supplemental Standard Toxi-      Plastic vial containing        6/15/88
                                          Discs No. SD-5 Catalog No. 235.  50 Standard Discs.                   
Toxi-Lab, Inc..........................  Supplemental Standard Toxi-      Plastic vial containing        6/15/88
                                          Discs No. SD-6 Catalog No. 236.  50 Standard Discs.                   
Toxi-Lab, Inc..........................  Toxi-Control...................  Plastic bottle containing      3/30/77
                                                                           50 ml.                               
Toxi-Lab, Inc..........................  Toxi-Control THC...............  Plastic bottle containing      10/5/83
                                                                           50 ml.                               
Toxi-Lab, Inc..........................  Toxi-Disc A Series.............  Plastic vial containing         5/6/75
                                                                           50 Standard Discs.                   
Toxi-Lab, Inc..........................  Toxi-Disc B Series.............  Plastic vial containing         5/6/75
                                                                           50 Standard Discs.                   
Toxi-Lab, Inc..........................  Toxi-Discs Library II, No 3      Plastic vial containing        6/15/88
                                          Catalog No. 131C.                50 Standard Discs.                   
Toxi-Lab, Inc..........................  Toxi-Discs Library II, No. 1     Plastic vial containing        6/15/88
                                          Catalog No. 131A.                50 Standard Discs.                   

[[Page 173]]

                                                                                                                
Toxi-Lab, Inc..........................  Toxi-Discs Library II, No. 10    Plastic vial containing        6/15/88
                                          Catalog No. 131K.                50 Standard Discs.                   
Toxi-Lab, Inc..........................  Toxi-Discs Library II, No. 11,   Plastic vial containing        6/15/88
                                          Catalog No. 131L.                50 Standard Discs.                   
Toxi-Lab, Inc..........................  Toxi-Discs Library II, No. 12    Plastic vial containing        6/15/88
                                          Catalog No. 131M.                50 Standard Discs.                   
Toxi-Lab, Inc..........................  Toxi-Discs Library II, No. 2     Plastic vial containing        6/15/88
                                          Catalog No. 131B.                50 Standard Discs.                   
Toxi-Lab, Inc..........................  Toxi-Discs Library II, No. 5     Plastic vial containing        6/15/88
                                          Catalog No. 131E.                50 Standard Discs.                   
Toxi-Lab, Inc..........................  Toxi-Discs Library II, No. 8     Plastic vial containing        6/15/88
                                          Catalog No. 131H.                50 Standard Discs.                   
Toxi-Lab, Inc..........................  Toxi-Discs THC.................  Plastic vial containing        10/5/83
                                                                           50 Standard Discs.                   
Toxi-Lab, Inc..........................  Toxi-Grams.....................  Glass jar containing 50        9/24/80
                                                                           or 100 Chromatograms.                
Toxi-Lab, Inc..........................  Toxi-Lab Cannabinoid (THC)       Kit: 50 tests............      10/5/83
                                          Screen.                                                               
Tudor Laboratories, Inc................  FPIA Phenobarbital Kit--Cat.     Kit: 100 tests...........     11/27/89
                                          No. 105.                                                              
Tudor Laboratories, Inc................  Phenobarbital Calibrator Kit     Kit: 6 vials.............     11/27/89
                                          Cat. No. 205.                                                         
Tudor Laboratories, Inc................  Phenobarbital Calibrators B, C,  Vial: 4.0 ml.............     11/27/89
                                          D, E, F.                                                              
Universal Reagents, Inc................  Drug Monitoring & Toxicology     Bottle: 10ml.............      10/9/90
                                          No. DM 90-5, DM-62.                                                   
Utak Laboratories......................  Toxicology Control-High Range    Bottle: 10ml.............      4/14/80
                                          Anticonvulsants No. 71910.                                            
Utak Laboratories......................  Toxicology Control-High Range    Bottle: 10ml.............      4/14/80
                                          Barbiturates No. 71916.                                               
Utak Laboratories......................  Toxicology Control-High Range    Bottle: 10ml.............      4/14/80
                                          Hypnotic Plus Acetaminophem,                                          
                                          No. 71918.                                                            
Utak Laboratories......................  Toxicology Control-High Range    Bottle: 10ml.............      4/14/80
                                          Hypnotic Plus Salicylate, No.                                         
                                          71920.                                                                
Utak Laboratories......................  Toxicology Control-Mid Range     Bottle: 10ml.............      4/14/80
                                          Anticonvulsants No. 71911.                                            
Utak Laboratories......................  Toxicology Control-Mid Range     Bottle: 10ml.............      4/14/80
                                          Barbiturates No. 71917.                                               
Utak Laboratories......................  Toxicology Control-Mid Range     Bottle: 10ml.............      4/14/80
                                          Hypnotic Plus Acetaminophem,                                          
                                          No. 71919.                                                            
Utak Laboratories......................  Toxicology Control-Mid Range     Bottle: 10ml.............      4/14/80
                                          Hypnotic Plus Salicylate, No.                                         
                                          71921.                                                                
Utak Laboratories......................  Toxicology Serum Control Dried   Bottle: 10ml.............      7/29/82
                                          #88112.                                                               
Utak Laboratories......................  Toxicology Serum Control Dried   Bottle: 10ml.............      7/29/82
                                          #88113.                                                               
Utak Laboratories......................  Toxicology Serum Control Dried   Bottle: 10ml.............      7/29/82
                                          #88120.                                                               
Utak Laboratories......................  Toxicology Serum Control-Dried   In Bottles...............      5/24/76
                                          Catalog Nos. 44610, 44612,                                            
                                          44632, 44635, 44636, 44637,                                           
                                          44642, 44645, 44646, 44647,                                           
                                          44658.                                                                
Utak Laboratories......................  Toxicology Urine Control Dried   Bottle: 20ml.............      7/29/82
                                          #88100.                                                               
Utak Laboratories......................  Toxicology Urine Control Dried   Bottle: 10ml.............      7/29/82
                                          #88121.                                                               
Utak Laboratories......................  Toxicology Urine Control-Dried   Bottle: 1 oz.............      5/24/76
                                          Catalog Nos. 44650, 44651,                                            
                                          44652, 44653.                                                         
Ventrex Laboratories, Inc..............  PTH Antiserum..................  Vial: 5ml................      4/12/90
Ventrex Laboratories, Inc..............  PTH Assay Buffer...............  Vial: 10ml...............      4/12/90
Ventrex Laboratories, Inc..............  PTH Omega Radioimmunoassay Kit.  Kit: 60 tests............      4/12/90
Ventrex Laboratories, Inc..............  PTH Second Antibody............  Vial: 10ml...............      4/12/90
Ventrex Laboratories, Inc..............  PTH Tracer Buffer..............  Vial: 5 ml...............      4/12/90
Wien Laboratories, Inc.................  3H Dihydrotestosterone Cat. No.  Vial: 5.5ml..............      2/21/91
                                          D-1916.                                                               
Wien Laboratories, Inc.................  3H Epi-Testosterone Cat. No. T-  Vial: 5.5ml..............      2/21/91
                                          1028.                                                                 
Wien Laboratories, Inc.................  3H Testosterone Cat. No. T-3027  Vial: 5.5ml..............      2/21/91
Wien Laboratories, Inc.................  ANS Buffer pH 8.6 Catalog No. T- Plastic Bottle: 100ml....      5/14/75
                                          5144.                                                                 
Wien Laboratories, Inc.................  Buffer Reagent pH 8.6 Catalog    Bottle: 4oz..............     12/22/72
                                          No. T-5065.                                                           
Wien Laboratories, Inc.................  Coated Charcoal Suspension No.   Bottle: 4oz..............     12/22/72
                                          T-5077.                                                               
Wien Laboratories, Inc.................  Dihydrotestosterone Standard     Vial: 5.5ml..............      2/21/91
                                          1ng/ml Cat. No. D-1928.                                               
Wien Laboratories, Inc.................  Epi-Testosterone Standard, 10ng/ Vial: 5.5ml..............      2/21/91
                                          ml Cat. No. T-1016.                                                   
Wien Laboratories, Inc.................  Epi-Testosterone Test Set Cat.   Kit: 2 Bottles...........      2/21/91
                                          No. TS-1010.                                                          
Wien Laboratories, Inc.................  Methamphetamine: HRP EIA         Vial: 5ml, 10ml..........      6/25/90
                                          Conjugate.                                                            
Wien Laboratories, Inc.................  T3 Buffer Reagent Catalog No. T- Plastic Vial: 20ml.......      9/13/78
                                          5156.                                                                 
Wien Laboratories, Inc.................  Testosterone Standard, 10ng/ml   Vial: 5.5ml..............      2/21/91
                                          Cat. No. T-3039.                                                      
Wien Laboratories, Inc.................  Testosterone Test Set Cat. No.   Kit: 2 Bottles...........      2/21/91
                                          TS-333.                                                               
Windsor Laboratories, Inc..............  Calibrators FPR Phenobarbital..  Kit: 6 Vials.............     10/30/86
Windsor Laboratories, Inc..............  Phenobarbital Fluorescence       Kit: 100 tests...........     11/20/86
                                          Polarization Immunoassay Kit.                                         
----------------------------------------------------------------------------------------------------------------


[[Page 174]]



    (j) The following substances are designated as exempt chemical 
preparations for the purposes set forth in this section.
    (1) Chloral. When packaged in a sealed, oxygen-free environment, 
under nitrogen pressure, safeguarded against exposure to the air.(2) 
EmitR Phenobarbital Enzyme Reagent B. In one liter quantities each 
with a 5 ml. retention sample for repackaging as an exempt chemical 
preparation only.

[38 FR 8255, Mar. 30, 1973]

    Editorial Note: For Federal Register citations affecting 
Sec. 1308.24, see the List of CFR Sections Affected in the Finding Aids 
section of this volume.

          Excluded Veterinary Anabolic Steroid Implant Products



Sec. 1308.25  Exclusion of a veterinary anabolic steroid implant product; application.

    (a) Any person seeking to have any anabolic steroid product, which 
is expressly intended for administration through implants to cattle or 
other nonhuman species and which has been approved by the Secretary of 
Health and Human Services for such administration, identified as being 
excluded from any schedule, pursuant to section 102(41)(B)(i) of the Act 
(21 U.S.C. 802(41)(B)(i)), may apply to the Administrator, Drug 
Enforcement Administration, Department of Justice, Washington, DC 20537.
    (b) An application for any exclusion under this section shall be 
submitted in triplicate and contain the following information:
    (1) The name and address of the applicant;
    (2) The name of the product;
    (3) The chemical structural formula or description for any anabolic 
steroid contained in the product;
    (4) A complete description of dosage and quantitative composition of 
the dosage form;.
    (5) The conditions of use including whether or not Federal law 
restricts this product to use by or on the order of a licensed 
veterinarian;
    (6) A description of the delivery system in which the dosage form 
will be distributed with sufficient detail to identify the product (e.g. 
20 cartridge brown plastic belt);
    (7) The label and labeling of the immediate container and the 
commercial containers, if any, of the product;.
    (8) The name and address of the manufacturer of the dosage form if 
different from that of the applicant; and
    (9) Evidence that the product has been approved by the Secretary of 
Health and Human Services for administration through implant to cattle 
or other nonhuman species.
    (c) Within a reasonable period of time after the receipt of an 
application for an exclusion under this section, the Administrator shall 
notify the applicant of his acceptance or nonacceptance of the 
application, and if not accepted, the reason therefore. The 
Administrator need not accept an application for filing if any of the 
requirements prescribed in paragraph (b) of this section is lacking or 
is not set forth as to be readily understood. The applicant may amend 
the application to meet the requirements of paragraph (b) of this 
section. If the application is accepted for filing, the Administrator 
shall issue and have published in the Federal Register his order on the 
application, which shall include a reference to the legal authority 
under which the order is issued and the findings of fact and conclusions 
of law upon which the order is based. This order shall specify the date 
on which it will take effect. The Administrator shall permit any 
interested person to file written comments on or objections to the order 
within 60 days of the date of publication in the Federal Register. If 
any such comments or objections raise significant issues regarding any 
finding of fact or conclusion of law upon which the order is based, the 
Administrator shall immediately suspend the effectiveness of the order 
until he may reconsider the application in light of the comments and 
objections filed. Thereafter, the Administrator shall reinstate, revoke, 
or amend his original order as he determines appropriate.
    (d) The Administrator may at any time revoke or modify any 
designation of excluded status granted pursuant to this section by 
following the procedures set forth in paragraph (c) of this section for 
handling an application for

[[Page 175]]

an exclusion which has been accepted for filing.

[56 FR 42936, Aug. 30, 1991]



Sec. 1308.26  Excluded veterinary anabolic steroid implant products.

    (a) The following anabolic steroid-containing products which are 
expressly intended for administration through implants to cattle or 
other nonhuman species and which as been approved by the Secretary of 
Health and Human Services for such administration are excluded from all 
schedules pursuant to section 102(41)(B)(i) of the Act (21 U.S.C. 
802(41)(B)(i):

                                             Table of Excluded Veterinary Anabolic Steroid Implant Products                                             
--------------------------------------------------------------------------------------------------------------------------------------------------------
             Trade name                      Company             NDC code         Delivery system           Ingredients                Quantity         
--------------------------------------------------------------------------------------------------------------------------------------------------------
F-TO...............................  Animal Health Div.         0009-3351-02  20 implant cartridge    testosterone            200 mg/implant            
                                      Upjohn International,                    belt 8 pellets/         propionate oestradiol  20 mg/implant.            
                                      Kalamazoo, MI.                           implant.                benzoate.                                        
Finaplix-H.........................  Hoechst-Roussel, Agri-     12799-807-10  10 implant cartridge    trenbolone acetate....  200 mg/implant            
                                      Vet Co., Somerville,                     10 pellets/implant.                            (20 mg/pellet).           
                                      NJ.                                                                                                               
Finaplix-S.........................  Hoechst-Roussel, Agri-     12799-807-07  10 implant cartridge 7  trenbolone acetate....  140 mg/implant            
                                      Vet Co., Somerville,                     pellets/implant.                               (20 mg/pellet).           
                                      NJ.                                                                                                               
Heifer-oid.........................  Anchor Division,                         single & 20 implant     testosterone            200 mg/implant            
                                      Boehringer Ingelheim,                    cartridge belts 8       propionate estradiol   20mg/implant.             
                                      St. Joseph, MO.                          pellets/implant.        benzoate.                                        
Heifer-oid.........................  Bio-Ceutic Division,                     20 implant cartridge    testosterone            200 mg/implant            
                                      Boehringer Ingelheim,                    belt 8 pellets/         propionate estradiol   20 mg/implant.            
                                      St. Joseph, MO.                          implant.                benzoate.                                        
Heifer-oid.........................  Ivy Laboratories,                        single & 20 implant     testosterone            200 mg/implant            
                                      Inc., Overland Park                      cartridge belts.        propionate.            (25 mg/pellet).           
                                      KS.                                                                                                               
                                                             ...............  8 pellets/implant.....  estradiol benzoate....  20 mg/implant             
                                                                                                                              (2.5 mg/pellet).          
ImplusTM-H.........................  The Upjohn Company,        0009-0434-01  20 implant belt 8       testosterone            200 mg/implant, 20 mg/    
                                      Kalamazoo, MI.                           pellets/implant.        propionate estradiol    implant                  
                                                                                                       benzoate.                                        
Revalor-s..........................  Hoechst-Roussel, Agri-     12799-809-07  10 implant cartridge 6  trenbolone acetate....  120 mg/implant            
                                      Vet Co., Somerville,                     pellets/implant.                               (20 mg/pellet).           
                                      NJ.                                                                                                               
                                                                                                      estradiol.............  24 mg/implant             
                                                                                                                              (4 mg/pellet).            
Synovex H..........................  Syntex Laboratories,                     10 implant clip 8       testosterone            200 mg/implant            
                                      Palo Alto, CA.                           pellets/implant.        propionate.            (25 mg/pellet).           
                                                                                                      estradiol benzoate....  20 mg/implant             
                                                                                                                              (2.5 mg/pellet).          
--------------------------------------------------------------------------------------------------------------------------------------------------------

    (b) In accordance with section 102(41)(B)(ii) of the Act (21 U.S.C. 
802(41)(B)(ii)) if any person prescribes, dispenses, or distributes a 
product listed in paragraph (a) of this section for human use, such 
person shall be considered to have prescribed, dispensed, or distributed 
an anabolic steroid within the meaning of section 102(41)(A) of the Act 
(21 U.S.C. 802(41)(A)).

[56 FR 42936, Aug. 30, 1991, as amended at 57 FR 19534, May 7, 1992; 58 
FR 15088, Mar. 19, 1993]

                     Exempted Prescription Products



Sec. 1308.31  Application for exemption of a nonnarcotic prescription product.

    (a) Any person seeking to have any compound, mixture, or preparation 
containing any nonnarcotic controlled substance listed in 
Sec. 1308.12(e), or in Sec. 1308.13 (b) or (c), or in Sec. 1308.14, or 
in Sec. 1308.15, exempted from application of all or any part of the Act 
pursuant to section 201(g)(3)(A), of the Act (21 U.S.C. 811(g)(3)(A). 
may apply to the Administrator, Drug Enforcement Administration, 
Washington, DC 20537, for such exemption.

[[Page 176]]

    (b) An application for an exemption under this section shall contain 
the following information:
    (1) The complete quantitative composition of the dosage form.
    (2) Description of the unit dosage form together with complete 
labeling.
    (3) A summary of the pharmacology of the product including animal 
investigations and clinical evaluations and studies, with emphasis on 
the psychic and/or physiological dependence liability (this must be done 
for each of the active ingredients separately and for the combination 
product).
    (4) Details of synergisms and antagonisms among ingredients.
    (5) Deterrent effects of the noncontrolled ingredients.
    (6) Complete copies of all literature in support of claims.
    (7) Reported instances of abuse.
    (8) Reported and anticipated adverse effects.
    (9) Number of dosage units produced for the past 2 years.
    (c) Within a reasonable period of time after the receipt of an 
application for an exemption under this section, the Administrator shall 
notify the applicant of his acceptance or non-acceptance of the 
application, and if not accepted, the reason therefor. The Administrator 
need not accept an application for filing if any of the requirements 
prescribed in paragraph (b) of this section is lacking or is not set 
forth so as to be readily understood. If the applicant desires, he may 
amend the application to meet the requirements of paragraph (b) of this 
section. If accepted for filing, the Administrator shall publish in the 
Federal Register general notice of this proposed rulemaking in granting 
or denying the application. Such notice shall include a reference to the 
legal authority under which the rule is proposed, a statement of the 
proposed rule granting or denying an exemption, and, in the discretion 
of the Administrator, a summary of the subjects and issues involved. The 
Administrator shall permit any interested person to file written 
comments on or objections to the proposal and shall designate in the 
notice of proposed rule making the time during which such filings may be 
made. After consideration of the application and any comments on or 
objections to his proposed rulemaking, the Administrator shall issue and 
publish in the Federal Register his final order on the application, 
which shall set forth the findings of fact and conclusions of law upon 
which the order is based. This order shall specify the date on which it 
shall take effect, which shall not be less than 30 days from the date of 
publication in the Federal Register unless the Administrator finds that 
conditions of public health or safety necessitate an earlier effective 
date, in which event the Administrator shall specify in the order his 
findings as to such conditions.
    (d) The Administrator may revoke any exemption granted pursuant to 
section 201(g)(3)(A) of the Act (21 U.S.C. 811(g)(3)(A)) by following 
the procedures set forth in paragraph (c) of this section for handling 
an application for an exemption which has been accepted for filing.

[38 FR 8254, Mar. 30, 1973. Redesignated at 38 FR 26609, Sept. 24, 1973, 
as amended at 44 FR 18968, Mar. 30, 1979; 52 FR 9803, Mar. 27, 1987]



Sec. 1308.32  Exempted prescription products.

    The following compounds, mixtures, or preparations which contain a 
non-narcotic controlled substance listed in Sec. 1308.12(e) or in 
Sec. 1308.13(b) or (c) or in Sec. 1308.14 or in Sec. 1308.15 listed in 
the Table of Exempted Prescription Products have been exempted by the 
Adminsitrator from the application of sections 302 through 305, 307 
through 309, 1002 through 1004 of the Act (21 U.S.C. 822-825, 827-829, 
and 952-954) and Secs. 1301.24, 1301.31, 1301.32, and Secs. 1301.71 
through 1301.76 of this chapter for administrative purposes only. Except 
that those products containing butalbital shall not be exempt from the 
requirements of 21 U.S.C. 952-954 concerning importation, exportation, 
transshipment and in-transit shipment of controlled substances. Any 
deviation from the quantitative composition of any of the listed drugs 
shall require a petition of exemption in order for the product to be 
exempted.

[[Page 177]]

                     Exempted Prescription Products

            Explanation of Column Headings and Abbreviations

    Company/Trade Name. Self explanatory.
    NDC Code. Refers to the specific National Drug Code listing for the 
particular formulated product.
    Form. Refers to the type of dosage formulation:
    CA=capsule
    DP=drops
    EL=elixir
    EC=enteric coated capsule
    ET=enteric coated tablet
    LQ=liquid
    SS=suspension
    SU=suppository
    TB=tablet
    WA=wafer
    XC=sustained release capsule
    XT=sustained release tablet
    Controlled Substance (mg or mg/ml). Refers to the type and amount of 
controlled substance present in the mixture. If the dosage formulation 
is solid (CA, EC, ET, SU, TB, WA, XC, or XT), the amount shown is 
milligrams per dosage unit. If the dosage formulation is liquid (DP, EL, 
LQ, or SS), the amount shown is milligrams per milliliter.

                                      Table of Exempt Prescription Products                                     
----------------------------------------------------------------------------------------------------------------
                                                                                         Controlled      (mg or 
            Company                  Trade Name           NDC Code          Form         Substance       mg/ml) 
----------------------------------------------------------------------------------------------------------------
Adria Laboratories.............  Axotal............         00013-1301  TB           Butalbital.......     50.00
Alpha Scriptics Inc............  Butacet Capsules..         53121-0133  CA           Butalbital.......     50.00
American Urologicals Inc.......  Butace............         00539-0906  CA           Butalbital.......     50.00
Apotheca.......................  Theophen..........         12634-0101  TB           Phenobarbital....      8.00
Arco Pharmaceuthcals...........  Arco-Lase Plus....         00275-0045  TB           Phenobarbital....      8.00
Arlo Interamerican.............  Espasmotex........         11475-0835  TB           Phenobarbital....     20.00
Ascher and Co..................  Anaspaz PB........         00225-0300  TB           Phenobarbital....     15.00
Ascot Pharmaceuticals..........  Antispasmodic              47679-0158  TB           Phenobarbital....     16.20
                                  Tablets.                                                                      
Ascot Pharmaceuticals..........  Chlordiazepoxide           47679-0268  CA           Chlordiazepoxide       5.00
                                  Hydrochloride +                                     HCl.                      
                                  Clidinium Bromide.                                                            
Ayerst Laboratories............  PMB-200...........         00046-0880  TB           Meprobamate......    200.00
Ayerst Laboratories............  PMB-400...........         00046-0881  TB           Meprobamate......    400.00
Barre Drug Co..................  Barophen..........         00472-0981  EL           Phenobarbital....      3.24
Barre Drug Co..................  Isolate Compound..         00472-0929  EL           Phenobarbital....      0.40
Baucum Laboratories Inc........  Butalbital,                54696-0513  TB           Butalbital.......     50.00
                                  Acetaminophen and                                                             
                                  Caffeine Tablets.                                                             
Beecham Laboratories...........  Hybephen..........         00029-2360  TB           Phenobarbital....     15.00
Bioline Labs Inc...............  Anti-Spas Elixir..         00719-4090  EL           Phenobarbital....      3.24
Bioline Labs Inc...............  Anti-Spas Tablets.         00719-1091  TB           Phenobarbital....     16.20
Bioline Labs Inc...............  Bel-Phen-Ergot-S           00719-1686  TB           Phenobarbital....     40.00
                                  Tablets.                                                                      
Bioline Labs Inc...............  Chlordinium.......         00719-1208  CA           Chlordiazepoxide       5.00
                                                                                      HCl.                      
Blaine Co......................  Spaslin...........         00165-0029  TB           Phenobarbital....     16.20
Blansett Pharm Co..............  Anolor 300                 51674-0009  CA           Butalbital.......     50.00
                                  Capsules.                                                                     
Bock Pharmacal Co..............  Broncholate.......         00563-0277  CA           Phenobarbital....      8.00
Bowman Pharmaceutical..........  Private Formula No         00252-3095  TB           Phenobarbital         15.00
                                  3095.                                               Sodium.                   
Breon Labs.....................  Isuprel Compound..         00057-0874  EL           Phenobarbital....      0.40
Caldwell & Bloor Co............  Hyosital White....         00361-2131  TB           Phenobarbital....     16.20
Carnrick Labs Inc..............  Phrenilin.........         00086-0050  TB           Butalbital.......     50.00
Carnrick Labs Inc..............  Phrenilin Forte...         00086-0056  CA           Butalbital.......     50.00
Carpenter Pharmacal Co.........  ALAGESIC Tablets..         55726-0300  TB           Butalbital.......     50.00
Chelsea Laboratories...........  Chlordiazepoxide           46193-0948  CA           Chlordiazepoxide       5.00
                                  with Clidinium                                      HCl.                      
                                  Bromide.                                                                      
Columbia Drug Co...............  Isopap Capsules...         11735-0400  CA           Butalbital.......     50.00
Consolidated Midland...........  Bellalphen........         00223-0425  TB           Phenobarbital....     16.20
Dorasol Laboratories...........  Donalixir.........         00471-0095  EL           Phenobarbital....      3.24
Dunhall Pharmacal Inc..........  Triaprin..........         00217-2811  CA           Butalbital.......     50.00
Econolab.......................  Micomp-PB Tablets.         55053-0525  TB           Pentobarbital         30.00
                                                                                      Sodium.                   
Equipharm Corp.................  EQUI-CET Tablets..         57779-0111  TB           Butalbital.......     50.00
Everett Laboratories Inc.......  Repan Capsules....         00642-0163  CA           Butalbital.......     50.00
Everett Laboratories Inc.......  Repan Tablets.....         00642-0162  TB           Butalbital.......     50.00
Forest Pharmacal Inc...........  Acetaminophen 325          00456-0674  TB           Butalbital.......     50.00
                                  mg/Butalbital 50                                                              
                                  mg.                                                                           
Forest Pharmacal Inc...........  Acetaminophen 500          00456-0671  TB           Butalbital.......     50.00
                                  mg/Butalbital 50                                                              
                                  mg.                                                                           
Forest Pharmacal Inc...........  Bancap............         00456-0546  CA           Butalbital.......     50.00
Forest Pharmacal Inc...........  ESGIC-PLUS........         00456-0678  TB           Butalbital.......     50.00
Forest Pharmacal Inc...........  Esgic Capsules....         00456-0631  CA           Butalbital.......     50.00
Forest Pharmacal Inc...........  Esgic Tablets.....         00456-0630  TB           Butalbital.......     50.00
Forest Pharmacal Inc...........  G.B.S.............         00456-0281  TB           Phenobarbital....      8.00
Forest Pharmacal Inc...........  Soniphen..........         00456-0429  ET           Phenobarbital....     16.00
Gen-King Products..............  Antispasmodic.....         03547-0777  TB           Phenobarbital....     16.20
Genetco Inc....................  Butalbital,                00302-0490  TB           Butalbital.......     50.00
                                  Acetaminophen and                                                             
                                  Caffeine Tablets.                                                             

[[Page 178]]

                                                                                                                
Genetco Inc....................  Butalbital, Apap           00302-0490  TB           Butalbital.......     50.00
                                  and Caffeine.                                                                 
Geneva Generics................  Phenobarbital,             00781-1701  TB           Phenobarbital....     40.00
                                  Ergotamine and                                                                
                                  Belladonna                                                                    
                                  Tablets.                                                                      
Geriatric Pharmacal Corp.......  Bilezyme Plus.....         00249-1112  TB           Phenobarbital....      8.00
Geriatric Pharmacal Corp.......  Gustase Plus......         00249-1121  TB           Phenobarbital....      8.00
Glenlawn Laboratories..........  Chlordinium                00580-0084  CA           Chlordiazepoxide       5.00
                                  Sealets.                                            HCl.                      
Goldline Laboratories..........  Antispasmodic              00182-0686  EL           Phenobarbital....      3.24
                                  Elixir.                                                                       
Goldline Laboratories..........  Antispasmodic              00182-0129  TB           Phenobarbital....     16.20
                                  Tablets.                                                                      
Goldline Laboratories..........  Bel-phen-ergot s           00182-1847  TB           Phenobarbital....     40.00
                                  Tablets.                                                                      
Goldline Laboratories..........  Butalbital, APAP           00182-1274  TB           Butalbital.......     50.00
                                  and Caffeine                                                                  
                                  Tablets.                                                                      
Goldline Laboratories..........  C.D.P. Plus                00182-1856  CA           Chlordiazepoxide       5.00
                                  Capsules.                                           HCl.                      
H.L. Moore Drug Exchange.......  Antispasmodic              00839-5055  TB           Phenobarbital....     16.00
                                  Tablets.                                                                      
H.L. Moore Drug Exchange.......  Bellamor Tablets..         00839-7370  TB           Phenobarbital....     40.00
H.L. Moore Drug Exchange.......  Theophenyllin.....         00839-5111  TB           Phenobarbital....      8.00
Halsey Drug Co Inc.............  Blue Cross                 00879-0567  TB           Butalbital.......     50.00
                                  Butalbital, APAP                                                              
                                  and Caffeine                                                                  
                                  Tablets.                                                                      
Halsey Drug Co Inc.............  Butalbital and             00879-0543  TB           Butalbital.......     50.00
                                  Acetaminophen                                                                 
                                  Tablets.                                                                      
Halsey Drug Co Inc.............  Clinoxide.........         00879-0501  CA           Chlordiazepoxide       5.00
                                                                                      HCl.                      
Halsey Drug Co Inc.............  Susano............         00879-0059  EL           Phenobarbital....      3.24
Halsey Drug Co Inc.............  Susano............         00879-0058  TB           Phenobarbital....     16.20
Horizon Products Co............  Spastrin Tablets..         54580-0124  TB           Phenobarbital....     40.00
Hyrex Pharmaceutical...........  Panzyme...........         00314-0310  TB           Phenobarbital....      8.10
Hyrex Pharmaceutical...........  Two-Dyne Revised..         00314-2229  TB           Butalbital.......     50.00
Interstate Drug Exchange.......  IDE-Cet Tablets...         00814-3820  TB           Butalbital.......     50.00
Interstate Drug Exchange.......  Spastolate........         00814-7088  TB           Phenobarbital....     16.20
Intetlab.......................  CON-TEN...........         11584-1029  CA           Butalbital.......     50.00
Kaiser Foundation Hosp.........  Belladonna                 00179-0045  EL           Phenobarbital....      3.24
                                  Alkaloids with                                                                
                                  Phenobarbital.                                                                
Keene Pharmacal Inc............  Endolar...........         00588-7777  CA           Butalbital.......     50.00
Knoll Pharmaceutical...........  Quadrinal                  00044-4580  SS           Phenobarbital....      2.40
                                  Suspension.                                                                   
Knoll Pharmaceutical...........  Quadrinal Tablets.         00044-4520  TB           Phenobarbital....     24.00
Kraft Pharmacal Co Inc.........  Digestokraft......         00796-0237  TB           Butabarbital           8.00
                                                                                      Sodium.                   
Kremers Urban Co...............  Levsin with                00091-4530  EL           Phenobarbital....      3.00
                                  Phenobarbital                                                                 
                                  Elixir.                                                                       
Kremers Urban Co...............  Levsin with                00091-3534  TB           Phenobarbital....     15.00
                                  Phenobarbital                                                                 
                                  Tablets.                                                                      
Kremers Urban Co...............  Levsin-PB.........         00091-4536  DP           Phenobarbital....     15.00
Kremers Urban Co...............  Levsinex with              00091-3539  XC           Phenobarbital....     45.00
                                  Phenobarbital.                                                                
Landry Pharmacal Inc...........  Febridyne Plain            05383-0001  CA           Butalbital.......     50.00
                                  Capsules.                                                                     
Lanpar Co......................  PB Phe-Bell.......         12908-7006  TB           Phenobarbital....     16.20
Lasalle Laboratories...........  Pacaps Modified            48534-0884  CA           Butalbital.......     50.00
                                  Formula.                                                                      
Lemmon Pharmacal Co............  Donphen...........         00093-0205  TB           Phenobarbital....     15.00
Life Laboratories..............  Belladonna                 00737-1283  EL           Phenobarbital....      3.00
                                  Alkaloids with                                                                
                                  Phenobarbital.                                                                
Lunsco Inc.....................  Pacaps Capsules...         10892-0116  CA           Butalbital.......     50.00
Major Pharmacal Corp...........  Bellamine Tablets.         00904-2548  TB           Phenobarbital....     40.00
Major Pharmacal Corp...........  Cafatine-PB                00904-1750  TB           Pentobarbital         30.00
                                  Tablets.                                            Sodium.                   
Major Pharmacal Corp...........  Fabophen Tablets..         00904-3280  TB           Butalbital.......     50.00
Mallard Inc....................  Anoquan Modified           00166-0881  CA           Butalbital.......     50.00
                                  Formula.                                                                      
Mallard Inc....................  Malatal...........         00166-0748  TB           Phenobarbital....     16.20
Marlop Pharmacal Inc...........  Broncomar.........         12939-0128  EL           Butabarbital.....      1.00
Marlop Pharmacal Inc...........  Dolmar............         12939-0812  CA           Butalbital.......     50.00
Marnel Pharmacal Inc...........  Margesic Capsules.         00682-0804  CA           Butalbital.......     50.00
Martec Pharmacal Inc...........  Butalbital,                52555-0079  TB           Butalbital.......     50.00
                                  Acetaminophen and                                                             
                                  Caffeine Tablets.                                                             
Mayrand Pharmacal Inc..........  B-A-C Tablets.....         00259-1256  TB           Butalbital.......     50.00
Mayrand Pharmacal Inc..........  Sedapap-10 Tablets         00259-1278  TB           Butalbital.......     50.00
Mead Johnson Pharmacal.........  Quibron Plus               00087-0518  CA           Butabarbital.....     20.00
                                  Capsules.                                                                     
Mead Johnson Pharmacal.........  Quibron Plus               00087-0511  EL           Butabarbital.....      1.33
                                  Elixir.                                                                       
Medco Supply Co................  Phenobarbital &            00764-2057  TB           Phenobarbital....     16.20
                                  Hyoscyamine                                                                   
                                  Sulfate.                                                                      

[[Page 179]]

                                                                                                                
Mikart Inc.....................  Butalbital and             46672-0099  TB           Butalbital.......     50.00
                                  Acetaminophen                                                                 
                                  Tablets 50/325.                                                               
Mikart Inc.....................  Butalbital and             46672-0098  TB           Butalbital.......     50.00
                                  Acetaminophen                                                                 
                                  Tablets 50/650.                                                               
Mikart Inc.....................  Butalbital,                46672-0228  CA           Butalbital.......     50.00
                                  Acetaminophen and                                                             
                                  Caffeine Capsules.                                                            
Mikart Inc.....................  Butalbital,                46672-0053  TB           Butalbital.......     50.00
                                  Acetaminophen and                                                             
                                  Caffeine Tablets.                                                             
Mikart Inc.....................  Butalbital,                46672-0059  TB           Butalbital.......     50.00
                                  Acetaminophen,                                                                
                                  and Caffeine                                                                  
                                  Tablets.                                                                      
Nejo Pharmaceutical............  Spasmalones.......         00653-0002  TB           Phenobarbital....     16.00
Parke-Davis & Co...............  Dilantin with              00071-0531  CA           Phenobarbital....     32.00
                                  Phenobarbital 1/2.                                                            
Parke-Davis & Co...............  Dilantin with              00071-0375  CA           Phenobarbital....     16.00
                                  Phenobarbital 1/4.                                                            
Parke-Davis & Co...............  Tedral SA.........         00071-0231  XT           Phenobarbital....     25.00
Parmed Pharmaceutical..........  Sedapar Elixir....         00349-4100  EL           Phenobarbital....      3.24
Parmed Pharmaceutical..........  Sedapar Tablets...         00349-2355  TB           Phenobarbital....     16.20
Pasadena Research..............  Seds..............         00418-4072  TB           Phenobarbital....     16.20
Pharmaceutical Basics Inc......  Antispasmodic              00832-8009  EL           Phenobarbital....      3.24
                                  Elixir.                                                                       
Pharmaceutical Basics Inc......  Butalbital,                00832-1102  TB           Butalbital.......     50.00
                                  Acetaminophen and                                                             
                                  Caffeine Tablets.                                                             
Pharmaceutical Basics Inc......  Clinibrax Capsules         00832-1054  CA           Chlordiazepoxide       5.00
                                                                                      HCl.                      
Poythress & Co Inc.............  Antrocol..........         00095-0041  CA           Phenobarbital....     16.00
Poythress & Co Inc.............  Antrocol Elixir...         00095-0042  EL           Phenobarbital....      3.00
Poythress & Co Inc.............  Antrocol Tablets..         00095-0040  TB           Phenobarbital....     16.00
Poythress & Co Inc.............  Mudrane...........         00095-0050  TB           Phenobarbital....      8.00
Poythress & Co Inc.............  Mudrane GG Elixir.         00095-0053  EL           Phenobarbital....      0.50
Poythress & Co Inc.............  Mudrane GG Tablets         00095-0051  TB           Phenobarbital....      8.00
Private Formula Inc............  Sangesic..........         00511-1627  TB           Butalbital.......     30.00
Qualitest Products Inc.........  Butalbital,                52446-0544  TB           Butalbital.......     50.00
                                  Acetaminophen and                                                             
                                  Caffeine Tablets.                                                             
Qualitest Products Inc.........  Chlordiazepoxide           52446-0096  CA           Chlordiazepoxide       5.00
                                  HCl 5 mg and                                        HCl.                      
                                  Clidinium Br 2.5                                                              
                                  mg.                                                                           
Redi-Med.......................  Butalbital                 53506-0103  CA           Butalbital.......     50.00
                                  Compound Capsules.                                                            
Rexar Pharmacal Corp...........  Rexatal Tablets...         00478-5477  TB           Phenobarbital....     16.52
Richlyn Laboratories...........  Aminophylline &            00115-2156  ET           Phenobarbital....     15.00
                                  Phenobarbital.                                                                
Richlyn Laboratories...........  Aminophylline &            00115-2154  TB           Phenobarbital....     15.00
                                  Phenobarbital                                                                 
                                  Tablets.                                                                      
Richlyn Laboratories...........  Bellophen.........         00115-2400  TB           Phenobarbital....     16.20
Richlyn Laboratories...........  Spasmolin.........         00115-4652  TB           Phenobarbital....     15.00
Robins A H Co Inc..............  Donnatal Capsules.         00031-4207  CA           Phenobarbital....     16.20
Robins A H Co Inc..............  Donnatal Elixir...         00031-4221  EL           Phenobarbital....      3.24
Robins A H Co Inc..............  Donnatal Extentabs         00031-4235  XT           Phenobarbital....     48.60
Robins A H Co Inc..............  Donnatal No 2.....         00031-4264  TB           Phenobarbital....     32.40
Robins A H Co Inc..............  Donnatal Tablets..         00031-4250  TB           Phenobarbital....     16.20
Robins A H Co Inc..............  Donnazyme.........         00031-4649  ET           Phenobarbital....      8.10
Roche Labs.....................  Librax............         00140-0007  CA           Chlordiazepoxide       5.00
                                                                                      HCl.                      
Roche Labs.....................  Menrium 10-4......         00140-0025  TB           Chlordiazepoxide.     10.00
Roche Labs.....................  Menrium 5-2.......         00140-0023  TB           Chlordiazepoxide.      5.00
Roche Labs.....................  Menrium 5-4.......         00140-0024  TB           Chlordiazepoxide.      5.00
Rondex Laboratories............  Antispasmodic.....         00367-4118  TB           Phenobarbital....     16.20
Rotex Pharmacal Inc............  Rogesic Capsules..         31190-0008  CA           Butalbital.......     50.00
Ruckstuhl Co...................  Sedarex No 3......         00144-1575  TB           Phenobarbital....     16.20
Rugby Laboratories Inc.........  Clindex...........         00536-3490  CA           Chlordiazepoxide       5.00
                                                                                      HCl.                      
Rugby Laboratories Inc.........  Ergocaff-PB                00536-3801  TB           Pentobarbital         30.00
                                  Tablets.                                            Sodium.                   
Rugby Laboratories Inc.........  Hyosophen Capsules         00536-3926  CA           Phenobarbital....     16.00
Rugby Laboratories Inc.........  Hyosophen Tablets.         00536-3920  TB           Phenobarbital....     16.20
Rugby Laboratories Inc.........  ISOCET Tablets....         00536-3951  TB           Butalbital.......     50.00
Rugby Laboratories Inc.........  Phenerbel-S                00536-4234  TB           Phenobarbital....     40.00
                                  Tablets.                                                                      
Rugby Laboratories Inc.........  Theodrine Tablets.         00536-4648  TB           Phenobarbital....      8.00
Russ Pharmacal Inc.............  FEMCET Capsules...         50474-0703  CA           Butalbital.......     50.00
Sandoz Pharmacal Corp..........  Belladenal........         00078-0028  TB           Phenobarbital....     50.00
Sandoz Pharmacal Corp..........  Belladenal-S......         00078-0027  XT           Phenobarbital....     50.00
Sandoz Pharmacal Corp..........  Bellergal-S.......         00078-0031  XT           Phenobarbital....     40.00
Sandoz Pharmacal Corp..........  Cafergot P-B               00078-0035  SU           Pentobarbital....     60.00
                                  Suppository.                                                                  

[[Page 180]]

                                                                                                                
Sandoz Pharmacal Corp..........  Cafergot P-B               00078-0036  TB           Pentobarbital         30.00
                                  Tablets.                                            Sodium.                   
Sandoz Pharmacal Corp..........  Fioricet..........         00078-0084  CA           Butalbital.......     50.00
Schein Henry Inc...............  Antispasmodic.....         00364-0020  TB           Phenobarbital....     16.00
Schein Henry Inc...............  Antispasmodic              00364-7002  EL           Phenobarbital....      3.20
                                  Elixir.                                                                       
Schein Henry Inc...............  Isolate Compound           00364-7029  EL           Phenobarbital....      0.40
                                  Elixir.                                                                       
Schein Henry Inc...............  T-E-P.............         00364-0266  TB           Phenobarbital....      8.10
Shoals Pharmacal Co............  Tencet............         47649-0370  TB           Butalbital.......     50.00
Shoals Pharmacal Co............  Tencet Capsules...         47649-0560  CA           Butalbital.......     50.00
Stewart-Jackson Pharmacal......  Ezol..............         45985-0578  CA           Butalbital.......     50.00
Stuart Pharmaceutical..........  Kinesed...........         00038-0220  TB           Phenobarbital....     16.00
Superpharm Laboratories........  Chlordiazepoxide           57247-1003  CA           Chlordiazepoxide       5.00
                                  HCl & Clidinium                                     HCl.                      
                                  Br.                                                                           
Towne Paulsen & Co.............  T. E. P...........         00157-0980  TB           Phenobarbital....      8.00
Trimen Labs....................  Amaphen Capsules           11311-0954  CA           Butalbital.......     50.00
                                  (reformulated).                                                               
Truxton C O Inc................  Atropine Sulfate           00463-6035  TB           Phenobarbital....     15.00
                                  with                                                                          
                                  Phenobarbital.                                                                
Truxton C O Inc................  Ephedrine with             00463-6086  TB           Phenobarbital....     15.00
                                  Phenobarbital.                                                                
Truxton C O Inc................  Spastemms Elixir..         00463-9023  EL           Phenobarbital....      3.24
Truxton C O Inc................  Spastemms Tablets.         00463-6181  TB           Phenobarbital....     15.00
U.S. Pharmaceuticals Inc.......  Medigesic Tablets.         52747-0311  TB           Butalbital.......     50.00
UAD Laboratories Inc...........  Bucet Capsules....         00785-2307  CA           Butalbital.......     50.00
UAD Laboratories Inc...........  Bucet Tablets.....         00785-2307  TB           Butalbital.......     50.00
UAD Laboratories Inc...........  Triad.............         00785-2306  TB           Butalbital.......     50.00
UAD Laboratories Inc...........  Triad Capsules....         00785-2305  CA           Butalbital.......     50.00
UDL Laboratories...............  Belladonna                 51079-0168  TB           Phenobarbital....     16.20
                                  Alkaloids with                                                                
                                  Phenobarbital.                                                                
United Research Labs Inc.......  Bel-Tabs..........         00677-1171  TB           Phenobarbital....     40.00
University of Iowa.............  Bladder Mixture            11326-1624  LQ           Phenobarbital....      2.92
                                  Plus                                                                          
                                  Phenobarbital.                                                                
Vale Chemical Co...............  Alkaloids of               00377-0527  TB           Phenobarbital....     16.20
                                  Belladonna and                                                                
                                  Phenobarbital.                                                                
Vale Chemical Co...............  Antispas..........         00377-0622  TB           Phenobarbital....     16.20
Vale Chemical Co...............  Barbeloid                  00377-0365  TB           Phenobarbital....     16.20
                                  (Revised) Green.                                                              
Vale Chemical Co...............  Barbeloid Yellow..         00377-0498  TB           Phenobarbital....     16.20
Vale Chemical Co...............  Charspast.........         00377-0500  TB           Phenobarbital....     16.20
Vale Chemical Co...............  Digestokraft......         00377-0460  TB           Butabarbital           8.00
                                                                                      Sodium.                   
Vale Chemical Co...............  Ephedrine & Sodium         00377-0109  TB           Phenobarbital         16.20
                                  Phenobarbital.                                      Sodium.                   
Vale Chemical Co...............  Panzyme...........         00377-0491  TB           Phenobarbital....      8.10
Vale Chemical Co...............  Pulsaphen.........         00377-0652  TB           Phenobarbital....     15.00
Vale Chemical Co...............  Truxaphen.........         00377-0541  TB           Phenobarbital....     16.20
Vale Chemical Co...............  Wescophen S-II....         00377-0628  TB           Phenobarbital....     30.00
Vale Chemical Co...............  Wesmatic Forte....         00377-0426  TB           Phenobarbital....      8.10
Vitarine Pharmacal Inc.........  E-Caff PB Tablets.         00185-0982  TB           Pentobarbital....     30.00
Vortech Pharmacal Co...........  Donna-Sed.........         00298-5054  EL           Phenobarbital....      3.24
Vortech Pharmacal Co...........  Hypnaldyne........         00298-1778  TB           Phenobarbital....     16.20
Vortech Pharmacal Co...........  Isophed...........         00298-5680  LQ           Phenobarbital....      0.40
Vortech Pharmacal Co...........  Phedral C. T......         00298-1173  TB           Phenobarbital....      8.10
W.E. Hauck Inc.................  G-1 Capsules......         43797-0244  CA           Butalbital.......     50.00
Wallace Laboratories...........  Barbidonna Elixir.         00037-0305  EL           Phenobarbital....      3.20
Wallace Laboratories...........  Barbidonna No 2...         00037-0311  TB           Phenobarbital....     32.00
Wallace Laboratories...........  Barbidonna Tablets         00037-0301  TB           Phenobarbital....     16.00
Wallace Laboratories...........  Butibel Elixir....         00037-0044  EL           Butabarbital           3.00
                                                                                      Sodium.                   
Wallace Laboratories...........  Butibel Tablets...         00037-0046  TB           Butabarbital          15.00
                                                                                      Sodium.                   
Wallace Laboratories...........  Lufyllin-EPG               00037-0565  EL           Phenobarbital....      1.60
                                  Elixir.                                                                       
Wallace Laboratories...........  Lufyllin-EPG               00037-0561  TB           Phenobarbital....     16.00
                                  Tablets.                                                                      
Wallace Laboratories...........  Milprem-200.......         00037-5501  TB           Meprobamate......    200.00
Wallace Laboratories...........  Milprem-400.......         00037-5401  TB           Meprobamate......    400.00
Wesley Pharmacal Co............  Hytrophen.........         00917-0244  TB           Phenobarbital....     16.20
Wesley Pharmacal Co............  Pulsaphen Gray....         00917-0113  TB           Phenobarbital....     15.00
Wesley Pharmacal Co............  Wescophen-S.......         00917-0135  TB           Phenobarbital....     30.00
Wesley Pharmacal Co............  Wesmatic Forte....         00917-0845  TB           Phenobarbital....      8.00
West-ward Inc..................  Belladonna                 00143-1140  TB           Phenobarbital....     16.20
                                  Alkaloids &                                                                   
                                  Phenobarbital.                                                                
West-ward Inc..................  Butalbital with            00143-1787  TB           Butalbital.......     50.00
                                  Acetaminophen and                                                             
                                  Caffeine Tablets.                                                             
West-ward Inc..................  Theophylline               00143-1695  TB           Phenobarbital....      8.00
                                  Ephedrine &                                                                   
                                  Phenobarbital.                                                                

[[Page 181]]

                                                                                                                
Winthrop Labs..................  Isuprel...........         00024-0874  EL           Phenobarbital....      0.40
Zenith Labs Inc................  Azpan.............         00172-3747  TB           Phenobarbital....      8.00
----------------------------------------------------------------------------------------------------------------

[52 FR 9803, Mar. 27, 1987, as amended at 53 FR 10861, April 1, 1988; 54 
FR 11520, Mar. 21, 1989; 55 FR 9114, Mar. 12, 1990; 57 FR 23301, June 3, 
1992]

                    Exempt Anabolic Steroid Products



Sec. 1308.33  Exemption of certain anabolic steroid products; application.

    (a) The Administrator, upon the recommendation of the Secretary of 
Health and Human Services, may, by regulation, exempt from the 
application of all or any part of the Act any compound, mixture, or 
preparation containing an anabolic steroid as defined in Sec. 1308.02 
if, because of its concentration, preparation, mixture or delivery 
system, it has no significant potential for abuse (Pub. L. 101-647 
section 1903(a)).
    (b) Any person seeking to have any compound, mixture, or preparation 
containing an anabolic steroid as defined in Sec. 1308.02 exempted from 
the application of all or any part of the Act, pursuant to paragraph (a) 
of this section, may apply to the Administrator, Drug Enforcement 
Administration, Department of Justice, Washington, DC 20537.
    (c) An application for an exemption under this section shall be 
submitted in triplicate and contain the following information:
    (1) The name and address of the applicant;
    (2) The name of the product;
    (3) The chemical structural formula or description for any anabolic 
steroid contained in the product;
    (4) The complete description of dosage and quantitative composition 
of the dosage form;
    (5) A description of the delivery system, if applicable;
    (6) The indications and conditions for use in which species, 
including whether or not this product is a prescription drug;
    (7) Information to facilitate identification of the dosage form, 
such as shape, color, coating, and scoring;
    (8) The label and labeling of the immediate container and the 
commercial containers, if any, of the product;
    (9) The units in which the dosage form is ordinarily available; and
    (10) The facts which the applicant believes justify:
    (i) A determination that the product has no significant potential 
for abuse and
    (ii) a granting of an exemption under this section.
    (d) Within a reasonable period of time after the receipt of the 
application for an exemption under this section, the Administrator shall 
notify the applicant of his acceptance or nonacceptance of the 
application, and if not accepted, the reason therefor. The Administrator 
need not accept an application for filing if any of the requirements 
prescribed in paragraph (c) of this section is lacking or is not set 
forth so as to be readily understood. The applicant may amend the 
application to meet the requirements of paragraph (c) of this section. 
If accepted for filing, the Administrator will request from the 
Secretary for Health and Human Services his recommendation, as to 
whether such product which contains an anabolic steroid should be 
considered for exemption from certain portions of the Controlled 
Substances Act. On receipt of the recommendation of the Secretary, the 
Administrator shall make a determination as to whether the evidence 
submitted or otherwise available sufficiently establishes that the 
product possesses no significant potential for abuse. The Administrator 
shall issue and publish in the Federal Register his order on the 
application, which shall include a reference to the legal authority 
under which the order is issued, and the findings of fact and 
conclusions of law upon which the order is based. This order shall 
specify

[[Page 182]]

the date on which it will take effect. The Administrator shall permit 
any interested person to file written comments on or objections to the 
order within 60 days of the date of publication of his order in the 
Federal Register. If any such comments or objections raise significant 
issues regarding any finding of fact or conclusion of law upon which the 
order is based, the Administrator shall immediately suspend the 
effectiveness of the order until he may reconsider the application in 
light of the comments and objections filed. Thereafter, the 
Administrator shall reinstate, revoke, or amend his original order as he 
determines appropriate.
    (e) The Administrator may revoke any exemption granted pursuant to 
section 1903(a) of Public Law 101-647 by following the procedures set 
forth in paragraph (d) of this section for handling an application for 
an exemption which has been accepted for filing.

[56 FR 42936, Aug. 30, 1991; 57 FR 10815, Mar. 31, 1992]



Sec. 1308.34  Exempt anabolic steroid products.

    The following anabolic steroid containing compounds, mixtures, or 
preparations have been exempted by the Administrator from application of 
sections 302 through 309 and 1002 through 1004 of the Act (21 U.S.C. 
822-829 and 952-954) and Secs. 1301.24, 1301.31, 1301.32, and 1301.71 
through 1301.76 of this chapter for administrative purposes only:

                                    Table of Exempt Anabolic Steroid Products                                   
----------------------------------------------------------------------------------------------------------------
          Trade name                Company           NDC No.           Form       Ingredients       Quantity   
----------------------------------------------------------------------------------------------------------------
Androgyn L.A.................  Forest            0456-1005........  Vial.......  Testosterone     90 mg/ml      
                                Pharmaceuticals                                   enanthate.      4 mg/ml       
                                , St. Louis, MO.                                 Estradiol                      
                                                                                  valerate.                     
Andro-Estro 90-4.............  Rugby             0536-1605........  Vial.......  Testosterone     90 mg/ml      
                                Laboratories,                                     enanthate.      4 mg/ml       
                                Rockville                                        Estradiol                      
                                Centre, NY.                                       valerate.                     
depANDROGYN..................  Forest            0456-1020........  Vial.......  Testosterone     50 mg/ml      
                                Pharmaceuticals                                   cypionate.      2 mg/ml       
                                , St. Louis, MO.                                 Estradiol                      
                                                                                  cypionate.                    
DEPO-T.E.....................  Quality Research  52765-257........  Vial.......  Testosterone     50 mg/ml      
                                Pharm., Carmel,                                   cypionate.      2 mg/ml       
                                IN.                                              Estradiol                      
                                                                                  cypionate.                    
depTESTROGEN.................  Martica           51698-257........  Vial.......  Testosterone     50 mg/ml      
                                Pharmaceuticals                                   cypionate.      2 mg/ml       
                                , Phoenix, AZ.                                   Estradiol                      
                                                                                  cypionate.                    
Duomone......................  Wintec            52047-360........  Vial.......  Testosterone     90 mg/ml      
                                Pharmaceutical,                                   enanthate.      4 mg/ml       
                                Pacific, MO.                                     Estradiol                      
                                                                                  valerate.                     
DURATESTRIN..................  W.E. Hauck,       43797-016........  Vial.......  Testosterone     50 mg/ml      
                                Alpharetta, GA.                                   cypionate.      2 mg/ml       
                                                                                 Estradiol                      
                                                                                  cypionate.                    
DUO-SPAN II..................  Primedics         0684-0102........  Vial.......  Testosterone     50 mg/ml      
                                Laboratories,                                     cyplonate.      2 mg/ml       
                                Gardena, CA.                                     Esterified                     
                                                                                  cypionate.                    
Estratest....................  Solvay            0032-1026........  TB.........  Esterified       1.25 mg       
                                Pharmaceuticals                                   estrogens.      2.5 mg        
                                , Marletta, GA.                                  Methyltestoster                
                                                                                  one.                          
Estratest HS.................  Solvay            0032-1023........  TB.........  Esterified       0.625 mg      
                                Pharmaceuticals                                   estrogens.      1.25 mg       
                                , Marletta, GA.                                  Methyltestoster                
                                                                                  one.                          
PAN ESTRA TEST...............  Pan American      0525-0175........  Vial.......  Testosterone     50 mg/ml      
                                Labs,                                             cypionate.      2 mg/ml       
                                Covington, LA.                                   Estradiol                      
                                                                                  cypionate.                    
Premarin with                  Ayerst Labs.      0046-0879........  TB.........  Conjugated       1.25 mg       
 Methyltestosterone.            Inc., New York,                                   estrogens.      10.0 mg       
                                NY.                                              Methyltestoster                
                                                                                  one.                          
Premarin with                  Ayerst Labs.      0046-0878........  TB.........  Conjugated       0.625 mg      
 Methyltestosterone.            Inc., New York,                                   estrogens.      5.0 mg        
                                NY.                                              Methyltestoster                
                                                                                  one.                          
Synovex H Pellets in process.  Syntex Animal     .................  Drum.......  Testosterone     25 mg.        
                                Health, Palo                                      propionate.     2.5 mg.       
                                Alto, CA.                                        Estradiol                      
                                                                                  benzoate.                     
Synovex H Pellets in process   Syntex Animal     .................  Drum.......  Testosterone     10 parts.     
 granulation.                   Health, Palo                                      propionate.     1 part.       
                                Alto, CA.                                        Estradiol                      
                                                                                  benzoate.                     
TEST-ESTRO Cypionates........  Rugby             0536-9470........  Vial.......  Testosterone     50 mg/ml      
                                Laboratories,                                     cypionate.      2 mg/ml       
                                Rockville                                        Estradiol                      
                                Centre, NY.                                       cypionate.                    
Testagen.....................  Clint             55553-257........  Vial.......  Testosterone     50 mg/ml.     
                                Pharmaceuticals                                   cypionate.      2 mg/ml.      
                                , Nashville, TN.                                 Estradiol                      
                                                                                  cypionate.                    
Testosterone Cyp 50 Estradiol  I.D.E.-           0814-7737........  Vial.......  Testosterone     50 mg/ml      
 Cyp 2.                         Interstate,                                       cypionate.      2 mg/ml       
                                Amityville, NY.                                  Estradiol                      
                                                                                  cypionate.                    

[[Page 183]]

                                                                                                                
Testosterone Cypionate--       Best Generics,    54274-530........  Vial.......  Testosterone     50 mg/ml      
 Estradiol Cypionate            No. Miami                                         cypionate.      2 mg/ml       
 Injection.                     Beach, FL.                                       Estradiol                      
                                                                                  cypionate.                    
Testosterone Cypionate--       Goldline Labs,    0182-3069........  Vial.......  Testosterone     50 mg/ml.     
 Estradiol Cypionate            Ft. Lauderdale,                                   cypionate.      2 mg/ml.      
 Injection.                     FL.                                              Estradiol                      
                                                                                  cypionate.                    
Testosterone Cypionate--       Schein            0364-6611........  Vial.......  Testosterone     50 mg/ml      
 Estradiol Cypionate            Pharmaceuticals                                   cypionate.      2 mg/ml       
 Injection.                     , Port                                           Estradiol                      
                                Washington, NY.                                   cypionate.                    
Testosterone Cypionate--       Steris Labs.      0402-0257........  Vial.......  Testosterone     50 mg/ml      
 Estradiol Cypionate            Inc., Phoenix,                                    cypionate.      2 mg/ml       
 Injection.                     AZ.                                              Estradiol                      
                                                                                  cypionate.                    
Testosterone Cypionate--       The Upjohn Co.,   0009-0253........  Vial.......  Testosterone     50 mg/ml.     
 Estradiol Cypionate            Kalamazoo, MI.                                    cypionate.      2 mg/ml.      
 Injection.                                                                      Estradiol                      
                                                                                  cypionate.                    
Testosterone Enanthate--       Goldline Labs,    0182-3073........  Vial.......  Testosterone     90 mg/ml.     
 Estradiol Valerate Injection.  Ft. Lauderdale,                                   enanthate.      4 mg/ml.      
                                FL.                                              Estradiol                      
                                                                                  valerate.                     
Testosterone Enanthate--       Schein            0364-6618........  Vial.......  Testosterone     90 mg/ml      
 Estradiol Valerate Injection.  Pharmaceuticals                                   enanthate.      4 mg/ml       
                                , Port                                           Estradiol                      
                                Washington, NY.                                   valerate.                     
Testosterone Enanthate--       Steris Labs.      0402-0360........  Vial.......  Testosterone     90 mg/ml      
 Estradiol Valerate Injection.  Inc., Phoenix,                                    enanthate.      4 mg/ml       
                                AZ.                                              Estradiol                      
                                                                                  valerate.                     
Tilapia Sex Reversal Feed      Zeigler           .................  Plastic      Methyltestoster  60 mg/1 kg.   
 (Investigational).             Brothers, Inc.,                      Bags.        one fish feed.                
                                Gardners, PA.                                                                   
----------------------------------------------------------------------------------------------------------------


[56 FR 42937, Aug. 30, 1991, as amended at 57 FR 55091, Nov. 24, 1992; 
58 FR 16773, Mar. 31, 1993; 58 FR 34708, June 29, 1993]

                                Hearings



Sec. 1308.41   Hearings generally.

    In any case where the Administrator shall hold a hearing on the 
issuance, amendment, or repeal of rules pursuant to section 201 of the 
Act, the procedures for such hearing and accompanying proceedings shall 
be governed generally by the rulemaking procedures set forth in the 
Administrative Procedure Act (5 U.S.C. 551-559) and specifically by 
section 201 of the Act (21 U.S.C. 811), by Secs. 1308.42-1308.51, and by 
Secs. 1316.41-1316.67 of this chapter.



Sec. 1308.42   Purpose of hearing.

    If requested by any interested person after proceedings are 
initiated pursuant to Sec. 1308.44, the Administrator shall hold a 
hearing for the purpose of receiving factual evidence and expert opinion 
regarding the issues involved in the issuance, amendment or repeal of a 
rule issuable pursuant to section 201(a) of the Act (21 U.S.C. 811(a)). 
Extensive argument should not be offered into evidence but rather 
presented in opening or closing statements of counsel or in memoranda or 
proposed findings of fact and conclusions of law.



Sec. 1308.43   Waiver or modification of Rules.

    The Administrator or the presiding officer (with respect to matters 
pending before him) may modify or waive any rule in this part by notice 
in advance of the hearing, if he determines that no party in the hearing 
will be unduly prejudiced and the ends of justice will thereby be 
served. Such notice of modification or waiver shall be made a part of 
the record of the hearing.



Sec. 1308.44   Initiation of proceedings for rulemaking.

    (a) Any interested person may submit a petition to initiate 
proceedings for the issuance, amendment, or repeal of any rule or 
regulation issuable pursuant to the provisions of section 201 of the 
Act.
    (b) Petitions shall be submitted in quintuplicate to the 
Administrator in the following form:

_______________________________________________________________________
(Date)
Administrator, Drug Enforcement
    Administration
Department of Justice,
Washington, DC 20537.


[[Page 184]]


    Dear Sir: The undersigned --------------- hereby petitions the 
Administrator to initiate proceedings for the issuance (amendment or 
repeal) of a rule or regulation pursuant to section 201 of the 
Controlled Substances Act.
    Attached hereto and constituting a part of this petition are the 
following:
    (A) The proposed rule in the form proposed by the petitioner. (If 
the petitioner seeks the amendment or repeal of an existing rule, the 
existing rule, together with a reference to the section in the Code of 
Federal Regulations where it appears, should be included.)
    (B) A statement of the grounds which the petitioner relies for the 
issuance (amendment or repeal) of the rule. (Such grounds shall include 
a reasonably concise statement of the facts relied upon by the 
petitioner, including a summary of any relevant medical or scientific 
evidence known to the petitioner.)
    All notices to be sent regarding this petition should be addressed 
to:

_______________________________________________________________________

                                 (Name)

_______________________________________________________________________

                            (Street Address)

_______________________________________________________________________

                            (City and State)

    Respectfully yours,

_______________________________________________________________________

                        (Signature of petitioner)

    (c) Within a reasonable period of time after the receipt of a 
petition, the Administrator shall notify the petitioner of his 
acceptance or nonacceptance of the petition, and if not accepted, the 
reason therefor. The Administrator need not accept a petition for filing 
if any of the requirements prescribed in paragraph (b) of this section 
is lacking or is not set forth so as to be readily understood. If the 
petitioner desires, he may amend the petition to meet the requirements 
of paragraph (b) of this section. If accepted for filing, a petition may 
be denied by the Administrator within a reasonable period of time 
thereafter if he finds the grounds upon which the petitioner relies are 
not sufficient to justify the initiation of proceedings.
    (d) The Administrator shall, before initiating proceedings for the 
issuance, amendment, or repeal of any rule either to control a drug or 
other substance, or to transfer a drug or other substance from one 
schedule to another, or to remove a drug or other substance entirely 
from the schedules, and after gathering the necessary data, request from 
the Secretary a scientific and medical evaluation and the Secretary's 
recommendations as to whether such drug or other substance should be so 
controlled, transferred, or removed as a controlled substance. The 
recommendations of the Secretary to the Administrator shall be binding 
on the Administrator as to such scientific and medical matters, and if 
the Secretary recommends that a drug or other substance not be 
controlled, the Administrator shall not control that drug or other 
substance.
    (e) If the Administrator determines that the scientific and medical 
evaluation and recommendations of the Secretary and all other relevant 
data constitute substantial evidence of potential for abuse such as to 
warrant control or additional control over the drug or other substance, 
or substantial evidence that the drug or other substances should be 
subjected to lesser control or removed entirely from the schedules, he 
shall initiate proceedings for control, transfer, or removal as the case 
may be.
    (f) If and when the Administrator determines to initiate 
proceedings, he shall publish in the Federal Register general notice of 
any proposed rule making to issue, amend, or repeal any rule pursuant to 
section 201 of the Act. Such published notice shall include a statement 
of the time, place, and nature of any hearings on the proposal in the 
event a hearing is requested pursuant to Sec. 1308.45. Such hearings may 
not be commenced until after the expiration of at least 30 days from the 
date the general notice is published in the Federal Register. Such 
published notice shall also include a reference to the legal authority 
under which the rule is proposed, a statement of the proposed rule, and, 
in the discretion of the Administrator, a summary of the subjects and 
issues involved.
    (g) The Administrator may permit any interested persons to file 
written comments on or objections to the proposal and shall designate in 
the notice of proposed rule making the time during which such filings 
may be made.

[[Page 185]]



Sec. 1308.45   Request for hearing or appearance; waiver.

    (a) Any interested person desiring a hearing on a proposed 
rulemaking, shall, within 30 days after the date of publication of 
notice of the proposed rulemaking in the Federal Register, file with the 
Administrator a written request for a hearing in the form prescribed in 
Sec. 1316.47 of this chapter.
    (b) Any interested person desiring to participate in a hearing 
pursuant to Sec. 1308.41 shall, within 30 days after the date of 
publication of the notice of hearing in the Federal Register, file with 
the Administrator a written notice of his intention to participate in 
such hearing in the form prescribed in Sec. 1316.48 of this chapter. Any 
person filing a request for a hearing need not also file a notice of 
appearance; the request for a hearing shall be deemed to be a notice of 
appearance.
    (c) Any interested person may, within the period permitted for 
filing a request for a hearing, file with the Administrator a waiver of 
an opportunity for a hearing or to participate in a hearing, together 
with a written statement regarding his position on the matters of fact 
and law involved in such hearing. Such statement, if admissible, shall 
be made a part of the record and shall be considered in light of the 
lack of opportunity for cross-examination in determining the weight to 
be attached to matters of fact asserted therein.
    (d) If any interested person fails to file a request for a hearing; 
or if he so files and fails to appear at the hearing, he shall be deemed 
to have waived his opportunity for the hearing or to participate in the 
hearing, unless he shows good cause for such failure.
    (e) If all interested persons waive or are deemed to waive their 
opportunity for the hearing or to participate in the hearing, the 
Administrator may cancel the hearing, if scheduled, and issue his final 
order pursuant to Sec. 1308.48 without a hearing.



Sec. 1308.46   Burden of proof.

    At any hearing, the proponent for the issuance, amendment, or repeal 
of any rule or regulation shall have the burden of proof.



Sec. 1308.47   Time and place of hearing.

    The hearing will commence at the place and time designated in the 
notice of proposed rulemaking published in the Federal Register but 
thereafter it may be moved to a different place and may be continued 
from day to day or recessed to a later day without notice other than 
announcement thereof by the presiding officer at the hearing.



Sec. 1308.48   Final order.

    As soon as practicable after the presiding officer has certified the 
record to the Administrator, the Administrator shall cause to be 
published in the Federal Register his order in the proceeding, which 
shall set forth the final rule and the findings of fact and conclusions 
of law upon which the rule is based. This order shall specify the date 
on which it shall take effect, which shall not be less than 30 days from 
the date of publication in the Federal Register unless the Administrator 
finds that conditions of public health or safety necessitate an earlier 
effective date, in which event the Administrator shall specify in the 
order his findings as to such conditions.



Sec. 1308.49   Control required under international treaty.

    Pursuant to section 201(d) of the Act (21 U.S.C. 811(d) ), where 
control of a substance is required by U.S. obligations under 
international treaties, conventions, or protocols in effect on May 1, 
1971, the Administrator shall issue and publish in the Federal Register 
an order controlling such substance under the schedule he deems most 
appropriate to carry out obligations. Issuance of such an order shall be 
without regard to the findings required by subsections 201(a) or 202(b) 
of the Act (21 U.S.C. 811(a) or 812(b)) and without regard to the 
procedures prescribed by Sec. 1308.41 or subsections 201 (a) and (b) of 
the Act (21 U.S.C. 811 (a) and (b)). An order controlling a substance 
shall become effective 30 days from the date of publication in the 
Federal Register, unless the Administrator finds that conditions of 
public health or safety necessitate an earlier effective date, in which 
event the Administrator shall specify in the order his findings as to 
such conditions.

[[Page 186]]



Sec. 1308.50   Control of immediate precursors.

    Pursuant to section 201(e) of the Act (21 U.S.C. 811(e)), the 
Administrator may, without regard to the findings required by subsection 
201(a) or 202 (b) of the Act (21 U.S.C. 811(a) or 812(b)) and without 
regard to the procedures prescribed by Sec. 1308.41 or subsections 201 
(a) and (b) of the Act (21 U.S.C. 811(a) and (b)), issue and publish in 
the Federal Register an order controlling an immediate precursor. The 
order shall designate the schedule in which the immediate precursor is 
to be placed, which shall be the same schedule in which the controlled 
substance of which it is an immediate precursor is placed or any other 
schedule with a higher numerical designation. An order controlling an 
immediate precursor shall become effective 30 days from the date of 
publication in the Federal Register, unless the Administrator finds that 
conditions of public health or safety necessitate an earlier effective 
date, in which event the Administrator shall specify in the order his 
findings as to such conditions.



Sec. 1308.51   Pending proceedings.

    All administrative proceedings pending before the Administration on 
the effective date of this part, including the matter of listing 
chlordiazepoxide and its salts and diazepam as drugs subject to control 
under the Drtg Abuse Control Amendments of 1965, shall be continued and 
brought to final determination in accord with the laws and regulations 
in effect prior to such effective date.



Sec. 1308.52  Emergency Scheduling.

    Pursuant to 21 U.S.C. 811(h) and withott regard to the requirements 
of 21 U.S.C. 811(b) relating to the scientific and medical evaluation of 
the Secretary of Health and Human Services, the Administrator may place 
a substance into Schedule I on a temporary basis, if he determines that 
such action is necessary to avoid an imminent hazard to the public 
safety. An order issued under this section may not be effective before 
the expiration of 30 days from:
    (a) The date of publication by the Administrator of a notice in the 
Federal Register of his intention to issue such order and the grounds 
upon which such order is to be issued, and
    (b) The date the Administrator has transmitted notification to the 
Secretary of Health and Human Services of his intention to issue such 
order. An order issued under this section shall be vacated upon the 
conclusion of a subsequent rulemaking proceeding initiated under section 
201(a) (21 U.S.C. 811(a)) with respect to such substance or at the end 
of one year from the effective date of the order scheduling the 
substance, except that during the pendency of proceedings under section 
201(a) (21 U.S.C. 811(a)) with respect to the substance, the 
Administrator may extend the temporary scheduling for up to six months.

[51 FR 15318, Apr. 23, 1986]

 PART 1309--REGISTRATION OF MANUFACTURERS, DISTRIBUTORS, IMPORTERS AND 
                      EXPORTERS OF LIST I CHEMICALS

                           General Information

Sec.
1309.01  Scope of part 1309.
1309.02  Definitions.
1309.03  Information; special instructions.

                Fees for Registration and Reregistration

1309.11  Fee amounts.
1309.12  Time and method of payment; refund.

                      Requirements for Registration

1309.21  Persons required to register.
1309.22  Separate registration for independent activities.
1309.23  Separate registration for separate locations.
1309.24  Exemption of agents and employees.
1309.25  Exemption of certain controlled substance registrants.
1309.26  Exemption of law enforcement officials.
1309.27  Exemption of certain manufacturers.

                      Application for Registration

1309.31  Time for application for registration; expiration date.
1309.32  Application forms; contents, signature.
1309.33  Filing of application; joint filings.

[[Page 187]]

1309.34  Acceptance for filing; defective applications.
1309.35  Additional information.
1309.36  Amendments to and withdrawals of applications.

  Action on Applications for Registration: Revocation or Suspension of 
                              Registration

1309.41  Administrative review generally.
1309.42  Certificate of registration; denial of registration.
1309.43  Suspension or revocation of registration.
1309.44  Suspension of registration pending final order.
1309.45  Extension of registration pending final order.
1309.46  Order to show cause.

                                Hearings

1309.51  Hearings generally.
1309.52  Purpose of hearing.
1309.53  Waiver or modification of rules.
1309.54  Request for hearing or appearance; waiver.
1309.55  Burden of proof.
1309.56  Time and place of hearing.
1309.57  Final order.

         Modification, Transfer and Termination of Registration

1309.61  Modification in registration.
1309.62  Termination of registration.
1309.63  Transfer of registration.

                          Security Requirements

1309.71  General security requirements.
1309.72  Felony conviction; employer responsibilities.
1309.73  Employee responsibility to report diversion.

    Authority: 21 U.S.C. 821, 822, 823, 824, 830, 871(b), 875, 877, 958.

    Source:  60 FR 32454, June 22, 1995, unless otherwise noted.

                           General Information

Sec. 1309.01  Scope of Part 1309.

    Procedures governing the registration of manufacturers, 
distributors, importers and exporters of List I chemicals pursuant to 
Sections 102, 302, 303, 1007 and 1008 of the Act (21 U.S.C. 802, 822, 
823, 957 and 958) are set forth generally by those sections and 
specifically by the sections of this part.



Sec. 1309.02  Definitions.

    (a) The term Act means the Controlled Substances Act (84 Stat. 1242; 
21 U.S.C. 801) and/or the Controlled Substances Import and Export Act 
(84 Stat. 1285; 21 U.S.C. 951).
    (b) The term hearing means any hearing held pursuant to the part for 
the granting, denial, revocation, or suspension of a registration 
pursuant to sections 303 and 304 of the Act (21 U.S.C. 823-824).
    (c) The term person includes any individual, corporation, government 
or governmental subdivision or agency, business trust, partnership, 
association, or other legal entity.
    (d) The term register and registration refer only to registration 
required and permitted by sections 302 and 1007 of the Act (21 U.S.C. 
822 and 957).
    (e) The term registrant means any person who is registered pursuant 
to either section 303 or section 1008 of the Act (21 U.S.C. 823 and 
958).
    (f) The term retail distributor means a distributor whose List I 
chemical activities are restricted to the sale of drug products that are 
regulated as List I chemicals pursuant to Section 1310.01(f)(1)(iv), 
directly to walk-in customers for personal use.
    (g) Any term not defined in this section shall have the definition 
set forth in section 102 of the Act (21 U.S.C. 802) or in Sections 
1310.01 and 1313.02 of this chapter.

[60 FR 32454, June 22, 1995; 60 FR 42436, Aug. 16, 1995]



Sec. 1309.03  Information; special instructions.

    Information regarding procedures under these rules and instructions 
supplementing these rules will be furnished upon request by writing to 
the Drug Enforcement Administration, Chemical Operations Section, Office 
of Diversion Control, Washington, D.C. 20537.

                Fees for Registration and Reregistration



Sec. 1309.11  Fee amounts.

    (a) For each initial registration to manufacture for distribution, 
distribute, import, or export, the applicant shall pay a fee of $595 for 
a annual registration.

[[Page 188]]

    (b) For each reregistration to manufacture for distribution, 
distribute, import, or export, the registrant shall pay a fee of $477 
for an annual registration.
    (c) For each initial registration to conduct business as a retail 
distributor the applicant shall pay an application processing fee of $7 
and an investigation fee of $248, for an annual registration.
    (d) For each reregistration to conduct business as a retail 
distributor the registrant shall pay a fee of $116.



Sec. 1309.12  Time and method of payment; refund.

    (a) For each application for registration or reregistration to 
manufacture for distribution, distribute, import, or export, the 
applicant shall pay the fee when the application for registration or 
reregistration is submitted for filing.
    (b) For retail the distributor initial applications, the applicant 
shall pay the application processing fee when the application for 
registration is submitted for filing. The investigation fee shall be 
paid within 30 days after DEA notifies the applicant that the 
preregistration investigation has been scheduled.
    (c) For retail distributor reregistration applications, the 
registrant shall pay the fee when the application for reregistration is 
submitted for filing.
    (d) Payments should be made in the form of a personal, certified, or 
cashier's check or money order made payable to ``Drug Enforcement 
Administration.'' Payments made in the form of stamps, foreign currency, 
or third party endorsed checks will not be accepted. These application 
fees are not refundable.

[60 FR 32454, June 22, 1995; 60 FR 36334, July 14, 1995]

                      Requirements for Registration



Sec. 1309.21  Persons required to register.

    (a) Every person who distributes, imports, or exports any List I 
chemical, other than those List I chemicals contained in a product 
exempted under Sec. 1310.01(f)(1)(iv), or who proposes to engage in the 
distribution, importation, or exportation of any List I chemical, shall 
obtain annually a registration specific to the List I chemicals to be 
handled, unless exempted by law or pursuant to Secs. 1309.24 through 
1309.27. Only persons actually engaged in such activities are required 
to obtain a registration; related or affiliated persons who are not 
engaged in such activities are not required to be registered. (For 
example, a stockholder or parent corporation of a corporation 
distributing List I chemicals is not required to obtain a registration.)
    (b) Every person who distributes or exports a List I chemical they 
have manufactured, other than a List I chemical contained in a product 
exempted under Sec. 1310.01(f)(1)(iv), or proposes to distribute or 
export a List I chemical they have manufactured, shall obtain annually a 
registration specific to the List I chemicals to be handled, unless 
exempted by law or pursuant to Secs. 1309.24 through 1309.27.



Sec. 1309.22  Separate registration for independent activities.

    (a) The following groups of activities are deemed to be independent 
of each other:
    (1) Retail distributing of List I chemicals;
    (2) Non-Retail distributing of List I chemicals;
    (3) Importing List I chemicals; and
    (4) Exporting List I chemicals.
    (b) Every person who engages in more than one group of independent 
activities shall obtain a separate registration for each group of 
activities, unless otherwise exempted by the Act or Secs. 1309.24 
through 1309.26, except that a person registered to import any List I 
chemical shall be authorized to distribute that List I chemical after 
importation, but no other chemical that the person is not registered to 
import.



Sec. 1309.23  Separate registration for separate locations.

    (a) A separate registration is required for each principal place of 
business at one general physical location where List I chemicals are 
distributed, imported, or exported by a person.
    (b) The following locations shall be deemed to be places not subject 
to the registration requirement:

[[Page 189]]

    (1) A warehouse where List I chemicals are stored by or on behalf of 
a registered person, unless such chemicals are distributed directly from 
such warehouse to locations other than the registered location from 
which the chemicals were originally delivered; and
    (2) An office used by agents of a registrant where sales of List I 
chemicals are solicited, made, or supervised but which neither contains 
such chemicals (other than chemicals for display purposes) nor serves as 
a distribution point for filling sales orders.



Sec. 1309.24  Exemption of agents and employees.

    The requirement of registration is waived for any agent or employee 
of a person who is registered to engage in any group of independent 
activities, if such agent or employee is acting in the usual course of 
his or her business or employment.



Sec. 1309.25  Exemption of certain controlled substance registrants.

    (a) The requirement of registration is waived for any person who 
distributes a product containing a List I chemical that is regulated 
pursuant to Sec. 1310.01(f)(1)(iv), if that person is registered with 
the Administration to manufacture, distribute or dispense a controlled 
substance.
    (b) The requirement of registration is waived for any person who 
imports or exports a product containing a List I chemical that is 
regulated pursuant to Sec. 1310.01(f)(1)(iv), if that person is 
registered with the Administration to engage in the same activity with a 
controlled substance.
    (c) The Administrator may, upon finding that continuation of the 
waiver would not be in the public interest, suspend or revoke a person's 
waiver pursuant to the procedures set forth in Secs. 1309.43 through 
1309.46 and 1309.51 through 1309.57. In considering the revocation or 
suspension of a person's waiver, the Administrator shall also consider 
whether action to revoke or suspend the person's controlled substance 
registration pursuant to 21 U.S.C. 824 is warranted.
    (d) Any person exempted from the registration requirement under this 
section shall comply with the security requirements set forth in 
Sections 1309.71-1309.73 and the recordkeeping and reporting 
requirements set forth under Parts 1310 and 1313 of this chapter.



Sec. 1309.26  Exemption of law enforcement officials.

    (a) The requirement of registration is waived for the following 
persons in the circumstances described in this section:
    (1) Any officer or employee of the Administration, any officer of 
the U.S. Customs Service, any officer or employee of the United States 
Food and Drug Administration, any other Federal officer who is lawfully 
engaged in the enforcement of any Federal law relating to listed 
chemicals, controlled substances, drugs or customs, and is duly 
authorized to possess and distribute List I chemicals in the course of 
official duties; and
    (2) Any officer or employee of any State, or any political 
subdivision or agency thereof, who is engaged in the enforcement of any 
State or local law relating to listed chemicals and controlled 
substances and is duly authorized to possess and distribute List I 
chemicals in the course of his official duties.
    (b) Any official exempted by this section may, when acting in the 
course of official duties, possess any List I chemical and distribute 
any such chemical to any other official who is also exempted by this 
section and acting in the course of official duties.



Sec. 1309.27  Exemption of certain manufacturers.

    The requirement of registration is waived for any manufacturer of a 
List I chemical, if that chemical is produced solely for internal 
consumption by the manufacturer and there is no subsequent distribution 
or exportation of the List I chemical.

                      Application for Registration



Sec. 1309.31  Time for application for registration; expiration date.

    (a) Any person who is required to be registered and who is not so 
registered may apply for registration at any time.

[[Page 190]]

No person required to be registered shall engage in any activity for 
which registration is required until the application for registration is 
approved and a Certificate of Registration is issued by the 
Administrator to such person.
    (b) Any person who is registered may apply to be reregistered not 
more than 60 days before the expiration date of his registration.
    (c) At the time a person is first registered, that person shall be 
assigned to one of twelve groups, which shall correspond to the months 
of the year. The expiration date of the registrations of all registrants 
within any group will be the last day of the month designated for that 
group. In assigning any of the above persons to a group, the 
Administration may select a group the expiration date of which is less 
than one year from the date such business activity was registered. If 
the person is assigned to a group which has an expiration date less than 
eleven months from the date of which the person is registered, the 
registration shall not expire until one year from that expiration date; 
in all other cases, the registration shall expire on the expiration date 
following the date on which the person is registered.



Sec. 1309.32  Application forms; contents; signature.

    (a) Any person who is required to be registered pursuant to Section 
1309.21 and is not so registered, shall apply on DEA Form 510.
    (b) Any person who is registered pursuant to Section 1309.21, shall 
apply for reregistration on DEA Form 510a.
    (c) DEA Form 510 may be obtained at any divisional office of the 
Administration or by writing to the Registration Unit, Drug Enforcement 
Administration, Department of Justice, Post Office Box 28083, Central 
Station, Washington, DC 20005. DEA Form 510a will be mailed to each List 
I chemical registrant approximately 60 days before the expiration date 
of his or her registration; if any registered person does not receive 
such forms within 45 days before the expiration date of the 
registration, notice must be promptly given of such fact and DEA Form 
510a must be requested by writing to the Registration Unit of the 
Administration at the foregoing address.
    (d) Each application for registration shall include the 
Administration Chemical Code Number, as set forth in Section 1310.02 of 
this chapter, for each List I chemical to be distributed, imported, or 
exported.
    (e) Registration shall not entitle a person to engage in any 
activity with any List I chemical not specified in his or her 
application.
    (f) Each application shall include all information called for in the 
form, unless the item is not applicable, in which case this fact shall 
be indicated.
    (g) Each application, attachment, or other document filed as part of 
an application, shall be signed by the applicant, if an individual; by a 
partner of the applicant, if a partnership; or by an officer of the 
applicant, if a corporation, corporate division, association, trust or 
other entity. An applicant may authorize one or more individuals, who 
would not otherwise be authorized to do so, to sign applications for the 
applicant by filing with the application or other document a power of 
attorney for each such individual. The power of attorney shall be signed 
by a person who is authorized to sign applications under this paragraph 
and shall contain the signature of the individual being authorized to 
sign the application or other document. The power of attorney shall be 
valid until revoked by the applicant.



Sec. 1309.33  Filing of application; joint filings.

    (a) All applications for registration shall be submitted for filing 
to the Registration Unit, Drug Enforcement Administration, Chemical 
Registration/ODC, Post Office Box 2427, Arlington, Virginia 22202-2427. 
The appropriate registration fee and any required attachments must 
accompany the application.
    (b) Any person required to obtain more than one registration may 
submit all applications in one package. Each application must be 
complete and must not refer to any accompanying application for required 
information.

[[Page 191]]



Sec. 1309.34  Acceptance for filing; defective applications.

    (a) Applications submitted for filing are dated upon receipt. If 
found to be complete, the application will be accepted for filing. 
Applications failing to comply with the requirements of this part will 
not generally be accepted for filing. In the case of minor defects as to 
completeness, the Administrator may accept the application for filing 
with a request to the applicant for additional information. A defective 
application will be returned to the applicant within 10 days of receipt 
with a statement of the reason for not accepting the application for 
filing. A defective application may be corrected and resubmitted for 
filing at any time.
    (b) Accepting an application for filing does not preclude any 
subsequent request for additional information pursuant to Section 
1309.35 and has no bearing on whether the application will be granted.



Sec. 1309.35  Additional information.

    The Administrator may require an applicant to submit such documents 
or written statements of fact relevant to the application as he deems 
necessary to determine whether the application should be granted. The 
failure of the applicant to provide such documents or statements within 
a reasonable time after being requested to do so shall be deemed to be a 
waiver by the applicant of an opportunity to present such documents or 
facts for consideration by the Administrator in granting or denying the 
application.



Sec. 1309.36  Amendments to and withdrawals of applications.

    (a) An application may be amended or withdrawn without permission of 
the Administration at any time before the date on which the applicant 
receives an order to show cause pursuant to Sec. 1309.46. An application 
may be amended or withdrawn with permission of the Administrator at any 
time where good cause is shown by the applicant or where the amendment 
or withdrawal is in the public interest.
    (b) After an application has been accepted for filing, the request 
by the applicant that it be returned or the failure of the applicant to 
respond to official correspondence regarding the application, including 
a request that the applicant submit the required fee, when sent by 
registered or certified mail, return receipt requested, shall be deemed 
to be a withdrawal of the application.

  Action on Applications for Registration: Revocation or Suspension of 
                              Registration



Sec. 1309.41  Administrative review generally.

    The Administrator may inspect, or cause to be inspected, the 
establishment of an applicant or registrant, pursuant to subpart A of 
Part 1316 of this chapter. The Administrator shall review the 
application for registration and other information gathered by the 
Administrator regarding an applicant in order to determine whether the 
applicable standards of Section 303 of the Act (21 U.S.C. 823) have been 
met by the applicant.



Sec. 1309.42  Certificate of registration; denial of registration.

    (a) The Administrator shall issue a Certificate of Registration (DEA 
Form 511) to an applicant if the issuance of registration or 
reregistration is required under the applicable provisions of section 
303 of the Act (21 U.S.C. 823). In the event that the issuance of 
registration or reregistration is not required, the Administrator shall 
deny the application. Before denying any application, the Administrator 
shall issue an order to show cause pursuant to Section 1309.46 and, if 
requested by the applicant, shall hold a hearing on the application 
pursuant to Sec. 1309.51.
    (b) The Certificate of Registration (DEA Form 511) shall contain the 
name, address, and registration number of the registrant, the activity 
authorized by the registration, the amount of fee paid, and the 
expiration date of the registration. The registrant shall maintain the 
certificate of registration at the registered location in a readily 
retrievable manner and shall permit inspection of the certificate by any 
official, agent or employee of the Administration or of any Federal,

[[Page 192]]

State, or local agency engaged in enforcement of laws relating to List I 
chemicals or controlled substances.



Sec. 1309.43  Suspension or revocation of registration.

    (a) The Administrator may suspend any registration pursuant to 
section 304(a) of the Act (21 U.S.C. 824(a)) for any period of time he 
determines.
    (b) The Administrator may revoke any registration pursuant to 
section 304(a) of the Act (21 U.S.C. 824(a)).
    (c) Before revoking or suspending any registration, the 
Administrator shall issue an order to show cause pursuant to Section 
1309.46 and, if requested by the registrant, shall hold a hearing 
pursuant to Section 1309.51. Notwithstanding the requirements of this 
Section, however, the Administrator may suspend any registration pending 
a final order pursuant to Sec. 1309.44.
    (d) Upon service of the order of the Administrator suspending or 
revoking registration, the registrant shall immediately deliver his or 
her Certificate of Registration to the nearest office of the 
Administration.



Sec. 1309.44  Suspension of registration pending final order.

    (a) The Administrator may suspend any registration simultaneously 
with or at any time subsequent to the service upon the registrant of an 
order to show cause why such registration should not be revoked or 
suspended, in any case where he finds that there is an imminent danger 
to the public health or safety. If the Administrator so suspends, he 
shall serve with the order to show cause pursuant to Sec. 1309.46 an 
order of immediate suspension that shall contain a statement of his 
findings regarding the danger to public health or safety.
    (b) Upon service of the order of immediate suspension, the 
registrant shall promptly return his Certificate of Registration to the 
nearest office of the Administration.
    (c) Any suspension shall continue in effect until the conclusion of 
all proceedings upon the revocation or suspension, including any 
judicial review thereof, unless sooner withdrawn by the Administrator or 
dissolved by a court of competent jurisdiction. Any registrant whose 
registration is suspended under this section may request a hearing on 
the revocation or suspension of his registration at a time earlier than 
specified in the order to show cause pursuant to Section 1309.46, which 
request shall be granted by the Administrator, who shall fix a date for 
such hearing as early as reasonably possible.



Sec. 1309.45  Extension of registration pending final order.

    In the event that an applicant for reregistration (who is doing 
business under a registration previously granted and not revoked or 
suspended) has applied for reregistration at least 45 days before the 
date on which the existing registration is due to expire, and the 
Administrator has issued no order on the application on the date on 
which the existing registration is due to expire, the existing 
registration of the applicant shall automatically be extended and 
continue in effect until the date on which the Administrator so issues 
his order. The Administrator may extend any other existing registration 
under the circumstances contemplated in this section even though the 
registrant failed to apply for reregistration at least 45 days before 
expiration of the existing registration, with or without request by the 
registrant, if the Administrator finds that such extension is not 
inconsistent with the public health and safety.



Sec. 1309.46  Order to show cause.

    (a) If, upon examination of the application for registration from 
any applicant and other information gathered by the Administration 
regarding the applicant, the Administrator is unable to make the 
determinations required by the applicable provisions of section 303 of 
the Act (21 U.S.C. 823) to register the applicant, the Administrator 
shall serve upon the applicant an order to show cause why the 
application for registration should not be denied.
    (b) If, upon information gathered by the Administration regarding 
any registrant, the Administrator determines that the registration of 
such registrant is subject to suspension or revocation pursuant to 
section 304 of the Act (21 U.S.C. 824), the Administrator shall

[[Page 193]]

serve upon the registrant an order to show cause why the registration 
should not be revoked or suspended.
    (c) The order to show cause shall call upon the applicant or 
registrant to appear before the Administrator at a time and place stated 
in the order, which shall not be less than 30 days after the date of 
receipt of the order. The order to show cause shall also contain a 
statement of the legal basis for such hearing and for the denial, 
revocation, or suspension of registration and a summary of the matters 
of fact and law asserted.
    (d) Upon Receipt of an order to show cause, the applicant or 
registrant must, if he desires a hearing, file a request for a hearing 
pursuant to Sec. 1309.54. If a hearing is requested, the Administrator 
shall hold a hearing at the time and place stated in the order, pursuant 
to Sec. 1309.51.
    (e) When authorized by the Administrator, any agent of the 
Administration may serve the order to show cause.

                                Hearings



Sec. 1309.51  Hearings generally.

    (a) In any case where the Administrator shall hold a hearing on any 
registration or application therefore, the procedures for such hearing 
shall be governed generally by the adjudication procedures set forth in 
the Administrative Procedure Act (5 U.S.C. 551-559) and specifically by 
sections 303 and 304 of the Act (21 U.S.C. 823-824), by Secs. 1309.52 
through 1309.57, and by the procedures for administrative hearings under 
the Act set forth in Secs. 1316.41 through 1316.67 of this chapter.
    (b) Any hearing under this part shall be independent of, and not in 
lieu of, criminal prosecutions or other proceedings under the Act or any 
other law of the United States.



Sec. 1309.52  Purpose of hearing.

    If requested by a person entitled to a hearing, the Administrator 
shall hold a hearing for the purpose of receiving factual evidence 
regarding the issues involved in the denial, revocation, or suspension 
of any registration. Extensive argument should not be offered into 
evidence but rather presented in opening or closing statements of 
counsel or in memoranda or proposed findings of fact and conclusions of 
law.



Sec. 1309.53  Waiver or modification of rules.

    The Administrator or the presiding officer (with respect to matters 
pending before him) may modify or waive any rule in this part by notice 
in advance of the hearing, if he determines that no party in the hearing 
will be unduly prejudiced and the ends of justice will thereby be 
served. Such notice of modification or waiver shall be made a part of 
the record of the hearing.



Sec. 1309.54  Request for hearing or appearance; waiver.

    (a) Any person entitled to a hearing pursuant to Secs. 1309.42 and 
1309.43 and desiring a hearing shall, within 30 days after the date of 
receipt of the order to show cause, file with the Administrator a 
written request for a hearing in the form prescribed in Sec. 1316.47 of 
this chapter.
    (b) Any person entitled to a hearing pursuant to Secs. 1309.42 and 
1309.43 may, within the period permitted for filing a request for a 
hearing, file with the Administrator a waiver of an opportunity for a 
hearing, together with a written statement regarding his position on the 
matters of fact and law involved in such hearing. Such statement, if 
admissible, shall be made a part of the record and shall be considered 
in light of the lack of opportunity for cross-examination in determining 
the weight to be attached to matters of fact asserted therein.
    (c) If any person entitled to a hearing pursuant to Secs. 1309.42 
and 1309.43 fails to file a request for a hearing, or if he so files and 
fails to appear at the hearing, he shall be deemed to have waived his 
opportunity for the hearing, unless he shows good cause for such 
failure.
    (d) If any person entitled to a hearing waives or is deemed to waive 
his or her opportunity for the hearing, the Administrator may cancel the 
hearing, if scheduled, and issue his final order pursuant to 
Sec. 1309.57 without a hearing.



Sec. 1309.55  Burden of proof.

    (a) At any hearing for the denial of a registration, the 
Administration shall

[[Page 194]]

have the burden of proving that the requirements for such registration 
pursuant to section 303 of the Act (21 U.S.C. 823) are not satisfied.
    (b) At any hearing for the revocation or suspension of a 
registration, the Administration shall have the burden of proving that 
the requirements for such revocation or suspension pursuant to section 
304(a) of the Act (21 U.S.C. 824(a)) are satisfied.



Sec. 1309.56  Time and place of hearing.

    The hearing will commence at the place and time designated in the 
order to show cause or notice of hearing published in the Federal 
Register (unless expedited pursuant to Section 1309.44(c)) but 
thereafter it may be moved to a different place and may be continued 
from day to day or recessed to a later day without notice other than 
announcement thereof by the presiding officer at the hearing.



Sec. 1309.57  Final order.

    As soon as practicable after the presiding officer has certified the 
record to the Administrator, the Administrator shall cause to be 
published in the Federal Register his final order in the proceeding, 
which shall set forth the final rule and the findings of fact and 
conclusions of law upon which the rule is based. This order shall 
specify the date on which it shall take effect, which date shall not be 
less than 30 days from the date of publication in the Federal Register 
unless the Administrator finds that the public interest in the matter 
necessitates an earlier effective date, in which case the Administrator 
shall specify in the order his findings as to the conditions which led 
him to conclude that an earlier effective date was required.

         Modification, Transfer and Termination of Registration



Sec. 1309.61  Modification in registration.

    Any registrant may apply to modify his or her registration to 
authorize the handling of additional List I chemicals or to change his 
or her name or address, by submitting a letter of request to the Drug 
Enforcement Administration, Chemical Registration/ODC, Post Office Box 
2427, Arlington, Virginia 22202-2427. The letter shall contain the 
registrant's name, address, and registration number as printed on the 
certificate of registration, and the List I chemicals to be added to his 
registration or the new name or address and shall be signed in 
accordance with Sec. 1309.32(g). No fee shall be required to be paid for 
the modification. The request for modification shall be handled in the 
same manner as an application for registration. If the modification in 
registration is approved, the Administrator shall issue a new 
certificate of registration (DEA Form 511) to the registrant, who shall 
maintain it with the old certificate of registration until expiration.



Sec. 1309.62  Termination of registration.

    The registration of any person shall terminate if and when such 
person dies, ceases legal existence, or discontinues business or 
professional practice. Any registrant who ceases legal existence or 
discontinues business or professional practice shall notify the 
Administrator promptly of such fact.



Sec. 1309.63  Transfer of registration.

    No registration or any authority conferred thereby shall be assigned 
or otherwise transferred except upon such conditions as the 
Administrator may specifically designate and then only pursuant to his 
written consent.

                          Security Requirements



Sec. 1309.71  General security requirements.

    (a) All applicants and registrants shall provide effective controls 
and procedures to guard against theft and diversion of List I chemicals. 
Specific attention shall be paid to storage of and controlling access to 
List I chemicals as follows:
    (1) Chemicals shall be stored in containers sealed in such a manner 
as to indicate any attempts at tampering with the container. Where 
chemicals cannot be stored in sealed containers, access to the chemicals 
should be controlled through physical means or through human or 
electronic monitoring.
    (2) In retail settings open to the public where drugs containing 
List I

[[Page 195]]

chemicals that are regulated pursuant to Sec. 1310.01(f)(1)(iv) are 
distributed, such drugs will be stocked behind a counter where only 
employees have access.
    (b) In evaluating the effectiveness of security controls and 
procedures, the Administrator shall consider the following factors:
    (1) The type, form, and quantity of List I chemicals handled;
    (2) The location of the premises and the relationship such location 
bears on the security needs;
    (3) The type of building construction comprising the facility and 
the general characteristics of the building or buildings;
    (4) The availability of electronic detection and alarm systems;
    (5) the extent of unsupervised public access to the facility;
    (6) The adequacy of supervision over employees having access to List 
I chemicals;
    (7) The procedures for handling business guests, visitors, 
maintenance personnel, and nonemployee service personnel in areas where 
List I chemicals are processed or stored;
    (8) The adequacy of the registrant's or applicant's systems for 
monitoring the receipt, distribution, and disposition of List I 
chemicals in its operations.
    (c) Any registrant or applicant desiring to determine whether a 
proposed system of security controls and procedures is adequate may 
submit materials and plans regarding the proposed security controls and 
procedures either to the Special Agent in Charge in the region in which 
the security controls and procedures will be used, or to the Chemical 
Operations Section Office of Diversion Control, Drug Enforcement 
Administration, Washington, D.C. 20537.



Sec. 1309.72  Felony conviction; employer responsibilities.

    (a) The registrant shall exercise caution in the consideration of 
employment of persons who will have access to listed chemicals, who have 
been convicted of a felony offense relating to controlled substances or 
listed chemicals, or who have, at any time, had an application for 
registration with the DEA denied, had a DEA registration revoked, or 
surrendered a DEA registration for cause. (For purposes of this 
subsection, the term ``for cause'' means a surrender in lieu of, or as a 
consequence of, any Federal or State administrative, civil or criminal 
action resulting from an investigation of the individual's handling of 
controlled substances or listed chemicals.) The registrant should be 
aware of the circumstances regarding the action against the potential 
employee and the rehabilitative efforts following the action. The 
registrant shall assess the risks involved in employing such persons, 
including the potential for action against the registrant pursuant to 
Sec. 1309.43, If such person is found to have diverted listed chemicals, 
and, in the event of employment, shall institute procedures to limit the 
potential for diversion of List I chemicals.
    (b) It is the position of DEA that employees who possess, sell, use 
or divert listed chemicals or controlled substances will subject 
themselves not only to State or Federal prosecution for any illicit 
activity, but shall also immediately become the subject of independent 
action regarding their continued employment. The employer will assess 
the seriousness of the employee's violation, the position of 
responsibility held by the employee, past record of employment, etc., in 
determining whether to suspend, transfer, terminate or take other action 
against the employee.



Sec. 1309.73  Employee responsibility to report diversion.

    Reports of listed chemical diversion by fellow employees is not only 
a necessary part of an overall employee security program but also serves 
the public interest at large. It is, therefore, the position of DEA that 
an employee who has knowledge of diversion from his employer by a fellow 
employee has an obligation to report such information to a responsible 
security official of the employer. The employer shall treat such 
information as confidential and shall take all reasonable steps to 
protect the confidentiality of the information and the identity of the 
employee furnishing information. A failure to report information of 
chemical diversion will be considered in determining the

[[Page 196]]

feasibility of continuing to allow an employee to work in an area with 
access to chemicals. The employer shall inform all employees concerning 
this policy.



PART 1310--RECORDS AND REPORTS OF LISTED CHEMICALS AND CERTAIN MACHINES--Table of Contents




Sec.
1310.01  Definitions.
1310.02  Substances covered.
1310.03  Persons required to keep records and file reports.
1310.04  Maintenance of records.
1310.05  Reports.
1310.06  Content of records and reports.
1310.07  Proof of identity.
1310.08  Excluded transactions.
1310.09  Temporary exemption from registration.
1310.10  Removal of the exemption of drugs distributed under the Food, 
          Drug and Cosmetic Act.
1310.11  Reinstatement of exemption for drug products distributed under 
          the Food, Drug and Cosmetic Act.
1310.14  Exemption of drug products containing ephedrine and 
          therapeutically significant quantities of another active 
          medicinal ingredient.
1310.15  Exempt drug products containing ephedrine and therapeutically 
          significant quantities of another active medicinal ingredient.

    Authority: 21 U.S.C. 802, 830, 871(b).

    Source: 54 FR 31665, Aug. 1, 1989, unless otherwise noted.



Sec. 1310.01  Definitions.

    As used in this part, the following terms shall have the meanings 
specified:
    (a) The term Act means the Controlled Substances Act, as amended (84 
Stat. 1242; 21 U.S.C. 801) and/or the Controlled Substances Import and 
Export Act, as amended (84 Stat. 1285; 21 U.S.C. 951).
    (b) The term listed chemical means any List I chemical or List II 
chemical.
    (c) The term List I chemical means a chemical specifically 
designated by the Administrator in Sec. 1310.02(a) that, in addition to 
legitimate uses, is used in manufacturing a controlled substance in 
violation of the Act and is important to the manufacture of a controlled 
substance.
    (d) The term List II chemical means a chemical, other than a List I 
chemical, specifically designated by the Administrator in Section 
1310.02(b) that, in addition to legitimate uses, is used in 
manufacturing a controlled substance in violation of the Act.
    (e) The term regulated person means any individual, corporation, 
partnership, association, or other legal entity who manufactures, 
distributes, imports, or exports a listed chemical, a tableting machine, 
or an encapsulating machine, or who acts as a broker or trader for an 
international transaction involving a listed chemical, tableting 
machine, or encapsulating machine.
    (f) The term regulated transaction means:
    (1) A distribution, receipt, sale, importation, or exportation of a 
listed chemical, or an international transaction involving shipment of a 
listed chemical, or if the Administrator establishes a threshold amount 
for a specific listed chemical, a threshold amount as determined by the 
Administrator, which includes a cumulative threshold amount for multiple 
transactions, of a listed chemical, except that such terms does not 
include:
    (i) A domestic lawful distribution in the usual course of business 
between agents or employees of a single regulated person; in this 
context, agents or employees means individuals under the direct 
management and control of the regulated person;
    (ii) A delivery of a listed chemical to or by a common or contract 
carrier for carriage in the lawful and usual course of the business of 
the common or contract carrier, or to or by a warehouseman for storage 
in the lawful and usual course of the business of the warehouseman, 
except that if the carriage or storage is in connection with the 
distribution, importation, or exportation of a listed chemical to a 
third person, this paragraph does not relieve a distributor, importer, 
or exporter from compliance with this part or parts 1309 and 1313 of 
this chapter;
    (iii) Any category of transaction or any category of transaction for 
a specific listed chemical or chemicals specified by regulation of the 
Administrator as excluded from this definition

[[Page 197]]

as unnecessary for enforcement of the Act;
    (iv) Any transaction in a listed chemical that is contained in a 
drug that may be marketed or distributed lawfully in the United States 
under the Federal Food, Drug, and Cosmetic Act unless--
    (A) The drug contains ephedrine or its salts, optical isomers, or 
salts of optical isomers as the only active medicinal ingredient or 
contains ephedrine or its salts, optical isomers or salts of optical 
isomers and therapeutically insignificant quantities of another active 
medicinal ingredient. For purposes of this paragraph, the term 
``therapeutically insignificant quantities'' shall apply if the product 
formulation (i.e., the qualitative and quantitative composition of 
active ingredients within the product) is not listed in American 
Pharmaceutical Association (Apha) Handbook of Nonprescription Drugs; 
Drug Facts and Comparisons (published by Wolters Kluwer Company); or USP 
DI (published by authority of the United States Pharmacopeial 
Convention, Inc.); or the product is not listed in Sec. 1310.15 as an 
exempt drug product. For drug products having formulations not found in 
the above compendiums, the Administrator shall determine, pursuant to a 
written request as specified in Sec. 1310.14, whether the active 
medicinal ingredients are present in quantities considered 
therapeutically significant for purposes of this paragraph; or
    (B) The Administrator has determined pursuant to the criteria in 
Sec. 1310.10 that:
    (1) The drug or group of drugs is being diverted to obtain the 
listed chemical for use in the illicit production of a controlled 
substance; and
    (2) The quantity of ephedrine or other listed chemical contained in 
the drug included in the transaction or multiple transactions equals or 
exceeds the threshold established for that chemical by the 
Administrator;
    (v) Any transaction in a chemical mixture listed in Sec. 1310.13.
    (2) A distribution, importation, or exportation of a tableting 
machine or encapsulating machine except that such term does not include 
a domestic lawful distribution in the usual course of business between 
agents and emploxees of a single regulated person; in this context, 
agents or employees means individuals under the direct management and 
control of the regulated person.
    (g) The term chemical mixture means a combination of two or more 
chemical substances, at least one of which is not a listed chemical, 
except that such term does not include any combination of a listed 
chemical with another chemical that is present solely as an impurity or 
which has been created to evade the requirements of the act.
    (h) The term retrievable means that records required by this section 
are kept by automatic data processing systems or other electronic or 
mechanized recordkeeping systems in such a manner that they can be 
readily retrieved and separated out from all other records in a 
reasonable time and/or records are kept on which the listed chemicals, 
tableting machines, and encapsulating machines are asterisked, redlined, 
or in some other manner visually identifiable apart from other items 
appearing on the records or the maintained separate from all other 
records.
    (i) The term tableting machine means any manual, semi-automatic, or 
fully automatic equipment which may be used for the compaction or 
molding of powdered or granular solids, or semi-solid material, to 
produce coherent solid tablets.
    (j) The term encapsulating machine means any manual, semi-automatic, 
or fully automatic equipment which may be used to fill shells or 
capsules with any powdered, granular, semi-solid, or liquid material.
    (k) The terms broker and trader mean any individual, corporation, 
corporate division, partnership, association, or other legal entity 
which assists in arranging an international transaction in a listed 
chemical by--
    (1) negotiating contracts;
    (2) serving as an agent or intermediary; or
    (3) fulfilling a formal obligation to complete the transaction by 
bringing together a buyer and seller, a buyer and transporter, or a 
seller and transporter, or by receiving any form of compensation for so 
doing.
    (l) The term international transaction means a transaction involving 
the

[[Page 198]]

shipment of a listed chemical across an international border (other than 
a United States border) in which a broker or trader located in the 
United States participates.
    (m) Any term not defined in this section shall have the definition 
set forth in section 102 and 1001 of the Act (21 U.S.C. 802 and 951) and 
Sec. 1301.02 of this chapter.

[60 FR 32454, June 22, 1995, as amended at 60 FR 32459, June 22, 1995]



Sec. 1310.02  Substances covered.

    The following chemicals have been specifically designated by the 
Administrator of the Drug Enforcement Administration as the listed 
chemicals subject to the provisions of this part and parts 1309 and 1313 
of this chapter. Each chemical has been assigned the DEA Chemical Code 
Number set forth opposite it.
    (a) List I chemicals

(1) Anthranilic acid, its esters, and its salts.....................8530
(2) Benzyl cyanide..................................................8735
(3) Ephedrine, its salts, optical isomers, and salts of optical isomers 
                                                                    8113
(4) Ergonovine and its salts........................................8675
(5) Ergotamine and its salts........................................8676
(6) N-Acetylanthranilic acid, its esters, and its salts.............8522
(7) Norpseudoephedrine, its salts, optical isomers, and salts of optical 
isomers.............................................................8317
(8) Phenylacetic acid, its esters, and its salts....................8791
(9) Phenylpropanolamine, its salts, optical isomers, and salts of 
optical isomers.....................................................1225
(10) Piperidine and its salts.......................................2704
(11) Pseudoephedrine, its salts, optical isomers, and salts of optical 
isomers.............................................................8112
(12) 3,4-Methylenedioxyphenyl-2-propanone...........................8502
(13) Methylamine and its salts......................................8520
(14) Ethylamine and its salts.......................................8678
(15) Propionic anhydride............................................8328
(16) Insosafrole (Isosafrole).......................................8704
(17) Safrole........................................................8323
(18) Piperonal......................................................8750
(19) N-Methylephedrine, its salts, optical isomers, and salts of optical 
isomers (N-Methylephedrine).........................................8115
(20) N-Methylpseudoephedrine, its salts, optical isomers, and salts of 
optical isomers.....................................................8119
(21) Hydriotic acid (Hydriodic Acid)................................6695
(22) Benzaldehyde...................................................8256
(23) Nitroethane....................................................6724
    (b) List II chemicals:

(1) Acetic anhydride................................................8519
(2) Acetone.........................................................6532
(3) Benzyl chloride.................................................8570
(4) Ethyl ether.....................................................6584
(5) Potassium permanganate..........................................6579
(6) 2-Butanone (or Methyl Ethyl Ketone or MEK)......................6714
(7) Toluene.........................................................6594
(8) Hydrochloric acid...............................................6545
(9) Sulfuric acid...................................................6552
(10) Methyl Isobutyl Ketone (MIBK)..................................6715
    (c) The Administrator may add or delete a substance as a listed 
chemical by publishing a final rule in the Federal Register following a 
proposal which shall be published at least 30 days prior to the final 
rule.
    (d) Any person may petition the Administrator to have any substance 
added or deleted from paragraphs (a) or (b) of this section.
    (e) Any petition under this section shall contain the following 
information:
    (1) The name and address of the petitioner;
    (2) The name of the chemical to which the petition pertains;
    (3) The name and address of the manufacturer(s) of the chemical (if 
known);
    (4) A complete statement of the facts which the petitioner believes 
justifies the addition or deletion of the substance from paragraphs (a) 
or (b) of this section;
    (5) The date of the petition.
    (f) The Administrator may require the petitioner to submit such 
documents or written statements of fact relevant to the petition as he 
deems necessary in making a determination.
    (g) Within a reasonable period of time after the receipt of the 
petition, the Administrator shall notify the petitioner of his decision 
and the reason therefor. The Administrator need not accept a petition if 
any of the requirements prescribed in paragraph (e) of this section or 
requested pursuant to paragraph (f) of this section are lacking or are 
not clearly set forth as to be readily understood. If the petitioner 
desires, he may amend and resubmit the petition to meet the requirements 
of paragraphs (e) and (f) of this section.

[[Page 199]]

    (h) If a petition is granted or the Administrator, upon his own 
motion, proposes to add or delete substances as listed chemicals as set 
forth in paragraph (c) of this section, he shall issue and publish in 
the Federal Register a proposal to add or delete a substance as a lhsted 
chemical. The Administrator shall permit any interested person to file 
written comments regarding the proposal within 30 days of the date of 
publication of his order in the Federal Register. The Administrator will 
consider any comments filed by interested persons and publish a final 
rule in accordance with his decision in the matter.

[54 FR 31665, Aug. 1, 1989, as amended at 56 FR 48733, Sept. 26, 1991; 
57 FR 43615, Sept. 22, 1992; 60 FR 19510, Apr. 19, 1995; 60 FR 32460, 
June 22, 1995]



Sec. 1310.03  Persons required to keep records and file reports.

    (a) Each regulated person who engages in a regulated transaction 
involving a listed chemical, a tableting machine, or an encapsulating 
machine shall keep a record of the transaction as specified by 
Sec. 1310.04 and file reports as specified by Sec. 1310.05. However, a 
non-regulated person who acquires listed chemicals for internal 
consumption or ``end use'' and becomes a regulated person by virtue of 
infrequent or rare distribution of a listed chemical from inventory, 
shall not be required to maintain receipt records of listed chemicals 
under this section.
    (b) Each regulated person who manufactures a List I or List II 
chemical shall file reports regarding such manufacture as specified in 
Section 1310.05.

[54 FR 31665, Aug. 1, 1989, as amended at 56 FR 8277, Feb. 28, 1991; 61 
FR 14023, Mar. 29, 1996]

    Effective Date Note:  At 61 FR 14023, March 29, 1996, Sec. 1310.03 
was amended by redesignating the existing text as paragraph (a) and 
adding paragraph (b), effective April 29, 1996.



Sec. 1310.04  Maintenance of records.

    (a) Every record required to be kept subject to Section 1310.03 for 
a List I chemical, a tableting machine, or an encapsulating machine 
shall be kept by the regulated person for four years after the date of 
the transaction.
    (b) Every record required to be kept subject to Section 1310.03 for 
List II chemical shall be kept by the regulated person for two years 
after the date of the transaction.
    (c) A record under this section shall be kept at the regulated 
person's place of business where the transaction occurred, except that 
records may be kept at a single, central location of the regulated 
person if the regulated person has notified the Administration of the 
intention to do so. Written notification must be submitted by registered 
or certified mail, return receipt requested, to the Special Agent in 
Charge of the DEA Divisional Office for the area in which the records 
are required to be kept.
    (d) The records required to be kept under this section shall be 
readily retrievable and available for inspection and copying by 
authorized employees of the Administration under the provisions of 21 
U.S.C. 880.
    (e) The regulated person with more than one place of business where 
records are required to be kept shall devise a system to detect any 
party purchasing from several individual locations of the regulated 
person thereby seeking to avoid the application of the cumulative 
threshold or evading the requirements of the Act.
    (f) For those listed chemicals for which thresholds have been 
established, the quantitative threshold or the cumulative amount for 
multiple transactions within a calendar month, to be utilized in 
determining whether a receipt, sale, importation or exportation is a 
regulated transaction is as follows:
    (1) List I Chemicals:

------------------------------------------------------------------------
               Chemical                     Threshold by base weight    
------------------------------------------------------------------------
(i) Anthranilic acid and its salts...  30 kilograms.                    
(ii) Benzyl cyanide..................  1 kilogram.                      
(iii) Ergonovine and its salts.......  10 grams.                        
(iv) Ergotamine and its salts........  20 grams.                        
(v) N-Acetylanthranilic acid and its   40 kilograms                     
 salts.                                                                 
(vi) Norpseudoephedrine, its salts,    2.5 kiloframs.                   
 optical isomers, and salts of                                          
 optical isomers.                                                       

[[Page 200]]

                                                                        
(vii) Phenylacetic acid and its salts  1 kilogram.                      
(viii) Phenylpropanolamine, its        2.5 kilograms.                   
 salts, optical isomers, and salts of                                   
 optical isomers.                                                       
(ix) Piperidine and its salts........  500 grams.                       
(x) Pseudoephedrine, its salts,        1 kilogram                       
 optical isomers, and salts of                                          
 optical isomers.                                                       
(xi) 3, 4-Methylenedioxyphenyl-2-      4 kilograms.                     
 propanone.                                                             
(xii) Methylamine and its salts......  1 kilogram.                      
(xiii) Ethylamine and its salts......  1 kilogram.                      
(xiv) Propionic anhydride............  1 gram.                          
(xv) Isosafrole......................  4 kilograms.                     
(xvi) Safrole........................  4 kilograms.                     
(xvii) Piperonal.....................  4 kilograms.                     
(xviii) N-Methylephedrine, its salts,  1 kilogram.                      
 optical isomers, and salts of                                          
 optical isomers.                                                       
(xix) N-Methylpseudoephedrine, its     1 kilogram.                      
 salts, optical isomers, and salts of                                   
 optical isomers.                                                       
(xx) Hydriotic acid (57%)............  1.7 kilograms (or 1 liter by     
                                        volume).                        
(xxi) Benzaldehyde...................  4 Kilograms.                     
(xxii) Nitroethane...................  2.5 Kilograms.                   
------------------------------------------------------------------------

    (2) List II Chemicals:
    (i) Imports and Exports

----------------------------------------------------------------------------------------------------------------
                Chemical                         Threshold by volume                  Threshold by weight       
----------------------------------------------------------------------------------------------------------------
(A) Acetic anhydride...................  250 gallons........................  1,023 kilograms.                  
(B) Acetone............................  500 gallons........................  1,500 kilograms.                  
(C) Benzyl chloride....................  N/A................................  4 kilograms.                      
(D) Ethyl ether........................  500 gallons........................  1,364 kilograms.                  
(E) Potassium permanganate.............  N/A................................  500 kilograms.                    
(F) 2-Butanone (MEK)...................  500 gallons........................  1,455 kilograms.                  
(G) Toluene............................  500 gallons........................  1,591 kilograms.                  
----------------------------------------------------------------------------------------------------------------

    (ii) Domestic Sales

----------------------------------------------------------------------------------------------------------------
                Chemical                         Threshold by volume                  Threshold by weight       
----------------------------------------------------------------------------------------------------------------
(A) Acetic anhydride...................  250 gallons........................  1,023 kilograms.                  
(B) Acetone............................  50 gallons.........................  150 kilograms.                    
(C) Benzyl chloride....................  N/A................................  1 kilogram.                       
(D) Ethyl ether........................  50 gallons.........................  135.8 kilograms.                  
(E) Potassium permanganate.............  N/A................................  55 kilograms.                     
(F) 2-Butanone (MEK)...................  50 gallons.........................  145 kilograms.                    
(G) Toluene............................  50 gallons.........................  159 kilograms.                    
----------------------------------------------------------------------------------------------------------------

    (iii) The cumulative threshold is not applicable to domestic sales 
of Acetone, 2-Butanone (MEK), and Toluene.
    (iv) Exports, transshipments and international transactions to 
Designated Countries set forth in Sec. 1310.08(b)
    (v) Export and International Transactions to Designated Countries, 
and Importations for Transshipment or Transfer to Designated Countries

------------------------------------------------------------------------
                                    Threshold by                        
            Chemical                   volume        Threshold by weight
------------------------------------------------------------------------
(A) Methyl Isobutyl Ketone       500 gallons.......  1523 kilograms.    
 (MIBK).                                                                
(B) Reserved.                                                           
------------------------------------------------------------------------

    (g) For listed chemicals for which no thresholds have been 
established, the size of the transaction is not a factor in determining 
whether the transaction meets the definition of a regulated transaction 
as set forth in Sec. 1310.01(f). All such transactions, regardless of 
size, are subject to recordkeeping and reporting requirements as set 
forth in this part 1310 and notification provisions as set forth in part 
1313 of this chapter.
    (1) Listed Chemicals For Which No Thresholds Have Been Established:
    (i) Ephedrine, its salts, optical isomers, and salts of optical 
isomers
    (ii) [Reserved]

[[Page 201]]

    (2) [Reserved]

[54 FR 31665, Aug. 1, 1989, as amended at 56 FR 48733, Sept. 26, 1991; 
57 FR 43615, Sept. 22, 1992; 59 FR 51367, Oct. 11, 1994; 60 FR 19510, 
Apr. 19, 1995; 60 FR 32460, June 22, 1995; 60 FR 42436, Aug. 16, 1995]



Sec. 1310.05  Reports.

    (a) Each regulated person shall report to the Special Agent in 
Charge of the DEA Divisional Office for the area in which the regulated 
person making the report is located, as follows:
    (1) Any regulated transaction involving an extraordinary quantity of 
a listed chemical, an uncommon method of payment or delivery, or any 
other circumstance that the regulated person believes may indicate that 
the listed chemical will be used in violation of this part.
    (2) Any proposed regulated transaction with a person whose 
description or other identifying characteristic the Administration has 
previously furnished to the regulated person.
    (3) Any unusual or excessive loss or disappearance of a listed 
chemical under the control of the regulated person. The regulated person 
responsible for reporting a loss in-transit is the supplier.
    (4) Any domestic regulated transaction in a tableting machine or an 
encapsulating machine.
    (b) Each report submitted pursuant to paragraph (a) of this section 
shall, whenever possible, be made orally to the DEA Divisional Office 
for the area in which the regulated person making the report is located 
at the earliest practicable opportunity after the regulated person 
becomes aware of the circumstances involved and as much in advance of 
the conclusion of the transaction as possible. Written reports of 
transactions listed in paragraphs (a)(1), (a)(3) and (a)(4) of this 
section will subsequently be filed as set forth in Sec. 1310.06 within 
15 days after the regulated person becomes aware of the circumstances of 
the event. A transaction may not be completed with a person whose 
description or identifying characteristic has previously been furnished 
to the regulated person by the Administration unless the transaction is 
approved by the Administration.
    (c) Each regulated person who imports or exports a tableting 
machine, as defined in Sec. 1310.01(i), or encapsulation machine, as 
defined in Sec. 1310.01(j), shall file a report (not a 486) of such 
importation or exportation with the Administration at the following 
address on or before the date of importation or exportation: Drug 
Enforcement Administration, P.O. Box 28346, Washington, DC 20038. In 
order to facilitate the importation or exportation of any tableting 
machine or encapsulating machine and implement the purpose of the Act, 
regulated persons may wish to report to the Administration as far in 
advance as possible. A copy of the report may be transmitted directly to 
the Drug Enforcement Administration through electronic facsimile media. 
Any tableting machine or encapsulating machine may be imported or 
exported if that machine is needed for medical, commercial, scientific, 
or other legitimate uses. However, an importation or exportation of a 
tableting machine or encapsulating machine may not be completed with a 
person whose description or identifying characteristic has previously 
been furnished to the regulated person by the Administration unless the 
transaction is approved by the Administration.
    (d) Each regulated bulk manufacturer of a listed chemical shall 
submit manufacturing, inventory and use data on an annual basis as set 
forth in Sec. 1310.06(h). This data shall be submitted annually to the 
Drug and Chemical Evaluation Section, Drug Enforcement Administration 
(DEA), Washington, D.C. 20537, on or before the 15th day of March of the 
year immediately following the calendar year for which submitted. A 
business entity which manufactures a listed chemical may elect to report 
separately by individual location or report as an aggregate amount for 
the entire business entity provided that they inform the DEA of which 
method they will use. This reporting requirement does not apply to drug 
or other products which are exempted under Secs. 1310.01(f)(1)(iv) or 
1310.01(f)(1)(v) except as set forth in Sec. 1310.06(h)(5). Bulk 
manufacturers that

[[Page 202]]

produce a listed chemical solely for internal consumption shall not be 
required to report for that listed chemical. For purposes of these 
reporting requirements, internal consumption shall consist of any 
quantity of a listed chemical otherwise not available for further resale 
or distribution. Internal consumption shall include (but not be limited 
to) quantities used for quality control testing, quantities consumed in-
house or production losses. Internal consumption does not include the 
quantities of a listed chemical consumed in the production of exempted 
products. If an existing standard industry report contains the 
information required in Sec. 1310.06(h) and such information is separate 
or readily retrievable from the report, that report may be submitted in 
satisfaction of this requirement. Each report shall be submitted to the 
DEA under company letterhead and signed by an appropriate, responsible 
official. For purposes of this paragraph only, the term regulated bulk 
manufacturer of a listed chemical means a person who manufactures a 
listed chemical by means of chemical synthesis or by extraction from 
other substances. The term bulk manufacturer does not include persons 
whose sole activity consists of the repackaging or relabeling of listed 
chemical products or the manufacture of drug dosage from products which 
contain a listed chemical.

[54 FR 31665, Aug. 1, 1989, as amended at 57 FR 2461, Jan. 22, 1992; 61 
FR 14024, Mar. 29, 1996]

    Effective Date Note:  At 61 FR 1404, March 29, 1996, Sec. 1310.05 
was amended by adding paragraph (d), effective April 29, 1996.



Sec. 1310.06  Content of records and reports.

    (a) Each record required by Sec. 1310.03 shall include the 
following:
    (1) The name, address, and, if required, DEA registration number of 
each party to the regulated transaction.
    (2) The date of the regulated transaction.
    (3) The name, quantity and form of packaging of the listed chemical 
or a description of the tableting machine or encapsulating machine 
(including make, model and serial number).
    (4) The method of transfer (company truck, picked up by customer, 
etc.).
    (5) The type of identification used by the purchaser and any unique 
number on that identification.
    (b) For purposes of this section, normal business records shall be 
considered adequate if they contain the information listed in paragraph 
(a) of this section and are readily retrievable from other business 
records of the regulated person. For prescription drug products, 
prescription and hospital records kept in the normal course of medical 
treatment shall be considered adequate.
    (c) Each report required by Section 1310.05(a) shall include the 
information as specified by Section 1310.06(a) and, where obtainable, 
the registration number of the other party, if such party is registered. 
A report submitted pursuant to Sec. 1310.05(a)(1) or (a)(4) must also 
include a description of the circumstances leading the regulated person 
to make the report, such as the reason that the method of payment was 
uncommon or the loss unusual. If the report is for a loss or 
disappearance under Sec. 1310.05(a)(4), the circumstances of such loss 
must be provided (in-transit, theft from premises, etc.)
    (d) A suggested format for the reports is provided below:

                                Supplier:

Registration Number_____________________________________________________
Name____________________________________________________________________
Business Address________________________________________________________
City____________________________________________________________________
State___________________________________________________________________
Zip_____________________________________________________________________
Business Phone__________________________________________________________

                               Purchaser:

Registration Number_____________________________________________________
Name____________________________________________________________________
Business Address________________________________________________________
City____________________________________________________________________
State___________________________________________________________________
Zip_____________________________________________________________________
Business Phone__________________________________________________________
Identification__________________________________________________________

         Shipping Address (if different than purchaser Address):

Street__________________________________________________________________
City____________________________________________________________________
State___________________________________________________________________
Zip_____________________________________________________________________
Date of Shipment________________________________________________________

[[Page 203]]

Name of Listed Chemical(s)______________________________________________
Quantity and Form of Packaging__________________________________________

                         Description of Machine:

Make____________________________________________________________________
Model___________________________________________________________________
Serial #________________________________________________________________
Method of Transfer______________________________________________________

                        If Loss or Disappearance:

Date of Loss____________________________________________________________
Type of Loss____________________________________________________________
Description of Circumstances____________________________________________

Public reporting burden for this collection of information is estimated 
to average ten minutes per response, including the time for reviewing 
instructions, searching existing data sources, gathering and maintaining 
the data needed, and completing and reviewing the collection of 
information. Send comments regarding this burden estimate or any other 
aspect of this collection of information, including suggestions for 
reducing this burden to the Drug Enforcement Administration, Records 
Management Section, Washington, D.C. 20537; and to the Office of 
Management and Budget, Paperwork Reduction Project No. 1117-0024, 
Washington, D.C. 20503.
    (e) Each report of an importation of a tableting machine or an 
encapsulating machine required by Sec. 1310.05(c) shall include the 
following information:
    (1) The name, address, telephone number, tdlex number, and, where 
available, the facsimile number of the regulated person; the name, 
address, telephone number, telex number, and, where available, the 
facsimile number of the import broker or forwarding agent, if any:
    (2) The description of each machine (including make, model, and 
serial number) and the number of machines being received;
    (3) The proposed import date, and the first U.S. Customs Port of 
Entry; and
    (4) The name, address, telephone number, telex number, and, where 
available, the facsimile number of the consignor in the foreign country 
of exportation.
    (f) Each report of an exportation of a tableting machine or an 
encapsulating machine required by Sec. 1310.05(c) shall include the 
following information:
    (1) The name, address, telephone number, telex number, and, where 
available, the facsimile number of the regulated person; the name, 
address, telephone number, telex number, and, where available, the 
facsimile number of the export broker, if any;
    (2) The description of each machine (including make, model, and 
serial number) and the number of machines being shipped;
    (3) The proposed export date, the U.S. Customs Port of exportation, 
and the foreign Port of Entry; and
    (4) The name, address, telephone, telex, and, where available, the 
facsimile number of the consignee in the country where the shipment is 
destined; the name(s) and address(es) of any intermediate consignee(s).
    (g) Declared exports of machines which are refused, rejected, or 
otherwise deemed undeliverable may be returned to the U.S. exporter of 
record. A brief written report outlining the circumstances must be sent 
to the Drug Enforcement Administration, P.O. Box 28346, Washington, DC 
20038, following the return within a reasonable time. This provision 
does not apply to shipments that have cleared foreign customs, been 
delivered, and accepted by the foreign consignee. Returns to third 
parties in the United States will be regarded as imports.
    (h) Each annual report required by Section 1310.05(d) shall provide 
the following information for each listed chemical manufactured:
    (1) The name, address and chemical registration number (if any) of 
the manufacturer and person to contact for information.
    (2) The aggregate quantity of each listed chemical that the company 
manufactured during the preceding calendar year.
    (3) The year-end inventory of each listed chemical as of the close 
of business on the 31st day of December of each year. (For each listed 
chemical, if the prior period's ending inventory has not previously been 
reported to DEA, this report should also detail the beginning inventory 
for the period.) For purposes of this requirement, inventory shall 
reflect the quantity of listed chemicals, whether in bulk or non-exempt 
product form, held in storage for

[[Page 204]]

later distribution. Inventory does not include waste material for 
destruction, material stored as an in-process intermediate or other in-
process material.
    (4) The aggregate quantity of each listed chemical used for internal 
consumption during the preceding calendar year, unless the chemical is 
produced solely for internal consumption.
    (5) The aggregate quantity of each listed chemical manufactured 
which becomes a component of a product exempted from Section 
1310.01(f)(1)(iv) or 1310.01(f)(1)(v) during the preceding calendar 
year.
    (6) Data shall identify the specific isomer, salt or ester when 
applicable but quantitative data shall be reported as anhydrous base or 
acid in kilogram units of measure.

[54 FR 31665, Aug. 1, 1989, as amended at 57 FR 2462, Jan. 22, 1992; 59 
FR 51364, Oct. 11, 1994; 60 FR 32461, June 22, 1995; 61 FR 14024, Mar. 
29, 1996]

    Effective Date Note:  At 61 FR 14024, March 29, 1996, Sec. 1310.06 
was amended by adding paragraph (h), effective April 29, 1996.



Sec. 1310.07  Proof of identity.

    (a) Each regulated person who engages in a regulated transaction 
must identify the other party to the transaction. For domestic 
transaction, this shall be accomplished by having the other party 
present documents which would verify the identity, or registration 
status if a registrant, of the other party to the regulated person at 
the time the order is placed. For export transactions, this shall be 
accomplished by good faith inquiry through reasonably available research 
documents or publicly available information which would indicate the 
existence of the foreign customer. No proof of identity is required for 
foreign suppliers.
    (b) The regulated person must verify the existence and apparent 
validity of a business entity ordering a listed chemical, tableting 
machine or encapsulating machine. For domestic transactions, this may be 
accomplished by such methods as checking the telephone directory, the 
local credit bureau, the local Chamber of Commerce or the local Better 
Business Bureau, or, if the business entity is a registrant, by 
verification of the registration. For export transactions, a good faith 
inquiry to verify the existence and apparent validity of a foreign 
business entity may be accomplished by such methods as verifying the 
business telephone listing through international telephone information, 
the firm's listing in international or foreign national chemical 
directories or other commerce directories or trade publications, 
confirmation through foreign subsidiaries of the U.S. regulated person, 
verification through the country of destination's embassy Commercial 
Attache, or official documents provided by the purchaser which confirm 
the existence and apparent validity of the business entity.
    (c) When transacting business with a new representative of a firm, 
the regulated person must verify the claimed agency status of the 
representative.
    (d) For sales to individuals or cash purchasers, the type of 
documents and other evidence of proof must consist of at least a 
signature of the purchaser, a driver's license and one other form of 
identification. Any exports to individuals or exports paid in cash are 
suspect and should be handled as such. For such exports, the regulated 
person shall diligently obtain from the purchaser or independently seek 
to confirm clear documentation which proves the person is properly 
identified such as through foreign identity documents, driver's license, 
passport information and photograph, etc. Any regulated person who fails 
to adequately prove the identity of the other party to the transaction 
may be subject to the specific penalties provided for violations of law 
related to regulated transactions in listed chemicals.
    (e) For a new customer who is not an individual or cash customer, 
the regulated person shall establish the identity of the authorized 
purchasing agent or agents and have on file that person's signature, 
electronic password, or other identification. Once the authorized 
purchasing agent has been established, the agent list may be updated 
annually rather than on each order. The regulated person must ensure 
that shipments are not made unless the order is placed by an authorized 
agent of record.

[[Page 205]]

    (f) With respect to electronic orders, the identity of the purchaser 
shall consist of a computer password, identification number or some 
other means of identification consistent with electronic orders and with 
Sec. 1310.07(e).

[54 FR 31665, Aug. 1, 1989, as amended at 60 FR 32461, June 22, 1995]



Sec. 1310.08  Excluded transactions.

    Pursuant to 21 U.S.C. 802(39)(A)(iii), regulation of the following 
transactions has been determined to be unnecessary for the enforcement 
of the Chemical Diversion and Trafficking Act and, therefore, they have 
been excluded from the definitions of regulated transactions contained 
in 21 CFR 1310.01(f) and 1313.02(d):
    (a) Domestic and import transactions of hydrochloric and sulfuric 
acids.
    (b) Exports, transshipments, and international transactions of 
hydrochloric and sulfuric acids, except for exports, transshipments and 
international transactions to the following countries:
    (1) Argentina
    (2) Bolivia
    (3) Brazil
    (4) Chile
    (5) Colombia
    (6) Ecuador
    (7) French Guiana
    (8) Guyana
    (9) Panama
    (10) Paraguay
    (11) Peru
    (12) Surinam
    (13) Uruguay
    (14) Venezuela
    (c) Domestic transactions of Methyl Isobutyl Ketone (MIBK).
    (d) Import transactions of Methyl Isobutyl Ketone (MIBK) destined 
for the United States.
    (e) Export transactions, international transactions, and import 
transactions for transshipment or transfer of Methyl Isobutyl Ketone 
(MIBK) destined for Canada or any country outside of the Western 
Hemisphere.

[57 FR 43615, Sept. 22, 1992, as amended at 60 FR 19510, Apr. 19, 1995; 
60 FR 32461, June 22, 1995]



Sec. 1310.09  Temporary exemption from registration.

    Each person required by section 3(b) of the Domestic Chemical 
Diversion Control Act of 1993 (Pub. L. 103-200, effective April 16, 
1994), to obtain a registration to manufacture, distribute, import, or 
export a list I chemical (other than those list I chemicals exempted 
under Sec. 1310.01(f)(1)(iv)), is temporarily exempted from the 
registration requirement. The exemption will remain in effect for each 
person until the person has made proper application for registration and 
the Administration has approved or denied such application, provided 
that the application is submitted on or before November 13, 1995. This 
exemption applies only to registration; all other chemical control 
requirements set forth in the Domestic Chemical Diversion Control Act of 
1993 and in parts 1310 and 1313 of this chapter remain in full force and 
effect.

[60 FR 53122, Oct. 12, 1995]



Sec. 1310.10  Removal of the exemption of drugs distributed under the Food, Drug and Cosmetic Act.

    (a) The Administrator may remove from exemption under 
1310.01(f)(1)(iv) any drug or group of drugs that the Administrator 
finds is being diverted to obtain a listed chemical for use in the 
illicit production of a controlled substance. In removing a drug or 
group of drugs from the exemption the Administrator shall consider:
    (1) the scope, duration, and significance of the diversion;
    (2) whether the drug or group of drugs is formulated in such a way 
that it cannot be easily used in the illicit production of a controlled 
substance; and
    (3) whether the listed chemical can be readily recovered from the 
drug or group of drugs.
    (b) Upon determining that a drug or group of drugs should be removed 
from the exemption under paragraph (a) of this section, the 
Administrator shall issue and publish in the Federal Register his 
proposal to remove the drug or group of drugs from the exemption, which 
shall include a reference to the legal authority under which the 
proposal is based. The Administrator shall permit any interested person 
to file

[[Page 206]]

written comments on or objections to the proposal. After considering any 
comments or objections filed, the Administrator shall publish in the 
Federal Register his final order.
    (c) The Administrator shall limit the removal of a drug or group of 
drugs from exemption under paragraph (a) of this section to the most 
identifiable type of the drug or group of drugs for which evidence of 
diversion exists unless there is evidence, based on the pattern of 
diversion and other relevant factors, that the diversion will not be 
limited to that particular drug or group of drugs.
    (d) Any manufacturer seeking reinstatement of a particular drug 
product that has been removed from an exemption under paragraph (a) of 
this section, may apply to the Administrator for reinstatement of the 
exemption for that particular drug product on the grounds that the 
particular drug product is manufactured and distributed in a manner that 
prevents diversion. In determining whether the exemption should be 
reinstated the Administrator shall consider:
    (1) the package sizes and manner of packaging of the drug product;
    (2) the manner of distribution and advertising of the drug product;
    (3) evidence of diversion of the drug product;
    (4) any actions taken by the manufacturer to prevent diversion of 
the drug product; and
    (5) such other factors as are relevant to and consistent with the 
public health and safety, including the factors described in paragraph 
(a) of this section as applied to the drug product.
    (e) Within a reasonable period of time after receipt of the 
application for reinstatement of the exemption, the Administrator shall 
notify the applicant of his acceptance or non-acceptance of his 
application, and if not accepted, the reason therefor. If the 
application is accepted for filing, the Administrator shall issue and 
publish in the Federal Register his order on the reinstatement of the 
exemption for the particular drug product, which shall include a 
reference to the legal authority under which the order is based. This 
order shall specify the date on which it shall take effect. The 
Administrator shall permit any interested person to file written 
comments on or objections to the order. If any such comments raise 
significant issues regarding any finding of fact or conclusion of law 
upon which the order is based, the Administrator shall immediately 
suspend the effectiveness of the order until he may reconsider the 
application in light of the comments and objections filed. Thereafter, 
the Administrator shall reinstate, revoke, or amend his original order 
as he determines appropriate.
    (f) Unless the Administrator has evidence that the drug product is 
being diverted, as determined by applying the factors set forth in 
paragraph (a) of this section, and the Administrator so notifies the 
applicant, transactions involving a specific drug product will not be 
considered regulated transactions during the following periods:
    (1) while a bonafide application for reinstatement of exemption 
under paragraph (d) of this section for the specific drug product is 
pending resolution, provided that the application for reinstatement is 
filed not later than 60 days after the publication of the final order 
removing the exemption; and
    (2) for a period of 60 days following the Administrator's denial of 
an application for reinstatement.
    (g) An order published by the Administrator in the Federal Register, 
pursuant to paragraph (e) of this section, to reinstate an exemption may 
be modified or revoked with respect to a particular drug product upon a 
finding that:
    (1) applying the factors set forth in paragraph (a) of this section 
to the particular drug product, the drug product is being diverted; or
    (2) there is a significant change in the data that led to the 
issuance of the final rule.

[60 FR 32461, June 22, 1995]



Sec. 1310.11  Reinstatement of exemption for drug products distributed under the Food, Drug and Cosmetic Act.

    (a) The Administrator has reinstated the exemption for the drug 
products listed in paragraph (e) of this section from application of 
sections 302, 303, 310, 1007, and 1008 of the Act (21 U.S.C. 822-823, 
830, and 957-958), to the extent

[[Page 207]]

described in paragraphs (b), (c), and (d) of this section.
    (b) No reinstated exemption granted pursuant to 1310.10 affects the 
criminal liability for illegal possession or distribution of listed 
chemicals contained in the exempt drug product.
    (c) Changes in exempt drug product compositions: Any change in the 
quantitative or qualitative composition, trade name or other designation 
of an exempt drug product listed in paragraph (d) requires a new 
application for reinstatement of the exemption.
    (d) The following drug products, in the form and quantity listed in 
the application submitted (indicated as the ``date'') are designated as 
reinstated exempt drug products for the purposes set forth in this 
section:

                                              Exempt Drug Products                                              
----------------------------------------------------------------------------------------------------------------
               Supplier                      Product name                 Form                     Date         
----------------------------------------------------------------------------------------------------------------
[Reserved]...........................  .......................  .......................  .......................
----------------------------------------------------------------------------------------------------------------


[60 FR 32462, June 22, 1995]



Sec. 1310.14  Exemption of drug products containing ephedrine and therapeutically significant quantities of another active medicinal ingredient.

    (a) Any manufacturer of a drug product containing ephedrine in 
combination with another active medicinal ingredient, the product 
formulation of which is not listed in the compendiums set forth in 
section 1310.01(f)(1)(iv)(A), may request that the Administrator exempt 
the product as one which contains ephedrine together with a 
therapeutically significant quantity of another active medicinal 
ingredient.
    (b) An application for an exemption under this section shall contain 
the following information:
    (1) The name and address of the applicant;
    (2) The exact trade name of the drug product for which exemption is 
sought;
    (3) The complete quantitative and qualitative composition of the 
drug product;
    (4) A brief statement of the facts which the applicant believes 
justify the granting of an exemption under this section; and
    (5) Certification by the applicant that the product may be lawfully 
marketed or distributed under the Food, Drug, and Cosmetic Act.
    (6) The identification of any information on the application which 
is considered by the applicant to be a trade secret or confidential and 
entitled to protection under U.S. laws restricting the public disclosure 
of such information by government employees.
    (c) The Administrator may require the applicant to submit such 
additional documents or written statements of fact relevant to the 
application which he deems necessary for determining if the application 
should be granted.
    (d) Within a reasonable period of time after the receipt of a 
completed application for an exemption under this section, the 
Administrator shall notify the applicant of acceptance or non-acceptance 
of the application. If the application is not accepted, an explanation 
will be provided. The Administrator is not required to accept an 
application if any of the information required in paragraph (b) of this 
section or requested pursuant to paragraph (c) of this section is 
lacking or not readily understood. The applicant may, however, amend the 
application to meet the requirements of paragraphs (b) and (c) of this 
section. If the application is accepted for filing, the Administrator 
shall issue and publish in the Federal Register an order on the 
application, which shall include a reference to the legal authority 
under which the order is based. This order shall specify the date on 
which it shall take effect. The Administrator shall permit any 
interested person to file written comments on or objections to the 
order. If any comments or objections raise significant issues regarding 
any findings of fact or law upon which the order is based, the 
Administrator shall immediately suspend the effectiveness of the order 
until he may reconsider the application in light of the comments and 
objections filed. Thereafter, the Administrator shall reinstate, revoke, 
or amend the original order as deemed appropriate.

[60 FR 32462, June 22, 1995]

[[Page 208]]



Sec. 1310.15  Exempt drug products containing ephedrine and therapeutically significant quantities of another active medicinal ingredient.

    (a) The drug products containing ephedrine and therapeutically 
significant quantities of another active medicinal ingredient listed in 
paragraph (e) of this section have been exempted by the Administrator 
from application of sections 302, 303, 310, 1007, and 1008 of the Act 
(21 U.S.C. 822-3, 830, and 957-8) to the extent described in paragraphs 
(b), (c), and (d) of this section.
    (b) No exemption granted pursuant to 1310.14 affects the criminal 
liability for illegal possession or distribution of listed chemicals 
contained in the exempt drug product.
    (c) Changes in drug product compositions: Any change in the 
quantitative or qualitative composition of an exempt drug product listed 
in paragraph (d) requires a new application for exemption.
    (d) In addition to the drug products listed in the compendium set 
forth in Sec. 1310.01(f)(1)(iv)(A), the following drug products, in the 
form and quantity listed in the application submitted (indicated as the 
``date'') are designated as exempt drug products for the purposes set 
forth in this section:

Exempt Drug Products Containing Ephedrine and Therapeutically Significant Quantities of Another Active Medicinal
                                                   Ingredient                                                   
----------------------------------------------------------------------------------------------------------------
               Supplier                      Product name                 Form                     Date         
----------------------------------------------------------------------------------------------------------------
[Reserved]...........................  .......................  .......................  .......................
----------------------------------------------------------------------------------------------------------------


[60 FR 32463, June 22, 1995]



PART 1311--REGISTRATION OF IMPORTERS AND EXPORTERS OF CONTROLLED SUBSTANCES--Table of Contents




                           General Information

Sec.
1311.01  Scope of Part 1311.
1311.02  Definitions.
1311.03  Information; special instructions.

                Fees for Registration and Reregistration

1311.11  Fee amounts.
1311.12  Time and method of payment; refund.

                      Requirements of Registration

1311.21  Persons required to register.
1311.22  Separate registration for independent activities.
1311.23  Separate registrations for separate locations.
1311.24  Exemption of certain military personnel.
1311.25  Exemption of law enforcement officials.
1311.26  Exemption for ocean vessels, commercial aircraft, and certain 
          other entities.
1311.27  Exemptions for personal medical use.

                      Applications for Registration

1311.31  Time for application for registration; expiration date.
1311.32  Application forms; contents; signature.
1311.33  Filing of application; acceptance for filing; additional 
          information; amendments to and withdrawals of applications.

  Action on Applications for Registration: Revocation or Suspension of 
                              Registration

1311.41  Administrative review generally.
1311.42  Application for importation of Schedule I and II substances.
1311.43  Certificate of registration; denial of registration.
1311.44  Suspension or revocation of registration.
1311.45  Suspension of registration pending final order.
1311.46  Extension of registration pending final order.
1311.47  Order to show cause.

                                Hearings

1311.51  Hearings generally.
1311.52  Hearings on application for importation of Schedule I and II 
          substances.
1311.53  Burden of proof.

         Modification, Transfer, and Termination of Registration

1311.61  Modification in registration.
1311.62  Termination of registration.
1311.63  Transfer of registration.
1311.64  Termination of provisional registration.

    Authority: 21 U.S.C. 952, 956, 957, 958, unless otherwise noted.

    Source: 36 FR 7812, Apr. 24, 1971, unless otherwise noted. 
Redesignated at 38 FR 26609, Sept. 24, 1973.

                           General Information



Sec. 1311.01   Scope of Part 1311.

    Procedures governing the registration of importers and exporters of 
controlled substances pursuant to sections

[[Page 209]]

1007 and 1008 of the Act (21 U.S.C. 957-958) are set forth generally by 
those sections and specifically by the sections of this part.



Sec. 1311.02   Definitions.

    As used in this part, the following terms shall have the meanings 
specified:
    (a) The term Act means the Controlled Substances Act (84 Stat. 1242; 
21 U.S.C. 801) and/or the Controlled Substances Import and Export Act 
(84 Stat. 1285; 21 U.S.C. 951).
    (b) The term customs territory of the United States means the 
several States, the District of Columbia, and Puerto Rico.
    (c) The term export means, with respect to any article, any taking 
out or removal of such article from the jurisdiction of the United 
States (whether or not such taking out or removal constitutes an 
exportation within the meaning of the customs and related laws of the 
United States).
    (d) The term exporter includes every person who exports, or who acts 
as an export broker for exportation of, controlled substances listed in 
any schedule.
    (e) The term hearing means any hearing held pursuant to this part 
for the granting, denial, revocation or suspension of a registration 
pursuant to section 1008 of the Act (21 U.S.C. 958).
    (f) The term import means, with respect to any article, any bringing 
in or introduction of such article into either the jurisdiction of the 
United States or the customs territory of the United States, and from 
the jurisdiction of the United States into the customs territory of the 
United States (whether or not such bringing in or introduction 
constitutes an importation within the meaning of the tariff laws of the 
United States).
    (g) The term importer includes every person who imports, or who acts 
as an import broker for importation of, controlled substances listed in 
any schedule.
    (h) The term jurisdiction of the United States means the customs 
territory of the United States, the Virgin Islands, the Canal Zone, 
Guam, American Samoa, and the Trust Territories of the Pacific Islands.
    (i) The terms register and registration refer only to registration 
required and permitted by section 1007 of the Act (21 U.S.C. 957).
    (j) The term registrant means any person who is registered pursuant 
to either section 303 or section 1008 of the Act (21 U.S.C. 823 or 958).
    (k) Any term not defined in this section shall have the definition 
set forth in section 1001 of the Act (21 U.S.C. 951) or Sec. 1301.02 of 
this chapter.

[36 FR 7812, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 52 FR 17288, May 7, 1987]



Sec. 1311.03   Information; special instructions.

    Information regarding procedures under these rules and instructions 
supplementing these rules will be furnished upon request by writing to 
the Registration Unit, Drug Enforcement Administration, Department of 
Justice, Post Office Box 28083, Central Station, Washington, DC 20005.

[36 FR 7815, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 51 FR 5319, Feb. 13, 1986]

                Fees for Registration and Reregistration



Sec. 1311.11  Fee amounts.

    (a) For each registration or reregistration to import controlled 
substances, the registrant shall pay an application fee of $438 for an 
annual registration.
    (b) For each registration or reregistration to export controlled 
substances, the registrant shall pay an application fee of $438 for an 
annual registration.

[58 FR 15274, Mar. 22, 1993]



Sec. 1311.12   Time and method of payment; refund.

    The time and method of payment of application fees and refunds of 
application fees shall be as provided in Sec. 1301.12 of this chapter.

[53 FR 4963, Feb. 19, 1988]

[[Page 210]]

                      Requirements of Registration



Sec. 1311.21   Persons required to register.

    Every person who imports any controlled substance, or who exports 
any controlled substance, or who proposes to engage in such importation 
or exportation, shall obtain annually a registration unless exempted by 
law or pursuant to Secs. 1311.24 through 1311.27. Only persons actually 
engaged in such activities are required to obtain registration; related 
or affiliated persons who are not engaged in such activities are not 
required to be registered. (For example, a stockholder or parent 
corporation importing controlled substances is not required to obtain a 
registration.)

[52 FR 17288, May 7, 1987]



Sec. 1311.22   Separate registration for independent activities.

    (a) Every person who engages in more than one group of independent 
activities, as described in Sec. 1301.22 of this chapter shall obtain a 
separate registration for each group of activities as required by that 
section.
    (b) A single registration to engage in any group of independent 
activities may include one or more controlled substancds listed in the 
schedules authorized in that group of independent activities. A person 
registered to conduct research with controlled substances listed in 
schedule I may conduct research with any substance listed in schedule I 
for which he has filed and had approved a research protocol.

[36 FR 7812, Apr. 24, 1971, as amended at 36 FR 18734, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1311.23   Separate registrations for separate locations.

    (a) A separate registration is required for each principal place of 
business at one general physical location where controlled substances 
are imported or exported by a person.
    (b) The following locations shall be deemed not to be places where 
controlled substances are imported or exported:
    (1) A warehouse where controlled substances are stored on behalf of 
a registered person, unless such substances are distributed directly 
from such warehouse to persons other than the registered person or 
persons not required to register by virtue of subsection 1007(b)(1)(B) 
(21 U.S.C. 957(b)(1)(B) ); and
    (2) An office used by agents of a registrant where sales of 
controlled substances are solicited, made, or supervised but which 
neither contains such substances (other than substances for display 
purposes) nor serves as a distribution point for filling sales orders.



Sec. 1311.24   Exemption of certain military personnel.

    The requirement of registration is waived for any official or agency 
of the U.S. Army, Navy, Marine Corps, Air Force, Coast Guard, or Public 
Health Service who or which is authorized to import or export controlled 
substances in the course of his official duties.

[36 FR 7812, Apr. 24, 1971, as amended at 36 FR 18734, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1311.25   Exemption of law enforcement officials.

    The requirement of registration is waived for any officer or 
employee of the Administration, any officer of the U.S. Customs Service, 
any officer or employee of the U.S. Food and Drug Administration, and 
any other Federal officer who is lawfully engaged in the enforcement of 
any Federal law relating to controlled substances, drugs or customs, and 
is duly authorized to possess, import or export controlled substances in 
the course of his official duties.



Sec. 1311.26   Exemption for ocean vessels, commercial aircraft, and certain other entities.

    Owners or operators of vessels, aircraft, or other entities 
described in Sec. 1301.28 of this chapter or in Article 32 of the Single 
Convention on Narcotic Drugs, 1961, or in Article 14 of the Convention 
on Psychotropic Substances, 1971, shall not be deemed to import or 
export any controlled substances purchased and stored in accordance with 
that section or applicable article.

[52 FR 17288, May 7, 1987]

[[Page 211]]



Sec. 1311.27   Exemptions for personal medical use.

    Any individual who has in his possession a controlled substance 
listed in schedules II, III, IV, or V, which he has lawfully obtained 
for his personal medical use, or for administration to an animal 
accompanying him, may enter or depart the United States with such 
substance notwithstanding sections 1002-1005 of the Act (21 U.S.C. 952-
955), providing the following conditions are met:
    (a) The controlled substance is in the original container in which 
it was dispensed to the individual; and
    (b) The individual makes a declaration to an appropriate official of 
the U.S. Customs Service stating:
    (1) That the controlled substance is possessed for his personal use, 
or for an animal accompanying him; and
    (2) The trade or chemical name and the symbol designating the 
schedule of the controlled substance if it appears on the container 
label, or, if such name does not appear on the label, the name and 
address of the pharmacy or practitioner who dispensed the substance and 
the prescription number, if any.

[36 FR 7812, Apr. 24, 1971, as amended at 36 FR 13387, July 21, 1971; 36 
FR 18734, Sept. 21, 1971. Redesignated at 37 FR 15922, Aug. 8, 1972, and 
at 38 FR 26609, Sept. 24, 1973]

                      Applications for Registration



Sec. 1311.31   Time for application for registration; expiration date.

    (a) Any person who is required to be registered and who is not so 
registered may apply for registration at any time. No person required to 
be registered shall engage in any activity for which registration is 
required until the application for registration is granted and a 
Certificate of Reghstration is issued by the Administrator of such 
person.
    (b) Any person who is registered may apply to be reregistered not 
more than 60 days before the expiration date of his registration.
    (c) At the time any person is first registered, he will be assigned 
to one of 12 groups in the same manner and with the same effect as 
provided in Sec. 1301.31 of this chapter.

[36 FR 7812, Apr. 24, 1971, as amended at 36 FR 18734, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1311.32   Application forms; contents; signature.

    (a) Any person who is required to be registered to import or export 
controlled substances, and who is not so registered, shall apply on DEA 
Form 225.
    (b) Any person who is registered to import or export controlled 
substances, shall apply for reregistration on DEA Form 225a.
    (c) DEA Form 225 may be obtained at any regional office of the 
Administration or by writing to the Registration Unit, Drug Enforcement 
Administration, Department of Justice, Post Office Box 28083, Central 
Station, Washington, DC 20005. DEA Form 225a will be mailed to each 
registered importer and exporter approximately 60 days before the 
expiration date of his registration; if any registered person does not 
receive such forms within 45 days before the expiration date of his 
registration, he must promptly give notice of such fact and request such 
forms by writing to the Registration Branch of the Administration at the 
foregoing address.
    (d) Each application for registration to import or export controlled 
substances shall include the Administration Controlled Substances Code 
Number, as set forth in part 1308 of this chapter, for each controlled 
substance whose importation or exportation is to be authorized by such 
registration.
    (e) Registration as an importer or exporter shall not entitle a 
registrant to import or export any controlled substance not specified in 
such registration.
    (f) Each application shall include all information called for in the 
form, unless the item is not applicable, in which case this fact shall 
be indicated.
    (g) Each application, attachment, or other document filed as part of 
an application, shall be signed by the applicant, if an individual; by a 
partner of the applicant, if a partnership; or by an officer of the 
applicant, if a corporation, association, trust or other entity.

[[Page 212]]

An applicant may authorize one or more individuals, who would not 
otherwise be authorized to do so, to filing applications for the 
applicant by filing with the Registration Unit of the Administration a 
power of attorney for each such individual. The power of attorney shall 
be signed by a person who is authorized to sign applications under this 
paragraph and shall contain the signature of the individual being 
authorized to sign applications. The power of attorney shall be valid 
until revoked by the applicant.

[36 FR 7812, Apr. 24, 1971, as amended at 36 FR 18734, Sept. 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 51 FR 5319 
and 5320, Feb. 13, 1986; 52 FR 17288, May 7, 1987; 53 FR 4963, Feb. 19, 
1988]



Sec. 1311.33   Filing of application; acceptance for filing; additional information; amendments to and withdrawals of applications.

    Applications for registration to import or export controlled 
substances shall be filed, accepted for filing, supplemented, amended 
and withdrawn as provided in Secs. 1301.34-1301.37 of this chapter.

  Action on Applications for Registration: Revocation or Suspension of 
                              Registration



Sec. 1311.41   Administrative review generally.

    The Administrator may inspect, or cause to be inspected, the 
establishment of an applicant or registrant, pursuant to subpart A of 
part 1316 of this chapter. The Administrator shall review the 
application for registration and other information gathered by the 
Administrator regarding an applicant in order to determine whether the 
applicable standards of section 1008 of the Act (21 U.S.C. 958) have 
been met by the applicant.



Sec. 1311.42   Application for importation of Schedule I and II substances.

    (a) In the case of an application for registration or reregistration 
to import a controlled substance lhsted in Schedule I or II, under the 
authority of section 1002(a)(2)(B) of the Act (21 U.S.C. 952(a)(2)(B)), 
the Administrator shall, upon the filing of such application, publish in 
the Federal Register a notice naming the applicant and stating that such 
applicant has applied to be registered as an importer of a Schedule I or 
II controlled substance, which substance shall be identified. A copy of 
said notice shall be mailed simultaneously to each person registered as 
a bulk manufacturer of that controlled substance and to any other 
applicant therefor. Any such person may, within 30 days from the date of 
publication of the notice in the Federal Register, file written comments 
on or objections to the issuance of the proposed registration, and may, 
at the same time, file a written request for a hearing on the 
application pursuant to Sec. 1301.54. If a hearing is requested, the 
Administrator shall hold a hearing on the application in accordance with 
Sec. 1301.54. Notice of the hearing shall be published in the Federal 
Register, and shall be mailed simultaneously to the applicant and to all 
persons to whom notice of the application was mailed. Any such person 
may participate in the hearing by filing a notice of appearance in 
accordance with Sec. 1301.54 of this chapter. Notice of the hearing 
shall contain a summary of all comments and objections filed regarding 
the application and shall state the time and place for the hearing, 
which shall not be less than 30 days after the date of publication of 
such notice in the Federal Register. A hearing pursuant to this section 
may be consolidated with a hearing held pursuant to Secs. 1311.43 or 
1311.44 of this part.
    (b) The Administrator shall register an applicant to import a 
controlled substance listed in Schedule I or II if he determines that 
such registration is consistent with the public interest and with U.S. 
obligations under international treaties, conventions, or protocols in 
effect on May 1, 1971. In determining the public interest, the following 
factors shall be considered:
    (1) Maintenance of effective controls against diversion of 
particular controlled substances and any controlled substance in 
Schedule I or II compounded therefrom into other than legitimate 
medical, scientific research, or industrial channels, by limiting the 
importation and bulk manufacture of such controlled substances to a 
number of establishments which can produce

[[Page 213]]

an adequate and uninterrupted supply of these substances under 
adequately competitive conditions for legitimate medical, scientific, 
research, and industrial purposes;
    (2) Compliance with applicable State and local law;
    (3) Promotion of technical advances in the art of manufacturing 
these substances and the development of new substances;
    (4) Prior conviction record of applicant under Federal and State 
laws relating to the manufacture, distribution, or dispensing of such 
substances;
    (5) Past experience in the manufacture of controlled substances, and 
the existence in the establishment of effective control against 
diversion;
    (6) That the applicant will be permitted to import only:
    (i) Such amounts of crude opium, poppy straw, concentrate of poppy 
straw, and coca leaves as the Administrator finds to be necessary to 
provide for medical, scientific, or other legitimate purposes; or
    (ii) Such amounts of any controlled substances listed in Schedule I 
or II as the Administrator shall find to be necessary to provide for the 
medical, scientific, or other legitimate needs of the United States 
during an emergency in which domestic supplies of such substances are 
found by the Administrator to be inadequate; or
    (iii) Such amounts of any controlled substance listed in Schedule I 
or II as the Administrator shall find to be necessary to provide for the 
medical, scientific, or other legitimate needs of the United States in 
any case in which the Administrator finds that competition among 
domestic manufacturers of the controlled substance is inadequate and 
will not be rendered adequate by the registration of additional 
manufacturers under section 303 of the Act (21 U.S.C. 823); or
    (iv) Such limited quantities of any controlled substance listed in 
Schedule I or II as the Administrator shall find to be necessary for 
scientific, analytical or research uses; and
    (7) Such other factors as may be relevant to and consistent with the 
public health and safety.
    (c) In determining whether the applicant can and will maintain 
effective controls against diversion within the meaning of paragraph 
(b), the Administrator shall consider among other factors:
    (1) Compliance with the security requirements set forth in 
Secs. 1301.71-1301.76 of this chapter; and
    (2) Employment of security procedures to guard against in-transit 
losses within and without of the jurisdiction of the United States.
    (d) In determining whether competition among the domestic 
manufacturers of a controlled substance is adequate within the meaning 
of paragraphs (b)(1) and (6)(iii) of this section, as well as section 
1002(a)(2)(B) of the Act (21 U.S.C. 952(a)(2)(B)), the Administrator 
shall consider:
    (1) The extent of price rigidity in the light of changes in (i) raw 
materials and other costs and (ii) conditions of supply and demand;
    (2) The extent of service and quality competition among the domestic 
manufacturers for shares of the domestic market including (i) shifts in 
market shares and (ii) shifts in individual customers among domestic 
manufacturers;
    (3) The existence of substantial differentials between (i) domestic 
prices and (ii) the higher of prices generally prevailing in foreign 
markets or the prices at which the applicant for registration to import 
is committed to undertake to provide such products in the domestic 
market in conformity with the Act. In determining the existence of 
substantial differentials hereunder, appropriate consideration should be 
given to any additional costs imposed on domestic manufacturers by the 
requirements of the Act and such other cost-related and other factors as 
the Administrator may deem relevant. In no event shall an importer's 
offering prices in the United States be considered if they are lower 
than those prevailing in the foreign market or markets from which the 
importer is obtaining his supply;
    (4) The existence of competitive restraints imposed upon domestic 
manufacturers by governmental regulations; and
    (5) Such other factors as may be relevant to the determinations 
required under this paragraph.

[[Page 214]]

    (e) In considering the scope of the domestic market, consideration 
shall be given to substitute products which are reasonably 
interchangeable in terms of price, quality and use.
    (f) The fact that the number of existing manufacturers is small 
shall not demonstrate, in and of itself, that adequate competition among 
them does not exist.

[36 FR 7812, Apr. 24, 1971, as amended at 36 FR 18734, Sept. 21, 1971; 
37 FR 15922, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 52 FR 17288, May 7, 1987]



Sec. 1311.43   Certificate of registration; denial of registration.

    (a) The Administrator shall issue a Certificate of Registration (DEA 
Form 223) to an applicant if the issuance of registration or 
reregistration is required under the applicable provisions of section 
1008 of the Act (21 U.S.C. 958). In the event the issuance of 
registration or reregistration is not required, the Administrator shall 
deny the application. Before denying any application, the Administrator 
shall issue an order to show cause pursuant to Sec. 1311.47 and, if 
requested by the applicant, shall hold a hearing on the application 
pursuant to Sec. 1311.51.
    (b) The Certificate of Registration (DEA Form 223) shall contain the 
information, and shall be maintained in the manner prescribed in 
Sec. 1301.44(b) of this chapter.

[36 FR 7812, Apr. 24, 1971, as amended at 37 FR 15922, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 53 FR 4963, 
Feb. 19, 1988]



Sec. 1311.44   Surpension or revocation of registration.

    (a) The Administrator may suspend any registration pursuant to 
section 1008(d) of the Act (21 U.S.C. 958(d)) for any period of time.
    (b) The Administrator may revoje or suspend a registration issued 
under section 1008(d) of the Act (21 U.S.C. 958(d)) if he determines 
that such registration is inconsistent with the public interest as 
defined in that section or with the United States obligations under 
international treaties, conventions, or protocols in effect on October 
12, 1984.
    (c) The Administrator may revoke or suspend a registration issued 
under section 1008(c) of the Act (21 U.S.C. 958(c)) if he determines 
that such registration is inconsistent with the public interest as 
defined in that section or with the United States obligations under 
international treaties, conventions, or protocols in effect on October 
12, 1984.
    (d) The Administrator may limit the revocation or suspension of a 
registration to the particular controlled substance, or substances, with 
respect to which grounds for revocation or suspension exist.
    (e) Before revoking or suspending any registration, the 
Administrator shall issue an order to show cause pursuant to 
Sec. 1311.47, and if requested by the registrant, shall hold a hearing 
pursuant to Sec. 1311.51. Notwithstanding the requirements of this 
section, however, the Administrator may suspend any registration pending 
a final order pursuant to Sec. 1311.45.
    (f) Upon service of the order of the Administrator suspending or 
revoking registration, the registrant shall immediately deliver his 
Certificate of Registration and any order forms and import or export 
permits in his possession to the nearest office of the Administrator. 
The suspension or revocation of a registration shall suspend or revoke 
any import or export permits issued pursuant to part 1312 of this 
chapter. Also, upon service of the order of the Administrator revoking 
or suspending registration, the registrant shall, as instructed by the 
Administrator:
    (1) Deliver all controlled substances in his possession to the 
nearest office of the Administration pursuant to section 1008(d)(6) of 
the Act (21 U.S.C. 958(d)(6)); or
    (2) Deliver all controlled substances in his possession to 
authorized agents of the Administration who will either remove the 
substances or place them under seal as described in section as described 
in section 1008(d)(6) of the Act (21 U.S.C. 1008(d)(6)).
    (g) In the event that revocation or suspension is limited to a 
particular controlled substance or substances, the registrant shall be 
given a new Certificate of Registration for all substances

[[Page 215]]

not affected by such revocation or suspension. The registrant shall 
deliver the old Certificate of Registration and, if appropriate, any 
order forms and import or export permits in his possession to the 
nearest office of the Administrator. Also, upon service of the order of 
the Administrator revoking or suspending registration, the registrant 
shall, as instructed by the Administrator:
    (1) Deliver to the nearest office of the Administration, pursuant to 
section 1008(d)(6) of the Act (21 U.S.C. 958(d)(6)), all of the 
particular controlled substance or substances affected by the revocation 
or suspension which are in his possession; or
    (2) Deliver all of such substances to authorized agents of the 
Administration who will either remove the substances or place them under 
seal as described in section 1008(d)(6) of the Act (21 U.S.C. 
958(d)(6)).

[36 FR 7812, Apr. 24, 1971, as amended at 36 FR 13387, July 21, 1971; 37 
FR 15922, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, 1973, and 
amended at 52 FR 17288, May 7, 1987]



Sec. 1311.45   Suspension of registration pending final order.

    (a) The Administrator may suspend any registration simultaneously 
with or at any time subsequent to the service upon the registrant of an 
order to show cause why such registration should not be revoked or 
suspended, in any case where he finds that there is an imminent danger 
to the public health or safety. If the Administrator so suspends, he 
shall serve with the order to show cause pursuant to Sec. 1311.47 an 
order of immediate suspension which shall contain a statement of his 
findings regarding the danger to public health or safety.
    (b) Upon receipt of the order of immediate suspension, the 
registrant shall promptly return his Certificate of Registration and any 
other forms and import or export permits in his possession to the 
nearest office of the Administrator. The suspension of any registration 
under this section shall suspend any import and export permits issued 
pursuant to part 1312 of this chapter.
    (c) Any suspension shall continue in effect until the conclusion of 
all proceedings upon revocation or suspension, including any judicial 
review thereof, unless sooner withdrawn by the Administrator or 
dissolved by a court of competent jurisdiction. Any registrant whose 
registration is suspended under this section may request a hearing on 
the revocation or suspension of his registration at a time earlier than 
specified in the order to show cause pursuant to Sec. 1311.47 which 
request shall be granted by the Administrator, who shall fix a date for 
such hearing as early as reasonably possible.



Sec. 1311.46   Extension of registration pending final order.

    An applicant for reregistration (who is doing business under a 
registration previously granted and not revoked or suspended) may have 
the existing registration extended and continue in effect until the date 
on which the Administrator issues his order on the application for 
reregistration as provided in Sec. 1301.47 of this chapter.



Sec. 1311.47   Order to show cause.

    (a) If, upon examination of the application for registration from 
any applicant and other information gathered by the Administration 
regarding the applicant, the Administrator is unable to make the 
determinations required by the applicable provisions of sections 303 and 
1008(d) of the Act (21 U.S.C. 823 and 958(d)) to register the applicant, 
the Administrator shall serve upon the applicant an order to show cause 
why the application for registration should not be denied, as provided 
in Sec. 1301.48 of this chapter.
    (b) If, upon information gathered by the Administration regarding 
any registrant, the Administrator determines that the registration of 
such registrant is subject to suspension or revocation pursuant to 
section 1008(d) of the Act (21 U.S.C. 958(d)), the Administrator shall 
serve upon the registrant an order to show cause why the registration 
should not be revoked or suspended, as provided in Sec. 1301.48 of this 
chapter.

[52 FR 17289, May 7, 1987]

[[Page 216]]

                                Hearings



Sec. 1311.51   Hearings generally.

    (a) In any case where the Administrator shall hold a hearing on any 
registration or application thereof, the procedures for such hearing 
shall be governed generally by the adjudication procedures set forth in 
the Administrative Procedure Act (5 U.S.C. 551-559) and specifically by 
section 1008 of the Act (21 U.S.C. 958), by Secs. 1311.52-1311.53, by 
the procedures for hearings pursuant to sections 303 and 304 of the Act 
(21 U.S.C. 823-824) set forth in Secs. 1301.51-1301.57 of this chapter, 
and by the procedures for administrative hearings under the Act set 
forth in Secs. 1316.41-1316.67 of this chapter.
    (b) Any hearing under this part shall be independent of, and not in 
lieu of, criminal prosecutions or other proceedings under the Act or any 
other law of the United States.

[36 FR 7812, Apr. 24, 1971, as amended at 36 FR 13387, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1311.52   Hearings on application for importation of Schedule I and II substances.

    A hearing on an application for registration to import a basic class 
of any controlled substance listed in Schedule I or II required by 
Sec. 1311.42 shall be held under the same procedures prescribed in 
Secs. 1301.51-1301.57 of this chapter for a hearing on an application 
for registration to manufacture in bulk a basic class of any controlled 
substance.

[36 FR 7812, Apr. 24, 1971, as amended at 36 FR 13387, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1311.53   Burden of proof.

    (a) At any hearing on the granting or denial of an application to be 
registered to import or export any controlled substance listed in 
Schedule I or II, the applicant shall have the burden of proving that 
the requirements for such registration pursuant to sections 1008 (a) and 
(d) of the Act (21 U.S.C. 958 (a) and (d)) are satisfied. Any other 
person participating in the hearing pursuant to Sec. 1311.42 shall have 
the burden of proving any propositions of fact or law asserted by him in 
the hearings.
    (b) At any other hearing for the denial of an application for 
registration, the Administration shall have the burden of proving that 
the requirements for such registration pursuant to sections 1008 (c) and 
(d) of the Act (21 U.S.C. 958 (c) and (d)) are not satisfied.
    (c) At any hearing for the revocation or suspension of a 
registration, the Administration shall have the burden of proving that 
the requirements for such revocation or suspension pursuant to section 
1008(d) of the Act (21 U.S.C. 958(d)) are satisfied.

[52 FR 17289, May 7, 1987]

         Modification, Transfer, and Termination of Registration



Sec. 1311.61   Modification in registration.

    Any registrant may apply to modify his registration to authorize the 
handling of additional controlled substances or to change his name or 
address, by submitting a letter of request to the Registration Unit, 
Drug Enforcement Administration, Department of Justice, Post Office Box 
28083, Central Station, Washington, DC 20005. The letter shall contain 
the registrant's name, address, and registratinn number as printed on 
the Certificate of Registration, and the substances (including the 
schedule and the Administration Controlled Substances Code Number, as 
set forth in part 1308 of this chapter, for those substances) to be 
added to his registration or the new name and address, and shall be 
signed in accordance with Sec. 1311.32(f). No fee is required for the 
modification. The request for modification shall be handled in the same 
manner as an application for registration. If the modification in 
registration is approved, the Administrator shall issue a new 
Certificate of Registration (DEA Form 223) to the registrant, who shall 
maintain it with the old Certificate of Registration until expiration.

[52 FR 17289, May 7, 1987]



Sec. 1311.62   Termination of registration.

    The registration of any person shall terminate if and when such 
person dies, ceases legal existence or discontinues business or 
professional practice. Any registrant who ceases legal existence

[[Page 217]]

or discontinues business or professional practice shall notify the 
Administrator promptly of such fact.

[37 FR 15923, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1311.63   Transfer of registration.

    No registration or any authority conferred thereby shall be assigned 
or otherwise transferred except upon such conditions as the 
Administrator may specifically designate and then only pursuant to his 
written consent.

[36 FR 18735, Sept. 21, 1971. Redesignated at 38 FR 26609, Sept. 24, 
1973]



PART 1312--IMPORTATION AND EXPORTATION OF CONTROLLED SUBSTANCES--Table of Contents




Sec.
1312.01  Scope of part 1312.
1312.02  Definitions.

                  Importation of Controlled Substances

1312.11  Requirement of authorization to import.
1312.12  Application for import permit.
1312.13  Issuance of import permit.
1312.14  Distribution of copies of import permit.
1312.15  Shipments in greater or less amount than authorized.
1312.16  Cancellation of permit; expiration date.
1312.17  Special report from importers.
1312.18  Contents of import declaration.
1312.19  Distribution of import declaration.

                  Exportation of Controlled Substances

1312.21  Requirement of authorization to export.
1312.22  Application for export permit.
1312.23  Issuance of export permit.
1312.24  Distribution of copies of export permit.
1312.25  Expiration date.
1312.26  Records required of exporter.
1312.27  Contents of special controlled substances invoice.
1312.28  Distribution of special controlled substances invoice.
1312.29  Domestic release prohibited.
1312.30  Schedule III, IV, and V non-narcotic controlled substances 
          requiring an import and export permit.

     Transshipment and In-Transit Shipment of Controlled Substances

1312.31  Schedule I: Application for prior written approval.
1312.32  Schedules II, III, IV: Advance Notice.

                                Hearings

1312.41  Hearings generally.
1312.42  Purpose of hearing.
1312.43  Waiver or modification of rules.
1312.44  Request for hearing or appearance; waiver.
1312.45  Burden of proof.
1312.46  Time and place of hearing.
1312.47  Final order.

    Authority: 21 U.S.C. 952, 953, 954, 957, 958.

    Source: 36 FR 7815, Apr. 24, 1971, unless otherwise noted. 
Redesignated at 38 FR 26609, Sept. 24, 1973.



Sec. 1312.01   Scope of part 1312.

    Procedures governing the importation, exportation, transshipment and 
intransit shipment of controlled substances pursuant to section 1002, 
1003, and 1004 of the Act (21 U.S.C. 952, 953, and 954) are governed 
generally by those sections and specifically by the sections of this 
part.



Sec. 1312.02   Definitions.

    As used in this part, the following terms shall have the meanings 
specified:
    (a) The term Act means the Controlled Substances Import and Export 
Act (84 Stat. 1285; 21 U.S.C. 951).
    (b) Any term not defined in this section shall have the definition 
set forth in sections 1001 and 102 of the Act (21 U.S.C. 951 and 802) 
and Sec. 1311.02 of this chapter.

[36 FR 7815, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 51 FR 5320, Feb. 13, 1986]

                  Importation of Controlled Substances



Sec. 1312.11   Requirement of authorization to import.

    (a) No person shall import or cause to be imported any controlled 
substance listed in Schedule I or II or any narcotic controlled 
substance listed in Schedule III, IV or V or any non-narcotic controlled 
substance in Schedule III which the Administrator has specifically 
designated by regulation in

[[Page 218]]

Sec. 1312.30 of this part or any non-narcotic controlled substance in 
Schedule IV or V which is also listed in Schedule I or II of the 
Convention on Psychotropic Substances unless and until such person is 
properly registered under the Act (or exempt from registration) and the 
Administrator has issued him a permit to do so pursuant to Sec. 1312.13 
of this part.
    (b) No person shall import or cause to be imported any non-narcotic 
controlled substance listed in Schedule III, IV or V, excluding those 
described in paragraph (a) of this section, unless and until such person 
is properly registered under the Act (or exempt from registration) and 
has filed an import declaration to do so with the Administrator, 
pursuant to Sec. 1312.18 of this part.
    (c) When an import permit or declaration is required, a separate 
permit or declaration must be obtained for each consignment of 
controlled substances to be imported.

[36 FR 7815, Apr. 24, 1971, as amended at 37 FR 15923, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 52 FR 17289, 
May 7, 1987]



Sec. 1312.12   Application for import permit.

    (a) An application for a permit to import controlled substances 
shall be made on DEA Form 357. DEA Form 357 may be obtained from, and 
shall be filed with, the Drug Enforcement Administration, Drug Control 
Section, 1405 I Street, NW., Washington, DC 20537. Each application 
shall show the date of execution; the registration number of the 
importer; a detailed description of each controlled substance to be 
imported including the drug name, dosage form, National Drug Code (NDC) 
number, the Administration Controlled Substance Code Number as set forth 
in part 1308 of this chapter, the number and size of packages or 
containers, the name and quantity of the controlled substance contained 
in any finished dosage units, and the net quantity of any controlled 
substance (expressed in anhydrous acid, base or alkaloid) given in 
kilograms or parts thereof. The application shall also include the 
following:
    (1) The name, address, and business of the consignor, if known at 
the time application is submitted, but if unknown at that time, the fact 
should be indicated and the name and address afterwards furnished to the 
Administrator as soon as ascertained by the importer;
    (2) The foreign port of exportation (i.e., the place where the 
article will begin its journey of exportation to the United States);
    (3) The port of entry into the United States;
    (4) The latest date said shipment will leave said foreign port;
    (5) The stock on hand of the controlled substance desired to be 
imported;
    (6) The name of the importing carrier or vessel (if known, or if 
unknown it should be stated whether shipment will be made by express, 
freight, or otherwise, imports of controlled substances in Schedules I 
or II and narcotic drugs in Schedules III, IV, or V by mail being 
prohibited);
    (7) The total tentative allotment to the importer of such controlled 
substance for the current calendar year;
    (8) The total number of kilograms of said allotment for which 
permits have previously been issued and the total quantity of controlled 
substance actually imported during the current year to date.
    (b) If desired, alternative foreign ports of exportation within the 
same country may be indicated upon the application (e.g., (1) Calcutta, 
(2) Bombay). If a formal permit is issued pursuant to such application, 
it will bear the names of the two ports in the order given in the 
application and will authorize shipment from either port. Alternate 
ports in different countries will not be authorized in the same permit.

[36 FR 7815, Apr. 24, 1971, as amended at 36 FR 13387, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 39 FR 43218, 
Dec. 11, 1974; 45 FR 74715, Nov. 12, 1980; 51 FR 5319 and 5320, Feb. 13, 
1986; 52 FR 17289, May 7, 1987]



Sec. 1312.13   Issuance of import permit.

    (a) The Administrator may authorize importation of any controlled 
substance listed in Schedule I or II or any narcotic drug listed in 
Schedule III, IV, or V if he finds:

[[Page 219]]

    (1) That the substance is crude opium, poppy straw, concentrate of 
poppy straw, or coca leaves, in such quantity as the Administrator finds 
necessary to provide for medical, scientific, or other legitimate 
purposes;
    (2) That the substance is necessary to provide for medical and 
scientific needs or other legitimate needs of the United States during 
an emergency where domestic supplies of such substance or drug are found 
to be inadequate, or in any case in which the Administrator finds that 
competition among domestic manufacturers of the controlled substance is 
inadequate and will not be rendered adequate by the registration of 
additional manufacturers under section 303 of the Controlled Substances 
Act (21 U.S.C. 823); or
    (3) That the domestic supply of any controlled substance is 
inadequate for scientific studies, and that the importation of that 
substance for scientific purposes is only for delivery to officials of 
the United Nations, of the United States, or of any State, or to any 
person registered or exempted from registration under sections 1007 and 
1008 of the Act (21 U.S.C. 957 and 958).
    (4) That the importation of the controlled substance is for 
ballistics or other analytical or scientific purposes, and that the 
importation of that substance is only for delivery to officials of the 
United Nations, of the United States, or of any State, or to any person 
registered or exempted from registration under sections 1007 and 1008 of 
the Act (21 U.S.C. 957 and 958).
    (b) The Administrator may require that such non-narcotic controlled 
substances in Schedule III as he shall designate by regulation in 
Sec. 1312.30 of this part be imported only pursuant to the issuance of 
an import permit. The Administrator may authorize the importation of 
such substances if he finds that the substance is being imported for 
medical, scientific or other legitimate uses.
    (c) If a non-narcotic substance listed in Schedule IV or V is also 
listed in Schedule I or II of the Convention on Psychotropic Substances, 
1971, it shall be imported only pursuant to the issuance of an import 
permit. The Administrator may authorize the importation of such 
substances if it is found that the substance is being imported for 
medical, scientific or other legitimate uses.
    (d) The Administrator may require an applicant to submit such 
documents or written statements of fact relevant to the application as 
he deems necessary to determine whether the application should be 
granted. The failure of the applicant to provide such documents or 
statements within a reasonable time after being requested to do so shall 
be deemed to be a waiver by the applicant of an opportunity to present 
such documents or facts for consideration by the Administrator in 
granting or denying the application.
    (e) Each import permit shall be issued in sextuplet and serially 
numbered, with all six copies bearing the same serial number and being 
designated ``original'' (Copy 1), ``duplicate'' (Copy 2), etc., 
respectively. All copies of import permits shall bear the signature of 
the Director or his delegate, and facsimiles of signatures shall not be 
used. No permit shall be altered or changed by any person after being 
signed by the Administrator or his delegate and any change or alteration 
upon the face of any permit after it shall have been signed by the 
Administrator or his delegate shall render it void and of no effect. 
Permits are not transferable. Each copy of the permit shall have printed 
or stamped thereon the disposition to be made thereof. Each permit shall 
be dated and shall certify that the importer named therein is thereby 
permitted as a registrant under the Act, to import, throtgh the port 
named, one shipment of not to exceed the specified quantity of the named 
controlled substances, shipment to be made before a specified date. Not 
more than one shipment shall be made on a single import permit. The 
permit shall state that the Administrator is satisfied that the 
consignment proposed to be imported is required for legitimate purposes.
    (f) Notwithstanding paragraphs (a)(1) and (a)(2) of this section, 
the Administrator shall permit, pursuant to 21

[[Page 220]]

U.S.C. 952(a)(1) or (a)(2)(A), the importation of approved narcotic raw 
material (opium, poppy straw and concentrate of poppy straw) having as 
its source:
    (1) Turkey,
    (2) India,
    (3) Yugoslavia,
    (4) France,
    (5) Poland,
    (6) Hungary, and
    (7) Australia.
    (g) At least eighty (80) percent of the narcotic raw material 
imported into the United States shall have as its original source Turkey 
and India. Except under conditions of insufficient supplies of narcotic 
raw materials, not more than twenty (20) percent of the narcotic raw 
material imported into the United States annually shall have as its 
source Yugoslavia, France, Poland, Hungary and Australia.

[36 FR 23624, Dec. 11, 1971, as amended at 37 FR 15923, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 46 FR 41776, 
Aug. 18, 1981; 52 FR 17289, May 7, 1987]



Sec. 1312.14   Distribution of copies of import permit.

    Copies of the import permit shall be distributed and serve purposes 
as follows:
    (a) The original and quintuplet copies (Copy 1 and Copy 5) shall be 
transmitted by the Administration to the importer, who shall retain the 
quintuplet copy (Copy 5) on file as his record of authority for the 
importation, and shall transmit the original copy (Copy 1) to the 
foreign exporter. The foreign exporter will submit the original copy 
(Copy 1) to the proper governmental authority in the exporting country, 
if required, as a prerequisite to the issuance of an export 
authorization. This copy of the permit will accompany the shipment. Upon 
arrival of the imported merchandise, the District Director of the U.S. 
Customs Service at the port of entry will, after appraising the 
merchandise, forward the original copy (Copy 1) to the Drug Control 
Section with a report on the reverse side of such copy, showing the name 
of the port of importation, date prepared, name and net quantity of each 
substance, and report of analysis of the merchandise entered.
    (b) The duplicate copy (Copy 2) shall be forwarded by the 
Administration to the proper governmental authorities of the exporting 
country.
    (c) The quadruplet copy (Copy 4) shall be forwarded by the 
Administration to the District Director of the U.S. Customs Service at 
the U.S. port of entry, which shall be the customs port of destination 
in the case of shipments transported under immediate transportation 
entries, in order that the District Director may compare it with the 
original copy (Copy 1) and the bill of lading upon arrival of the 
merchandise. If a discrepancy is noted between corresponding items upon 
different copies of a permit bearing the same serial number when 
compared by the District Director, he shall refuse to permit entry of 
the merchandise until the facts are communicated to the Administration 
and further instructions are received.
    (d) The triplicate copy (Copy 3) and sextuplet copy (Copy 6) shall 
be retained by the Administration.

[36 FR 7815, Apr. 24, 1971, as amended at 36 FR 13387, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and further amended at 45 
FR 74715, Nov. 12, 1980; 51 FR 5319, Feb. 13, 1986; 53 FR 48244, Nov. 
30, 1988]



Sec. 1312.15   Shipments in greater or less amount than authorized.

    (a) If the shipment made under an import permit is greater than the 
maximum amount authorized to be imported under the permit, as determined 
at the weighing by the District Director of the U.S. Customs Service, 
such difference shall be seized subject to forfeiture, pending an 
explanation; except that shipments of substances exceeding the maximum 
authorized amount by less than 1 percent may be released to the importer 
upon the filing by him of an amended import permit. If the substance is 
included in Schedule I, it will be summarily forfeited to the 
Government.
    (b) If the shipment made under the permit is less than the maximum 
amount authorized to be imported under the permit as determined at the 
weighing by the District Director of the U.S. Customs Service, such 
difference, when ascertained by the Administration, shall be recredited 
to the

[[Page 221]]

tentative allotment against which the quantity covered by the permit was 
charged, and the balance of any such tentative allotment with any such 
recredits will remain available to the importer to whom made (unless 
previously revoked in whole or in part), for importations pursuant to 
any permit or permits as are requested and issued during the remainder 
of the calendar year to which the allotment is applicable. No permit 
shall be issued for importation of a quantity of controlled substances 
as a charge against the tentative allotment for a given calendar year, 
after the close of such calendar year, unless the Director of the 
Administration decides to make an exception for good cause shown.

[36 FR 7815, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 46 FR 28841, May 29, 1981]



Sec. 1312.16   Cancellation of permit; expiration date.

    (a) A permit may be canceled after being issued, at the request of 
the importer, provided no shipment has been made thereunder. In the 
event that a permit is lost, the Administrator may, upon the production 
by the importer of satisfactory proof, by affidavit or otherwise, issue 
a duplicate permit. Nothing in this part shall affect the right, hereby 
reserved by the Administrator, to cancel a permit at any time for proper 
cause.
    (b) An import permit shall not be valid after the date specified 
therein, and in no event shall the date be subsequent to 6 months after 
the date the permit is issued. Any unused import permit shall be 
returned for cancellation by the registrant to the Drug Enforcement 
Administration, Drug Control Section, 1405 Eye Street, N.W., Washington, 
DC 20537.

[36 FR 7815, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 45 FR 74715, Nov. 12, 1980; 51 FR 5319, Feb. 13, 1986; 53 
FR 48244, Nov. 30, 1988]



Sec. 1312.17   Special report from importers.

    Whenever requested by the Administrator, importers shall render to 
him not later than 30 days after receipt of the request therefor a 
statement under oath of the stocks of controlled substances on hand as 
of the date specified by the Administrator in his request, and, if 
desired by the Administrator, an estimate of the probable requirements 
for legitimate uses of the importer for any subsequent period that may 
be designated by the Administrator. In lieu of any special statement 
that may be considered necessary, the Administrator may accept the 
figures given upon the reports subsequent by said importer under part 
304 of this chapter.



Sec. 1312.18   Contents of import declaration.

    (a) Any non-narcotic controlled substance listed in Schedule III, 
IV, or V, not subject to the requirement of an import permit pursuant to 
Sec. 1312.13 (b) or (c) of this chapter, may be imported if that 
substance is needed for medical, scientific or other legitimate uses in 
the United States, and will be imported pursuant to a controlled 
substances import declaration.
    (b) Any person registered or authorized to import and desiring to 
import any non-narcotic controlled substance in Schedules III, IV, or V 
which is not subject to the requirement of an import permit as described 
in paragraph (a) of this section, must furnish a controlled substances 
import declaration on DEA Form 236 to the Drug Enforcement 
Administration, Drug Control Section, 1405 Eye Street, NW., Washington, 
DC 20537, not later than 15 calendar days prior to the proposed date of 
importation and distribute four copies of same as hereinafter directed 
in Sec. 1312.19.
    (c) DEA (or BND) Form 236 must be executed in quintuplicate and will 
include the following information:
    (1) The name, address, and registration number of the importer; and 
the name and address and registration number of the import broker, if 
any; and
    (2) A complete description of the controlled substances to be 
imported, including drug name, dosage form, National Drug Code (NDC) 
number, the Administration Controlled Substances Code Number as set 
forth in part 1308 of this chapter, the number and size of packages or 
containers, the name and quantity of the controlled substance

[[Page 222]]

contained in any finished dosage units, and the net quantity of any 
controlled substance (expressed in anhydrous acid, base, or alkaloid) 
given in kilograms or parts thereof; and
    (3) The proposed import date, the foreign port of exportation to the 
United States, the port of entry, and the name, address, and 
registration number of the recipient in the United States; and
    (4) The name and address of the consignor in the foreign country of 
exportation, and any registration or license numbers if the consignor is 
required to have such numbers either by the country of exportation or 
under U.S. law.
    (d) Notwithstanding the time limitations included in paragraph (a) 
of this section, an applicant may obtain a special waiver of these time 
limitations in emergency or unusual instances, provided that a specific 
confirmation is received from the Administrator or his delegate advising 
the registrant to proceed pursuant to the special waiver.

[36 FR 7815, Apr. 24, 1971, as amended at 37 FR 15923, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 45 FR 74715, 
Nov. 12, 1980; 51 FR 5319, Feb. 13, 1986; 52 FR 17290, May 7, 1987]



Sec. 1312.19   Distribution of import declaration.

    The required five copies of the controlled substances import 
declaration will be distributed as follows:
    (a) Copy 1, Copy 2, and Copy 3 shall be transmitted to the foreign 
shipper. The foreign shipper will submit Copy 1 to the proper 
governmental authority in the foreign country, if required as a 
prerequisite to export authorization. Copy 1 will then accompany the 
shipment to its destination, and shall be retained on file by the 
importer. Copy 2 shall be detached and retained by the appropriate 
customs official of the foreign country. Copy 3 shall be removed by the 
District Director of the U.S. Customs Service at the port of entry, who 
shall sign and date the certification of customs on Copy 3, noting any 
changes from the entries made by the importer, and shall then forward 
that copy to the Drug Control Section of the Administration.
    (b) Copy 4 shall be forwarded, within the time limit required in 
Sec. 1312.18, directly to the Drug Enforcement Administration, Drug 
Control Section, 1405 Eye Street, N.W., Washington, DC 20537.
    (c) Copy 5 shall be retained by the importer on file as his record 
of authority for the importation.

[36 FR 7815, Apr. 24, 1971, as amended at 36 FR 13387, July 21, 1971; 37 
FR 15923, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, 1973, and 
further amended at 45 FR 74715, Nov. 12, 1980; 51 FR 5319, Feb. 13, 
1986; 53 FR 48244, Nov. 30, 1988]

                  Exportation of Controlled Substances



Sec. 1312.21   Requirement of authorization to export.

    (a) No person shall in any manner export or cause to be exported 
from the United States any controlled substance listed in Schedule I or 
II, or any narcotic substance listed in Schedule III or IV, or any non-
narcotic substance in Schedule III which the Administrator has 
specifically designated by regulation in Sec. 1312.30 of this part or 
any non-narcotic substance in Schedule IV or V which is also listed in 
Schedule I or II of the Convention on Psychotropic Substances unless and 
until such person is properly registered under the Act (or exempted from 
registration) and the Administrator has issued a permit pursuant to 
Sec. 1312.23 of this part.
    (b) No person shall in any manner export or cause to be exported 
from the United States any non-narcotic controlled substance listed in 
Schedule III, IV, or V, excluding those described in paragraph (a) of 
this section, or any narcotic controlled substance listed in Schedule V, 
unless and until such person is properly registered under the Act (or 
exempted from registration) and has furnished a special controlled 
substance export invoice as provided by section 1003 of the Act (21 
U.S.C. 953(e)) to the Administrator pursuant to Sec. 1312.28 of this 
part.
    (c) A separate authorization repuest is obtained for each 
consignment of such controlled substances to be exported.

[36 FR 7815, Apr. 24, 1971, as amended at 37 FR 15923, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 52 FR 17290, 
May 7, 1987]

[[Page 223]]



Sec. 1312.22   Application for export permit.

    (a) An application for a permit to export controlled substances 
shall be made on DEA Form 161 which may be obtained from, and shall be 
filed with, the Drug Enforcement Administration, Drug Control Section, 
1405 I Street, NW., Washington, DC 20537. Each application shall show 
the exporter's name, address, and registration number; a detailed 
description of each controlled substance desired to be exported 
including the drug name, dosage form, National Drug Code (NDC) number, 
the Administration Controlled Substance Code Number as set forth in part 
1308 of this chapter, the number and size of packages or containers, the 
name and quantity of the controlled substance contained in any finished 
dosage units, and the quantity of any controlled substance (expressed in 
anhydrous acid, base, or alkaloid) given in kilograms or parts thereof. 
The application shall include the name, address, and business of the 
consignee, foreign port of entry, the port of exportation, the 
approximate date of exportation, the name of the exporting carrier or 
vessel (if known, or if unknown it should be stated whether shipment 
will be made by express, freight, or otherwise, exports of controlled 
substances by mail being prohibited), the date and number, if any, of 
the supporting foreign import license or permit accompanying the 
application, and the authority by whom such foreign license or permit 
was issued. The application shall also contain an affidavit that the 
packages are labeled in conformance with obligations of the United 
States under international treaties, conventions, or protocols in effect 
on May 1, 1971, and that, to the best of affiant's knowledge and belief, 
the controlled substances therein are to be applied exclusively to 
medical or scientific uses within the country to which exported, will 
not be reexported therefrom and that there is an actual need for the 
controlled substance for medical or scientific uses within such country. 
In the case of exportation of crude cocaine, the affidavit may state 
that to the best of knowledge and belief, the controlled substances will 
be processed within the country to which exported, either for medical or 
scientific use within that country or for reexportation in accordance 
with the laws of that country to another for medical or scientific use 
within that country. The application shall be signed and dated by the 
exporter and shall contain the address from which the substances will be 
shipped for exportation.
    (b) There shall also be submitted with the application any import 
license or permit (and a translation thereof if in a foreign language) 
or a certified copy of any such license or permit issued by competent 
authorities in the country of destination, or other documentary evidence 
deemed adequate by the Administrator, showing that the merchandise is 
consigned to an authorized permittee, that it is to be applied 
exclusively to medical or scientific use within the country of 
destination, that it will not be reexported from such country, and that 
there is an actual need for the controlled substance for medical or 
scientific use within such country. (In the case of exportation of bulk 
coca leaf alkaloid, the submitted evidence need only show the material 
outlined in paragraph (a) of this section for such exportations.)

[36 FR 7815, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 52 FR 17290, May 7, 1987]



Sec. 1312.23   Issuance of export permit.

    (a) The Administrator may authorize exportation of any controlled 
substance listed in Schedule I or II or any narcotic controlled 
substance listed in Schedule III or IV if he finds that such exportation 
is permitted by subsections 1003(a), (b), (c), or (d) of the Act (21 
U.S.C. 953 (a), (b), (c), or (d).
    (b) The Administrator may require that such non-narcotic controlled 
substances in Schedule III as shall be designated by regulation in 
Sec. 1312.30 of this part be exported only pursuant to the issuance of 
an export permit. The Administrator may authorize the exportation of 
such substances if he finds that such exportation is permitted by 
section 1003(e) of the Act (21 U.S.C. 953(e)).
    (c) If a non-narcotic substance listed in Schedule IV or V is also 
listed in Schedule I or II of the Convention on Psychotropic Substances, 
it shall be

[[Page 224]]

exported only pursuant to the issuance of an export permit. The 
Administrator may authorize the exportation of such substances if he 
finds that such exportation is permitted by section 1003(e) of the Act 
(21 U.S.C. 953(e)).
    (d) The Administrator may require an applicant to submit such 
documents or written statements of fact relevant to the application as 
he deems necessary to determine whether the application should be 
granted. The failure of the applicant to provide such documents or 
statements within a reasonable time after being requested to do so shall 
be deemed to be a waiver by the applicant of an opportunity to present 
such documents or facts for consideration by the Administrator in 
granting or denying the application.
    (e) Each export permit shall be issued in septuplet and serially 
numbered, with all seven copies bearing the same serial number and being 
designated ``original'' (Copy 1), ``duplicate'' (Copy 2), etc., 
respectively. Each export permit shall be predicated upon an import 
certificate or other documentary evidence. Export permits are not 
transferable.
    (f) No export permit shall be issued for the exportation of any 
narcotic drug to any country when the Administrator has information to 
show that the estimates submitted with respect to that country for the 
current period, under the Narcotic Limitation Convention of 1931, or the 
Single Convention on Narcotic Drugs of 1961, have been, or, considering 
the quantity proposed to be imported, will be exceeded. If it shall 
appear through subsequent advice received from the International 
Narcotic Control Board of the United Nations that the estimates of the 
country of destination have been adjusted to permit further importation 
of the narcotic drug, an export permit may then be issued if otherwise 
permissible.

[36 FR 23625, Dec. 11, 1971, as amended at 37 FR 15923, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 52 FR 17290, 
May 7, 1987]



Sec. 1312.24   Distribution of copies of export permit.

    Copies of the export permit shall be distributed and serve purposes 
as follows:
    (a) The original, duplicate, and triplicate copies (Copy 1, Copy 2, 
and Copy 3) shall be transmitted by the Bureau to the exporter who will 
retain the triplicate copy (Copy 3) as his record of authority for the 
exportation. The exporter shall present to the District Director of the 
U.S. Customs Service at the port of export and at the time of shipment, 
the original and duplicate copies (Copy 1 and Copy 2). After endorsing 
the port of export on the reverse side of the original and duplicate 
copies (Copy 1 and Copy 2) the District Director shall forward the 
endorsed original copy (Copy 1) with the shipment, and return the 
endorsed duplicate copy (Copy 2) to the Drug Enforcement Administration, 
Drug Control Section, 1405 Eye Street, N.W., Washington, DC 20537.
    (b) The quadruplet copy (Copy 4) shall be forwarded by the 
Administrator to the District Director of the U.S. Customs Service at 
the port of export for comparison with the original copy (Copy 1) and 
for retention for the customs record.
    (c) The quintuplet copy (Copy 5) shall be forwarded by the 
Administration to the officer in the country of destination who issued 
the import certificate, or other documentary evidence upon which the 
export permit is founded.
    (d) The sextuplet and septuplet copies (Copy 6 and Copy 7) shall be 
retained by the Administration.

[36 FR 7815, Apr. 24, 1971, as amended at 36 FR 13387, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 45 FR 74715, 
Nov. 12, 1980; 51 FR 5319, Feb. 13, 1986; 53 FR 48244, Nov. 30, 1988]



Sec. 1312.25   Expiration date.

    An export permit shall not be valid after the date specified 
therein, which date shall conform to the expiration date specified in 
the supporting import certificate or other documentary evidence upon 
which the export permit is

[[Page 225]]

founded, but in no event shall the date be subsequent to 6 months after 
the date the permit is issued. Any unused export permit shall be 
returned by the permittee to the Drug Control Section for cancellation.

[36 FR 7815, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 45 FR 74715, Nov. 12, 1980; 51 FR 5319, Feb. 13, 1986; 53 
FR 48244, Nov. 30, 1988]



Sec. 1312.26   Records required of exporter.

    The exporter shall keep a record of any serial numbers that might 
appear on packages of narcotic drugs in quantities of one ounce or more 
in such a manner as will identify the foreign consignee, along with Copy 
3 of the export permit.



Sec. 1312.27   Contents of special controlled substances invoice.

    (a) A person regirtered or authorized to export any non-narcotic 
controlled substance listed in Schedule III, IV, or V, which is not 
subject to the requirement of an export permit pursuant to Sec. 1312.23 
(b) or (c), or any person registered or authorized to export any 
controlled substance in Schedule V, must furnish a special controlled 
substances export invoice on DEA Form 236 to the Drug Enforcement 
Administration, Drug Control Section, 1405 I Street, NW., Washington, DC 
20537, not less than 15 calendar days prior to the proposed date of 
exportation, and distribute four copies of same as hereinafter directed 
in Sec. 1312.28 of this part.
    (b) This invoice must be executed by the exporter in quintuplicate 
and include the following information.
    (1) The name, address, and registration number, if any, of the 
exporter; and the name, address and registration number of the exporter 
broker, if any; and
    (2) A complete description of the controlled substances to be 
exported including the drug name, dosage form, National Drug Code (NDC) 
number, the Administration Controlled Substances Code Number as set 
forth in part 1308 of this chapter, the number and size of packages or 
containers, the name and quantity of the controlled substance contained 
in finished dosage units, and the net quantity of any controlled 
substance (expressed in anhydrous acid, base, or alkaloid) given in 
kilograms or parts thereof; and
    (3) The proposed export date, the port of exportation, the foreign 
port of entry, the carriers and shippers involved, method of shipment, 
the name of the vessel if applicable, and the name, address, and 
reghstration number, if any, of any forwarding agent utilized; and
    (4) The name and address of the consignee in the country of 
destination, and any registration or license number if the consignee is 
required to have such numbers either by the country of destination or 
under United States law. In addition, documentation must be provided to 
show that:
    (i) The consignee is authorized under the laws and regulations of 
the country of destination to receive the controlled substances, and 
that
    (ii) The substance is being imported for consumption within the 
importing country to satisfy medical, scientific or other legitimate 
purposes, and that
    (5) The reexport of non-narcotic controlled substances in Schedules 
III and IV, and controlled substances in Schedule V is not permitted 
under the authority of 21 U.S.C. 953(e), except as provided below:
    (i) Bulk substances will not be reexported in the same form as 
exported from the United States, i.e, the material must undergo further 
manufacturing process. This further manufactured material may only be 
reexported to a country of ultimate consumption.
    (ii) Finished dosage units, if reexported, will be in a commercial 
package, properly sealed and labeled for legitimate medical use in the 
country of destination.
    (iii) Any reexportation be made known to DEA at the time the inital 
DEA Form 236, Controlled Substances Import/Export Declaration is 
completed, by checking the box marked ``other'' on the certification. 
The following information will be furnished in the remarks section:
    (A) Indicate ``for reexport''.
    (B) Indicate if reexport is bulk or finished dosage units.
    (C) Indicate product name, dosage strength, commercial package size, 
and quantity.

[[Page 226]]

    (D) Indicate name of consignee, complete address, and expected 
shipment date, as well as, the name and address of the ultimate 
consignee in the country to where the substances will be reexported.
    (E) A statement that the consignee in the country of ultimate 
destination is authorized under the laws and regulations of the country 
of ultimate destination to receive the controlled substances.
    (iv) Shipments which have been exported from the United States and 
are refused by the consignee in the country of destination, or are 
otherwise unacceptable or undeliverable, may be returned to the 
registered exporter in the United States upon authorization of the Drug 
Enforcement Administration. In this circumstance, the exporter in the 
United States shall file a written request for reexport, along with a 
completed DEA Form 236, Import Declaration with the Drug Enforcement 
Administration, Drug Control Section, 1405 I Street, NW., Washington, DC 
20537. A brief summary of the facts that warrant the return of the 
substance to the United States along with an authorization from the 
country of export will be included with the request. DEA will evaluate 
the request after considering all the facts as well as the exporter's 
registration status with DEA. The substance may be returned to the 
United States only after affirmative authorization is issued in writing 
by DEA.
    (c) Notwithstanding the time limitations included in paragraph (a) 
of this section, a registrant may obtain a special waiver of these time 
limitations in emergency or unusual instances; provided that a specific 
confirmation is received from the Administrator or his delegate advising 
the registrant to proceed pursuant to the special waiver.

[36 FR 7815, Apr. 24, 1971, as amended at 37 FR 15923, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 45 FR 74715, 
Nov. 12, 1980; 51 FR 5319, Feb. 13, 1986; 52 FR 17290, May 7, 1987]



Sec. 1312.28   Distribution of special controlled substances invoice.

    The required five copies of the special controlled substances export 
invoice, DEA (or BND) Form 236, will be distributed as follows:
    (a) Copy 1 shall accompany the shipment and remain with the shipment 
to its destination.
    (b) Copy 2 shall accompany the shipment and will be detached and 
retained by appropriate customs officials at the foreign country of 
destination.
    (c) Copy 3 shall accompany the shipment and will be detached by the 
District Director of the U.S. Customs Service at the port of 
exportation, who shall sign and date the certification of customs on 
such Copy 3, noting any changes from the entries made by the exporter, 
and shall then promptly forward Copy 3 to the Drug Control Section of 
the Administration.
    (d) Copy 4 shall be forwarded, within the time limit required in 
Sec. 1312.27 of this part, directly to the Drug Enforcement 
Administration, Drug Control Section, 1405 I Street, NW., Washington, DC 
20537. The documentation required by Sec. 1327.27(b)(4) of this part 
must be attached to this copy.
    (e) Copy 5 shall be retained by the exporter on file as his record 
of authority for the exportation.

[36 FR 7815, Apr. 24, 1971, as amended at 36 FR 13387, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 45 FR 74715, 
Nov. 12, 1980; 51 FR 5319, Feb. 13, 1986; 52 FR 17291, May 7, 1987; 53 
FR 48244, Nov. 30, 1988]



Sec. 1312.29   Domestic release prohibited.

    An exporter or a forwarding agent acting for an exporter must either 
deliver the controlled substances to the port or border, or deliver the 
controlled substances to a bonded carrier approved by the consignor for 
delivery to the port or border, and may not, under any other 
circumstances, release a shipment of controlled substances to anyone, 
including the foreign consignee or his agent, within the United States.



Sec. 1312.30  Schedule III, IV, and V non-narcotic controlled substances requiring an import and export permit.

    The following Schedule III, IV, and V non-narcotic controlled 
substances have been specifically designated by

[[Page 227]]

the Administrator of the Drug Enforcement Administration as requiring 
import and export permits pursuant to sections 1002(b)(2) and 1003(e)(3) 
of the Act (21 U.S.C. 952(b)(2) and 953(e)(3)):
    (a) [Reserved]

[52 FR 17291, May 7, 1987]

     Transshipment and In-Transit Shipment of Controlled Substances



Sec. 1312.31   Schedule I: Application for prior written approval.

    (a) A controlled substance listed in schedule I may be imported into 
the United States for transshipment, or may be transferred or 
transshipped within the United States for immediate exportation, 
provided that:
    (1) The controlled substance is necessary for scientific, medical, 
or other legitimate purposes in the country of destination, and
    (2) A transshipment permit has been issued by the Administrator.
    (b) An application for a transshipment permit must be submitted to 
the Drug Enforcement Administration, Drug Control Section, 1405 Eye 
Street, N.W., Washington, DC 20537, at least 30 days, or in the case of 
an emergency as soon as practicable, prior to the expected date of 
importation, transfer or transshipment. Each application shall contain 
the following:
    (1) The date of execution;
    (2) The identification and description of the controlled substance;
    (3) The net quantity thereof;
    (4) The number and size of the controlled substance containers;
    (5) The name, address, and business of the foreign exporter;
    (6) The foreign port of exportation;
    (7) The approximate date of exportation;
    (8) The identification of the exporting carrier;
    (9) The name, address and business of the importer, transferor, or 
transshipper;
    (10) The registration number, if any, of the importer, transferor or 
transshipper;
    (11) The U.S. port of entry;
    (12) The approximate date of entry;
    (13) The name, address and business of the consignee at the foreign 
port of entry;
    (14) The shipping route from the U.S. port of exportation to the 
foreign port of entry;
    (15) The approximate date of receipt by the consignee at the foreign 
port of entry; and
    (16) The signature of the importer, transferor or transshipper, or 
his agent accompanied by the agent's title.
    (c) An application shall be accompanied by an export license, 
permit, or a certified copy of the export license, permit, or other 
authorization, issued by a competent authority of the country of origin 
(or other documentary evidence deemed adequate by the Administrator).
    (d) An application shall be accompanied by an import license or 
permit or a certified copy of such license or permit issued by a 
competent authority of the country of destination (or other documentary 
evidence deemed adequate by the Administrator), indicating that the 
controlled substance:
    (1) Is to be applied exclusively to scientific, medical or other 
legitimate uses within the country of destination;
    (2) Will not be exported from such country; and
    (3) Is needed therein because there is an actual shortage thereof 
and a demand therefor for scientific, medical or other legitimate uses 
within such country.
    (e) Verification by an American consular officer of the signatures 
on a foreign import license or permit shall be required, if such license 
or permit does not bear the seal of the authority signing them.
    (f) The Administrator may require an applicant to submit such 
documents or written statements of fact relevant to the application as 
he deems necessary to determine whether the application should be 
granted. The failure of the applicant to provide such documents or 
statements within a reasonable time after being requested to do so shall 
be deemed to be a waiver by the applicant of an opportunity to present 
such documents or facts for consideration by the Administrator in 
granting or denying the application.
    (g) The Administrator shall, within 21 days from the date of receipt 
of the application, either grant or deny the

[[Page 228]]

application. The applicant shall be accorded an opportunity to amend the 
application, with the Administrator either granting or denying the 
amended application within 7 days of its receipt. If the Administrator 
does not grant or deny the application within 21 days of its receipt, or 
in the case of an amended application, within 7 days of its receipt, the 
application shall be deemed approved and the applicant may proceed.

[36 FR 7815, Apr. 24, 1971, as amended at 37 FR 15923, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and further amended at 45 
FR 74715, Nov. 12, 1980; 51 FR 5319, Feb. 13, 1986; 53 FR 48244, Nov. 
30, 1988]



Sec. 1312.32   Schedules II, III, IV: Advance Notice.

    (a) A controlled substance listed in Schedules II, III, or IV may be 
imported into the United States for transshipment, or may be transferred 
or transshipped within the United States for immediate exportation, 
provided that written notice is submitted to the Drug Enforcement 
Administration, Drug Control Section, 1405 Eye Street, N.W., Washington, 
DC 20537, at least 15 days prior to the expected date of importation, 
transfer or transshipment.
    (b) Each advance notice shall contain those items required by 
Sec. 1312.31 (b) and (c).

[36 FR 7815, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 45 FR 74715, Nov. 12, 1980; 51 FR 5319, Feb. 13, 1986; 53 
FR 48244, Nov. 30, 1988]

                                Hearings



Sec. 1312.41   Hearings generally.

    (a) In any case where the Administrator shall hold a hearing 
regarding the denial of an application for an import, export or 
transshipment permit, the procedures for such hearing shall be governed 
generally by the adjudication procedures set forth in the Administrative 
Procedure Act (5 U.S.C. 551-559) and specifically by sections 1002 and 
1003 of the Act (21 U.S.C. 952 and 953), by Secs. 1312.42-1312.47, and 
by the procedures for administrative hearings under the Act set forth in 
Secs. 1316.41- 1316.67 of this chapter.

[36 FR 23625, Dec. 11, 1971, as amended at 37 FR 15923, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1312.42   Purpose of hearing.

    (a) If requested by a person applying for an import, export, or 
transshipment permit, the Administrator shall hold a hearing for the 
purpose of receiving factual evidence regarding the issues involved in 
the issuance or denial of such permit to such person.
    (b) Extensive argument should not be offered into evidence but 
rather presented in opening or closing statements of counsel or in 
memoranda or proposed findings of fact and conclusions of law.

[36 FR 23625, Dec. 11, 1971, as amended at 37 FR 15923, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1312.43   Waiver or modification of rules.

    The Administrator of the presiding officer (with respect to matters 
pending before him) may modify or waive any rule in this part by notice 
in advance of the hearing, if he determines that no party in the hearing 
will be unduly prejudiced and the ends of justice will thereby be 
served. Such notice of modification or waiver shall be made a part of 
the record of the hearing.

[36 FR 23625, Dec. 11, 1971. Redesignated at 38 FR 26609, Sept. 24, 
1973]



Sec. 1312.44   Request for hearing or appearance; waiver.

    (a) Any applicant entitled to a hearing pursuant to Sec. 1312.42 and 
who desires a hearing on the denial of his application for an import, 
export, or transshipment permit shall, within 30 days after the date of 
receipt of the denial of his application, file with the Administrator a 
written request for a hearing in the form prescribed in Sec. 1316.47 of 
this chapter.
    (b) Any applicant entitled to a hearing pursuant to Sec. 1312.42 
may, within the period permitted for filing a request for a hearing, 
file with the Administrator a waiver of an opportunity for a hearing, 
together with a written

[[Page 229]]

statement regarding his position on the matters of fact and law involved 
in such hearing. Such statement, if admissible, shall be made a part of 
the record and shall be considered in light of the lack of opportunity 
for cross-examination in determining the weight to be attached to 
matters of fact asserted therein.
    (c) If any applicant entitled to a hearing pursuant to Sec. 1312.42 
fails to appear at the hearing, he shall be deemed to have waived his 
opportunity for the hearing unless he shows good cause for such failure.
    (d) If the applicant waives or is deemed to have waived this 
opportunity for the hearing, the Administrator may cancel the hearing, 
if scheduled, and issue his final order pursuant to Sec. 1312.47 without 
a hearing.

[37 FR 15923, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1312.45   Burden of proof.

    At any hearing on the denial of an application for an import, 
export, or transshipment permit, the Administrator shall have the burden 
of proving that the requirements for such permit pursuant to sections 
1002, 1003, and 1004 of the Act (21 U.S.C. 952, 953, and 954) are not 
satisfied.

[37 FR 15924, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1312.46   Time and place of hearing.

    (a) If any applicant for an import, export, or transshipment permit 
requests a hearing on the issuance or denial of his application, the 
Administrator shall hold such hearing. Notice of the hearing shall be 
given to the applicant of the time and place at least 30 days prior to 
the hearing, unless the applicant waives such notice and requests the 
hearing be held at an earlier time, in which case the Administrator 
shall fix a date for such hearing as early as reasonably possible.
    (b) The hearing will commence at the place and time designated in 
the notice given pursuant to paragraph (a) of this section but 
thereafter it may be moved to a different place and may be continued 
from day to day or recessed to a later day without notice other than 
announcement thereof by the presiding officer at the hearing.

[37 FR 15924, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1312.47   Final order.

    As soon as practicable after the presiding officer has certified the 
record to the Administrator, the Administrator shall issue his order on 
the issuance or denial of the application for and import, export, or 
transshipment permit. The order shall include the findings of fact and 
conclusions of law upon which the order is based. The Administrator 
shall serve one copy of his order upon the applicant.

[37 FR 15924, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, 1973]



PART 1313--IMPORTATION AND EXPORTATION OF PRECURSORS AND ESSENTIAL CHEMICALS--Table of Contents




Sec.
1313.01  Scope.
1313.02  Definitions.

                     Importation of Listed Chemicals

1313.12  Requirement of authorization to import.
1313.13  Contents of import declaration.
1313.14  Distribution of import declaration.
1313.15  Waiver of 15-day advance notice for regular importers.

                     Exportation of Listed Chemicals

1313.21  Requirement of authorization to export.
1313.22  Contents of export declaration.
1313.23  Distribution of export declaration.
1313.24  Waiver of 15-day advance notice for chemical exporters.
1313.25  Foreign import restrictions.

  Transshipments, In-Transit Shipments and International Transactions 
                       Involving Listed Chemicals

1313.31  Advance notice of importation for transshipment or transfer.
1313.32  Requirement of authorization for international transactions.
1313.33  Contents of an international transaction declaration.
1313.34  Distribution of the international transaction declaration.
1313.41  Suspension of shipments.

                                Hearings

0313.51  Hearings generally.
1313.52  Purpose of hearing.

[[Page 230]]

1313.53  Waiver of modification of rules.
1313.54  Request for hearing.
1313.55  Burden of proof.
1313.56  Time and place of hearing.
1313.57  Final order.

    Authority: 21 U.S.C. 802, 830, 871(b), 971.

    Source:  54 FR 31665, Aug. 1, 1989, unless otherwise noted.



Sec. 1313.01  Scope.

    Procedures governing the importation, exportation, transshipment and 
in-transit shipment of listed chemicals pursuant to section 1018 of the 
Act (21 U.S.C. 971) are governed generally by that section and 
specifically by the sections of this part.

[54 FR 31665, Aug. 1, 1989, as amended at 60 FR 32465, June 22, 1995]



Sec. 1313.02  Definitions.

    (a) The term chemical export means transferring ownership or 
control, or the sending or taking of threshold quantities of listed 
chemicals out of the United States (whether or not such sending or 
taking out constitutes an exportation within the meaning of the Customs 
and related laws of the United States).
    (b) The term chemical exporter is a regulated person who, as the 
principal party in interest in the export transaction, has the power and 
responsibility for determining and controlling the sending of the listed 
chemical out of the United States.
    (c) The term regulated person means any individual, corporation, 
partnership, association, or other legal entity who manufactures, 
distributes, imports, or exports a listed chemical, a tableting machine, 
or an encapsulating machine, or who acts as a broker or trader for an 
international transaction involving a listed chemical, a tableting 
machine, or an encapsulating machine.
    (d) The term regulated transaction means:
    (1) A distribution, receipt, sale, importation, exportation, or 
international transaction of a listed chemical, or if the Administrator 
establishes a threshold amount for a specific listed chemical, a 
threshold amount as determined by the Administrator, which includes a 
cumulative threshold amount for multiple transactions, of a listed 
chemical, except that such term does not include:
    (i) A domestic lawful distribution in the usual course of business 
between agents or employees of a single regulated person; in this 
context, agents or employees means individuals under the direct 
management and control of the regulated person;
    (ii) A delivery of a listed chemical to or by a common or contract 
carrier for carriage in the lawful and usual course of the business of 
the common or contract carrier, or to or by a warehouseman for storage 
in the lawful and usual course of the business of the warehouseman, 
except that if the carriage or storage is in connection with the 
distribution, importation, or exportation of a listed chemical to a 
third person, this paragraph does not relieve a distributor, importer, 
or exporter from compliance with this part or parts 1309 and 1310 of 
this chapter;
    (iii) Any category of transaction or any category of transaction for 
a specific listed chemical or chemicals specified by regulation of the 
Administrator as excluded from this definition as unnecessary for 
enforcement of the Act;
    (iv) Any transaction in a listed chemical that is contained in a 
drug that may be marketed or distributed lawfully in the United States 
under the Federal Food, Drug, and Cosmetic Act unless)--
    (A) The drug contains ephedrine or its salts, optical isomers, or 
salts of optical isomers as the only active medicinal ingredient or 
contains ephedrine or its salts, optical isomers or salts of optical 
isomers and therapeutically insignificant quantities of another active 
medicinal ingredient (for purposes of this paragraph, the term 
``therapeutically insignificant quantities'' shall apply if the product 
formulation (i.e., the qualitative and quantitative composition of 
active ingredients within the product) is not listed in American 
Pharmaceutical Association (Apha) Handbook of Nonprescription Drugs; 
Drug Facts and Comparisons (published by Wolters Kluwer Company); or USP 
DI (published by authority of the United States Pharmacopeial 
Convention, Inc.); or the product is not listed in

[[Page 231]]

Section 1310.15 as an exempt drug product. For drug products having 
formulations not found in the above compendiums, the Administrator shall 
determine, pursuant to a written request as specified in Section 
1310.14, whether the active medicinal ingredients are present in 
quantities considered therapeutically significant for purposes of this 
paragraph; or
    (B) The Administrator has determined pursuant to the criteria in 
Section 1310.10 that:
    (1) The drug or group of drugs is being diverted to obtain the 
listed chemical for use in the illicit production of a controlled 
substance; and
    (2) The quantity of ephedrine or other listed chemical contained in 
the drug included in the transaction or multiple transactions equals or 
exceeds the threshold established for that chemical by the 
Administrator;
    (v) Any transaction in a chemical mixture listed in Section 1310.13.
    (2) A distribution, importation, or exportation of a tableting 
machine or encapsulating machine except that such term does not include 
a domestic lawful distribution in the usual course of business between 
agents and employees of a single regulated person; in this context, 
agents or employees means individuals under the direct management and 
control of the regulated person.
    (e) The term chemical import means with respect to a listed 
chemical, any bringing in or introduction of such listed chemical into 
either the jurisdiction of the United States or into the Customs 
territory of the United States (whether or not such bringing in or 
introduction constitutes an importation within the meaning of the tariff 
laws of the United States).
    (f) The term chemical importer is a regulated person who, as the 
principal party in interest in the import transaction, has the power and 
responsibility for determining and controlling the bringing in or 
introduction of the listed chemical into the United States.
    (g) The term regular customer means a person with whom the regulated 
person has an established business relationship for a specified listed 
chemical or chemicals that has been reported to the Administration 
subject to the criteria established in Sec. 1313.02(j).
    (h) The term regular importer means, with respect to a listed 
chemical, a person that has an established record as an importer of that 
listed chemical that is reported to the Administrator.
    (i) The term established record as an importer means that the 
regulated person has imported a listed chemical at least once within the 
past six months, or twice within the past twelve months from a foreign 
supplier. The term also means that the regulated person has provided the 
Administration with the following information in accordance with the 
waiver of the 15-day advance notice requirements of Section 1313.15:
    (1) the name, DEA registration number (where applicable), street 
address, telephone number, telex number, and, where available, the 
facsimile number of the regulated person and of each foreign supplier; 
and
    (2) the frequency and number of transactions occurring during the 
preceding 12-month period.
    (j) The term established business relationship with a foreign 
customer means the regulated person has exported a listed chemical at 
least once within the past six months, or twice within the past twelve 
months to a foreign manufacturer, distributor, or end user of the 
chemical that has an established business in the foreign country with a 
fixed street address. A person or business which functions as a broker 
or intermediary is not a customer within the meaning of this section. 
The term also means that the regulated person has provided the 
Administration with the following information in accordance with the 
Waiver of 15-day advance notice requirements of Sec. 1313.24:
    (1) The name and street address of the chemical exporter and of each 
regular customer;
    (2) The telephone number, telex number, contact person, and where 
available, the facsimile number for the chemical exporter and for each 
regular customer;
    (3) The nature of the regular customer's business (i.e., importer, 
exporter, distributor, manufacturer, etc.), and if known, the use to 
which the listed chemical or chemicals will be applied;
    (4) The duration of the business relationship;

[[Page 232]]

    (5) The frequency and number of transactions occurring during the 
preceding 12-month period;
    (6) The amounts and the listed chemical or chemicals involved in 
regulated transactions between the chemical exporter and the regular 
customer;
    (7) The method of delivery (direct shipment or through a broker or 
forwarding agent); and
    (8) Other information that the chemical exporter considers relevant 
for determining whether a customer is a regular customer.
    (k) The term Customs territory of the United States means the 
several states, the District of Columbia, and Puerto Rico.
    (l) The term jurisdiction of the United States means the Customs 
territory of the United States, the Virgin Islands, the Canal Zone, 
Guam, American Samoa, and Palau.
    (m) The terms broker and trader mean any individual, corporation, 
corporate division, partnership, association, or other legal entity 
which assists in arranging an international transaction in a listed 
chemical by--
    (1) negotiating contracts;
    (2) serving as an agent or intermediary; or
    (3) fulfilling a formal obligation to complete the transaction by 
bringing together a buyer and seller, a buyer and transporter, or a 
seller and transporter, or by receiving any form of compensation for so 
doing.
    (n) The term international transaction means a transaction involving 
the shipment of a listed chemical across an international border (other 
than a United States border) in which a broker or trader located in the 
United States participates.
    (o) Any term not defined in this section shall have the definition 
set forth in sections 102 and 1001 of the Act (21 U.S.C. 802 and 951), 
and Sec. 1301.02 and Sec. 1310.01 of this chapter.

[54 FR 31665, Aug. 1, 1989, as amended at 60 FR 32463, June 22, 1995]

                     Importation of Listed Chemicals



Sec. 1313.12  Requirement of authorization to import.

    (a) Each regulated person who imports a listed chemical that meets 
or exceeds the threshold quantities identified in Sec. 1310.04(f) or is 
a listed chemical for which no threshold has been established as 
identified in Sec. 1310.04(g) of this chapter, shall notify the 
Administrator of the importation not later than 15 days before the 
transaction is to take place.
    (b) A completed DEA Form 486 must be received at the following 
address not later than 15 days prior to the importation:

Drug Enforcement Administration, P.O. Box 28346, Washington, DC 20038.

    A copy of the completed DEA Form 486 may be transmitted directly to 
the Drug Enforcement Administration, Drug Control Section, through 
electronic facsimile media not later than 15 days prior to the 
importation.
    (c) The 15-day advance notification requirement for listed chemical 
imports may be waived for:
    (1) Any regulated person who has satisfied the requirements for 
reporting to the Administration as a regular importer of such listed 
chemicals; or
    (2) A specific listed chemical, as set forth in paragraph (f) of 
this section, for which the Administrator determines that advance 
notification is not necessary for effective chemical diversion control.
    (d) For imports where advance notification is waived pursuant to 
paragraph (c)(1) of this section, the DEA Form 486 must be received by 
the Drug Enforcement Administration, Chemical Operations Section, on or 
before the date of importation through use of the mailing address listed 
in Sec. 1313.12(b) or through use of electronic facsimile media.
    (e) For importations where advance notification is waived pursuant 
to paragraph (c)(2) of this section no DEA Form 486 is required, 
however, the regulated person shall submit quarterly reports to the Drug 
Enforcement Administration, Chemical Operations Section, P.O. Box 28346, 
Washington,

[[Page 233]]

DC 20038, by no later than the 15th day of the month following the end 
of each quarter. The report shall contain the following information 
regarding each individual importation:
    (1) The name of the listed chemical;
    (2) The quantity and date imported;
    (3) The name and full business address of the supplier;
    (4) The foreign port of embarkation; and
    (5) The port of entry.
    (f) The 15 day advance notification requirement set forth in 
paragraph (a) has been waived for imports of the following listed 
chemicals:
    (1) [Reserved]

[54 FR 31665, Aug. 1, 1989, as amended at 59 FR 51367, Oct. 11, 1994; 60 
FR 32464, June22, 1995]



Sec. 1313.13  Contents of import declaration.

    (a) Any List I or List II chemical listed in Sec. 1310.02 of this 
chapter may be imported if that chemical is necessary for medical, 
commercial, scientific, or other legitimate uses within the United 
States. Chemical importations into the United States for immediate 
transfer/transshipment outside the United States must comply with the 
procedures set forth in Sec. 1313.31.
    (b) Any regulated person who desires to import a threshold or 
greater quantity of a listed chemical shall notify the Administration 
through procedures set forth in Sec. 1313.12 and distribute three copies 
of DEA Form 486 as directed in Sec. 1313.14.
    (c) The DEA Form 486 must be executed in triplicate and must include 
the following information:
    (1) The name, address, telephone number, telex number, and, where 
available, the facsimile number of the chemical importer; the name, 
address, telephone, telex, and where available, the facsmile number of 
the broker or forwarding agent (if any); and
    (2) The name and description of each listed chemical as it appears 
on the label or container, the name of each chemical as it is designated 
in 1310.02 of this chapter, the size or weight of container, the number 
of containers, the net weight of each listed chemical given in kilograms 
or parts thereof; and the gross weight of the shipment given in 
kilograms or parts thereof; and
    (3) The proposed import date, the foreign port of exportation and 
the first U.S. Customs Port of Entry; and
    (4) The name, address, telephone number, telex number, and, where 
available, the facsmile number of the consignor in the foreign country 
of exportation.

[54 FR 31665, Aug. 1, 1989, as amended at 60 FR 32465, June 22, 1995]



Sec. 1313.14  Distribution of import declaration.

    The required three copies of the listed chemical import declaration 
(DEA Form 486) will be distributed as follows:
    (a) Copy 1 shall be retained on file by the regulated person as the 
official record of import. Import declaration forms involving a List I 
chemical must be retained for four years; declaration forms for List II 
chemical must be retained for two years.
    (b) Copy 2 is the Drug Enforcement Administration copy used to 
fulfill the notification requirements of Section 6053 of the Chemical 
Diversion and Trafficking Act of 1988, as specified in Sec. 1313.12.
    (c) Copy 3 shall be presented to the U.S. Customs Sevice along with 
the customs entry. If the import is a regulated transaction for which 
the 15-day advance notice requirement has been waived, the regulated 
person shall declare this information to the U.S. Customs Service 
Official by checking the block on the DEA Form 486 designated for this 
purpose.

[54 FR 31665, Aug. 1, 1989, as amended at 60 FR 32465, June 22, 1995]



Sec. 1313.15  Waiver of 15-day advance notice for regular importers.

    (a) Each regulated person seeking designation as a ``regular 
importer'' shall provide, by certified mail return receipt requested, to 
the Administration such information as is required under 
Sec. 1313.02(i), documenting their status as a regular importer.
    (b) Each regulated person making application under paragraph (a) of 
this section shall be considered a ``regular importer'' for purposes of 
waiving the

[[Page 234]]

15-day advance notice, 30 days after receipt of the application by the 
Administration, as indicated on the return receipt, unless the regulated 
person is otherwise notified in writing by the Administration.
    (c) The Administrator, may, at any time, disqualify a regulated 
person's status as a regular importer on the grounds that the chemical 
being imported may be diverted to the clandestine manufacture of a 
controlled substance.
    (d) Unless the Administration notifies the chemical importer to the 
contrary, the qualification of a regular importer of any one of these 
three chemicals, acetone, 2-Butanone (MEK), or toluene, qualifies that 
importer as a regular importer of all three of these chemicals.
    (e) All chemical importers shall be required to file a DEA Form 486 
as required by Section 1313.12.

[60 FR 32464, June 22, 1995]

                     Exportation of Listed Chemicals



Sec. 1313.21  Requirement of authorization to export.

    (a) No person shall export or cause to be exported from the United 
States any chemical listed in Sec. 1310.02 of this chapter, which meets 
or exceeds the threshold quantities identified in Sec. 1310.04(f) or is 
a listed chemical for which no threshold has been established as 
identified in Sec. 1310.04(g) of this chapter, until such time as the 
Administrator has been notified. Notification must be made not later 
than 15 days before the transaction is to take place. In order to 
facilitate the export of listed chemicals and implement the purpose of 
the Act, regulated persons may wish to provide notification to the 
Administration as far in advance of the 15 days as possible.
    (b) A completed DEA Form 486 must be received at the following 
address not later than 15 days prior to the exportation:

    Drug Enforcement Administration, P.O. Box 28346, Washington, DC 
20038.

    A copy of the completed DEA Form 486 may be transmitted directly to 
the Drug Enforcement Administration, Drug Control Section, through 
electronic facsimile media not later than 15 days prior to the 
exportation.
    (c) The 15-day advance notification requirement for listed chemical 
exports may be waived for:
    (1) any regulated person who has satisfied the requirements of 
Section 1313.24 for reporting to the Administration an established 
business relationship with a foreign customer as defined in 
Sec. 1313.02(j).
    (2) A specific listed chemical to a specified country, as set forth 
in paragraph (f) of this section, for which the Administrator determines 
that advance notification is not necessary for effective chemical 
diversion control.
    (d) For exports where advance notification is waived pursuant to 
paragraph (c)(1) of this section, the DEA Form 486 must be received by 
the Drug Enforcement Administration, Chemical Operations Section, on or 
before the date of exportation through use of the mailing address listed 
in Section 1313.12(b) or through use of electronic facsimile media.
    (e) For exportations where advance notification is waived pursuant 
to paragraph (c)(2) of this section, the regulated person shall file 
quarterly reports to the Drug Enforcement Administration, Chemical 
Operations Section, P.O. Box 28346, Washington, DC 20038, by no later 
than the 15th day of the month following the end of each quarter. The 
report shall contain the following information regarding each individual 
importation:
    (1) The name of the listed chemical;
    (2) The quantity and date exported;
    (3) The name and full business address of the foreign customer;
    (4) The port of embarkation; and
    (5) The foreign port of entry.
    (f) The 15 day advance notification requirement set forth in 
paragraph (a) of this section has been waived for exports of the 
following listed chemicals to the following countries:

------------------------------------------------------------------------
             Name of Chemical                          Country          
------------------------------------------------------------------------
[Reserved]................................  ............................
------------------------------------------------------------------------

    (g) No person shall export or cause to be exported any listed 
chemical, knowing or having reasonable cause to believe the export is in 
violation of the

[[Page 235]]

laws of the country to which the chemical is exported or the chemical 
will be used to manufacture a controlled substance in violation of the 
Act or the laws of the country to which the chemical is exported. The 
Administration will publish a notice of foreign import restrictions for 
listed chemicals of which DEA has knowledge as provided in Sec. 1313.25.

[54 FR 31665, Aug. 1, 1989, as amended at 59 FR 51367, Oct. 11, 1994; 60 
FR 32464, June 22, 1995]



Sec. 1313.22  Contents of export declaration.

    (a) Any List I or List II chemical listed in Sec. 1310.02 of this 
chapter which meets or exceeds the quantitative threshold criteria 
established in Sec. 1310.04(f) of this chapter may be exported if that 
chemical is needed for medical, commercial, scientific, or other 
legitimate uses.
    (b) Any regulated person who desires to export a threshold or 
greater quantity of a listed chemical shall notify the Administration 
through procedures outlined in Sec. 1313.21 and distribute three copies 
of DEA Form 486 as directed in Sec. 1313.23.
    (c) The DEA Form 486 must be executed in triplicate and must include 
all the following information:
    (1) The name, address, telephone number, telex number, and, where 
available, the facsimile number of the chemical exporter; the name, 
address, telephone number, telex number, and, where available, the 
facsimile number of the export broker, if any;
    (2) The name and description of each listed chemical as it appears 
on the label or container, the name of each listed chemical as it is 
designated in Sec. 1310.02 of this chapter, the size or weight of 
container, the number of containers, the net weight of each listed 
chemical given in kilograms or parts thereof, and the gross weight of 
the shipment given in kilograms or parts thereof;
    (3) The proposed export date, the U.S. Customs port of exportation, 
and the foreign port of entry; and
    (4) The name, address, telephone, telex, and where available, the 
facsimile number of the consignee in the country where the chemical 
shipment is destined; the name(s) and address(es) of any intermediate 
consignee(s).
    (d) Notwithstanding the time limitations included in paragraph (b) 
of this section, a regulated person may receive a waiver of the 15-day 
advance notification requirement following the procedures outlined in 
Sec. 1313.24.
    (e) Declared exports of listed chemicals which are refused, 
rejected, or otherwise deemed undeliverable may be returned to the U.S. 
chemical exporter of record. A brief written notification (this does not 
require a DEA Form 486) outlining the circumstances must be sent to the 
Drug Enforcement Administration, P.O. Box 28346, Washington, DC 20038, 
following the return within a reasonable time. This provision does not 
apply to shipments that have cleared foreign customs, been delivered, 
and accepted by the foreign consignee. Returns to third parties in the 
United States will be regarded as imports.

[54 FR 31665, Aug. 1, 1989, as amended at 60 FR 32465, June 22, 1995]



Sec. 1313.23  Distribution of export declaration.

    The required three copies of the listed chemical export declaration 
(DEA Form 486) will be distributed as follows:
    (a) Copy 1 shall be retained on file by the chemical exporters as 
the official record of export. Export declaration forms involving a List 
I chemical must be retained for four years; declaration forms for list 
II chemical must be retained for two years.
    (b) Copy 2 is the Drug Enforcement Administration copy used to 
fulfill the notification requirements of Section 6053 of the Chemical 
Diversion and Trafficking Act of 1988, as specified in Sec. 1313.21
    (c) Copy 3 shall be prerented to the U.S. Customs Service at the 
port of exit along with the Shippers Export Declaration for each export 
of a listed chemical or chemicals.

[54 FR 31665, Aug. 1, 1989, as amended at 60 FR 32465, June 22, 1995]



Sec. 1313.24  Waiver of 15-day advance notice for chemical exporters.

    (a) Each regulated person shall provide to the Administration the 
identity

[[Page 236]]

and information listed in Sec. 1313.02(j) for an established business 
relationship with a foreign customer not later than August 31, 1989.
    (b) Not later than October 31, 1989, each regular customer so 
identified in notifications made under Sec. 1313.24(a) shall be a 
regular customer for purposes of waiving the 15-day advance notice 
requirement, unless the regulated person is otherwise notified in 
writing by the Administration.
    (c) Each foreign customer identified on an initial DEA Form 486 
submitted after the effective date of the implementation of part 1313 
shall, after the expiration of the 15-day period, qualify as a regular 
customer, unless the Administration otherwise notifies the regulated 
person in writing.
    (d) Unless the Administration notifies the chemical exporter to the 
contrary, the qualification of a regular customer for any one of these 
three chemicals, acetone, 2-Butanone (MEK), or toluene, qualifies that 
customer as a regular customer for all three of these chemicals.
    (e) The Administrator may notify any chemical exporter that a 
regular customer has been disqualified or that a new customer for whom a 
notification has been submitted is not to be accorded the status of a 
regular customer. In the event of a disqualification of an established 
regular customer, the chemical exporter will be notified in writing of 
the reasons for such action.

Public reporting (one-time) burden for this collection of information is 
estimated to average four hours per response, including the time for 
reviewing instructions, searching existing data sources, gathering and 
maintaining the data needed, and completing and reviewing and collection 
of information. Send comments regarding this burden estimate or any 
other aspect of this collection of information, including suggestions 
for reducing this burden to the Drug Enforcement Administration, Records 
Management Section, Washington, DC 20537; and to the Office of 
Management and Budget, Paperwork Reduction Project No. 1117-0025, 
Washington, DC 20503.

[54 FR 31665, Aug. 1, 1989, as amended at 56 FR 55077, Oct. 24, 1991]



Sec. 1313.25  Foreign import restrictions.

    Any export from the United States in violation of the law of the 
country to which the chemical is exported is subject to the penalties of 
Title 21 United States Code 960(d).

  Transshipments, In-Transit Shipments and International Transactions 
                       Involving Listed Chemicals



Sec. 1313.31  Advance notice of importation for transshipment or transfer.

    (a) A quantity of a chemical listed in Sec. 1310.02 of this chapter 
that meets or exceeds the threshold reporting requirements found in 
Sec. 1310.04(f) of this chapter may be imported into the United States 
for transshipment, or may be transferred or transshipped within the 
United States for immediate exportation, provided that advance notice is 
given to the Administration.
    (b) Advance notification must be provided to the Drug Enforcement 
Administration, P.O. Box 28346, Washington, DC 20038, not later than 15 
days prior to the proposed date the listed chemical will transship or 
transfer through the United States. The written notification (not a DEA 
Form 486) shall contain the following information:
    (1) The date the notice was executed;
    (2) The complete name and description of the listed chemical as it 
appears on the label or container.
    (3) The name of the listed chemical as designated by Sec. 1310.02 of 
this chapter.
    (4) The number of containers and the size or weight of the container 
for each listed item;
    (5) The new weight of each listed chemical given in kilograms or 
parts thereof;
    (6) The gross weight of the shipment given in kilograms or parts 
thereof;
    (7) The name, address, telephone number, telex number, business of 
the foreign exporter and, where available, the facsimile number;
    (8) The foreign port of exportation;
    (9) The approxhmate date of exportation;
    (10) The complete identification of the exporting carrier;
    (11) The name, address, business, telephone number, telex number, 
and, where available, the facsimile number

[[Page 237]]

of the importer, transferor, or transshipper;
    (12) The U.S. port of entry;
    (13) The approximate date of entry;
    (14) The name, address, telephone number, telex number, business of 
the consignee and, where available, facsimile number of the consignee at 
the foreign port of entry;
    (15) The shipping route from the U.S. port of exportation to the 
foreign port of entry at final destination;
    (16) The approximate date of receipt by the consignee at the foreign 
port of entry; and
    (17) The signature of the importer, transferor or transshipper, or 
his agent, accompanied by the agent's title.
    (c) Unless notified to the contrary prior to the expected date of 
delivery, the importation for transshipment or transfer is considered 
approved.
    (d) No waiver of the 15-day advance notice will be given for imports 
of listed chemicals in quantities meeting or exceeding threshold 
quantities for transshipment or transfer outside the United States.



Sec. 1313.32  Requirement of authorization for international transactions.

    (a) A broker or trader shall notify the Administrator prior to an 
international transaction involving a listed chemical which meets or 
exceeds the threshold amount identified in Section 1310.04 of this 
chapter, in which the broker or trader participates. Notification must 
be made no later than 15 days before the transaction is to take place. 
In order to facilitate an international transaction involving listed 
chemicals and implement the purpose of the Act, regulated persons may 
wish to provide advance notification to the Administration as far in 
advance of the 15 days as possible.
    (b) (1) A completed DEA Form 486 must be received at the following 
address not later than 15 days prior to the international transaction:

    Drug Enforcement Administration, P.O. Box 28346, Washington, D.C. 
20038

    (2) A copy of the DEA Form 486 may be transmitted directly to the 
Drug Enforcement Administration, Chemical Operations Section, through 
electronic facsimile media not later than 15 days prior to the 
exportation.
    (c) No person shall serve as a broker or trader for an international 
transaction involving a listed chemical knowing or having reasonable 
cause to believe that the transaction is in violation of the laws of the 
country to which the chemical is exported or the chemical will be used 
to manufacture a controlled substance in violation of the laws of the 
country to which the chemical is exported. The Administration will 
publish a notice of foreign import restrictions for listed chemicals of 
which DEA has knowledge as provided in Section 1313.25.

[60 FR 32465, June 22, 1995]



Sec. 1313.33  Contents of an international transaction declaration.

    (a) An international transaction involving a chemical listed in 
Sec. 1310.02 of this chapter which meets the threshold criteria 
established in Sec. 1310.04 of this chapter may be arranged by a broker 
or trader if the chemical is needed for medical, commercial, scientific, 
or other legitimate uses.
    (b) Any broker or trader who desires to arrange an international 
transaction involving a listed chemical which meets the criteria set 
forth in Section 1310.04 shall notify the Administration through the 
procedures outlined in Section 1313.32(b).
    (c) The DEA Form 486 must be executed in triplicate and must include 
all the following information:
    (1) The name, address, telephone number, telex number, and, where 
available, the facsimile number of the chemical exporter; the name, 
address, telephone number, telex number, and, where available, the 
facsimile number of the chemical importer;
    (2) The name and description of each listed chemical as it appears 
on the label or container, the name of each listed chemical as it is 
designated in Section 1310.02 of this chapter, the size or weight of 
container, the number of containers, the net weight of each listed 
chemical given in kilograms or parts thereof, and the gross weight of 
the shipment given in kilograms or parts thereof;

[[Page 238]]

    (3) The proposed export date, the port of exportation, and the port 
of importation; and
    (4) The name, address, telephone, telex, and where available, the 
facsimile number, of the consignee in the country where the chemical 
shipment is destined; the name(s) and address(es) of any intermediate 
consignee(s).

[60 FR 32465, June 22, 1995]



Sec. 1313.34  Distribution of the international transaction declaration.

    The required three copies of the DEA Form 486 will be distributed as 
follows:
    (a) Copies 1 and 3 shall be retained on file by the broker or trader 
as the official record of the international transaction. Declaration 
forms involving List I chemicals shall be retained for List II chemicals 
shall be retained for four years; declaration forms for two years.
    (b) Copy 2 is the Drug Enforcement Administration copy used to 
fulfill the notification requirements of Section 1313.32.

[60 FR 32465, June 22, 1995; 60 FR 36334, July 14, 1995]



Sec. 1313.41  Suspension of shipments.

    (a) The Administrator may suspend any importation or exportation of 
a chemical listed in Sec. 1310.02 of this chapter based on evidence that 
the chemical proposed to be imported or exported may be diverted to the 
clandestine manufacture of a controlled substance. If the Administrator 
so suspends, he shall provide written notice of such suspension to the 
regulated person. Such notice shall contain a statement of the legal and 
factual basis for the order.
    (b) Upon service of the order of suspension, the regulated person to 
whom the order applies under paragraph (a) of this section must, if he 
desires a hearing, file a written request for a hearing pursuant to 
Secs. 1313.51-1313.57.

                                Hearings



Sec. 1313.51  Hearings generally.

    In any case where a regulated person requests a hearing regarding 
the suspension of a shipment of a listed chemical, the procedures for 
such hearing shall be governed generally by the procedures set forth in 
the Administrative Procedure Act (5 U.S.C. 551-559) and specifically by 
section 6053 of the Chemical Diversion and Trafficking Act (Pub. L. 100-
690), by 21 CFR 1313.52-1313.57, and by the procedures for 
administrative hearings under the Controlled Substances Act set forth in 
Secs. 1316.41-1316.67 of this chapter.



Sec. 1313.52  Purpose of hearing.

    If requested by a person entitled to a hearing, the Administrator 
shall cause a hearing to be held for the purpose of receiving factual 
evidence regarding the issues involved in the suspension of shipments 
within 45 days of the date of the request, unless the requesting party 
requests an extension of time.



Sec. 1313.53  Waiver of modification of rules.

    The Administrator or the presiding officer (with respect to matters 
pending before him) may modify or waive any rule in this part by notice 
in advance of the hearing, if he determines that no party in the hearing 
will be unduly prejudiced and the ends of justice will thereby be 
served. Such notice of modification or waiver shall be made a part of 
the record of the hearing.



Sec. 1313.54  Request for hearing.

    (a) Any person entitled to a hearing pursuant to Sec. 1313.52 and 
desiring a hearing shall, within 30 days after receipt of the notice to 
suspend the shipment, file with the Administrator a written request for 
a hearing in the form prescribed in Sec. 1316.47 of this chapter.
    (b) If any person entitled to a hearing or to participate in a 
hearing pursuant to Sec. 1313.41 fails to file a request for a hearing 
or a notice of appearance, or if he so files and fails to appear at the 
hearing, he shall be deemed to have waived his opportunity for the 
hearing or to participate in the hearing, unless he shows good cause for 
such failure.
    (c) If all persons entitled to a hearing or to participate in a 
hearing waive or are deemed to waive their opportunity for the hearing 
or to participate in the hearing, the Administrator may cancel the 
hearing, if scheduled, and issue his final order pursuant to 
Sec. 1313.57.

[[Page 239]]



Sec. 1313.55  Burden of proof.

    At any hearing regarding the suspension of shipments, the Agency 
shall have the burden of proving that the requirements of this part for 
such suspension are satisfied.



Sec. 1313.56  Time and place of hearing.

    (a) If any regulated person requests a hearing on the suspension of 
shipments, a hearing will be scheduled no later than 45 days after the 
request is made, unless the regulated person requests an extension to 
this date.
    (b) The hearing will commence at the place and time designated in 
the notice given pursuant to paragraph (a) of this section but 
thereafter it may be moved to a different place and may be continued 
from day to day or recessed to a later day without notice other than 
announcement thereof by the presiding officer at the hearing.



Sec. 1313.57  Final order.

    As soon as practicable after the presiding officer has certified the 
record to the Administrator, the Administrator shall issue his order 
regarding the suspension of shipment. The order shall include the 
findings of fact and conclusions of law upon which the order is based. 
The Administrator shall serve one copy of his order upon each party in 
the hearing.



PARTS 1314-1315--[RESERVED]--Table of Contents






PART 1316--ADMINISTRATIVE FUNCTIONS, PRACTICES, AND PROCEDURES--Table of Contents




                  Subpart A--Administrative Inspections

Sec.
1316.01  Scope of Subpart A.
1316.02  Definitions.
1316.03  Authority to make inspections.
1316.04  Exclusion from inspection.
1316.05  Entry.
1316.06  Notice of inspection.
1316.07  Requirement for administrative inspection warrant; exceptions.
1316.08  Consent to inspection.
1316.09  Application for administrative inspection warrant.
1316.10  Administrative probable cause.
1316.11  Execution of warrants.
1316.12  Refusal to allow inspection with an administrative warrant.
1316.13  Frequency of administrative inspections.

       Subpart B--Protection of Researchers and Research Subjects

1316.21  Definitions.
1316.22  Exemption.
1316.23  Confidentiality of identity of research subjects.
1316.24  Exemption from prosecution for researchers.

                   Subpart C--Enforcement Proceedings

1316.31  Authority for enforcement proceeding.
1316.32  Notice of proceeding; time and place.
1316.33  Conduct of proceeding.
1316.34  Records of proceeding.

                   Subpart D--Administrative Hearings

1316.41  Scope of Subpart D.
1316.42  Definitions.
1316.43  Information; special instructions.
1316.44  Waiver or modification of rules.
1316.45  Filings; address; hours.
1316.46  Inspection of record.
1316.47  Request for hearing.
1316.48  Notice of appearance.
1316.49  Waiver of hearing.
1316.50  Appearance; representation; authorization.
1316.51  Conduct of hearing and parties; ex parte communications.
1316.52  Presiding officer.
1316.53  Time and place of hearing.
1316.54  Prehearing conference.
1316.55  Prehearing ruling.
1316.56  Burden of proof.
1316.57  Submission of documentary evidence and affidavits and 
          identification of witnesses subsequent to prehearing 
          conference.
1316.58  Summary of testimony; affidavits.
1316.59  Submission and receipt of evidence.
1316.60  Objections; offer of proof.
1316.61  Exceptions to rulings.
1316.62  Appeal from ruling of presiding officer.
1316.63  Official transcript; index; corrections.
1316.64  Proposed findings of fact and conclusions of l`w.
1316.65  Report and record.
1316.66  Exceptions.
1316.67  Final order.
1316.68  Copies of petitions for judicial review.

       Subpart E--Seizure, Forfeiture, and Disposition of Property

1316.71  Definitions.
1316.72  Officers who will make seizures.

[[Page 240]]

1316.73  Custody and other duties.
1316.74  Appraisement.
1316.75  Advertisement.
1316.76  Requirements as to claim and bond.
1316.77  Administrative forfeiture.
1316.78  Judicial forfeiture.
1316.79  Petitions for remission or mitigation of forfeiture.
1316.80  Time for filing petitions.
1316.81  Handling of petitions.

    Subpart F--Expedited Forfeiture Proceedings for Certain Property

1316.90  Purpose and scope.
1316.91  Definitions.
1316.92  Petition for expedited release in an administrative forfeiture 
          action.
1316.93  Ruling on petition for expedited release in an administrative 
          forfeiture action.
1316.94  Posting of substitute res in an administrative forfeiture 
          action.
1316.95  Petition for expedited release of a conveyance in a judicial 
          forfeiture action.
1316.96  Ruling on a petition for expedited release of a conveyance in a 
          judicial forfeiture action.
1316.97  Initiating judicial forfeiture proceeding against a conveyance 
          within 60 days of the filing of a claim and cost bond.
1316.98  Substitute res bond in a judicial forfeiture action againrt a 
          conveyance.
1316.99  Notice provisions.

    Source: 36 FR 7820, Apr. 24, 1971, unless otherwise noted. 
Redesignated at 38 FR 26609, Sept. 24, 1973.



                  Subpart A--Administrative Inspections

    Authority: 21 U.S.C. 822(f), 830(a), 871(b), 880, 958(f), 965.



Sec. 1316.01   Scope of Subpart A.

    Procedures regarding administrative inspections and warrants 
pursuant to sections 302(f), 510, 1008(d), and 1015 of the Act (21 
U.S.C. 822(f), 880, 958(d), and 965) are governed generally by those 
sections and specifically by the sections of this subpart.



Sec. 1316.02   Definitions.

    As used in this subpart, the following terms shall have the meanings 
specified:
    (a) The term Act means the Controlled Substances Act (84 Stat. 1242; 
21 U.S.C. 801) and/or the Controlled Substances Import and Export Act 
(84 Stat. 1285; 21 U.S.C. 951).
    (b) The term Administration means the Drug Enforcement 
Administration.
    (c) The term controlled premises means--(1) Places where original or 
other records or documents required under the Act are kept or required 
to be kept, and
    (2) Places, including factories, warehouses, or other establishments 
and conveyances, where persons registered under the Act or exempted from 
registration under the Act, or regulated persons may lawfully hold, 
manufacture, or distribute, dispense, administer, or otherwise dispose 
of controlled substances or listed chemicals or where records relating 
to those activities are maintained.
    (d) The term Administrator means the Administrator of the 
Administration. The Administrator has been delegated authority under the 
Act by the Attorney General (28 CFR 0.100).
    (e) The term inspector means an officer or employee of the 
Administration authorized by the Administrator to make inspections under 
the Act.
    (f) The term register and registration refer to registration 
required and permitted by sections 303 and 1008 of the Act (21 U.S.C. 
823 and 958).
    (g) Any term not defined in this section shall have the definition 
set forth in sections 102 and 1001 of the Act (21 U.S.C. 802 and 951).

[36 FR 7820, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
as amended at 60 FR 32465, June 22, 1995; 60 FR 36334, July 14, 1995]



Sec. 1316.03   Authority to make inspections.

    In carrying out his functions under the Act, the Administrator, 
through his inspectors, is authorized in accordance with sections 510 
and 1015 of the Act (21 U.S.C. 880 and 965) to enter controlled premises 
and conduct administrative inspections thereof, for the purpose of:
    (a) Inspecting, copying, and verifying the correctness of records, 
reports, or other documents reqtired to be kept or made under the Act 
and regulations promulgated under the Act, including, but not limited 
to, inventory and other records required to be kept pursuant to part 
1304 of this chapter, order form

[[Page 241]]

records required to be kept pursuant to part 1305 of this chapter, 
prescription and distribution records required to be kept pursuant to 
part 1306 of this chapter, records of listed chemicals, tableting 
machines, and encapsulating machines required to be kept pursuant to 
part 1310 of this chapter, import/export records of listed chemicals 
required to be kept pursuant to part 1313 of this chapter, shipping 
records identifying the name of each carrier used and the date and 
quantity of each shipment, and storage records identifying the name of 
each warehouse used and the date and quantity of each storage.
    (b) Inspecting within reasonable limits and to a reasonable manner 
all pertinent equipment, finished and unfinished controlled substances, 
listed chemicals, and other substances or materials, containers, and 
labeling found at the controlled premises relating to this Act;
    (c) Making a physical inventory of all controlled substances and 
listed chemicals on-hand at the premises;
    (d) Collecting samples of controlled substances or listed chemicals 
(in the event any samples are collected during an inspection, the 
inspector shall issue a receipt for such samples on DEA Form 84 to the 
owner, operator, or agent in charge of the premises);
    (e) Checking of records and information on distribution of 
controlled substances or listed chemicals by the registrant or regulated 
person (i.e., has the distribution of controlled substances or listed 
chemicals increased markedly within the past year, and if so why);
    (f) Except as provided in Sec. 1316.04, all other things therein 
(including records, files, papers, processes, controls and facilities) 
appropriate for verification of the records, reports, documents referred 
to above or otherwise bearing on the provisions of the Act and the 
regulations thereunder.

[36 FR 7820, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 51 FR 5319, Feb. 13, 1986; 55 FR 50827, Dec. 11, 1990; 60 
FR 32465, June 22, 1995]



Sec. 1316.04   Exclusion from inspection.

    (a) Unless the owner, operator or agent in charge of the controlled 
premises so consents in writing, no inspection authorized by these 
regulations shall extend to:
    (1) Financial data:
    (2) Sales data other than shipping data; or
    (3) Pricing data.



Sec. 1316.05   Entry.

    An inspection shall be carried out by an inspector. Any such 
inspector, upon (a) stating his purpose and (b) presenting to the owner, 
operator or agent in charge of the premises to be inspected (1) 
appropriate credentials, and (2) written notice of his inspection 
authority under Sec. 1314.06 of this chapter, and (c) receiving informed 
consent under Sec. 1316.08 or through the use of administrative warrant 
issued under Secs. 1316.09-1316.14, shall have the right to enter such 
premises and conduct inspections at reasonable times and in a reasonable 
manner.

[36 FR 7820, Apr. 24, 1971, as amended at 36 FR 13387, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, l973]



Sec. 1316.06   Notice of inspection.

    The notice of inspection (DEA (or DNB) Form 82) shall contain:
    (a) The name and title of the owner, operator, or agent in charge of 
the controlled premises;
    (b) The controlled premises name;
    (c) The address of the controlled premises to be inspected;
    (d) The date and time of the inspection;
    (e) A statement that a notice of inspection is given pursuant to 
section 510 of the Act (21 U.S.C. 880);
    (f) A reproduction of the pertinent parts of section 510 of the Act; 
and
    (g) The signature of the inspector.



Sec. 1316.07   Requirement for administrative inspection warrant; exceptions.

    In all cases where an inspection is contemplated, an administrative 
inspection warrant is required pursuant to section 510 of the Act (21 
U.S.C. 880), except that such warrant shall not be required for 
establishments applying for initial registration under the Act, for the 
inspection of books and records pursuant to an administrative subpoena 
issued in accordance with section 506 of the Act (21 U.S.C. 876) nor

[[Page 242]]

for entries in administrative inspections (including seizures of 
property):
    (a) With the consent of the owner, operator, or agent in charge of 
the controlled premises as set forth in Sec. 1316.08;
    (b) In situations presenting imminent danger to health or safety;
    (c) In situations involving inspection of conveyances where there is 
reasonable cause to obtain a warrant;
    (d) In any other exceptional or emergency circumstance or time or 
opportunity to apply for a warrant is lacking; or
    (e) In any other situations where a warrant is not constitutionally 
required.



Sec. 1316.08   Consent to inspection.

    (a) An administrative inspection warrant shall not be required if 
informed consent is obtained from the owner, operator, or agent in 
charge of the controlled premises to be inspected.
    (b) Wherever possible, informed consent shall consist of a written 
statement signed by the owner, operator, or agent in charge of the 
premises to be inspected and witnessed by two persons. The written 
consent shall contain the following information:
    (1) That he (the owner, operator, or agent in charge of the 
premises) has been informed of his constitutional right not to have an 
administrative inspection made without an administrative inspection 
warrant;
    (2) That he has right to refuse to consent to such an inspection;
    (3) That anything of an incriminating nature which may be found may 
be seized and used against him in a criminal prosecution;
    (4) That he has been presented with a notice of inspection as set 
forth in Sec. 1316.06;
    (5) That the consent is given by him is voluntary and without 
threats of any kind; and
    (6) That he may withdraw his consent at any time during the course 
of inspection.
    (c) The written consent shall be produced in duplicate and be 
distributed as follows:
    (1) The original will be retained by the inspector; and
    (2) The duplicate will be given to the person inspected.

[36 FR 7820, Apr. 24, 1971, as amended at 37 FR 15924, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1316.09   Application for administrative inspection warrant.

    (a) An administrative inspection warrant application shall be 
submitted to any judge of the United States or of a State court of 
record, or any United States magistrate and shall contain the following 
information:
    (1) The name and address of the controlled premises to be inspected;
    (2) A statement of statutory authority for the administrative 
inspection warrant, and that the fact that the particular inspection in 
question is designed to insure compliance with the Act and the 
regulations promulgated thereunder;
    (3) A statement relating to the nature and extent of the 
administrative inspection, including, where necessary, a request to 
seize specified items and/or to collect samples of finished or 
unfinished controlled substances or listed chemicals;
    (4) A statement that the establishment either:
    (i) Has not been previously inspected, or
    (ii) Was last inspected on a particular date.
    (b) The application shall be submitted under oath to an appropriate 
judge or magistrate.

[36 FR 7820, Apr. 24, 1971, as amended at 36 FR 13387, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973; 60 FR 32466, June 22, 1995]



Sec. 1316.10   Administrative probable cause.

    If the judge or magistrate is satisfied that ``administrative 
probable cause,'' as defined in section 510(d)(1) of the Act (21 U.S.C. 
880(d)(1)) exists, he shall issue an administrative warrant. 
Administrative probable cause shall not mean criminal probable cause as 
defined by Federal statute or case law.



Sec. 1316.11   Execution of warrants.

    An administrative inspection warrant shall be executed and returned 
as

[[Page 243]]

required by, and any inventory or seizure made shall comply with the 
requirements of, section 510(d) (3) of the Act (21 U.S.C. 880(d)(3)). 
The inspection shall begin as soon as is practicable after the issuance 
of the administrative inspection warrant and shall be completed with 
reasonable promptness. The inspection shall be conducted during regular 
business hours and shall be completed in a reasonable manner.



Sec. 1316.12   Refusal to allow inspection with an administrative warrant.

    If a registrant or any person subject to the Act refuses to permit 
execution of an administrative warrant or impedes the inspector in the 
execution of that warrant, he shall be advised that such refusal or 
action constitutes a violation of section 402(a)(6) of the Act (21 
U.S.C. (a)(6)). If he persists and the circumstances warrant, he shall 
be arrested and the inspection shall commence or continue.



Sec. 1316.13   Frequency of administrative inspections.

    Except where circumstances otherwise dictate, it is the intent of 
the Administration to inspect all manufacturers of controlled substances 
listed in Schedules I and II and distributors of controlled substances 
listed in Schedule I once each year; and to inspect all distributors of 
controlled substances listed in Schedules II through V and manufacturers 
of controlled substances listed in schedules III through V once every 3 
years.



       Subpart B--Protection of Researchers and Research Subjects

    Authority: 21 U.S.C. 830, 871(b).



Sec. 1316.21  Definitions.

    As used in this part, the following terms shall have the meanings 
specified:
    (a) The term investigative personnel includes managers, Diversion 
Investigators, attorneys, analysts and support personnel employed by the 
Drug Enforcement Administration who are involved in the processing, 
reviewing and analyzing of declarations and other relevant documents or 
data relative to regulated transactions or are involved in conducting 
investigations initiated pursuant to the receipt of such declarations, 
documents or data.
    (b) The term law enforcement personnel means Special Agents employed 
by the Drug Enforcement Administration who, in the course of their 
official duties, gain knowledge of information which is confidential 
under such section.

[54 FR 31670, Aug. 1, 1989]



Sec. 1316.22  Exemption.

    (a) Any person who is aggrieved by a disclosure of information in 
violation of subsection (c)(1) of Section 310 of the Controlled 
Substances Act (21 U.S.C. 830) may bring a civil action against the 
violator for appropriate relief.
    (b) Notwithstanding the provision of paragraph (a), a civil action 
may not be brought under such paragraph against investigative or law 
enforcement personnel of the Drug Enforcement Administration.


[54 FR 31670, Aug. 1, 1989]



Sec. 1316.23   Confidentiality of identity of research subjects.

    (a) Any person conducting a bona fide research project directly 
related to the enforcement of the laws under the jurisdiction of the 
Attorney General concerning drugs or other substances which are or may 
be subject to control under the Controlled Substances Act (84 Stat. 
1242; 21 U.S.C. 801) who intends to maintain the confidentiality of the 
identity of those persons who are the subjects of such research may 
petition the Administrator of the Drug Enforcement Administration for a 
grant of confidentiality: Providing, That:
    (1) The Attorney General is authorized to carry out such research 
under the provisions of Section 502(a) (2-6) of the Controlled 
Substances Act of 1970 (21 U.S.C. 872(a) (2-6)); and the research is 
being conducted with funds provided in whole or part by the Department 
of Justice; or
    (2) The research is of a nature that the Attorney General would be 
authorized to carry out under the provisions of Section 502(a) (2-6) of 
the Controlled Substances Act (21 U.S.C. 872(a) (2-6),

[[Page 244]]

and is being conducted with funds provided from sources outside the 
Department of Justice.
    (b) All petitions for Grants of Confidentiality shall be addressed 
to the Administrator, Drug Enforcement Administration, 1405 I Street 
NW., Washington, DC 20537, and shall contain the following:
    (1) A statement as to whether the research protocol requires the 
manufacture, production, import, export, distribution, dispensing, 
administration, or possession of controlled substances, and if so the 
researcher's registration number or a statement that an application for 
such registration has been submitted to DEA;
    (2) The location of the research project;
    (3) The qualifications of the principal investigator;
    (4) A general description of the research or a copy of the research 
protocol;
    (5) The source of funding for the research project;
    (6) A statement as to the risks posed to the research subjects by 
the research procedures and what protection will be afforded to the 
research subjects;
    (7) A statement as to the risks posed to society in general by the 
research procedures and what measures will be taken to protect the 
interests of society;
    (8) A specific request to withhold the names and/or any other 
identifying characteristics of the research subjects; and
    (9) Statements establishing that a grant of confidentiality is 
necessary to the successful completion of the research project.
    (c) The grant of confidentiality of identity of research subjects 
shall consist of a letter issued by the Administrator, which shall 
include:
    (1) The researcher's name and address.
    (2) The researcher's registration number, if applicable.
    (3) The title and purpose of the research.
    (4) The location of the research project.
    (5) An authorization for all persons engaged in the research to 
withhold the names and identifying characteristics of persons who are 
the subjects of such research, stating that persons who obtain this 
authorization may not be compelled in any Federal, State, or local 
civil, criminal, administrative, legislative, or other proceeding to 
identify the subjects of such research for which this authorization was 
obtained.
    (6) The limits of this authorization, if any.
    (7) A statement to the effect that the grant of confidentiality of 
identity of research subjects shall be perpetual but shall pertain only 
to the subjects of the research described in the research protocol, the 
description of the research submitted to DEA, or as otherwise 
established by DEA.
    (d) Within 30 days of the date of completion of the research 
project, the researcher shall so notify the Administrator. The 
Administrator shall issue another letter including the information 
required in paragraph (c) of this section and stating the starting and 
finishing dates of the research for which the confidentiality of 
identity of research subjects was granted; upon receipt of this letter, 
the research shall return the original letter of exemption.

[42 FR 54946, Oct. 12, 1977. Redesignated at 54 FR 31670, Aug. 1, 1989]



Sec. 1316.24  Exemption from prosecution for researchers.

    (a) Upon registration of an individual to engage in research in 
controlled substances under the Controlled Substances Act (84 Stat. 
1242; 21 U.S.C. 801), the Administrator of the Drug Enforcement 
Administration, on his own motion or upon request in writing from the 
Secretary or from the researcher or researching practitioner, may exempt 
the registrant when acting within the scope of his registration, from 
prosecution under Federal, State, or local laws for offenses relating to 
possession, distribution or dispensing of those controlled substances 
within the scope of his exemption. However, this exemption does not 
diminish any requirement of compliance with the Federal Food, Drug and 
Cosmetic Act (21 U.S.C. 301).

[[Page 245]]

    (b) All petitions for Grants of Exemption from Prosecution for the 
Researcher shall be addressed to the Administrator, Drug Enforcement 
Administration, 1405 I Street NW., Washington, DC 20537 and shall 
contain the following:
    (1) The researcher's registration number if any, for the project;
    (2) The location of the research project;
    (3) The qualifications of the principal investigator;
    (4) A general description of the research or a copy of the research 
protocol;
    (5) The source of funding for the research project;
    (6) A statement as to the risks posed to the research subjects by 
the research procedures and what protection will be afforded to the 
research subjects;
    (7) A statement as to the risks posed to society in general by the 
research procedures and what measures will be taken to protect the 
interests of society;
    (8) A specific request for exemption from prosecution by Federal, 
State, or local authorities for offenses related to the possession, 
distribution, and dispensing of controlled substances in accord with the 
procedures described in the research protocol;
    (9) A statement establishing that a grant of exemption from 
prosecution is necessary to the successful completinn of the research 
project.
    (c) Any researcher or practitioner proposing to engage in research 
requesting both exemption from prosecution and confidentiality of 
identity of research subjects may submit a single petition incorporating 
the information required in Sec. Sec. 1316.21(b) and 1316.22(b).
    (d) The exemption shall consist of a letter issued by the 
Administrator, which shall include:
    (1) The researcher's name and address;
    (2) The researcher's registration number for the research project;
    (3) The location of the research project;
    (4) A concise statement of the scope of the researcher's 
registration;
    (5) Any limits of the exemption; and
    (6) A statement that the exemption shall apply to all acts done in 
the scope of the exemption while the exemption is in effect. The 
exemption shall remain in effect until completion of the research 
project or until the registration of the researcher is either revoked or 
suspended or his renewal of registration is denied. However, the 
protection afforded by the grant of exemption from prosecution during 
the research period shall be perpetual.
    (e) Within 30 days of the date of completion of the research 
project, the researcher shall so notify the Administrator. The 
Administrator shall issue another letter including the information 
required in paragraph (d) of this section and stating the date of which 
the period of exemption concluded; upon receipt of this letter the 
researcher shall return the original letter of exemption.

[42 FR 54946, Oct. 12, 1977. Redesignated at 54 FR 31670, Aug. 1, 1989]



                   Subpart C--Enforcement Proceedings

    Authority: 21 U.S.C. 871(b), 883.



Sec. 1316.31   Authority for enforcement proceeding.

    A hearing may be ordered or granted by any Special Agent in Charge 
of the Drug Enforcement Administration, at his discretion, to permit any 
person against whom criminal and/or civil action is contemplated under 
the Controlled Substances Act (84 Stat. 1242; 21 U.S.C. 801) or the 
Controlled Substances Import and Export Act (84 Stat. 1285; 21 U.S.C. 
951) an opportunity to present his views and his proposals for bringing 
his alleged violations into compliance with the law. Such hearing will 
also permit him to show cause why prosecution should not be instituted, 
or to present his views on the contemplated proceeding.

[36 FR 7820, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 47 FR 41735, Sept. 22, 1982]



Sec. 1316.32   Notice of proceeding; time and place.

    Appropriate notice designating the time and place for the hearing 
shall be given to the person. Upon request,

[[Page 246]]

timely and properly made, by the person to whom notice has been given, 
the time or place of the hearing, or both, may be changed if the request 
states reasonable grounds for such change. Such request shall be 
addressed to the Special Agent in Charge who issued the notice.

[36 FR 7820, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 47 FR 41735, Sept. 22, 1982]



Sec. 1316.33   Conduct of proceeding.

    Presentation of views at a hearing under this subpart shall be 
private and informal. The views presented shall be confined to matters 
relevant to bringing violations into compliance with the Act or to other 
contemplated proceedings under the Act. These views may be presented 
orally or in writing by the person to whom the notice was given, or by 
his authorized representative.



Sec. 1316.34   Records of proceeding.

    A formal record, either verbatim or summarized, of the hearing may 
be made at the discretion of the Special Agent in Charge. If a verbatim 
record is to be made, the person attending the hearing will be so 
advised prior to the start of the hearing.

[37 FR 15924, Aug. 8, 1972. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 47 FR 41735, Sept. 22, 1982]



                   Subpart D--Administrative Hearings

    Authority: 21 U.S.C. 811, 812, 871(b), 875, 958(d), 965.



Sec. 1316.41   Scope of Subpart D.

    Procedures in any administrative hearing held under the Act are 
governed generally by the rule making and/or adjudication procedures set 
forth in the Administrative Procedure Act (5 U.S.C. 551-559) and 
specifically by the procedures set forth in this subpart, except where 
more specific regulations (set forth in Secs. 1301.51-1301.57, 
Secs. 1303.41-1303.47, Secs. 1308.41-1308.51, Secs. 1311.51-1311.53, or 
Secs. 1312.41-1312.47) apply.

[36 FR 7820, Apr. 24, 1971, as amended at 37 FR 15924, Aug. 8, 1972. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1316.42   Definitions.

    As used in this subpart, the following terms shall have the meanings 
specified:
    (a) The term Act means the Controlled Substances Act (84 Stat. 1242; 
21 U.S.C. 801) and/or the Controlled Substances Import and Export Act 
(84 Stat. 1285; 21 U.S.C. 951).
    (b) The term Administrator means the Administrator of the 
Administration. The Administrator has been delegated authority under the 
Act by the Attorney General (28 CFR 0.100).
    (c) The term hearing means any hearing held pursuant to the Act.
    (d) The term Hearing Clerk means the hearing clerk of the 
Administration.
    (e) The term person includes an individual, corporation, government 
or governmental subdivision or agency, business trust, partnership, 
association or other legal entitx.
    (f) The term presiding officer means an administrative law judge 
qualified and appointed as provided in the Administrative Procedure Act 
(5 U.S.C. 556).
    (g) The term proceeding means all actions involving a hearing, 
colmencing with the publication by the Administrator of the notice of 
proposed rule making or the issuance of an order to show cause.
    (h) Any term not defined in this section shall have the definition 
set forth in section 102 of the Act (21 U.S.C. 802) and in Sec. 1301.02 
of this chapter.

[36 FR 7820, Apr. 24, 1971, as amended at 38 FR 757, Jan. 4, 1973. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1316.43   Information; special instructions.

    Information regarding procedure under these rules and instructions 
supplementing these rules in special instances will be furnished by the 
Hearing Clerk upon request.



Sec. 1316.44   Waiver or modification of rules.

    The Administrator or the presiding officer (with respect to matters 
pending before him) may modify or waive any rule in this subpart by 
notice in advance of the hearing, if he determines that no party in the 
hearing will be unduly prejudiced and the ends of

[[Page 247]]

justice will thereby be served. Such notice of modification or waiver 
shall be made a part of the record of the hearing.



Sec. 1316.45   Filings; address; hours.

    Documents required or permitted to be filed in, and correspondence 
relating to, hearhngs governed by the regulations in this chapter shall 
be filed with the Hearing Clerk, Drug Enforcement Administration, 
Department of Justice, Washington, DC 20537. This office is open Monday 
through Friday from 8:30 a.m. to 5 p.m. eastern standard or daylight 
saving time, whichever is effective in the District of Columbia at the 
time, except on national legal holidays. Documents shall be dated and 
deemed filed upon receipt by the Hearing Clerk.

[36 FR 7820, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 55 FR 27464, July 3, 1990]



Sec. 1316.46   Inspection of record.

    (a) The record bearing on any proceeding, except for material 
described in subsection (b) of this section, shall be available for 
inspection and copying by any person entitled to participate in such 
proceeding, during office hours in the office of the Hearing Clerk, Drug 
Enforcement Administration, Department of Justice, Washington, DC 20537.
    (b) The following material shall not be available for inspection as 
part of the record:
    (1) A research protocol filed with an application for registration 
to conduct research with controlled substances listed in Schedule I, 
pursuant to Sec. 1301.32 (a) (3) of this chapter, if the applicant 
requests that the protocol be kept confidential;
    (2) An outline of a production or manufacturing process filed with 
an application for registration to manufacture a new narcotic controlled 
substance, pursuant to Sec. 1301.33 of this chapter, if the applicant 
requests that the outline be kept confidential;
    (3) Any confidential or trade secret information disclosed in 
conjunction with an application for registration, or in reports filed 
while registered, or acquired in the course of an investigation, 
entitled to protection under subsection 402(a) (8) of the Act (21 U.S.C. 
842(a) (8)) or any other law restricting public disclosure of 
information; and
    (4) Any material contained in any investigatory report, memorandum, 
or file, or case report compiled by the Administration.



Sec. 1316.47   Request for hearing.

    (a) Any person entitled to a hearing and desiring a hearing shall, 
within the period permitted for filing, file a request for a hearing in 
the following form:

------------ (Date)

Administrator, Drug Enforcement Administration, United States Department 
of Justice, Washington, DC 20537, Attention: DEA Federal Register 
Representative.

    Dear Sir: The undersigned -------------------- (Name of person) 
hereby requests a hearing in the matter of: ------------------------ 
(Identification of the proceeding).
    (A) (State with particularity the interest of the person in the 
proceeding.)
    (B) (State with particularity the objections or issues, if any, 
concerning which the person desires to be heard.)
    (C) (State briefly the position of the person with regard to the 
particular objections or issues.)
    All notices to be sent pursuant to the proceeding should be 
addressed to:
_______________________________________________________________________

                                 (Name)

_______________________________________________________________________

                            (Street address)

_______________________________________________________________________

                            (City and State)

    Respectfully yours,
_______________________________________________________________________

                          (Signature of person)

    (b) The Administrative Law Judge, upon request and showing of good 
cause, may grant a reasonable extension of the time allowed for response 
to an Order to Show Cause.

[36 FR 7820, Apr. 24, 1971, as amended at 36 FR 13387, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]

    Editorial Note: For FR citations affecting Sec. 1316.47, see the 
List of CFR Sections Affected in the Finding Aids section of this 
volume.

[[Page 248]]



Sec. 1316.48   Notice of appearance.

    Any person entitled to a hearing and desiring to appear in any 
hearing, shall, if he has not filed a request for hearing, file within 
the time specified in the notice of proposed rule making, a written 
notice of appearance in the following form:

------------ (Date)

Administrator, Drug Enforcement Administration, United States Department 
of Justice, Washington, DC 20537, Attention: DEA Federal Register 
Representative.

    Dear Sir: Please take notice that -------------------- (Name of 
person) will appear in the matter of: ------------------------ 
(Identification of the proceeding).
    (A) (State with particularity the interest of the person in the 
proceeding.)
    (B) (State with particularity the objections or issues, if any, 
concerning which the person desires to be heard.)
    (C) (State briefly the position of the person with regard to the 
particular objections or issues.)
    All notices to be sent pursuant to this appearance should be 
addressed to:
_______________________________________________________________________

                                 (Name)

_______________________________________________________________________

                            (Street address)

_______________________________________________________________________

                            (City and State)

    Respectfully yours,
_______________________________________________________________________

                          (Signature of person)

[36 FR 7820, Apr. 24, 1971, as amended at 36 FR 13387, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 40 FR 57210, 
Dec. 8, 1975]



Sec. 1316.49   Waiver of hearing.

    Any person entitled to a hearing may, within the period permitted 
for filing a request for hearing or notice of appearance, waiver of an 
opportunity for a hearing, together with a written statement regarding 
his position on the matters of fact and law involved in such hearing. 
Such statement, if admissible, shall be made a part of the record and 
shall be considered in light of the lack of opportunity for crors-
examination in determining the weight to be attached to matters of fact 
asserted therein.



Sec. 1316.50   Appearance; representation; authorization.

    Any person entitled to appear in a hearing may appear in person or 
by a representative in any proceeding or hearing and may be heard with 
respect to matters relevant to the issues under consideration. A 
representative must either be an employee of the person or an attorney 
at law who is a member of the bar, in good standing, of any State, 
territory, or the District of Columbia, and admitted to practice before 
the highest court of that jurisdiction. Any representative may be 
required by the Administrator or the presiding officer to present a 
notarized power of attorney showing his authority to act in such 
representative capacity and/or an affidavit or certificate of admission 
to practice.

[36 FR 7820, Apr. 24, 1971, as amended at 36 FR 13387, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1316.51   Conduct of hearing and parties; ex parte communications.

    (a) Hearings shall be conducted in an informal but orderly manner in 
accordance with law and the directions of the presiding officer.
    (b) Participants in any hearing and their representatives, whether 
or not members of the bar, shall conduct themselves in accordance with 
judicial standards of practice and ethics and the directions of the 
presiding officer. Refusal to comply with this section shall constitute 
grounds for immediate exclusion from any hearing.
    (c) If any official of the Administration is contacted by any 
individual in private or public life concerning any substantive matter 
which is the subject of any hearing, at any time after the date on which 
the proceedings commence, the official who is contacted shall prepare a 
memorandum setting forth the substance of the conversation and shall 
file this memorandum in the appropriate public docket file. The 
presiding officer and employees of the Administration shall comply with 
the requirements of 5 U.S.C. 554(d) regarding ex parte communications 
and participation in any hearing.

[[Page 249]]



Sec. 1316.52   Presiding officer.

    A presiding officer, designated by the Administrator, shall preside 
over all hearings. The functions of the presiding officer shall commence 
upon his designation and terminate upon the certification of the record 
to the Administrator. The presiding officer shall have the duty to 
conduct a fair hearing, to take all necessary action to avoid delay, and 
to maintain order. He shall have all powers necessary to these ends, 
including (but not limited to) the power to:
    (a) Arrange and change the date, time, and place of hearings (other 
than the time and place prescribed in Sec. 1301.60) and prehearing 
conferences and issue notice thereof.
    (b) Hold conferences to settle, simplify, or determine the issues in 
a hearing, or to consider other matters that may aid in the expeditious 
disposition of the hearing.
    (c) Require parties to state their position in writing with respect 
to the various issues in the hearing and to exchange such statements 
with all other parties.
    (d) Sign and issue subpoenas to compel the attendance of witnesses 
and the production of documents and materials to the extent necessary to 
conduct administrative hearings pending before him.
    (e) Examine witnesses and direct witnesses to testify.
    (f) Receive, rule on, exclude, or limit evidence.
    (g) Rule on procedural items pending before him.
    (h) Take any action permitted to the presiding officer as authorized 
by this part or by the provisions of the Administrative Procedure Act (5 
U.S.C. 551-559).

[36 FR 7820, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 42 FR 57457, Nov. 3, 1977]



Sec. 1316.53   Time and place of hearing.

    The hearing will commence at the place and time designated in the 
notice of hearing published in the Federal Register but thereafter it 
may be moved to a different place and may be continued from day to day 
or recessed to a later day without notice other than announcement 
thereof by the presiding officer at the hearing.



Sec. 1316.54   Prehearing conference.

    The presiding officer on his own motion, or on the motion of any 
party for good cause shown, may direct all parties to appear at a 
specified time and place for a conference for:
    (a) The simplification of the issues.
    (b) The possibility of obtaining stipulations, admission of facts, 
and documents.
    (c) The possibility of limiting the number of expert witnesses.
    (d) The identification and, if practicable, the scheduling of all 
witnesses to be called.
    (e) The advance submission at the prehearing conference of all 
documentary evidence and affidavits to be marked for identification.
    (f) Such other matters as may aid in the expeditious disposition of 
the hearing.



Sec. 1316.55   Prehearing ruling.

    The presiding officer may have the prehearing conference reported 
verbatim and shall make a ruling reciting the action taken at the 
conference, the agreements made by the partier, the schedule of 
witnesses, and a statement of the issues for hearing. Such ruling shall 
control the subsequent course of the hearing unless modified by a 
subsequent ruling.



Sec. 1316.56   Burden of proof.

    At any hearing, the proponent for the issuance, amendment, or repeal 
of any rule shall have the burden of proof.



Sec. 1316.57   Submission of documentary evidence and affidavits and identification of witnesses subsequent to prehearing conference.

    All documentary evidence and affidavits not submitted and all 
witnesses not identified at the prehearing conference shall be submitted 
or identified to the presiding officer as soon as possible, with a 
showing that the offering party had good cause for failing to so submit 
or identify at the prehearing conference. If the presiding officer 
determines that good cause does exist, the documents or affidavits shall 
be submitted or witnesses identified to all

[[Page 250]]

parties sufficiently in advance of the offer of such documents or 
affidavits or witnesses at the hearing to avoid prejudice or surprise to 
the other parties. If the presiding officer determines that good cause 
does not exist, he may refuse to admit as evidence such documents or 
affidavits or the testimony of such witnesses.



Sec. 1316.58   Summary of testimony; affidavits.

    (a) The presiding officer may direct that summaries of the direct 
testimony of witnesses be prepared in writing and served on all parties 
in advance of the hearing. Witnesses will not be permitted to read 
summaries of their testimony into the record and all witnesses shall be 
available for cross-examination. Each witness shall, before proceeding 
to testify, be sworn or make affirmation.
    (b) Affidavits submitted at the prehearing conference or pursuant to 
Sec. 1316.57 with good cause may be examined by all parties and opposing 
affidavits may be submitted to the presiding officer within a perhod of 
time fixed by him. Affidavits admitted into evidence shall be considered 
in light of the lack of opportunity for cross-examination in determining 
the weight to be attached to statements made therein.

[36 FR 7820, Apr. 24, 1971, as amended at 36 FR 13387, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973]



Sec. 1316.59   Submission and receipt of evidence.

    (a) The presiding officer shall admit only evidence that is 
competent, relevant, material and not unduly repetitious.
    (b) Opinion testimony shall be admitted when the presiding officer 
is satisfied that the witness is properly qualified.
    (c) The authenticity of all documents submitted in advance shall be 
deemed admitted unless written objection thereto is filed with the 
presiding officer, except that a party will be permitted to challenge 
such authenticity at a later time upon a showing of good cause for 
failure to have filed such written objection.
    (d) Samples, if otherwise admissible into evidence, may be displayed 
at the hearing and may be described for purposes of the record, or may 
be admitted in evidence as exhibits.
    (e) Where official notice is taken or is to be taken of a material 
fact not appearing in the evidence of record, any party, on timely 
request, shall be afforded opportunity to controvert such fact.
    (f) The presiding officer shall file as exhibits copies of the 
folloving documents:
    (1) The order to show cause or notice of hearing;
    (2) Any notice of waiver or modification of rules made pursuant to 
Sec. 1316.44 or otherwise;
    (3) Any waiver of hearing (together with any statement filed 
therewith) filed pursuant to Sec. 1316.49 or otherwise;
    (4) The prehearing ruling, if any, made pursuant to Sec. 1316.55;
    (5) Any other document necessary to show the basis for the hearing.



Sec. 1316.60   Objections; offer of proof.

    If any party in the hearing objects to the admission or rejection of 
any evidence or to other limitation of the scope of any examination or 
cross-examination, he shall state briefly the grounds for such objection 
without extended argument or debate thereon except as permitted by the 
presiding officer. A ruling of the presiding officer on any such 
objection shall be a part of the transcript together with such offer of 
proof as has been made if a proper foundation has been laid for its 
admission. An offer of proof made in connection with an objection taken 
to any ruling of the presiding officer rejecting or excluding proffered 
oral testimony shall consist of a statement of the substance of the 
evidence which the party contends would be adduced by such testimony; 
and, if the excluded evidence consists of evidence in documentary or 
written form a copy of such evidence shall be marked for identification 
and shall accompany the records as the offer of proof.



Sec. 1316.61   Exceptions to rulings.

    Exceptions to rulings of the presiding officer are unnecessary. It 
is sufficient that a party, at the time the ruling of the presiding 
officer is sought, makes knovn the action that he desires the

[[Page 251]]

presiding officer to take, or his objection to an action taken, and his 
grounds therefor.



Sec. 1316.62   Appeal from ruling of presiding officer.

    Rulings of the presiding officer may not be appealed to the 
Administrator prior to his consideration of the entire hearing, except 
with the consent of the presiding officer and where he certifies on the 
record or in writing that the allowance of an interlocutory appeal is 
clearly necessary to prevent exceptional delay, expense, or prejudice to 
any party or substantial detriment to the public interest. If an appeal 
is allowed, any party in the hearing may file a brief in quintuplicate 
with the Administrator within such period that the presiding officer 
directs. No oral argument will be heard unless the Administrator directs 
otherwise.



Sec. 1316.63   Official transcript; index; corrections.

    (a) Testimony given at a hearing shall be reported verbatim. The 
Administration will make provision for a stenographic record of the 
testimony and for such copies of the transcript thereof as it requires 
for its own purpose.
    (b) At the close of the hearing, the presiding officer shall afford 
the parties and witnesses time (not longer than 30 days, except in 
unusual cases) in which to submit written proposed corrections of the 
transcript, pointing out errors that may have been made in transcribing 
the testimony. The presiding officer shall promptly thereafter order 
such corrections made as in his judgment are required to make the 
transcript conform to the testimony.

[36 FR 7820, Apr. 24, 1971, as amended at 36 FR 13387, July 21, 1971. 
Redesignated at 38 FR 26609, Sept. 24, 1973, and amended at 50 FR 2046, 
Jan. 15, 1985]



Sec. 1316.64   Proposed findings of fact and conclusions of law.

    Any party in the hearing may file in quintuplicate proposed findings 
of fact and conclusions of law within the time fixed by the presiding 
officer. Any party so filing shall also serve one copy of his proposed 
findings and conclusion upon each other party in the hearing. The party 
shall include a statement of supporting reasons for the proposed 
findings and conclusions, together with evidence of record (including 
specific and complete citations of the pages of the transcript and 
exhibits) and citations of authorities relied upon.



Sec. 1316.65   Report and record.

    (a) As soon as practicable after the time for the parties to file 
proposed findings of fact and conclusions of law has expired, the 
presiding officer shall prepare a report containing the following:
    (1) His recommended rulings on the proposed findings of fact and 
conclusions of law;
    (2) His recommended findings of fact and conclusions of law, with 
the reasons therefore; and
    (3) His recommended decision.
    (b) The presiding officer shall serve a copy of his report upon each 
party in the hearing. The report shall be considered to have been served 
when it is mailed to such party or its attorney of record.
    (c) Not less than twenty-five days after the date on which he caused 
copies of his report to be served upon the parties, the presiding 
officer shall certify to the Administrator the record, which shall 
contain the transcript of testimony, exhibits, the findings of fact and 
conclusions of law proposed by the parties, the presiding officer's 
report, and any exceptions thereto which may have been filed by the 
parties.

[36 FR 7778, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973 
and amended at 44 FR 55332, Sept. 26, 1979]



Sec. 1316.66  Exceptions.

    (a) Within twenty days after the date upon which a party is served a 
copy of the report of the presiding officer, such party may file with 
the Hearing Clerk, Office of the Administrative Law Judge, exceptions to 
the recommended decision, findings of fact and conclusions of law 
contained in the report. The party shall include a statement of 
supporting reasons for such exceptions, together with evidence of record 
(including specific and complete citations of the pages of the 
transcript and exhibits) and citations of the authorities relied upon.

[[Page 252]]

    (b) The Hearing Clerk shall cause such filings to become part of the 
record of the proceeding.
    (c) The Administrative Law Judge may, upon the request of any party 
to a proceeding, grant time beyond the twenty days provided in paragraph 
(a) of this section for the filing of a response to the exceptions filed 
by another party if he determines that no party in the hearing will be 
unduly prejudiced and that the ends of justice will be served thereby. 
Provided however, that each party shall be entitled to only one filing 
under this section; that is, either a set of exceptions or a response 
thereto.

[44 FR 55332, Sept. 26, 1979]



Sec. 1316.67  Final order.

    As soon as practicable after the presiding officer has certified the 
record to the Administrator, the Administrator shall cause to be 
published in the Federal Register his final order in the proceeding, 
which shall set forth the final rule and the findings of fact and 
conclusions of law upon which the rule is based. This order shall 
specify the date on which it shall take effect, which date shall not be 
less than 30 days from the date of publication in the Federal Register 
unless the Administrator finds that the public interest in the matter 
necessitates an earlier effective date, in which event the Administrator 
shall specify in the order his findings as to the conditions which led 
him to conclude that an earlier effective date was required.

[44 FR 42179, July 19, 1979, as amended at 44 FR 55332, Sept. 26, 1979]



Sec. 1316.68   Copies of petitions for judicial review.

    Copies of petitions for judicial review, filed pursuant to section 
507 of the Act (21 U.S.C. 877) shall be delivered to and served upon the 
Administrator in quintuplicate. The Administrator shall certify the 
record of the hearing and shall file the certified record in the 
appropriate U.S. Court of Appeals.

[36 FR 7820, Apr. 24, 1971. Redesignated at 44 FR 42179, July 19, 1979]



       Subpart E--Seizure, Forfeiture, and Disposition of Property

    Authority: 21 U.S.C 871(b), 881, 965, 19 U.S.C. 1606, 1607, 1608, 
1610, 1613, 1618, 28 U.S.C. 509, 510.



Sec. 1316.71   Definitions.

    As used in this subpart, the following terms shall have the meanings 
specified:
    (a) The term Act means the Controlled Substances Act (84 Stat. 1242; 
21 U.S.C. 801) and/or the Controlled Substances Import and Export Act 
(84 Stat. 1285; 21 U.S.C. 951).
    (b) The term custodian means the officer required under Sec. 1316.72 
to take custody of particular property which has been seized pursuant to 
the Act.
    (c) The term property means a controlled substance, raw material, 
product, container, equipment, money or other asset, vessel, vehicle, or 
aircraft within the scope of the Act.
    (d) The terms seizing officer, officer seizing, etc., mean any 
officer, authorized and designated by Sec. 1316.72 to carry out the 
provisions of the Act, who initially seizes property or adopts a seizure 
initially made by any other officer or by a private person.
    (e) The term Special Agents-in-Charge means Drug Enforcement 
Administration Special Agents-in-Charge or Resident Agents in Charge and 
Federal Bureau of Investigation Special Agents-in-Charge.
    (f) Any term not defined in this section shall have the definition 
set forth in sections 102 and 1001 of the Act (21 U.S.C. 802 and 951) 
and in Sec. 1301.02 of this chapter.

[36 FR 7820, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 45 FR 20096, Mar. 27, 1980; 47 FR 43370, Oct. 1, 1982; 49 
FR 28701, July 16, 1984]



Sec. 1316.72   Officers who will make seizures.

    For the purpose of carrying out the provisions of the Act, all 
special agents of the Drug Enforcement Administration and the Federal 
Bureau of Investigation are authorized and designated to seize such 
property as may be subject to seizure.

[47 FR 43370, Oct. 1, 1982]

[[Page 253]]



Sec. 1316.73   Custody and other duties.

    An officer seizing property under the Act shall store the property 
in a location designated by the custodian, generally in the judicial 
district of seizure. The Special Agents-in-Charge are designated as 
custodians to receive and maintain in storage all property seized 
pursuant to the Act, are authorized to dispose of any property pursuant 
to the Act and any other applicable statutes or regulations relative to 
disposal, and to perform such other duties regarding such seized 
property as are appropriate, including the impound release of property 
pursuant to 28 CFR 0.101(c).

[47 FR 43370, Oct. 1, 1982]



Sec. 1316.74   Appraisement.

    The custodian shall appraise the property to determine the domestic 
value at the time and place of seizure. The domestic value shall be 
considered the price at which such or similar property is freely offered 
for sale. If there is no market for the property at the place of 
seizure, the domestic value shall be considered the value in the 
principal market nearest the place of seizure.

(Sec. 606, 46 Stat. 754 (19 U.S.C. 1606))

[36 FR 7820, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 52 FR 41418, Oct. 28, 1987]



Sec. 1316.75   Advertisement.

    (a) If the appraised value does not exceed the monetary amount set 
forth in title 19, United States Code, Section 1607; the seized 
merchandise is any monetary instrument within the meaning of section 
5312(a)(3) of title 31 of the United States Code; or if a conveyance 
used to import, export or otherwise transport or store any controlled 
substance is involved, the custodian or DEA Asset Forfeiture Section 
shall cause a notice of the seizure and of the intention to forfeit and 
sell or otherwise dispose of the property to be published once a week 
for at least 3 successive weeks in a newspaper of general circulation in 
the judicial district in which the processing for forfeiture is brought.
    (b) The notice shall: (1) Describe the property seized and show the 
motor and serial numbers, if any; (2) state the time, cause, and place 
of seizure; and (3) state that any person desiring to claim the property 
may, within 20 days from the date of first publication of the notice, 
file with the custodian or DEA Asset Forfeiture Section a claim to the 
property and a bond with satisfactory sureties in the sum of $5,000 or 
ten percent of the value of the claimed property whichever is lower, but 
not less than $250.

(Sec. 607, 46 Stat. 754, as amended (19 U.S.C. 1607); Pub. L. 98-473, 
Pub. L. 98-573)

[36 FR 7820, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973 
and amended at 44 FR 56324, Oct. 1, 1979; 49 FR 1178, Jan. 10, 1984; 49 
FR 50643, Dec. 31, 1984; 52 FR 24446, July 1, 1987; 56 FR 8686, Mar. 1, 
1991]



Sec. 1316.76  Requirements as to claim and bond.

    (a) The bond shall be rendered to the United States, with sureties 
to be approved by the custodian or DEA Asset Forfeiture Section, 
conditioned that in the case of condemnation of the property the obligor 
shall pay all costs and expenses of the proceedings to obtain such 
condemnation. When the claim and bond are received by the custodian or 
DEA Asset Forfeiture Section, he shall, after finding the documents in 
proper form and the sureties satisfactory, transmit the documents, 
together with a description of the property and a complete statement of 
the facts and circumstances surrounding the seizure, to the United 
States Attorney for the judicial district in which the proceeding for 
forfeiture is brought. If the documents are not in satisfactory 
condition when first received, a reasonable time for correction may be 
alloved. If correction is not made within a reasonable time the 
documents may be treated as nugatory, and the case shall proceed as 
though they had not been tendered.
    (b) The filing of the claim and the posting of the bond does not 
entitle the claimant to possession of the property, however, it does 
stop the administrative forfeiture proceedings. The bond posted to cover 
corts may be in cash, certified check, or satisfactory sureties. The 
costs and expenses secured by the bond are such as are incurred after 
the filing of the bond including storage

[[Page 254]]

cost, safeguarding, court fees, marshal's costs, etc.

(Sec. 608, 46 Stat. 755 (19 U.S.C. 1608); Pub. L. 98-473, Pub. L. 98-
573)

[36 FR 7820, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973 
and amended at 49 FR 1178, Jan. 10, 1984; 49 FR 50643, Dec. 31, 1984; 56 
FR 8686, Mar. 1, 1991]



Sec. 1316.77  Administrative forfeiture.

    (a) For property seized by officers of the Drug Enforcement 
Administration, if the appraised value does not exceed the 
jurisdictional limits in Sec. 1316.75(a), and a claim and bond are not 
filed within the 20 days hereinbefore mentioned, the DEA Special Agent-
in-Charge or DEA Asset Forfeiture Section shall declare the property 
forfeited. The DEA Special Agent-in-Charge or DEA Asset Forfeiture 
Section shall prepare the Declaration of Forfeiture and fovard it to the 
Administrator of the Administration as notification of the action he has 
taken. Thereafter, the property shall be retained in the district of the 
DEA Special Agent-in-Charge or DEA Asset Forfeiture Section or delivered 
elsewhere for official use, or otherwise disposed of, in accordance with 
official instructions received by the DEA Special Agent-in-Charge or DEA 
Asset Forfeiture Section.
    (b) For property seized by officers of the Federal Bureau of 
Investigation, if the appraised value does not exceed the jurisdictional 
limits in Sec. 1316.75(a), and a claim and bond are not filed within the 
20 days hereinbefore mentioned, the FBI Property Management Officer 
shall declare the property forfeited. The FBI Property Management 
Officer shall prepare the Declaration of Forfeiture. Thereafter, the 
property shall be retained in the field office or delivered elsewhere 
for official use, or otherwise disposed of, in accordance with the 
official instructions of the FBI Property Management Officer.

(28 U.S.C. 509 and 510; 21 U.S.C. 871 and 881(d); Pub. L. 98-473, Pub. 
L. 98-573)

[48 FR 35087, Aug. 3, 1983, as amended at 49 FR 1178, Jan. 10, 1984; 49 
FR 50643, Dec. 31, 1984; 56 FR 8686, Mar. 1, 1991]



Sec. 1316.78   Judicial forfeiture.

    If the appraised value is greater than the jurisdictional limits in 
Sec. 1316.75(a) or a claim and satisfactory bond have been received for 
property the jurisdictional limits in Sec. 1316.76, the custodian or DEA 
Asset Forfeiture Section shall transmit a description of the property 
and a complete statement of the facts and circumstances surrounding the 
seizure to the U.S. Attorney for the judicial district in which the 
proceeding for forfeiture is sought for the purpose of instituting 
condemnation proceedings. The U.S. Attorney shall also be furnished the 
newspaper advertisements required by Sec. 1316.75. The Forfeiture 
Counsel of DEA shall make applications to the U.S. District Courts to 
place property in official DEA use.

(Sec. 610, 46 Stat. 755 (19 U.S.C. 1610); Pub. L. 98-473, Pub. L. 98-
573)

[36 FR 7820, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973 
and amended at 44 FR 56324, Oct. 1, 1979; 49 FR 1178, Jan. 10, 1984; 49 
FR 32174, Aug. 13, 1984; 49 FR 50643, Dec. 31, 1984; 56 FR 8686, Mar. 1, 
1991]



Sec. 1316.79  Petitions for remission or mitigation of forfeiture.

    (a) Any person interested in any property which has been seized, or 
forfeited either administratively or by court proceedings, may file a 
petition for remission or mitigation of the forfeiture. Such petition 
shall be filed in triplicate with the DEA Asset Forfeiture Section or 
Special Agent-in-Charge of the DEA or FBI, depending upon which agency 
seized the property, for the judicial district in which the proceeding 
for forfeiture is brought. It shall be addressed to the Director of the 
FBI or the Administrator of the DEA, depending upon which agency seized 
the property, if the property is subject to administrative forfeiture 
pursuant to Sec. 1316.77, and addressed to the Attorney General if the 
property is subject to judicial forfeiture pursuant to Sec. 1316.78. The 
petition must be executed and sworn to by the person alleging interest 
in the property.
    (b) The petition shall include the following: (1) A complete 
description of the property, including motor and serial numbers, if any, 
and the date and place of seizure; (2) the petitioner's interest in the 
property, which shall be

[[Page 255]]

supported by bills of sale, contracts, mortgages, or other satisfactory 
documentary evidence; and, (3) the facts and circumstances, to be 
established by satisfactory proof, relied upon by the petitioner to 
justify remission or mitigation.
    (c) Where the petition is for restoration of the proceeds of sale, 
or for value of the property placed in official use, it must be 
supported by satisfactory proof that the petitioner did not know of the 
seizure prior to the declaration of condemnation of forfeiture and was 
in such circumstances as prevented him from knowing of the same.

(Secs. 613, 618, 46 Stat. 756, 757, as amended (19 U.S.C. 1613, 1618; 28 
U.S.C. 509 and 510; 21 U.S.C. 871 and 881(d)); Pub. L. 98-473, Pub. L. 
98-573)

[36 FR 7820, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 48 FR 35088, Aug. 3, 1983; 49 FR 1178, Jan. 10, 1984; 49 
FR 50643, Dec. 31, 1984; 56 FR 8686, Mar. 1, 1991]



Sec. 1316.80   Time for filing petitions.

    (a) In order to be considered as seasonably filed, a petition for 
remission or mitigation of forfeiture should be filed within 30 days of 
the receipt of the notice of seizure. If a petition for remission or 
mitigation of forfeiture has not been received within 30 days of the 
notice of seizure, the property will either be placed in official 
service or sold as soon as it is forfeited. Once property is placed in 
official use, or is sold, a petition for remission or mitigation of 
forfeiture can no longer be accepted.
    (b) A petition for restoration of proceeds of sale, or for the value 
of property placed in official use, must be filed within 90 days of the 
sale of the property, or within 90 days of the date the property is 
placed in official use.

(Secs. 613, 618, 46 Stat. 756, 757, as amended (19 U.S.C. 1613, 1618); 
Pub. L. 98-473, Pub. L. 98-573)

[36 FR 7820, Apr. 24, 1971. Redesignated at 38 FR 26609, Sept. 24, 1973, 
and amended at 49 FR 50643, Dec. 31, 1984]



Sec. 1316.81   Handling of petitions.

    Upon receipt of a petition, the custodian or DEA Asset Forfeiture 
System shall request an appropriate investigation. The petition and the 
report of investigation shall be forwarded to the Director of the FBI or 
to the Administrator of the DEA, depending upon which agency seized the 
property. If the petition involves a case which has been referred to the 
U.S. Attorney for the institution of court proceedings, the custodian or 
DEA Asset Forfeiture System shall transmit the petition to the U.S. 
Attorney for the judicial district in which the proceeeding for 
forfeiture is brought. He shall notify the petitioner of this action.

(28 U.S.C. 509 and 510; 21 U.S.C. 871 and 881(d); Pub. L. 98-473, Pub. 
L. 98-573)

[48 FR 35088, Aug. 3, 1983, as amended at 49 FR 1178, Jan. 10, 1984; 49 
FR 50643, Dec. 31, 1984; 56 FR 8686, Mar. 1, 1991]



    Subpart F--Expedited Forfeiture Proceedings for Certain Property

    Authority: 21 U.S.C. 822, 871, 872, 880, 881, 881-1, 883, 958, 965; 
19 U.S.C. 1606, 1607, 1608, 1610, 1613, 1618; 28 U.S.C. 509, 510; Pub. 
L. No. 100-690, sec. 6079, 6080.

    Source: 54 FR 37610, Sept. 11, 1989, unless otherwise noted.



Sec. 1316.90  Purpose and scope.

    (a) The following definitions, regulations, and criteria are 
designed to establish and implement procedures required by sections 6079 
and 6080 of the Anti-Drug Abuse Act of 1988, Public Law No. 100-690 (102 
Stat. 4181). They are intended to supplement existing law and procedures 
relative to the forfeiture of property under the identified statutory 
authority. The provisions of these regulations do not affect the 
existing legal and equitable rights and remedies of those with an 
interest in property seized for forfeiture, nor do these provisions 
relieve interested parties from their existing obligations and 
responsibilities in pursuing their interests through such courses of 
action. These regulations are intended to reflect the intent of Congress 
to minimize the adverse impact on those entitled to legal or equitable 
relief occasioned by the prolonged detention of property subject to 
forfeiture due to violations of law involving personal use quantities of 
controlled substances, and conveyances seized for drug-related offenses. 
The definition of personal use

[[Page 256]]

quantities of a controlled substance as contained herein is intended to 
distinguish between those quantities small in amount which are generally 
considered to be possessed for personal consumption and not for further 
distribution, and those larger quantities generally considered to be 
subject to further distribution.
    (b) In this regard, for violations involving the porsession of 
personal use quantities of a controlled substance, section 6079(b)(2) 
requires either that administrative forfditure be completed within 21 
days of the seizure of the property, or alternatively, that procedures 
are established that provide a means by which an individual entitled to 
relief may initiate an expedited administrative review of the legal and 
factual basis of the seizure for forfeiture. Should an individual 
request relief pursuant to these regulations and be entitled to the 
return of the seized property, such property shall be returned 
immediately following that determination, and the administrative 
forfeiture process shall cease. Should the individual not be entitled to 
the return of the seized property, however, the administrative 
forfeiture of that property shall proceed. The owner may, in any event, 
obtain release of property pending the administrative forfeiture by 
submitting to the agency making the determination, property sufficient 
to preserve the government's vested interest for purposes of the 
administrative forfeiture.
    (c) Section 6080 requires a similar expedited review by the Attorney 
General or his representative in those instances where a conveyance is 
being forfeited in a civil judicial proceeding following its seizure for 
a drug-related offense.



Sec. 1316.91  Definitions.

    As used in this subpart, the following terms shall have the meanings 
specified:
    (a) The term Appraised Value means the estimated domestic price at 
the time of seizure at which such or similar property is freely offered 
for sale.
    (b) The term Commercial Fishing Industry Vessel means a vessel that:
    (1) Commercially engages in the catching, taking, or harvesting of 
fish or an activity that can reasonably be expected to result in the 
catching, taking, or harvesting of fish;
    (2) Commercially prepares fish or fish products other than by 
gutting, decapitating, gilling, skinning, shucking, icing, freezing, or 
brine chilling; or
    (3) Commercially supplies, stores, refrigerates, or transports fish, 
fish products, or materials directly related to fishing or the 
preparation of fish to or from a fishing, fish processing, or fish 
tender vessel or fish processing facility.
    (c) The term Controlled Substance has the meaning given in section 
802 of title 21, United States Code (U.S.C.).
    (d) The term Drug-Related Offense means any proscribed offense which 
involves the possession, distribution, manufacture, cultivation, sale, 
transfer, or the attempt or conspiracy to possess, distribute, 
manufacture, cultivate, sell or transfer any substance the possession of 
which is prohibited by Title 21, U.S.C.
    (e) The term Immediately means within 20 days of the filing of a 
petition for expedited release by an owner.
    (f) The term Interested Party means one who was in legal possession 
of the property at the time of seizure and is entitled to legal 
possdssion at the time of the granting of the petition for expedited 
release. This includes a lienholder (to the extent of his interest in 
the property) whose claim is in writing (except for a maritime lien 
which need not be in writing), unless the collateral is in the 
porsession of the secured party. The agreement securing such lien must 
create or provide for a security interest in the collateral, describe 
the collateral, and be signed by the debtor.
    (g) The term Legal and Factual Basis of the Seizure means a 
statement of the applicable law under which the property is seized, and 
a statement of the circumstances of the seizure sufficiently precise to 
enable an owner or other interested party to identify the date, place, 
and use or acquisition which makes the property subject to forfeiture.
    (h) The term Normal and Customary Manner means that inquiry 
suggested by particular facts and circumstances

[[Page 257]]

which would customarily be undertaken by a reasonably prudent individual 
in a like or similar situation. Actual knowledge of such facts and 
circumstances is unnecessary, and implied, imputed, or constructive 
knowledge is sufficient. An established norm, standard, or custom is 
persuasive but not conclusive or controlling in determining whether an 
owner acted in a normal and customary manner to ascertain how property 
would be used by another legally in possession of the property. The 
failure to act in a normal and customary manner as defined herein will 
result in the denial of a petition for expedited release of the property 
and is intended to have the desirable effect of inducing owners of the 
property to exercise greater care in transferring possession of their 
property.
    (i) The term Owner means one having a legal and possessory interest 
in the property seized for forfeiture. Even though one may hold primary 
and direct title to the property seized, such person may not have 
sufficient actual beneficial interest in the property to support a 
petition as owner if the facts indicate that another person had dominion 
and control over the property.
    (j) The term Personal Use Quantities means possession of controlled 
substances in circumstances where there is no other evidence of an 
intent to distribute, of to facilitate the manufacturing, compounding, 
processing, delivering, importing or exporting of any controlled 
substance. Evidence of personal use quantities shall not include 
sweepings or other evidence of possession of quantities of a controlled 
substance for other than personal use.
    (1) Such other evidence shall include:
    (i) Evidence, such as drug scales, drug distribution paraphernalia, 
drug records, drug packaging material, method of drug packaging, drug 
``cutting'' agents and other equipment, that indicates an intent to 
process, package or distribute a controlled substance;
    (ii) Information from reliable sources indicating possession of a 
controlled substance with intent to distribute;
    (iii) The arrest and/or conviction record of the person or persons 
in actual or constructive possession of the controlled substance for 
offenses under Federal, State or local law that indicates an intent to 
distribute a controlled substance;
    (iv) The controlled substance is related to large amounts of cash or 
any amount of prerecorded government funds;
    (v) The controlled substance is possessed under circumstances that 
indicate such a controlled substance is a sample intended for 
distribution in anticipation of a transaction involving large 
quantities, or is part of a larger delivery; or
    (vi) Statements by the possessor, or otherwise attributable to the 
possessor, including statements of conspirators, that indicate 
possession with intent to distribute.
    (2) Possession of a controlled substance shall be presumed to be for 
personal use when there are no indicia of illicit drug trafficking or 
distribution such as, but not limited to, the factors listed above and 
the amounts do not exceed the following quantities:
    (i) One gram of a mixture of substance containing a detectable 
amount of heroin;
    (ii) One gram of a mixture or substance containing a detectable 
amount of--
    (A) Coca leaves, except coba leaves and extracts of coca leaves frol 
which cocaine, ecgonine, and derivations of ecgonine or their salts have 
been removed;
    (B) Cocaine, its salts, optical and geometric isomers, and salts of 
isomers;
    (C) Ecgonine, its derivatives, their salts, isomers, and salts of 
isomers; or
    (D) Any compound, mixture or preparation which contains any quantity 
of any of the substances referred to in paragraphs (j)(2)(ii)(A) through 
(j)(2)(ii)(C) of this section;
    (iii) \1/10\th gram of a mixture or substance described in paragraph 
(j)(2)(ii) of this section which contains cocaine base;
    (iv) \1/10\th gram of a mixture or substance containing a detectable 
amount of phencyclidine (PCP);
    (v) 500 micrograms of a mixture or substance containing a detectable 
amount of lysergic acid diethylamide (LSD);

[[Page 258]]

    (vi) One ounce of a mixture of substance containing a detectable 
amount of marihuana;
    (vii) One gram of methamphetamine, its salts, isomers, and salts of 
its isomers, or one gram of a mixture or substance containing a 
detectable amount of methamphetamine, its salts, isomers, or salts of 
its isomers.
    (3) The possession of a narcotic, a depressant, a stimulant, a 
hallucinogen or cannabis-controlled substance will be considered in 
excess of personal use quantities if the dosage unit amount possessed 
provides the same or greater equivalent efficacy as described in 
paragraph (j)(2) of this section.
    (k) The term Property means property subject to forfeiture under 
title 21, U.S.C., sections 881(a) (4), (6), and (7); title 19, U.S.C., 
section 1595a, and; title 49, U.S.C. App., section 782.
    (l) The term Seizing Agency means the Federal agency which has 
seized the property or adopted the seizure of another agency, and has 
the responsibility for administratively forfeiting the property;
    (m) The term Statutory Rights or Defenses to the Forfeiture means 
all legal and equitable rights and remedies available to a claimant of 
property seized for forfeiture.
    (n) The term Sworn to as used in Secs. 1316.92(e) and 1316.95(c) 
refers to the oath as provided by Title 28, U.S.C., section 1746.



Sec. 1316.92  Petition for expedited release in an administrative forfeiture action.

    (a) Where property is seized for administrative forfeiture involving 
controlled substances in personal use quantities the owner may petition 
the seizing agency for expedited release of the property.
    (b) Where property described in paragraph (a) of this section is a 
commercial fishing industry vessel proceeding to or from a fishing area 
or intermediate port of call or actually engaged in fishing operations, 
which would be subject to seizure for administrative forfeiture for a 
violation of law involving controlled substances in personal use 
quantities, a summons to appear shall be isrued in lieu of a physical 
seizure. The vessel shall report to the port designated in the summons. 
The seizing agency shall be authorized to effect administrative 
forfeiture as if the vessel had been physically seized. Upon answering 
the summons to appear on or prior to the last reporting date specified 
in the summons, the owner of the vessel may file a petition for 
expedited release pursuant to paragraph (a) of this section and the 
provisions of paragraph (a) of this section and other provishons in this 
subpart pertaining to a petition for expedited release shall apply as if 
the vessel had been physically seized.
    (c) The owner filing the petition for expedited release shall 
establish the following:
    (1) The owner has a valid, good faith interest in the seized 
property as owner or otherwise;
    (2) The owner reasonably attempted to ascertain the use of the 
property in a normal and customary manner; and
    (3) The owner did not know or consent to the illegal use of the 
property, or in the event that the owner knew or should have known of 
the illegal use, the owner did what reasonably could be expected to 
prevent the violation.
    (d) In addition to those factors listed in paragraph (c) of this 
section, if an owner can demonstrate that the owner has other statutnry 
rights or defenses that would cause the owner to prevail on the issue of 
forfeiture, such factors shall also be considered in ruling on the 
petition for expedited release.
    (e) A petition for expedited release must be filed in a timely 
manner to be considered by the seizing agency. In order to be filed in a 
timely manner, the petition must be received by the appropriate seizing 
agency within 20 days from the date of the first publication of the 
notice of seizure. The petition must be executed and sworn to by the 
owner and both the envelope and the request must be clearly marked 
``PETITION FOR EXPEDITED RELEASE.'' Such petition shall be filed in 
triplicate with the Special Agent in Charge of the Drug Enforcement 
Administration (DEA) or Federal Bureau of Investigation (FBI) field 
office in the judicial district in which the property was seized, 
depending upon which agency seized the property. The petition shall be 
addressed to the Director of

[[Page 259]]

the FBI or to the Administrator of the DEA, depending upon which agency 
seized the property.
    (f) The petition shall include the following:
    (1) A complete description of the property, including identification 
numbers, if any, and the date and place of seizure;
    (2) The petitioner's interest in the property, which shall be 
supported by title documentation, bills of sale, contracts, mortgages, 
or other satisfactory documentary evidence; and
    (3) A statement of the facts and circumstances, to be established by 
satisfactory proof, relied upon by the petitioner to justify expedited 
release of the seized property.



Sec. 1316.93  Ruling on petition for expedited release in an administrative forfeiture action.

    (a) Upon receipt of a petition for expedited release filed pursuant 
to Sec. 1316.92(a), the seizing agency shall determine first whether a 
final administrative determination of the case, without regard to the 
provisions of this subpart, can be made within 21 days of the seizure. 
If such a final administrative determination is made within 21 days, no 
further action need be taken under this subpart.
    (b) If no such final administrative determination is made within 21 
days of the seizure, the following procedure shall apply. The seizing 
agency shall, within 20 days after the receipt of the petition for 
expedited release, determine whether the petition filed by the owner has 
established the factors listed in Sec. 1316.92(c) and:
    (1) If the seizing agency determines that those factors have been 
established, it shall terminate the administrative proceedings and 
return the property to the owner (or in the case of a commercial fishing 
industry vessel for which a summons has been issued shall dismiss the 
summons), except where it is evidence of a violation of law; or
    (2) If the seizing agency determines that those factors have not 
been established, the agency shall proceed with the administrative 
forfeiture.



Sec. 1316.94  Posting of substitute res in an administrative forfeiture action.

    (a) Where property is seized for administrative forfeiture involving 
controlled substances in personal use quantities, the owner may obtain 
release of the property by posting a substitute res with the seizing 
agency. The property will be released to the owner upon the payment of 
an amount equal to the appraised value of the property if it is not 
evidence of a violation of law or has design or other characteristics 
that particularly suit it for use in illegal activities. This payment 
must be in the form of a traveler's check, a money order, a cashier's 
check or an irrevocable letter of credit made payable to the seizing 
agency. A bond in the form of a cashier's check will be considered as 
paid once the check has been accepted for payment by the financial 
institution which issued the check.
    (b) If a substitute res is posted and the property is 
administratively forfeited, the seizing agency will forfeit the 
substitute res in lieu of the property.



Sec. 1316.95  Petition for expedited release of a conveyance in a judicial forfeiture action.

    (a) Where a conveyance has been seized and is being forfeited in a 
judicial proceeding for a drug-related offense, the owner may petition 
the United States Attorney for an expedited release of the conveyance.
    (b) The owner filing the petition for expedited release shall 
establish the following:
    (1) The owner has a valid, good faith interest in the seized 
conveyance as owner or otherwise;
    (2) The owner has statutory rights or defenses that would show to a 
substantial probability that the owner would prevail on the issue of 
forfeiture;
    (3) The owner reasonably attempted to ascertain the use of the 
conveyance in a normal and customary manner; and
    (4) The owner did not know or consent to the illegal use of the 
conveyance; or in the event that the owner knew or should have known of 
the illegal use, the owner did what reasonably could be expected to 
prevent the violation.

[[Page 260]]

    (c) A petition for expedited release must be filed in a timely 
manner in order to be considered by the United States Attorney. To be 
considered as filed in a timely manner, the petition must be received by 
the appropriate United States Attorney within 20 days from the date of 
the first publication of the notice of the action and arrest of the 
property, or within 30 days after filing of the claim, whichever occurs 
later. The petition must be executed and sworn to by the owner, and both 
the envelope and the request must be clearly marked ``PETITION FOR 
EXPEDITED RELEASE.'' Such petition shall be filed in triplicate and 
addressed to and filed with the United States Attorney prosecuting the 
conveyance for forfeiture with a copy to the seizing agency.
    (d) The petition shall include the following:
    (1) A complete description of the conveyance, including the 
identification number, and the date and place of seizure;
    (2) The petitioner's interest in the conveyance, which shall be 
supported by bills of sale, contracts, mortgages, or other satisfactory 
documentary evidence; and,
    (3) The facts and circumstances, to be established by satisfactory 
proof, relied upon by the petitioner to justify expedited release of the 
seized conveyance.



Sec. 1316.96  Ruling on a petition for expedited release of a conveyance in a judicial forfeiture action.

    (a) Upon receipt of a petition for expedited release filed pursuant 
to Sec. 1316.95, the United States Attorney shall rule on the petition 
within 20 days of receipt. A petition shall be deemed filed on the date 
it is received by the United States Attorney.
    (b) If the United States Attorney does not rule on the petition for 
expedited release within 20 days after the date on which it is filed, 
the conveyance shall be returned to the owner or interested party 
pending further forfeiture proceedings, except where it is evidence of a 
violation of law. Release of conveyance under provisions of this 
paragraph shall not affect the forfeiture action with respect to that 
conveyance.
    (c) Upon a favorable ruling on the petition for expedited release, 
the United States Attorney shall, where necessary, move to terminate the 
judicial proceedings against the conveyance and immediately direct the 
return of the conveyance except where it is evidence of a violation of 
law.
    (d) If, within 20 days, the United States Attorney denies the 
petition for expedited release, the government shall retain possession 
of the conveyance until the owner provides a substitute res bond 
pursuant to Sec. 1316.98 or the forfeiture is finalized.



Sec. 1316.97  Initiating judicial forfeiture proceeding against a conveyance within 60 days of the filing of a claim and cnrt bond.

    (a) The United States Attorney shall file a complaint for forfeiture 
of the conveyance within 60 days of the filing of the claim and cost 
bond.
    (b) Upon the failure of the United States Attorney to file a 
complaint for forfeiture of a conveyance within 60 days unless the court 
extends the 60-day period following a showing of good cause, or unless 
the owner and the United States Attorney agree to such an extension, the 
court shall order the return of the conveyance and the return of any 
bond.



Sec. 1316.98  Substitute res bond in a judicial forfeiture action against a conveyance.

    (a) Where a conveyance is being forfeited in a judicial proceeding 
for a drug-related offense, the owner may obtain release of the property 
by filing a substitute res bond with the seizing agency. The conveyance 
will be released to the owner upon the payment of a bond in the amount 
of the appraised value of the conveyance if it is not evidence of a 
violation of law or has design or other characteristics that 
particularly suit it for use in illegal activities. This bond must be in 
the form of a traveler's check, a money order, a cashier's check or an 
irrevocable letter of credit made payable to the Department of Justice 
or to the United States Customs Service depending on which agency seized 
the conveyance. A bond in the form of a cashier's check will be 
considered as paid once the check has

[[Page 261]]

been accepted for payment by the financial institution which issued the 
check.
    (b) If a substitute res bond is filed and the conveyance is 
judicially forfeited, the court will forfeit the bond in lieu of the 
property.



Sec. 1316.99  Notice provisions.

    (a) Special notice provision. At the time of seizure of property 
defined in Sec. 1316.91 for violations involving the possession of 
personal use quantities of a controlled substance and conveyances seized 
pursuant to Sec. 1316.95, written notice must be provided to the 
possessor of the property regarding applicable statutes and Federal 
regulations including the procedures established for the filing of a 
petition for expedited release and for the posting of a substitute res 
bond as set forth in sections 6079 and 6080 of the Anti-Drug Abuse Act 
of 1988 and implementing regulations.
    (b) Standard notice provision. The standard notice to the owner as 
required by title 19, U.S.C., section 1607 and applicable regulations, 
shall be made at the earliest practicable opportunity after determining 
ownership of the seized property or conveyance and shall include the 
legal and factual basis of the seizure.

[[Page 263]]





CHAPTER III--OFFICE OF NATIONAL DRUG CONTROL POLICY




  --------------------------------------------------------------------

Part                                                                Page
1400            [Reserved]..................................
1401            Public availability of information..........
1402            Mandatory declassification review...........
1403            Uniform administrative requirements for 
                    grants and cooperative agreements to 
                    State and local governments.............
1404            Governmentwide debarment and suspension 
                    (nonprocurement) and governmentwide 
                    requirements for drug-free workplace 
                    (grants)................................
1405-1499  
[Reserved]

[[Page 264]]





PART 1400--[RESERVED]--Table of Contents






PART 1401--PUBLIC AVAILABILITY OF INFORMATION--Table of Contents




Sec.
1401.1  Purpose.
1401.2  The Office of National Drug Control Policy--Organization and 
          functions.
1401.3  Definitions.
1401.4  Records of other agencies.
1401.5  How to request records--form and content.
1401.6  Initial determination.
1401.7  Prompt response.
1401.8  Responses--form and content.
1401.9  Appeal procedures.
1401.10  Fee schedule.
1401.11  Payment of fees.
1401.12  Waiver of fees.
1401.13  Aggregation of requests.
1401.14  Records that are exempt from disclosure.
1401.15  Deletion of exempted information.

    Authority: 5 U.S.C. 552, as amended.

    Source: 57 FR 59803, Dec. 16. 1992, unless otherwise noted.



Sec. 1401.1  Purpose.

    The purpose of this part is to prescribe rules, guidelines and 
procedures to implement the Freedom of Information Act (FOIA), 5 U.S.C. 
552, as amended.



Sec. 1401.2  The Office of National Drug Control Policy--Organization and functions.

    (a) The Office of National Drug Control Policy (ONDCP) was created 
by the Anti-Drug Abuse Act of 1988, 21 U.S.C. 1501 et seq. The mission 
of ONDCP is to coordinate the anti-drug efforts of the various agencies 
and departments of the Federal government, to consult with States and 
localities and assist their anti-drug efforts, and to annually 
promulgate the National Drug Control Strategy. ONDCP is headed by the 
Director of National Drug Control Policy. The Director is assisted by a 
Deputy Director for Supply Reduction, a Deputy Director for Demand 
Reduction, and an Associate Director for State and Local Affairs.
    (b) ONDCP has an Office of Public Affairs that is responsible for 
providing information to the press and to the general public. If members 
of the public have general questions about ONDCP that can be answered by 
telephone, they may call the Office of Public Affairs at (202) 467-9890. 
This number should not be used to make FOIA requests. All oral requests 
for information under FOIA will be rejected.



Sec. 1401.3  Definitions.

    As used in this part, the following definitions shall apply:
    (a) Commercial-use request means a request from or on behalf of one 
who seeks information for a cause or purpose that furthers the 
commercial, trade or profit interests of the requester or the person or 
institution on whose behalf the request is made. In determining whether 
a requester properly belongs in this category, ONDCP will consider how 
the requester intends to use the documents.
    (b) Direct costs means those expenditures that ONDCP actually incurs 
in searching for and duplicating (and in the case of commercial 
requesters, reviewing) documents to respond to a FOIA request. Direct 
costs include, for example, the salary of the employee performing work 
(the basic rate of pay for the employee plus 16 percent of that rate to 
cover benefits) and the cost of operating duplicating machinery. Not 
included in direct costs are overhead expenses such as costs of space, 
and heating or lighting the facility in which the records are stored.
    (c) Duplication means the process of making a copy of a document in 
response to a FOIA request. Such copies can take the form of paper copy, 
microform, audio-visual materials, or machine readable documentation. 
ONDCP will provide a copy of the material in a form that is usable by 
the requester unless it is administratively burdensome to do so.
    (d) Educational institution means preschool, a public or private 
elementary or secondary school, an institution of graduate higher 
education, an institution of undergraduate higher education, an 
institution of professional education, or an institution of vocational 
education, which operates a program or programs of scholarly research.
    (e) Noncommercial scientific institution means an institution that 
is not operated on a ``commercial'' basis as that

[[Page 265]]

term is referenced above, and that is operated solely for the purpose of 
conducting scientific research the results of which are not intended to 
promote any particular product or industry.
    (f) Records and/or information means all books, papers, manuals, 
maps, photographs, or other documentary materials, regardless of 
physical form or characteristics, made or received by ONDCP and 
preserved or appropriate for preservation by ONDCP as evidence of the 
organization, functions, policies, decisions, procedures, operations, or 
other activities of the Government or because of the information value 
of the data in them, but does not include books, magazines or other 
material acquired solely for library purposes and through other sources, 
and does not include analyses, computations, or compilations of 
information not extant at the time of the request. The term ``records'' 
does not include objects or articles such as structures, furniture, 
paintings, sculptures, three-dimensional models, vehicles, and 
equipment.
    (g) Representative of the news media means any person actively 
gathering news for an entity that is organized and operated to publish 
or broadcast news to the public. The term ``news'' means information 
that is about current events or that would be of current interest to the 
public. Examples of news media include television or radio stations 
broadcasting to the public at large, and publishers of periodicals (but 
only in those instances when they can qualify as disseminators of 
``news'') that make their products available for purchase or 
subscription by the general public. Freelance journalists may be 
regarded as working for a news organization if they can demonstrate a 
reasonable basis for expecting publication through that organization, 
even though not actually employed by it.
    (h) Request means a letter or other written communication seeking 
records or information under FOIA.
    (i) Review means the process of examining documents located in 
response to a commercial-use request to determine if that document or 
any portion of that document is permitted to be withheld. It also 
includes processing any document for disclosure (i.e., doing all that is 
necessary to excise those portions of the document not subject to 
disclosure under FOIA and otherwise preparing them for release). Review 
does not include time spent resolving general legal or policy issues 
regarding the application of exemptions.
    (j) Search means all time spent looking for material that is 
responsive to a request, including page-by-page or line-by-line 
identification of material within documents. Searches should be 
performed in the most efficient and least expensive manner so as to 
minimize costs for both ONDCP and the requester; for example, line-by-
line searches should not be undertaken when it would be more efficient 
to duplicate the entire document. Searches should be distinguished from 
``review'' of material in order to determine whether the material is 
exempt from disclosure. Searches may be done manually or by computer 
using existing programming.



Sec. 1401.4  Records of other agencies.

    Requests for records that originated in another agency and are in 
the custody of ONDCP shall be referred to the originating agency for 
processing, and the person submitting the request shall be so notified. 
Any decision made by the originating agency with respect to such records 
will be honored by ONDCP.



Sec. 1401.5  How to request records--form and content.

    (a) Requests for records under FOIA must be submitted in writing, 
addressed to: Office of the General Counsel, Office of National Drug 
Control Policy, Executive Office of the President, Washington, DC 20500. 
The words ``FOIA REQUEST'' or ``REQUEST FOR RECORDS'' must be clearly 
marked on both the letter and the envelope. If the request is not so 
marked and addressed, the 10-day time limit imposed by Sec. 1401.7 of 
this part shall not begin to run until the request has been received by 
the Office of the General Counsel and identified as a FOIA request. Due 
to security requirements, FOIA requests may not be delivered in person.
    (b) Any ONDCP employee who receives a request shall promptly forward 
it to the Office of the General Counsel. Any ONDCP employee who receives 
an

[[Page 266]]

oral request made under the FOIA shall inform the person making the 
request of the provisions of this part requiring a written request.
    (c) Each request must reasonably describe the record(s) sought, 
including when known: The specific event or action to which the request 
refers, if any; the name of the agency, office, organization or person 
that originated the record; the date or time period to which the request 
refers; the subject matter of the records requested; the type of 
document requested; the location of the record(s) requested; and any 
other pertinent information that would assist in promptly locating the 
record(s).
    (d) When a request is not considered reasonably descriptive, or 
requires the production of voluminous records, or places an 
extraordinary burden on ONDCP, seriously interfering with its normal 
functioning to the detriment of the business of the Government, ONDCP 
may require the person or agent making the FOIA request to confer with 
an ONDCP representative in order to attempt to verify, and, if possible, 
narrow the scope of the request.
    (e) Upon initial receipt of a request, the Office of the General 
Counsel shall determine which official or officials within ONDCP shall 
have the primary responsibility for collecting and reviewing the 
requested information and drafting a proposed response.



Sec. 1401.6  Initial determination.

    The General Counsel or his or her designee shall have the authority 
to approve or deny requests received pursuant to these regulations. The 
decision of the General Counsel shall be final, subject only to 
administrative review as provided in Sec. 1401.9.



Sec. 1401.7  Prompt response.

    (a) The General Counsel or his or her designee shall either approve 
or deny a request for records within 10 working days (excluding 
Saturday, Sunday and Federal holidays) after receipt of the request 
unless additional time is required for one of the following reasons:
    (1) It is necessary to search for, collect, and appropriately 
examine a voluminous amount of separate and distinct records that are 
demanded in a single request; or
    (2) It is necessary to consult with another agency having a 
substantial interest in the determination of the request or among two or 
more components of ONDCP that have a substantial interest in the subject 
matter of the request.
    (b) When additional time is required for one of the reasons stated 
in paragraph (a) of this section, the General Counsel or his or her 
designee shall acknowledge receipt of the request within the 10 working 
day period and include a brief explanation of the reason for delay, 
indicating the date by which a determination will be forthcoming. An 
extended deadline adopted for one of the reasons set forth above may not 
exceed 10 additional working days.



Sec. 1401.8  Responses--form and content.

    (a) When a requested record has been identified and is available, 
the General Counsel or his or her designee shall notify the person 
making the request as to where and when the record will be available for 
inspection or the copies will be available. The notification shall also 
advise the person making the request of any fees assessed under 
Sec. 1401.10 of this part.
    (b) A denial or partial denial of a request for a record shall be in 
writing signed by the General Counsel or his or her designee and shall 
include:
    (1) The name and title of the person making the determination;
    (2) Either a reference to the specific exemption under FOIA 
authorizing the withholding of the record and a brief explanation of how 
the exemption applies to the record withheld, or a statement that, after 
diligent effort, the requested records have not been found or have not 
been adequately examined during the time allowed by Sec. 1401.7, and 
that the denial will be reconsidered as soon as the search or 
examination is complete; and
    (3) A statement that the denial may be appealed to the Director 
within 30 days of its receipt by the requester.
    (c) If a requested record cannot be located from the information 
supplied, or is known to have been destroyed or otherwise disposed of, 
the person making the request shall be so notified and

[[Page 267]]

the legal authority for disposition shall be cited.



Sec. 1401.9  Appeal procedures.

    (a) When the General Counsel or his or her designee denies a request 
for records in whole or in part, the person making the request may, 
within 30 days of receipt of the notice of denial, appeal the denial to 
the Director of ONDCP. The appeal must be in writing, addressed to the 
Director, Office of National Drug Control Policy, Executive Office of 
the President, Washington, DC 20500. The envelope should be clearly 
labeled as a ``Freedom of Information Act Appeal.''
    (b) The Director will act upon the appeal within 20 working days of 
its receipt. The Director may extend the 20-day period of time by any 
number of working days which could have been used by the General Counsel 
or his or her designee under Sec. 1401.7 but which were not used in 
making the initial determination. The Director's action on an appeal 
shall be in writing and signed.
    (c) If the decision is in favor of the requester, the Director shall 
order records promptly made available to the requester.
    (d) A denial in whole or in part of a request on appeal shall set 
forth a brief explanation of the reasons for the decision, and shall 
inform the requester of his or her right to seek judicial review of the 
denial and ruling on appeal as provided in 5 U.S.C. 552(a)(4).
    (e) No personal appearance, oral argument or hearing will ordinarily 
be permitted in connection with an appeal to the Director.



Sec. 1401.10  Fee schedule.

    (a) There are four categories of requesters: Commercial use 
requesters; educational and non-commercial scientific institutions; 
representatives of the news media; and all other requesters. FOIA 
prescribes different levels of fees for each of these categories.
    (1) Commercial use requesters. When a request for records is made 
for commercial use, charges will be assessed to cover all the costs of 
searching for, reviewing for release, and duplicating the records 
sought.
    (2) Educational and non-commercial scientific institutions. When a 
request for records is made by an educational or a non-commercial 
scientific institution in furtherance of scholarly or scientific 
research, charges will be assessed to cover the cost of duplication 
alone, excluding charges for duplication of the first 100 pages.
    (3) Requests by representatives of the news media. When a request 
for records is made by a representative of the news media for the 
purpose of news dissemination, charges will be assessed to cover the 
cost of duplication alone, excluding charges for duplication of the 
first 100 pages.
    (4) All other requests. When a request for records is made by a 
requester who does not fit into any of the preceding categories, charges 
will be assessed to cover the costs of searching for and duplicating the 
records sought, excluding charges for the first two hours of search time 
and the duplication of the first 100 pages. Moreover, requests from 
individuals for records about themselves will be treated under the 
Privacy Act of 1974, 5 U.S.C. 552a, which permits the assessment of fees 
for duplication costs only, regardless of the requester's 
characterization of the search.
    (b) Fees for searches, review of records and duplication of records 
are charged as follows:
    (1) Search for records. The charge for a manual search is calculated 
by determining the search time to the nearest quarter hour and 
multiplying that figure by the sum of the basic rate of pay per hour of 
the employee conducting the search plus 16 percent of that rate. The 
charge for a computer search is calculated by determining the search 
time to the nearest quarter hour and multiplying that figure by the sum 
of the basic rate of pay per hour of the employee conducting the search, 
plus 16 percent of that rate, plus the direct cost of the operation of 
the computer for that portion of time attributable to the search.
    (2) Review of records. Only requesters who are seeking documents for 
commercial use will be charged for time spent reviewing records to 
determine whether they are exempt from mandatory disclosure. Charges 
will be

[[Page 268]]

assessed only for the initial review; i.e., the review undertaken the 
first time ONDCP analyzes the applicability of a specific exemption to a 
particular record or portion of a record. Charges will not be assessed 
for review at the administrative appeal level of the exemption(s) 
already applied. The cost for review will be calculated based on the 
salary of the category of the employee who actually performed the review 
plus 16 percent of that rate.
    (3) Duplication of records. Copies made by routine photostatic 
copying shall be charged at the rate of $0.15 per page. If copies need 
to be made by other methods, the direct costs of such copies will be 
charged to the requester, as determined by the General Counsel.
    (4) Unsuccessful searches. Requesters may be charged for 
unsuccessful or unproductive searches or for searches when records 
located are determined to be exempt from disclosure.
    (5) Other charges. ONDCP will recover the direct costs of providing 
special services such as certifying that records are true copies, and 
sending records by special methods such as express mail.
    (c) No fee will be charged by ONDCP when the routine costs of 
collecting and processing the fee equal to or exceed the amount of the 
fee. For purposes of this section, the routine costs of collecting and 
processing a fee chargeable under FOIA are estimated to be $15.00 for 
each FOIA request.



Sec. 1401.11  Payment of Fees.

    (a) The requester must agree to pay all fees that are chargeable 
under this section prior to issuance of the requested copies.
    (b) Payment of fees shall be in the form either of a personal check 
or bank draft drawn on a bank in the United States, or a postal money 
order. Remittances shall be made payable to the order of the Treasurer 
of the United States and mailed to the General Counsel, Office of 
National Drug Control Policy, Executive Office of the President, 
Washington, DC 20500.
    (c) If it is anticipated that the fees chargeable under this section 
will amount to more than $25.00, and the requester has not indicated in 
advance his willingness to pay such fees, the requester shall be 
promptly notified of the amount of the anticipated fee or such portion 
thereof as can readily be estimated. In instances where the estimated 
fees will exceed $250.00, an advance deposit may be required. The notice 
or request for an advance deposit shall extend to the requester an offer 
to consult with ONDCP personnel in order to reformulate the request in a 
manner which will reduce the fees. A reformulated request shall be 
considered a new request, thus beginning a new 10 workday period for 
responding to the request.
    (d) When a requester has previously failed to pay a fee in a timely 
fashion (i.e., within 30 days of the date of the billing), ONDCP may 
require the requester to demonstrate that he or she has, in fact, paid 
any outstanding fees from past requests, and to make an advance payment 
of the full amount of the estimated fee for the present request before 
ONDCP responds to that request.
    (e) Interest charges on an unpaid bill may be assessed starting on 
the 31st day following the day on which the billing was sent. Interest 
shall be assessed at the rate prescribed in 31 U.S.C. 3717, and shall 
accrue from the date of the billing. The fact that a fee has been 
received by ONDCP, even if not processed, will suffice to stay the 
accrual of interest.
    (f) To encourage the repayment of delinquent fees, ONDCP shall use 
the procedures described in the Debt Collection Act of 1982, 31 U.S.C. 
3716-3719, including the use of collection agencies and disclosure to 
consumer reporting agencies.



Sec. 1401.12  Waiver of fees.

    (a) Records shall be furnished without charge, or at a reduced 
charge, upon a determination by the General Counsel of ONDCP that:
    (1) Waiver or reduction of the fees is in the public interest 
because release of the requested information is likely to contribute 
significantly to public understanding of the operations or activities of 
ONDCP and is not primarily in the commercial interest of the requester; 
or
    (2) Assessment of fees is not feasible.
    (b) Upon written request, a written explanation will be provided as 
to why

[[Page 269]]

a request for waiver or reduction of FOIA fees was not granted.
    (c) There is no right to an administrative appeal from a decision 
not to waive or reduce fees.



Sec. 1401.13  Aggregation of requests.

    (a) When the General Counsel reasonably believes that a requester, 
or a group of requesters acting in concert, is attempting to break down 
a request into a series of requests for the purpose of evading the 
assessment of fees, such requests may be aggregated and fees may be 
charged accordingly.
    (b) In determining whether a series of requests shall be aggregated, 
the General Counsel will consider two factors: whether the requests 
concern a single subject or two or more closely related subjects; and 
whether the requests were all made within a 30-day period. If a series 
of requests is made by multiple requesters, the General Counsel will 
also consider whether there is substantial evidence to support the 
conclusion that the requesters are acting in concert.



Sec. 1401.14  Records that are exempt from disclosure.

    (a) Records described in 5 U.S.C. 552(b) are exempt from disclosure 
under FOIA. These include the following categories of records:
    (1) Records that are specifically authorized under criteria 
established by an Executive order to be kept secret in the interest of 
national defense or foreign policy and are in fact properly classified 
pursuant to such Executive order;
    (2) Records related solely to the internal personnel rules and 
practices of an agency;
    (3) Records specifically exempted from disclosure by statute (other 
than 5 U.S.C. 552b), provided that such statute:
    (i) requires that the matters be withheld from the public in such a 
manner as to leave no discretion on the issue, or
    (ii) establishes particular criteria for withholding or refers to 
particular types of matters to be withheld;
    (4) Records of trade secrets and commercial or financial information 
obtained from a person and privileged or confidential;
    (5) Inter-agency or intra-agency memoranda or letters which would 
not be available by law to a party other than in litigation with the 
agency;
    (6) Personnel and medical files and similar files the disclosure of 
which would constitute a clearly unwarranted invasion of personal 
privacy; and
    (7) Records or information compiled for law enforcement purposes, 
but only to the extent that the production of such law enforcement 
records or information:
    (i) Could reasonably be expected to interfere with enforcement 
proceedings,
    (ii) Would deprive a person of a right to a fair trial or an 
impartial adjudication,
    (iii) Could reasonably be expected to constitute an unwarranted 
invasion of personal privacy,
    (iv) Could reasonably be expected to disclose the identity of a 
confidential source including a state, local, or foreign agency or 
authority or any private institution which furnished information on a 
confidential basis, and, in the case of a record compiled by a criminal 
law enforcement authority in the course of a criminal investigation, or 
by an agency conducting a lawful national security intelligence 
investigation, information furnished by a confidential source,
    (v) Would disclose techniques and procedures for law enforcement 
investigations or prosecutions, or would disclose guidelines for law 
enforcement investigations or prosecutions if such disclosure could 
reasonably be expected to risk circumvention of the law, or
    (vi) Could reasonably be expected to endanger the life or physical 
safety of any individual.



Sec. 1401.15  Deletion of exempted information.

    When requested records contain matters that are exempted under 5 
U.S.C. 552(b), but such exempted matters are reasonably segregable from 
the remainder of the records, the records shall be disclosed by ONDCP 
with the necessary deletions. ONDCP shall attach to each such record a 
written

[[Page 270]]

justification for making the deletion or deletions. A single such 
justification shall suffice for deletions made in a group of similar or 
related records.



PART 1402--MANDATORY DECLASSIFICATION REVIEW--Table of Contents




Sec.
1402.1  Purpose.
1402.2  Responsibility.
1402.3  Information in the custody of ONDCP.
1402.4  Information classified by another agency.
1402.5  Appeal procedure.
1402.6  Fees.
1402.7  Suggestions and complaints.

    Authority: Section 3.4, E.O. 12356 (3 CFR, 1982 Comp., p. 166), and 
Information Security Oversight Office Directive No. 1 (32 CFR 2001.32).

    Source: 57 FR 55089, Nov. 24, 1992, unless otherwise noted.



Sec. 1402.1  Purpose.

    Other government agencies, U.S. citizens or permanent resident 
aliens may request that classified information in files of the Office of 
National Drug Control Policy (ONDCP) be reviewed for possible 
declassification and release. This part prescribes the procedures for 
such review and subsequent release or denial.



Sec. 1402.2  Responsibility.

    All requests for the mandatory declassification review of classified 
information in ONDCP files should be addressed to the Security Officer, 
Office of National Drug Control Policy, Executive Office of the 
President, Washington, DC 20500, who will acknowledge receipt of the 
request. When a request does not reasonably describe the information 
sought, the requester shall be notified that unless additional 
information is provided, or the scope of the request is narrowed, no 
further action will be taken.



Sec. 1402.3  Information in the custody of ONDCP.

    Information contained in ONDCP files and under the exclusive 
declassification jurisdiction of ONDCP will be reviewed by the Director 
of the Office of Planning, Budget, and Administration of ONDCP and/or 
the office of primary interest to determine whether, under the 
declassification provisions of section 3.1 of Executive Order 12356 (3 
CFR, 1982 Comp., p. 166), the requested information may be declassified. 
If the information may not be released, in whole or in part, the 
requester shall be given a brief statement as to the reasons for denial, 
a notice of the right to appeal the determination to the Director of 
ONDCP, and a notice that such an appeal must be filed within 60 days in 
order to be considered.



Sec. 1402.4  Information classified by another agency.

    When a request is received for information that was classified by 
another agency, the Director of the Office of Planning, Budget, and 
Administration of ONDCP will forward the request and a copy of the 
document(s) along with any other related materials, to the appropriate 
agency for review and determination as to release. Recommendations as to 
release or denial may be made if appropriate. The requester will be 
notified of the referral, unless the receiving agency objects on the 
grounds that its association with the information requires protection.



Sec. 1402.5  Appeal procedure.

    Appeals reviewed as a result of a denial will be routed to the 
Director of ONDCP, who will take action as necessary to determine 
whether any part of the information may be declassified. If so, the 
Director shall notify the requester of this determination and shall make 
any information available that is declassified and is otherwise 
releasable. If continued classification is required, the requester shall 
be notified by the Director of ONDCP of the reasons therefore.



Sec. 1402.6  Fees.

    There will normally be no fees charged for the mandatory review of 
classified material for declassification under this part.



Sec. 1402.7  Suggestions and complaints.

    Suggestions and complaints regarding the information security 
program of ONDCP should be submitted, in writing, to the Security 
Officer, Office of

[[Page 271]]

National Drug Control Policy, Washington, DC 20500.



PART 1403--UNIFORM ADMINISTRATIVE REQUIREMENTS FOR GRANTS AND COOPERATIVE AGREEMENTS TO STATE AND LOCAL GOVERNMENTS--Table of Contents




                           Subpart A--General

Sec.
1403.1  Purpose and scope of this part.
1403.2  Scope of subpart.
1403.3  Definitions.
1403.4  Applicability.
1403.5  Effect on other issuances.
1403.6  Additions and exceptions.

                    Subpart B--Pre-Award Requirements

1403.10  Forms for applying for grants.
1403.11  State plans.
1403.12  Special grant or subgrant conditions for ``high-risk'' 
          grantees.

                   Subpart C--Post-Award Requirements

                        Financial Administration

1403.20  Standards for financial management systems.
1403.21  Payment.
1403.22  Allowable costs.
1403.23  Period of availability of funds.
1403.24  Matching or cost sharing.
1403.25  Program income.
1403.26  Non-Federal audit.

                    Changes, Property, and Subawards

1403.30  Changes.
1403.31  Real property.
1403.32  Equipment.
1403.33  Supplies.
1403.34  Copyrights.
1403.35  Subawards to debarred and suspended parties.
1403.36  Procurement.
1403.37  Subgrants.

              Reports, Records, Retention, and Enforcement

1403.40  Monitoring and reporting program performance.
1403.41  Financial reporting.
1403.42  Retention and access requirements for records.
1403.43  Enforcement.
1403.44  Termination for convenience.

                 Subpart D--After-the-Grant Requirements

1403.50  Closeout.
1403.51  Later disallowances and adjustments.
1403.52  Collection of amounts due.

                   Subpart E--Entitlement  [Reserved]

Appendix A to Part 1403--OMB Circular A-128, ``Audit of State and Local 
          Governments''

    Authority: 5 U.S.C. 301.

    Source: 57 FR 55092, Nov. 24, 1992, unless otherwise noted.



                           Subpart A--General



Sec. 1403.1  Purpose and scope of this part.

    This part establishes uniform administrative rules for Federal 
grants and cooperative agreements and subawards to State, local and 
Indian tribal governments.



Sec. 1403.2  Scope of subpart.

    This subpart contains general rules pertaining to this part and 
procedures for control of exceptions from this part.



Sec. 1403.3  Definitions.

    As used in this part:
    Accrued expenditures mean the charges incurred by the grantee during 
a given period requiring the provision of funds for:
    (1) Goods and other tangible property received;
    (2) Services performed by employees, contractors, subgrantees, 
subcontractors, and other payees; and
    (3) Other amounts becoming owed under programs for which no current 
services or performance is required, such as annuities, insurance 
claims, and other benefit payments.
    Accrued income means the sum of:
    (1) Earnings during a given period from services performed by the 
grantee and goods and other tangible property delivered to purchasers, 
and
    (2) Amounts becoming owed to the grantee for which no current 
services or performance is required by the grantee.
    Acquisition cost of an item of purchased equipment means the net 
invoice unit price of the property including the cost of modifications, 
attachments, accessories, or auxiliary apparatus necessary to make the 
property usable for the purpose for which it was acquired. Other charges 
such as the cost of installation, transportation,

[[Page 272]]

taxes, duty or protective in-transit insurance, shall be included or 
excluded from the unit acquisition cost in accordance with the grantee's 
regular accounting practices.
    Administrative requirements mean those matters common to grants in 
general, such as financial management, kinds and frequency of reports, 
and retention of records. These are distinguished from ``programmatic'' 
requirements, which concern matters that can be treated only on a 
program-by-program or grant-by-grant basis, such as kinds of activities 
that can be supported by grants under a particular program.
    Awarding agency means:
    (1) With respect to a grant, the Federal agency, and
    (2) With respect to a subgrant, the party that awarded the subgrant.
    Cash contributions means the grantee's cash outlay, including the 
outlay of money contributed to the grantee or subgrantee by other public 
agencies and institutions, and private organizations and individuals. 
When authorized by Federal legislation, Federal funds received from 
other assistance agreements may be considered as grantee or subgrantee 
cash contributions.
    Contract means (except as used in the definitions for ``grant'' and 
``subgrant'' in this section and except where qualified by ``Federal'') 
a procurement contract under a grant or subgrant, and means a 
procurement subcontract under a contract.
    Cost sharing or matching means the value of the third party in-kind 
contributions and the portion of the costs of a federally assisted 
project or program not borne by the Federal Government.
    Cost-type contract means a contract or subcontract under a grant in 
which the contractor or subcontractor is paid on the basis of the costs 
it incurs, with or without a fee.
    Equipment means tangible, nonexpendable, personal property having a 
useful life of more than one year and an acquisition cost of $5,000 or 
more per unit. A grantee may use its own definition of equipment 
provided that such definition would at least include all equipment 
defined above.
    Expenditure report means:
    (1) For nonconstruction grants, the SF-269 ``Financial Status 
Report'' (or other equivalent report);
    (2) For construction grants, the SF-271 ``Outlay Report and Request 
for Reimbursement'' (or other equivalent report).
    Federally recognized Indian tribal government means the governing 
body or a governmental agency of any Indian tribe, band, nation, or 
other organized group or community (including any Native village as 
defined in section 3 of the Alaska Native Claims Settlement Act, 85 
Stat. 688) certified by the Secretary of the Interior as eligible for 
the special programs and services provided by him through the Bureau of 
Indian Affairs.
    Government means a State or local government or a federally 
recognized Indian tribal government.
    Grant means an award of financial assistance, including cooperative 
agreements, in the form of money, or property in lieu of money, by the 
Federal Government to an eligible grantee. The term does not include 
technical assistance which provides services instead of money, or other 
assistance in the form of revenue sharing, loans, loan guarantees, 
interest subsidies, insurance, or direct appropriations. Also, the term 
does not include assistance, such as a fellowship or other lump sum 
award, which the grantee is not required to account for.
    Grantee means the government to which a grant is awarded and which 
is accountable for the use of the funds provided. The grantee is the 
entire legal entity even if only a particular component of the entity is 
designated in the grant award document.
    Local government means a county, municipality, city, town, township, 
local public authority (including any public and Indian housing agency 
under the United States Housing Act of 1937) school district, special 
district, intrastate district, council of governments (whether or not 
incorporated as a nonprofit corporation under state law), any other 
regional or interstate government entity, or any agency or 
instrumentality of a local government.
    Obligations means the amounts of orders placed, contracts and 
subgrants awarded, goods and services received,

[[Page 273]]

and similar transactions during a given period that will require payment 
by the grantee during the same or a future period.
    OMB means the United States Office of Management and Budget.
    Outlays (expenditures) means charges made to the project or program. 
They may be reported on a cash or accrual basis. For reports prepared on 
a cash basis, outlays are the sum of actual cash disbursement for direct 
charges for goods and service, the amount of indirect expense incurred, 
the value of in-kind contributions applied, and the amount of cash 
advances and payments made to contractors and subgrantees. For reports 
prepared on an accrued expenditure basis, outlays are the sum of actual 
cash disbursements, the amount of indirect expense incurred, the value 
of in-kind contributions applied, and the new increase (or decrease) in 
the amounts owed by the grantee for goods and other property received, 
for services performed by employees, contractors, subgrantees, 
subcontractors, and other payees, and other amounts becoming owed under 
programs for which no current services or performance are required, such 
as annuities, insurance claims, and other benefit payments.
     Percentage of completion method refers to a system under which 
payments are made for construction work according to the percentage of 
completion of the work, rather than to the grantee's cost incurred.
    Prior approval means documentation evidencing consent prior to 
incurring specific cost.
    Real property means land, including land improvements, structures 
and appurtenances thereto, excluding movable machinery and equipment.
    Share, when referring to the awarding agency's portion of real 
property, equipment or supplies, means the same percentage as the 
awarding agency's portion of the acquiring party's total costs under the 
grant to which the acquisition costs under the grant to which the 
acquisition cost of the property was charged. Only costs are to be 
counted--not the value of third-party in-kind contributions.
    State means any of the several States of the United States, the 
District of Columbia, the Commonwealth of Puerto Rico, any territory or 
possession of the United States, or any agency or instrumentality of a 
State exclusive of local governments. The term does not include any 
public and Indian housing agency under United States Housing Act of 
1937.
    Subgrant means an award of financial assistance in the form of 
money, or property in lieu of money, made under a grant by a grantee to 
an eligible subgrantee. The term includes financial assistance when 
provided by contractual legal agreement, but does not include 
procurement purchases, nor does it include any form of assistance which 
is excluded from the definition of ``grant'' in this part.
    Subgrantee means the government or other legal entity to which a 
subgrant is awarded and which is accountable to the grantee for the use 
of the funds provided.
    Supplies means all tangible personal property other than 
``equipment'' as defined in this part.
    Suspension means depending on the context, either
    (1) Temporary withdrawal of the authority to obligate grant funds 
pending corrective action by the grantee or subgrantee or a decision to 
terminate the grant, or
    (2) In action taken by a suspending official in accordance with 
agency regulations implementing E.O. 12549 to immediately exclude a 
person from participating in grant transactions for a period, pending 
completion of an investigation and such legal or debarment proceedings 
as may ensue.
    Termination means permanent withdrawal of the authority to obligate 
previously-awarded grant funds before that authority would otherwise 
expire. It also means the voluntary relinquishment of that authority by 
the grantee or subgrantee. ``Termination'' does not include:
    (1) Withdrawal of funds awarded on the basis of the grantee's 
underestimate of the unobligated balance in a prior period;
    (2) Withdrawal of the unobligated balance as of the expiration of a 
grant;
    (3) Refusal to extend a grant or award additional funds, to make a 
competing or noncompeting continuation,

[[Page 274]]

renewal, extension, or supplemental award; or
    (4) Voiding of a grant upon determination that the award was 
obtained fraudulently, or was otherwise illegal or invalid from 
inception.
    Terms of a grant or subgrant mean all requirements of the grant or 
subgrant, whether in statute, regulations, or the award document.
    Third party in-kind contributions mean property or services which 
benefit a federally assisted project or program and which are 
contributed by non-Federal third parties without charge to the grantee, 
or a cost-type contractor under the grant agreement.
    Unliquidated obligations for reports prepared on a cash basis mean 
the amount of obligations incurred by the grantee that has not been 
paid. For reports prepared on an accrued expenditure basis, they 
represent the amount of obligations incurred by the grantee for which an 
outlay has not been recorded.
    Unobligated balance means the portion of the funds authorized by the 
Federal agency that has not been obligated by the grantee and is 
determined by deducting the cumulative obligations from the cumulative 
funds authorized.



Sec. 1403.4  Applicability.

    (a) General. Subparts A-D of this part apply to all grants and 
subgrants to governments, except where inconsistent with Federal 
statutes or with regulations authorized in accordance with the exception 
provision of Sec. 1403.6, or:
    (1) Grants and subgrants to State and local institutions of higher 
education or State and local hospitals;
    (2) The block grants authorized by the Omnibus Budget Reconciliation 
Act of 1981 (Community Services; Preventive Health and Health Services; 
Alcohol, Drug Abuse, and Mental Health Services; Maternal and Child 
Health Services; Social Services; Low-Income Home Energy Assistance; 
States' Program of Community Development Block Grants for Small Cities; 
and Elementary and Secondary Education other than programs administered 
by the Secretary of Education under title V, subtitle D, chapter 2, 
section 583--the Secretary's discretionary grant program) and titles I-
III of the Job Training Partnership Act of 1982 and under the Public 
Health Services Act (Section 1921), Alcohol and Drug Abuse Treatment and 
Rehabilitation Block Grant and part C of title V, Mental Health Service 
for the Homeless Block Grant);
    (3) Entitlement grants to carry out the following programs of the 
Social Security Act:
    (i) Aid to Needy Families with Dependent Children (title IV-A of the 
Act, not including the Work Incentive Program (WIN) authorized by 
section 402(a)19(G); HHS grants for WIN are subject to this part);
    (ii) Child Support Enforcement and Establishment of Paternity (title 
IV-D of the Act);
    (iii) Foster Care and Adoption Assistance (title IV-E of the Act);
    (iv) Aid to the Aged, Blind, and Disabled (titles I, X, XIV, and 
XVI-AABD of the Act); and
    (v) Medical Assistance (Medicaid) (title XIX of the Act) not 
including the State Medicaid Fraud Control program authorized by section 
1903(a)(6)(B);
    (4) Entitlement grants under the following programs of The National 
School Lunch Act:
    (i) School Lunch (section 4 of the Act),
    (ii) Commodity Assistance (section 6 of the Act),
    (iii) Special Meal Assistance (section 11 of the Act),
    (iv) Summer Food Service for Children (section 13 of the Act), and
    (v) Child Care Food Program (section 17 of the Act);
    (5) Entitlement grants under the following programs of The Child 
Nutrition Act of 1966:
    (i) Special Milk (section 3 of the Act), and
    (ii) School Breakfast (section 4 of the Act);
    (6) Entitlement grants for State Administrative expenses under The 
Food Stamp Act of 1977 (section 16 of the Act);
    (7) A grant for an experimental, pilot, or demonstration project 
that is also supported by a grant listed in paragraph (a)(3) of this 
section;
    (8) Grant funds awarded under subsection 412(e) of the Immigration 
and

[[Page 275]]

Nationality Act (8 U.S.C. 1522(e)) and subsection 501(a) of the Refugee 
Education Assistance Act of 1980 (Pub. L. 96-422, 94 Stat. 1809), for 
cash assistance, medical assistance, and supplemental security income 
benefits to refugees and entrants and the administrative costs of 
providing the assistance and benefits;
    (9) Grants to local education agencies under 20 U.S.C. 236 through 
241-1(a), and 242 through 244 (portions of the Impact Aid program), 
except for 20 U.S.C. 238(d)(2)(c) and 240(f) (Entitlement Increase for 
Handicapped Children); and
    (10) Payments under the Veterans Administration's State Home Per 
Diem Program (38 U.S.C. 641(a)).
    (b) Entitlement programs. Entitlement programs enumerated above in 
Sec. 1403.4(a) (3) through (8) are subject to subpart E.



Sec. 1403.5  Effect on other issuances.

    All other grants administration provisions of codified program 
regulations, program manuals, handbooks and other nonregulatory 
materials which are inconsistent with this part are superseded, except 
to the extent they are required by statute, or authorized in accordance 
with the exception provision in Sec. 1403.6.



Sec. 1403.6  Additions and exceptions.

    (a) For classes of grants and grantees subject to this part, Federal 
agencies may not impose additional administrative requirements except in 
codified regulations published in the Federal Register.
    (b) Exceptions for classes of grants or grantees may be authorized 
only by OMB.
    (c) Exceptions on a case-by-case basis and for subgrantees may be 
authorized by the affected Federal agencies.



                    Subpart B--Pre-Award Requirements



Sec. 1403.10  Forms for applying for grants.

    (a) Scope. (1) This section prescribes forms and instructions to be 
used by governmental organizations (except hospitals and institutions of 
higher education operated by a government) in applying for grants. This 
section is not applicable, however, to formula grant programs which do 
not require applicants to apply for funds on a project basis.
    (2) This section applies only to applications to Federal agencies 
for grants, and is not required to be applied by grantees in dealing 
with applicants for subgrants. However, grantees are encouraged to avoid 
more detailed or burdensome application requirements for subgrants.
    (b) Authorized forms and instructions for governmental 
organizations. (1) In applying for grants, applicants shall only use 
standard application forms or those prescribed by the granting agency 
with the approval of OMB under the Paperwork Reduction Act of 1980.
    (2) Applicants are not required to submit more than the original and 
two copies of preapplications or applications.
    (3) Applicants must follow all applicable instructions that bear OMB 
clearance numbers. Federal agencies may specify and describe the 
programs, functions, or activities that will be used to plan, budget, 
and evaluate the work under a grant. Other supplementary instructions 
may be issued only with the approval of OMB to the extent required under 
the Paperwork Reduction Act of 1980. For any standard form, except the 
SF-424 facesheet, Federal agencies may shade out or instruct the 
applicant to disregard any line item that is not needed.
    (4) When a grantee applies for additional funding (such as a 
continuation or supplemental award) or amends a previously submitted 
application, only the affected pages need be submitted. Previously 
submitted pages with information that is still current need not be 
resubmitted.



Sec. 1403.11  State plans.

    (a) Scope. The statutes for some programs require States to submit 
plans before receiving grants. Under regulations implementing Executive 
Order 12372, ``Intergovernmental Review of Federal Programs,'' States 
are allowed to simplify, consolidate and substitute plans. This section 
contains additional provisions for plans that are subject to regulations 
implementing the Executive Order.

[[Page 276]]

    (b) Requirements. A State need meet only Federal administrative or 
programmatic requirements for a plan that are in statutes or codified 
regulations.
    (c) Assurances. In each plan the States will include an assurance 
that the State shall comply with all applicable Federal statutes and 
regulations in effect with respect to the periods for which it receives 
grant funding. For this assurance and other assurances required in the 
plan, the State may:
    (1) Cite by number the statutory or regulatory provisions requiring 
the assurances and affirm that it gives the assurances required by those 
provisions,
    (2) Repeat the assurance language in the statutes or regulations, or
    (3) Develop its own language to the extent permitted by law.
    (d) Amendments. A State will amend a plan whenever necessary to 
reflect: (1) New or revised Federal statutes or regulations or (2) a 
material change in any State law, organization, policy, or State agency 
operation. The State will obtain approval for the amendment and its 
effective date but need submit for approval only the amended portions of 
the plan.



Sec. 1403.12  Special grant or subgrant conditions for ``high-risk'' grantees.

    (a) A grantee or subgrantee may be considered ``high risk'' if an 
awarding agency determines that a grantee or subgrantee:
    (1) Has a history of unsatisfactory performance, or
    (2) Is not financially stable, or
    (3) Has a management system which does not meet the management 
standards set forth in this part, or
    (4) Has not conformed to terms and conditions of previous awards, or
    (5) Is otherwise not responsible; and if the awarding agency 
determines that an award will be made, special conditions and/or 
restrictions shall correspond to the high risk condition and shall be 
included in the award.
    (b) Special conditions or restrictions may include:
    (1) Payment on a reimbursement basis;
    (2) Withholding authority to proceed to the next phase until receipt 
of evidence of acceptable performance within a given funding period;
    (3) Requiring additional, more detailed financial reports;
    (4) Additional project monitoring;
    (5) Requiring the grantee or subgrantee to obtain technical or 
management assistance; or
    (6) Establishing additional prior approvals;
    (c) If an awarding agency decides to impose such conditions, the 
awarding official will notify the grantee or subgrantee as early as 
possible, in writing, of:
    (1) The nature of the special conditions/restrictions;
    (2) The reason(s) for imposing them;
    (3) The corrective actions which must be taken before they will be 
removed and the time allowed for completing the corrective actions; and
    (4) The method of requesting reconsideration of the conditions/
restrictions imposed.



                   Subpart C--Post-Award Requirements

                        Financial Administration



Sec. 1403.20  Standards for financial management systems.

    (a) A State must expend and account for grant funds in accordance 
with State laws and procedures for expending and accounting for its own 
funds. Fiscal control and accounting procedures of the State, as well as 
its subgrantees and cost-type contractors, must be sufficient to--
    (1) Permit preparation of reports required by this part and the 
statutes authorizing the grant, and
    (2) Permit the tracing of funds to a level of expenditures adequate 
to establish that such funds have not been used in violation of the 
restrictions and prohibitions of applicable statutes.
    (b) The financial management systems of other grantees and 
subgrantees must meet the following standards:
    (1) Financial reporting. Accurate, current, and complete disclosure 
of the financial results of financially assisted activities must be made 
in accordance with the financial reporting requirements of the grant or 
subgrant.

[[Page 277]]

    (2) Accounting records. Grantees and subgrantees must maintain 
records which adequately identify the source and application of funds 
provided for financially-assisted activities. These records must contain 
information pertaining to grant or subgrant awards and authorizations, 
obligations, unobligated balances, assets, liabilities, outlays or 
expenditures, and income.
    (3) Internal control. Effective control and accountability must be 
maintained for all grant and subgrant cash, real and personal property, 
and other assets. Grantees and subgrantees must adequately safeguard all 
such property and must assure that it is used solely for authorized 
purposes.
    (4) Budget control. Actual expenditures or outlays must be compared 
with budgeted amounts for each grant or subgrant. Financial information 
must be related to performance or productivity data, including the 
development of unit cost information whenever appropriate or 
specifically required in the grant or subgrant agreement. If unit cost 
data are required, estimates based on available documentation will be 
accepted whenever possible.
    (5) Allowable cost. Applicable OMB cost principles, agency program 
regulations, and the terms of grant and subgrant agreements will be 
followed in determining the reasonableness, allowability, and 
allocability of costs.
    (6) Source documentation. Accounting records must be supported by 
such source documentation as canceled checks, paid bills, payrolls, time 
and attendance records, contract and subgrant award documents, etc.
    (7) Cash management. Procedures for minimizing the time elapsing 
between the transfer of funds from the U.S. Treasury and disbursement by 
grantees and subgrantees must be followed whenever advance payment 
procedures are used. Grantees must establish reasonable procedures to 
ensure the receipt of reports on subgrantees' cash balances and cash 
disbursements in sufficient time to enable them to prepare complete and 
accurate cash transactions reports to the awarding agency. When advances 
are made by letter-of-credit or electronic transfer of funds methods, 
the grantee must make drawdowns as close as possible to the time of 
making disbursements. Grantees must monitor cash drawdowns by their 
subgrantees to assure that they conform substantially to the same 
standards of timing and amount as apply to advances to the grantees.
    (c) An awarding agency may review the adequacy of the financial 
management system of any applicant for financial assistance as part of a 
preaward review or at any time subsequent to award.



Sec. 1403.21  Payment.

    (a) Scope. This section prescribes the basic standard and the 
methods under which a Federal agency will make payments to grantees, and 
grantees will make payments to subgrantees and contractors.
    (b) Basic standard. Methods and procedures for payment shall 
minimize the time elapsing between the transfer of funds and 
disbursement by the grantee or subgrantee, in accordance with Treasury 
regulations at 31 CFR part 205.
    (c) Advances. Grantees and subgrantees shall be paid in advance, 
provided they maintain or demonstrate the willingness and ability to 
maintain procedures to minimize the time elapsing between the transfer 
of the funds and their disbursement by the grantee or subgrantee.
    (d) Reimbursement. Reimbursement shall be the preferred method when 
the requirements in paragraph (c) of this section are not met. Grantees 
and subgrantees may also be paid by reimbursement for any construction 
grant. Except as otherwise specified in regulation, Federal agencies 
shall not use the percentage of completion method to pay construction 
grants. The grantee or subgrantee may use that method to pay its 
construction contractor, and if it does, the awarding agency's payments 
to the grantee or subgrantee will be based on the grantee's or 
subgrantee's actual rate of disbursement.
    (e) Working capital advances. If a grantee cannot meet the criteria 
for advance payments described in paragraph (c) of this section, and the 
Federal agency has determined that reimbursement is not feasible the 
grantee lacks sufficient working capital, the

[[Page 278]]

awarding agency may provide cash or a working capital advance basis. 
Under this procedure the awarding agency shall advance cash to the 
grantee to cover its estimated disbursement needs for an initial period 
generally geared to the grantee's disbursing cycle. Thereafter, the 
awarding agency shall reimburse the grantee for its actual cash 
disbursements. The working capital advance method of payment shall not 
be used by grantees or subgrantees if the reason for using such method 
is the unwillingness or inability of the grantee to provide timely 
advances to the subgrantee to meet the subgrantee's actual cash 
disbursements.
    (f) Effect of program income, refunds, and audit recoveries on 
payment. (1) Grantees and subgrantees shall disburse repayments to and 
interest earned on a revolving fund before requesting additional cash 
payments for the same activity.
    (2) Except as provided in paragraph (f)(1) of this section, grantees 
and subgrantees shall disburse program income, rebates, refunds, 
contract settlements, audit recoveries and interest earned on such funds 
before requesting additional cash payments.
    (g) Withholding payments. (1) Unless otherwise required by Federal 
statute, awarding agencies shall not withhold payments for proper 
charges incurred by grantees or subgrantees unless----
    (i) The grantee or subgrantee has failed to comply with grant award 
conditions or
    (ii) The grantee or subgrantee is indebted to the United States.
    (2) Cash withheld for failure to comply with grant award condition, 
but without suspension of the grant, shall be released to the grantee 
upon subsequent compliance. When a grant is suspended, payment 
adjustments will be made in accordance with Sec. 1403.43(c).
    (3) A Federal agency shall not make payment to grantees for amounts 
that are withheld by grantees or subgrantees from payment to contractors 
to assure satisfactory completion of work. Payments shall be made by the 
Federal agency when the grantees or subgrantees actually disburse the 
withheld funds to the contractors or to escrow accounts established to 
assure satisfactory completion of work.
    (h) Cash depositories. (1) Consistent with the national goal of 
expanding the opportunities for minority business enterprises, grantees 
and subgrantees are encouraged to use minority banks (a bank which is 
owned at least 50 percent by minority group members). A list of minority 
owned banks can be obtained from the Minority Business Development 
Agency, Department of Commerce, Washington, DC 20230.
    (2) A grantee or subgrantee shall maintain a separate bank account 
only when required by Federal-State agreement.
    (i) Interest earned on advances. Except for interest earned on 
advances of funds exempt under the Intergovernmental Cooperation Act (31 
U.S.C. 6501 et seq.) and the Indian Self-Determination Act (23 U.S.C. 
450), grantees and subgrantees shall promptly, but at least quarterly, 
remit interest earned on advances to the Federal agency. The grantee or 
subgrantee may keep interest amounts up to $100 per year for 
administrative expenses.



Sec. 1403.22  Allowable costs.

    (a) Limitation on use of funds. Grant funds may be used only for:
    (1) The allowable costs of the grantees, subgrantees and cost-type 
contractors, including allowable costs in the form of payments to fixed-
price contractors; and
    (2) Reasonable fees or profit to cost-type contractors but not any 
fee or profit (or other increment above allowable costs) to the grantee 
or subgrantee.
    (b) Applicable cost principles. For each kind of organization, there 
is a set of Federal principles for determining allowable costs. 
Allowable costs will be determined in accordance with the cost 
principles applicable to the organization incurring the costs. The 
following chart lists the kinds of organizations and the applicable cost 
principles.

------------------------------------------------------------------------
           For the costs of a--                Use the principles in--  
------------------------------------------------------------------------
State, local or Indian tribal government..  OMB Circular A-87.          
Private nonprofit organization other than   OMB Circular A-122.         
 (1) institution of higher education, (2)                               
 hospital, or (3) organization named in                                 
 OMB Circular A-122 as not subject to that                              
 circular.                                                              

[[Page 279]]

                                                                        
Educational institutions..................  OMB Circular A-21.          
For-profit organizations other than a       48 CFR part 31. Contract    
 hospital and an organization named in OMB   Cost Principles and        
 Circular A-122 as not subject to that       Procedures, or uniform cost
 circular.                                   accounting standards that  
                                             comply with cost principles
                                             acceptable to the Federal  
                                             agency.                    
------------------------------------------------------------------------



Sec. 1403.23  Period of availability of funds.

    (a) General. Where a funding period is specified, a grantee may 
charge to the award only costs resulting from obligations of the funding 
period unless carryover of unobligated balances is permitted, in which 
case the carryover balances may be charged for costs resulting from 
obligations of the subsequent funding period.
    (b) Liquidation of obligations. A grantee must liquidate all 
obligations incurred under the award not later than 90 days after the 
end of the funding period (or as specified in a program regulation) to 
coincide with the submission of the annual Financial Status Report (SF-
269). The Federal agency may extend this deadline at the request of the 
grantee.



Sec. 1403.24  Matching or cost sharing.

    (a) Basic rule: Costs and contributions acceptable. With the 
qualifications and exceptions listed in paragraph (b) of this section, a 
matching or cost sharing requirement may be satisfied by either or both 
of the following:
    (1) Allowable costs incurred by the grantee, subgrantee or a cost-
type contractor under the assistance agreement. This includes allowable 
costs borne by non-Federal grants or by others cash donations from non-
Federal third parties.
    (2) The value of third party in-kind contributions applicable to the 
period to which the cost sharing or matching requirements applies.
    (b) Qualifications and exceptions--(1) Costs borne by other Federal 
grant agreements. Except as provided by Federal statute, a cost sharing 
or matching requirement may not be met by costs borne by another Federal 
grant. This prohibition does not apply to income earned by a grantee or 
subgrantee from a contract awarded under another Federal grant.
    (2) General revenue sharing. For the purpose of this section, 
general revenue sharing funds distributed under 31 U.S.C. 6702 are not 
considered Federal grant funds.
    (3) Cost or contributions counted towards other Federal cost-sharing 
requirements. Neither costs nor the values of third party in-kind 
contributions may count towards satisfying a cost sharing or matching 
requirement of a grant agreement if they have been or will be counted 
towards satisfying a cost sharing or matching requirement of another 
Federal grant agreement, a Federal procurement contract, or any other 
award of Federal funds.
    (4) Costs financed by program income. Costs financed by program 
income, as defined in Sec. 1403.25, shall not count towards satisfying a 
cost sharing or matching requirement unless they are expressly permitted 
in the terms of the assistant agreement. (This use of general program 
income is described in Sec. 1403.25(g).)
    (5) Services or property financed by income earned by contractors. 
Contractors under a grant may earn income from the activities carried 
out under the contract in addition to the amounts earned from the party 
awarding the contract. No costs of services or property supported by 
this income may count toward satisfying cost sharing or matching 
requirement unless other provisions of the grant agreement expressly 
permit this kind of income to be used to meet the requirement.
    (6) Records. Costs and third party in-kind contributions counting 
towards satisfying a cost sharing or matching requirement must be 
verifiable from the records of grantees and subgrantee or cost-type 
contractors. These records must show how the value placed on third party 
in-kind contributions was derived. To the extent feasible, volunteer 
services will be supported by the same methods that the organization 
uses to support the allocability of regular personnel costs.
    (7) Special standards for third party in-kind contributions. (i) 
Third party in-kind contributions count towards satisfying a cost 
sharing or matching requirement only where, if the party receiving the 
contributions were to pay

[[Page 280]]

for them, the payments would be allowable costs.
    (ii) Some third party in-kind contributions are goods and services 
that, if the grantee, subgrantee, or contractor receiving the 
contribution had to pay for them, the payments would have been an 
indirect costs. Costs sharing or matching credit for such contributions 
shall be given only if the grantee, subgrantee, or contractor has 
established, along with its regular indirect cost rate, a special rate 
for allocating to individual projects or programs the value of the 
contributions.
    (iii) A third party in-kind contribution to a fixed-price contract 
may count towards satisfying a cost sharing or matching requirement only 
if it results in:
    (A) An increase in the services or property provided under the 
contract (without additional cost to the grantee or subgrantee) or
    (B) A cost savings to the grantee or subgrantee.
    (iv) The values placed on third party in-kind contributions for cost 
sharing or matching purposes will conform to the rules in the succeeding 
sections of this part. If a third party in-kind contribution is a type 
not treated in those sections, the value placed upon it shall be fair 
and reasonable.
    (c) Valuation of donated services--(1) Volunteer services. Unpaid 
services provided to a grantee or subgrantee by individuals will be 
valued at rates consistent with those ordinarily paid for similar work 
in the grantee's or subgrantee's organization. If the grantee or 
subgrantee does not have employees performing similar work, the rates 
will be consistent with those ordinarily paid by other employers for 
similar work in the same labor market. In either case, a reasonable 
amount for fringe benefits may be included in the valuation.
    (2) Employees of other organizations. When an employer other than a 
grantee, subgrantee, or cost-type contractor furnishes free of charge 
the services of an employee in the employee's normal line of work, the 
services will be valued at the employee's regular rate of pay exclusive 
of the employee's fringe benefits and overhead costs. If the services 
are in a different line of work, paragraph (c)(1) of this section 
applies.
    (d) Valuation of third party donated supplies and loaned equipment 
or space. (1) If a third party donates supplies, the contribution will 
be valued at the market value of the supplies at the time of donation.
    (2) If a third party donates the use of equipment or space in a 
building but retains title, the contribution will be valued at the fair 
rental rate of the equipment or space.
    (e) Valuation of third party donated equipment, buildings, and land. 
If a third party donates equipment, buildings, or land, and title passes 
to a grantee or subgrantee, the treatment of the donated property will 
depend upon the purpose of the grant or subgrant, as follows:
    (1) Awards for capital expenditures. If the purpose of the grant or 
subgrant is to assist the grantee or subgrantee in the acquisition of 
property, the market value of that property at the time of donation may 
be counted as cost sharing or matching.
    (2) Other awards. If assisting in the acquisition of property is not 
the purpose of the grant or subgrant, paragraphs (e)(2) (i) and (ii) of 
this section apply:
    (i) If approval is obtained from the awarding agency, the market 
value at the time of donation of the donated equipment or buildings and 
the fair rental rate of the donated land may be counted as cost sharing 
or matching. In the case of a subgrant, the terms of the grant agreement 
may require that the approval be obtained from the Federal agency as 
well as the grantee. In all cases, the approval may be given only if a 
purchase of the equipment or rental of the land would be approved as an 
allowable direct cost. If any part of the donated property was acquired 
with Federal funds, only the non-federal share of the property may be 
counted as cost-sharing or matching.
    (ii) If approval is not obtained under paragraph (e)(2)(i) of this 
section, no amount may be counted for donated land, and only 
depreciation or use allowances may be counted for donated equipment and 
buildings. The depreciation or use allowances for this property are not 
treated as third party in-kind

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contributions. Instead, they are treated as costs incurred by the 
grantee or subgrantee. They are computed and allocated (usually as 
indirect costs) in accordance with the cost principles specified in 
Sec. 1403.22, in the same way as depreciation or use allowances for 
purchased equipment and buildings. The amount of depreciation or use 
allowances for donated equipment and buildings is based on the 
property's market value at the time it was donated.
    (f) Valuation of grantee or subgrantee donates real property for 
construction/acquisition. If a grantee or subgrantee donates real 
property for a construction or facilities acquisition project, the 
current market value of that property may be counted as cost sharing or 
matching. If any part of the donated property was acquired with Federal 
funds, only the non-federal share of the property may be counted as cost 
sharing or matching.
    (g) Appraisal of real property. In some cases under paragraphs (d), 
(e) and (f) of this section, it will be necessary to establish the 
market value of land or a building or the fair rental rate of land or of 
space in a building. In these cases, the Federal agency may require the 
market value or fair rental value be set by an independent appraiser, 
and that the value or rate be certified by the grantee. This requirement 
will also be imposed by the grantee on subgrantees.



Sec. 1403.25  Program income.

    (a) General. Grantees are encouraged to earn income to defray 
program costs. Program income includes income from fees for services 
performed, from the use of rental of real or personal property acquired 
with grant funds, from the sale of commodities or items fabricated under 
a grant agreement, and from payments of principal and interest on loans 
made with grant funds. Except as otherwise provided in regulations of 
the Federal agency, program income does not include interest on grant 
funds, rebates, credits, discounts, refunds, etc., and interest earned 
on any of them.
    (b) Definition of program income. Program income means gross income 
received by the grantee or subgrantee directly generated by a grant 
supported activity, or earned only as a result of the grant agreement 
during the grant period. ``During the grant period'' is the time between 
the effective date of the award and the ending date of the award 
reflected in the final financial report.
    (c) Cost of generating program income. If authorized by Federal 
regulations or the grant agreement, costs incident to the generation of 
program income may be deducted from gross income to determine program 
income.
    (d) Governmental revenues. Taxes, special assessments levies, fines, 
and other such revenues raised by a grantee or subgrantee are not 
program income unless the revenues are specifically identified in the 
grant agreement or Federal agency regulations as program income.
    (e) Royalties. Income from royalties and license fees for 
copyrighted material, patents, and inventions developed by a grantee or 
subgrantee is program income only if the revenues are specifically 
identified in the grant agreement or Federal agency regulations as 
program income. (See Sec. 1403.34.)
    (f) Property. Proceeds from the sale of real property or equipment 
will be handled in accordance with the requirements of Sec. 1403.31 and 
Sec. 1403.32.
    (g) Use of program income. Program income shall be deducted from 
outlays which may be both Federal and non-Federal as described below, 
unless the Federal agency regulations or the grant agreement specify 
another alternative (or a combination of the alternatives). In 
specifying alternatives, the Federal agency may distinguish between 
income earned by the grantee and income earned by subgrantees and 
between the sources, kinds, or amounts of income. When Federal agencies 
authorize the alternatives in paragraphs (g) (2) and (3) of this 
section, program income in excess of any limits stipulated shall also be 
deducted from outlays.
    (1) Deduction. Ordinarily program income shall be deducted from 
total allowable costs to determine the net allowable costs. Program 
income shall be used for current costs unless the Federal agency 
authorizes otherwise. Program income which the grantee did not 
anticipate at the time of the award shall be used to reduce the Federal

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agency and grantee contributions rather than to increase the funds 
committed to the project.
    (2) Addition. When authorized, program income may be added to the 
funds committed to the grant agreement by the Federal agency and the 
grantee. The program income shall be used for the purposes and under the 
conditions of the grant agreement.
    (3) Cost sharing or matching. When authorized, program income may be 
used to meet the cost sharing or matching requirement of the grant 
agreement. The amount of the Federal grant award remains the same.
    (h) Income after the award period. There are no Federal requirements 
governing the disposition of program income earned after the end of the 
award period (i.e., until the ending date of the final financial report, 
see paragraph (a) of this section), unless the terms of the agreement or 
the Federal agency regulations provide otherwise.



Sec. 1403.26  Non-Federal audit.

    (a) Basic rule. Grantees and subgrantees are responsible for 
obtaining audits in accordance with the Single Audit Act of 1984 (31 
U.S.C. 7501-7) and Federal agency implementing regulations. The audits 
shall be made by an independent auditor in accordance with generally 
accepted government auditing standards covering financial and compliance 
audits.
    (b) Subgrantees. State or local governments, as those terms are 
defined for purposes of the Single Audit Act, that receive Federal 
financial assistance and provide $25,000 or more of it in a fiscal year 
to a subgrantee shall:
    (1) Determine whether State or local subgrantees have met the audit 
requirements of the Act and whether subgrantees covered by OMB Circular 
A-110, ``Uniform Requirements for Grants and Other Agreements with 
Institutions of Higher Education, Hospitals and Other Nonprofit 
Organizations'' have met the audit requirement. Commercial contractors 
(private for profit and private and governmental organizations) 
providing goods and services to State and local governments are not 
required to have a single audit performed. State and local governments 
should use their own procedures to ensure that the contractor has 
complied with laws and regulations affecting the expenditure of Federal 
funds;
    (2) Determine whether the subgrantee spent Federal assistance funds 
provided in accordance with applicable laws and regulations. This may be 
accomplished by reviewing an audit of the subgrantee made in accordance 
with the Act, Circular A-110, or through other means (e.g., program 
reviews) if the subgrantee has not had such an audit;
    (3) Ensure that appropriate corrective action is taken within six 
months after receipt of the audit report in instance of noncompliance 
with Federal laws and regulations;
    (4) Consider whether subgrantee audits necessitate adjustment of the 
grantee's own records; and
    (5) Require each subgrantee to permit independent auditors to have 
access to the records and financial statements.
    (c) Auditor selection. In arranging for audit services, Sec. 1403.36 
shall be followed.

                    Changes, Property, and Subawards



Sec. 1403.30  Changes.

    (a) General. Grantees and subgrantees are permitted to rebudget 
within the approved direct cost budget to meet unanticipated 
requirements and may make limited program changes to the approved 
project. However, unless waived by the awarding agency, certain types of 
post-award changes in budgets and projects shall require the prior 
written approval of the awarding agency.
    (b) Relation to cost principles. The applicable cost principles (see 
Sec. 1403.22) contain requirements for prior approval of certain types 
of costs. Except where waived, those requirements apply to all grants 
and subgrants even if paragraphs (c) through (f) of this section do not.
    (c) Budget changes--(1) Nonconstruction projects. Except as stated 
in other regulations or an award document, grantees or subgrantees shall 
obtain the prior approval of the awarding agency whenever any of the 
following changes is anticipated under a nonconstruction award:

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    (i) Any revision which would result in the need for additional 
funding.
    (ii) Unless waived by the awarding agency, cumulative transfers 
among direct cost categories, or, if applicable, among separately 
budgeted programs, projects, functions, or activities which exceed or 
are expected to exceed ten percent of the current total approved budget, 
whenever the awarding agency's share exceeds $100,000.
    (iii) Transfer of funds allotted for training allowances (i.e., from 
direct payments to trainees to other expense categories).
    (2) Construction projects. Grantees and subgrantees shall obtain 
prior written approval for any budget revision which would result in the 
need for additional funds.
    (3) Combined construction and nonconstruction projects. When a grant 
or subgrant provides funding for both construction and nonconstruction 
activities, the grantee or subgrantee must obtain prior written approval 
from the awarding agency before making any fund or budget transfer from 
nonconstruction to construction or vice versa.
    (d) Programmatic changes. Grantees or subgrantees must obtain the 
prior approval of the awarding agency whenever any of the following 
actions is anticipated:
    (1) Any revision of the scope or objectives of the project 
(regardless of whether there is an associated budget revision requiring 
prior approval).
    (2) Need to extend the period of availability of funds.
    (3) Changes in key persons in cases where specified in an 
application or a grant award. In research projects, a change in the 
project director or principal investigator shall always require approval 
unless waived by the awarding agency.
    (4) Under nonconstruction projects, contracting out, subgranting (if 
authorized by law) or otherwise obtaining the services of a third party 
to perform activities which are central to the purposes of the award. 
This approval requirement is in addition to the approval requirements of 
Sec. 1403.36 but does not apply to the procurement of equipment, 
supplies, and general support services.
    (e) Additional prior approval requirements. The awarding agency may 
not require prior approval for any budget revision which is not 
described in paragraph (c) of this section.
    (f) Requesting prior approval. (1) A request for prior approval of 
any budget revision will be in the same budget format the grantee used 
in its application and shall be accompanied by a narrative justification 
for the proposed revision.
    (2) A request for a prior approval under the applicable Federal cost 
principles (see Sec. 1403.22) may be made by letter.
    (3) A request by a subgrantee for prior approval will be addressed 
in writing to the grantee. The grantee will promptly review such request 
and shall approve or disapprove the request in writing. A grantee will 
not approve any budget or project revision which is inconsistent with 
the purpose or terms and conditions of the Federal grant to the grantee. 
If the revision requested by the subgrantee would result in a change to 
the grantee's approved project which requires Federal prior approval, 
the grantee will obtain the Federal agency's approval before approving 
the subgrantee's request.



Sec. 1403.31  Real property.

    (a) Title. Subject to the obligations and conditions set forth in 
this section, title to real property acquired under a grant or subgrant 
will vest upon acquisition in the grantee or subgrantee respectively.
    (b) Use. Except as otherwise provided by Federal statutes, real 
property will be used for the originally authorized purposes as long as 
needed for those purposes, and the grantee or subgrantee shall not 
dispose of or encumber its title or other interests.
    (c) Disposition. When real property is no longer needed for the 
originally authorized purpose, the grantee or subgrantee will request 
disposition instructions from the awarding agency. The instructions will 
provide for one of the following alternatives:
    (1) Retention of title. Retain title after compensating the awarding 
agency. The amount paid to the awarding agency will be computed by 
applying the

[[Page 284]]

awarding agency's percentage of participation in the cost of the 
original purchase to the fair market value of the property. However, in 
those situations were a grantee or subgrantee is disposing of real 
property acquired with grant funds and acquiring replacement real 
property under the same program, the net proceeds from the disposition 
may be used as an offset to the cost of the replacement property.
    (2) Sale of property. Sell the property and compensate the awarding 
agency. The amount due to the awarding agency will be calculated by 
applying the awarding agency's percentage of participation in the cost 
of the original purchase to the proceeds of the sale after deduction of 
any actual and reasonable selling and fixing-up expenses. If the grant 
is still active, the net proceeds from sale may be offset against the 
original cost of the property. When a grantee or subgrantee is directed 
to sell property, sales procedures shall be followed that provide for 
competition to the extent practicable and result in the highest possible 
return.
    (3) Transfer of title. Transfer title to the awarding agency or to a 
third-party designated/approved by the awarding agency. The grantee or 
subgrantee shall be paid an amount calculated by applying the grantee or 
subgrantee's percentage of participation in the purchase of the real 
property to the current fair market value of the property.



Sec. 1403.32  Equipment.

    (a) Title. Subject to the obligations and conditions set forth in 
this section, title to equipment acquired under a grant or subgrant will 
vest upon acquisition in the grantee or subgrantee respectively.
    (b) States. A State will use, manage, and dispose of equipment 
acquired under a grant by the State in accordance with State laws and 
procedures. Other grantees and subgrantees will follow paragraphs (c) 
through (e) of this section.
    (c) Use. (1) Equipment shall be used by the grantee or subgrantee in 
the program or project for which it was acquired as long as needed, 
whether or not the project or program continues to be supported by 
Federal funds. When no longer needed for the original program or 
project, the equipment may be used in other activities currently or 
previously supported by a Federal agency.
    (2) The grantee or subgrantee shall also make equipment available 
for use on other projects or programs currently or previously supported 
by the Federal Government, providing such use will not interfere with 
the work on the projects or program for which it was originally 
acquired. First preference for other use shall be given to other 
programs or projects supported by the awarding agency. User fees should 
be considered if appropriate.
    (3) Notwithstanding the encouragement in Sec. 1403.25(a) to earn 
program income, the grantee or subgrantee must not use equipment 
acquired with grant funds to provide services for a fee to compete 
unfairly with private companies that provide equivalent services, unless 
specifically permitted or contemplated by Federal statute.
    (4) When acquiring replacement equipment, the grantee or subgrantee 
may use the equipment to be replaced as a trade-in or sell the property 
and use the proceeds to offset the cost of the replacement property, 
subject to the approval of the awarding agency.
    (d) Management requirements. Procedures for managing equipment 
(including replacement equipment), whether acquired in whole or in part 
with grant funds, until disposition takes place will, as a minimum, meet 
the following requirements:
    (1) Property records must be maintained that include a description 
of the property, a serial number or other identification number, the 
source of property, who holds title, the acquisition date, and cost of 
the property, percentage of Federal participation in the cost of the 
property, the location, use and condition of the property, and any 
ultimate disposition data including the date of disposal and sale price 
of the property.
    (2) A physical inventory of the property must be taken and the 
results reconciled with the property records at least once every two 
years.
    (3) A control system must be developed to ensure adequate safeguards 
to prevent loss, damage, or theft of the

[[Page 285]]

property. Any loss, damage, or theft shall be investigated.
    (4) Adequate maintenance procedures must be developed to keep the 
property in good condition.
    (5) If the grantee or subgrantee is authorized or required to sell 
the property, proper sales procedures must be established to ensure the 
highest possible return.
    (e) Disposition. When original or replacement equipment acquired 
under a grant or subgrant is no longer needed for the original project 
or program or for other activities currently or previously supported by 
a Federal agency, disposition of the equipment will be made as follows:
    (1) Items of equipment with a current per-unit fair market value of 
less than $5,000 may be retained, sold or otherwise disposed of with no 
further obligation to the awarding agency.
    (2) Items of equipment with a current per unit fair market value in 
excess of $5,000 may be retained or sold and the awarding agency shall 
have a right to an amount calculated by multiplying the current market 
value or proceeds from sale by the awarding agency's share of the 
equipment.
    (3) In cases where a grantee or subgrantee fails to take appropriate 
disposition actions, the awarding agency may direct the grantee or 
subgrantee to take excess and disposition actions.
    (f) Federal equipment. In the event a grantee or subgrantee is 
provided federally-owned equipment:
    (1) Title will remain vested in the Federal Government.
    (2) Grantees or subgrantees will manage the equipment in accordance 
with Federal agency rules and procedures, and submit an annual inventory 
listing.
    (3) When the equipment is no longer needed, the grantee or 
subgrantee will request disposition instructions from the Federal 
agency.
    (g) Right to transfer title. The Federal awarding agency may reserve 
the right to transfer title to the Federal Government or a third party 
named by the awarding agency when such a third party is otherwise 
eligible under existing statutes. Such transfers shall be subject to the 
following standards:
    (1) The property shall be identified in the grant or otherwise made 
known to the grantee in writing.
    (2) The Federal awarding agency shall issue disposition instruction 
within 120 calendar days after the end of the Federal support of the 
project for which it was acquired. If the federal awarding agency fails 
to issue disposition instructions within the 120 calendar-day period the 
grantee shall follow Sec. 1403.32(e).
    (3) When title to equipment is transferred, the grantee shall be 
paid an amount calculated by applying the percentage of participation in 
the purchase to the current fair market value of the property.



Sec. 1403.33  Supplies.

    (a) Title. Title to supplies acquired under a grant or subgrant will 
vest, upon acquisition, in the grantee or subgrantee respectively.
    (b) Disposition. If there is a residual inventory of unused supplies 
exceeding $5,000 in total aggregate fair market value upon termination 
or completion of the award, and if the supplies are not needed for any 
other federally sponsored programs or projects, the grantee or 
subgrantee shall compensate the awarding agency for its share.



Sec. 1403.34  Copyrights.

    The Federal awarding agency reserves a royalty-free, nonexclusive, 
and irrevocable license to reproduce, publish or otherwise use, and to 
authorize others to use, for Federal Government purposes:
    (a) The copyright in any work developed under a grant, subgrant, or 
contract under a grant or subgrant; and
    (b) Any rights of copyright to which a grantee, subgrantee or a 
contractor purchases ownership with grant support.



Sec. 1403.35  Subawards to debarred and suspended parties.

    Grantees and subgrantees must not make any award or permit any award 
(subgrant or contract) at any tier to any party which is debarred or 
suspended or is otherwise excluded from or ineligible for participation 
in Federal assistance programs under Executive

[[Page 286]]

Order 12549, ``Debarment and Suspension.''



Sec. 1403.36  Procurement.

    (a) States. When procuring property and services under a grant, a 
State will follow the same policies and procedures it uses for 
procurements from its non-Federal funds. The State will ensure that 
every purchase order or other contract includes any clauses required by 
Federal statutes and executive orders and their implementing 
regulations. Other grantees and subgrantees will follow paragraphs (b) 
through (i) of this section.
    (b) Procurement standards. (1) Grantees and subgrantees will use 
their own procurement procedures which reflect applicable State and 
local laws and regulations, provided that the procurements conform to 
applicable Federal law and the standards identified in this section.
    (2) Grantees and subgrantees will maintain a contract administration 
system which ensures that contractors perform in accordance with the 
terms, conditions, and specifications of their contracts or purchase 
orders.
    (3) Grantees and subgrantees will maintain a written code of 
standards of conduct governing the performance of their employees 
engaged in the award and administration of contracts. No employee, 
officer or agent of the grantee or subgrantee shall participate in 
selection, or in the award or administration of a contract supported by 
Federal funds if a conflict of interest, real or apparent, would be 
involved. Such a conflict would arise when:
    (i) The employee, officer or agent,
    (ii) Any member of his immediate family,
    (iii) His or her partner, or
    (iv) An organization which employs, or is about to employ, any of 
the above, has a financial or other interest in the firm selected for 
award. The grantee's or subgrantee's officers, employees or agents will 
neither solicit nor accept gratuities, favors or anything of monetary 
value from contractors, potential contractors, or parties to 
subagreements. Grantee and subgrantees may set minimum rules where the 
financial interest is not substantial or the gift is an unsolicited item 
of nominal intrinsic value. To the extent permitted by State or local 
law or regulations, such standards or conduct will provide for 
penalties, sanctions, or other disciplinary actions for violations of 
such standards by the grantee's and subgrantee's officers, employees, or 
agents, or by contractors or their agents. The awarding agency may in 
regulation provide additional prohibitions relative to real, apparent, 
or potential conflicts of interest.
    (4) Grantee and subgrantee procedures will provide for a review of 
proposed procurements to avoid purchase of unnecessary or duplicative 
items. Consideration should be given to consolidating or breaking out 
procurements to obtain a more economical purchase. Where appropriate, an 
analysis will be made of lease versus purchase alternatives, and any 
other appropriate analysis to determine the most economical approach.
    (5) To foster greater economy and efficiency, grantees and 
subgrantees are encouraged to enter into State and local 
intergovernmental agreements for procurement or use of common goods and 
services.
    (6) Grantees and subgrantees are encouraged to use Federal excess 
and surplus property in lieu of purchasing new equipment and property 
whenever such use is feasible and reduces project costs.
    (7) Grantees and subgrantees are encouraged to use value engineering 
clauses in contracts for construction projects of sufficient size to 
offer reasonable opportunities for cost reductions. Value engineering is 
a systematic and creative analysis of each contract item or task to 
ensure that its essential function is provided at the overall lower 
cost.
    (8) Grantees and subgrantees will make awards only to responsible 
contractors possessing the ability to perform successfully under the 
terms and conditions of a proposed procurement. Consideration will be 
given to such matters as contractor integrity, compliance with public 
policy, record of past performance, and financial and technical 
resources.
    (9) Grantees and subgrantees will maintain records sufficient to 
detail

[[Page 287]]

the significant history of a procurement. These records will include, 
but are not necessarily limited to the following: rationale for the 
method of procurement, selection of contract type, contractor selection 
or rejection, and the basis for the contract price.
    (10) Grantees and subgrantees will use time and material type 
contracts only--
    (i) After a determination that no other contract is suitable, and
    (ii) If the contract includes a ceiling price that the contractor 
exceeds at its own risk.
    (11) Grantees and subgrantees alone will be responsible, in 
accordance with good administrative practice and sound business 
judgment, for the settlement of all contractual and administrative 
issues arising out of procurements. These issues include, but are not 
limited to source evaluation, protests, disputes, and claims. These 
standards do not relieve the grantee or subgrantee of any contractual 
responsibilities under its contracts. Federal agencies will not 
substitute their judgment for that of the grantee or subgrantee unless 
the matter is primarily a Federal concern. Violations of law will be 
referred to the local, State, or Federal authority having proper 
jurisdiction.
    (12) Grantees and subgrantees will have protest procedures to handle 
and resolve disputes relating to their procurements and shall in all 
instances disclose information regarding the protest to the awarding 
agency. A protestor must exhaust all administrative remedies with the 
grantee and subgrantee before pursuing a protest with the Federal 
agency. Reviews of protests by the Federal agency will be limited to:
    (i) Violations of Federal law or regulations and the standards of 
this section (violations of State or local law will be under the 
jurisdiction of State or local authorities) and
    (ii) Violations of the grantee's or subgrantee's protest procedures 
for failure to review a complaint or protest. Protests received by the 
Federal agency other than those specified above will be referred to the 
grantee or subgrantee.
    (c) Competition. (1) All procurement transactions will be conducted 
in a manner providing full and open competition consistent with the 
standards of Sec. 1403.36. Some of the situations considered to be 
restrictive of competition include but are not limited to:
    (i) Placing unreasonable requirements on firms in order for them to 
qualify to do business,
    (ii) Requiring unnecessary experience and excessive bonding,
    (iii) Noncompetitive pricing practices between firms or between 
affiliated companies,
    (iv) Noncompetitive awards to consultants that are on retainer 
contracts,
    (v) Organizational conflicts of interest,
    (vi) Specifying only a ``brand name'' product instead of allowing 
``an equal'' product to be offered and describing the performance of 
other relevant requirements of the procurement, and
    (vii) Any arbitrary action in the procurement process.
    (2) Grantees and subgrantees will conduct procurements in a manner 
that prohibits the use of statutorily or administratively imposed in-
State or local geographical preferences in the evaluation of bids or 
proposals, except in those cases where applicable Federal statutes 
expressly mandate or encourage geographic preference. Nothing in this 
section preempts State licensing laws. When contracting for 
architectural and engineering (A/E) services, geographic location may be 
a selection criteria provided its application leaves an appropriate 
number of qualified firms, given the nature and size of the project, to 
compete for the contract.
    (3) Grantees will have written selection procedures for procurement 
transactions. These procedures will ensure that all solicitations:
    (i) Incorporate a clear and accurate description of the technical 
requirements for the material, product, or service to be procured. Such 
description shall not, in competitive procurements, contain features 
which unduly restrict competition. The description may include a 
statement of the qualitative nature of the material, product or service 
to be procured, and when necessary, shall set forth those minimum 
essential characteristics and standards to which it must conform if it 
is to satisfy its intended use. Detailed product specifications should 
be

[[Page 288]]

avoided if at all possible. When it is impractical or uneconomical to 
make a clear and accurate description of the technical requirements, a 
``brand name or equal'' description may be used as a means to define the 
performance or other salient requirements of a procurement. The specific 
features of the named brand which must be met by offerors shall be 
clearly stated; and
    (ii) Identify all requirements which the offerors must fulfill and 
all other factors to be used in evaluating bids or proposals.
    (4) Grantees and subgrantees will ensure that all prequalified lists 
of persons, firms, or products which are used in acquiring goods and 
services are current and include enough qualified sources to ensure 
maximum open and free competition. Also, grantees and subgrantees will 
not preclude potential bidders from qualifying during the solicitation 
period.
    (d) Methods of procurement to be followed. (1) Procurement by small 
purchase procedures. Small purchase procedures are those relatively 
simple and informal procurement methods for securing services, supplies, 
or other property that do not cost more than the simplified acquisition 
threshold fixed at 41 U.S.C. 403(11) (currently set at $100,000). If 
small purchase procedures are used, price or rate quotations shall be 
obtained from an adequate number of qualified sources.
    (2) Procurement by sealed bids (formal advertising). Bids are 
publicly solicited and a firm-fixed-price contract (lump sum or unit 
price) is awarded to the responsible bidder whose bid, conforming with 
all the material terms and conditions of the invitation for bids, is the 
lowest in price. The sealed bid method is the preferred method for 
procuring construction, if the conditions in Sec. 1403.36(d)(2)(i) 
apply.
    (i) In order for sealed bidding to be feasible, the following 
conditions should be present:
    (A) A complete, adequate, and realistic specification or purchase 
description is available;
    (B) Two or more responsible bidders are willing and able to compete 
effectively and for the business; and
    (C) The procurement lends itself to a firm fixed price contract and 
the selection of the successful bidder can be made principally on the 
basis of price.
    (ii) If sealed bids are used, the following requirements apply:
    (A) The invitation for bids will be publicly advertised and bids 
shall be solicited from an adequate number of known suppliers, providing 
them sufficient time prior to the date set for opening the bids;
    (B) The invitation for bids, which will include any specifications 
and pertinent attachments, shall define the items or services in order 
for the bidder to properly respond;
    (C) All bids will be publicly opened at the time and place 
prescribed in the invitation for bids;
    (D) A firm fixed-price contract award will be made in writing to the 
lowest responsive and responsible bidder. Where specified in bidding 
documents, factors such as discounts, transportation cost, and life 
cycle costs shall be considered in determining which bid is lowest. 
Payment discounts will only be used to determine the low bid when prior 
experience indicates that such discounts are usually taken advantage of; 
and
    (E) Any or all bids may be rejected if there is a sound documented 
reason.
    (3) Procurement by competitive proposals. The technique of 
competitive proposals is normally conducted with more than one source 
submitting an offer, and either a fixed-price or cost-reimbursement type 
contract is awarded. It is generally used when conditions are not 
appropriate for the use of sealed bids. If this method is used, the 
following requirements apply:
    (i) Requests for proposals will be publicized and identify all 
evaluation factors and their relative importance. Any response to 
publicized requests for proposals shall be honored to the maximum extent 
practical;
    (ii) Proposals will be solicited from an adequate number of 
qualified sources;
    (iii) Grantees and subgrantees will have a method for conducting 
technical evaluations of the proposals received and for selecting 
awardees;
    (iv) Awards will be made to the responsible firm whose proposal is 
most advantageous to the program, with price and other factors 
considered; and

[[Page 289]]

    (v) Grantees and subgrantees may use competitive proposal procedures 
for qualifications-based procurement of architectural/engineering (A/E) 
professional services whereby competitors' qualifications are evaluated 
and the most qualified competitor is selected, subject to negotiation of 
fair and reasonable compensation. The method, where price is not used as 
a selection factor, can only be used in procurement of A/E professional 
services. It cannot be used to purchase other types of services though 
A/E firms are a potential source to perform the proposed effort.
    (4) Procurement by noncompetitive proposals is procurement through 
solicitation of a proposal from only one source, or after solicitation 
of a number of sources, competition is determined inadequate.
    (i) Procurement by noncompetitive proposals may be used only when 
the award of a contract is infeasible under small purchase procedures, 
sealed bids or competitive proposals and one of the following 
circumstances applies:
    (A) The item is available only from a single source;
    (B) The public exigency or emergency for the requirement will not 
permit a delay resulting from competitive solicitation;
    (C) The awarding agency authorizes noncompetitive proposals; or
    (D) After solicitation of a number of sources, competition is 
determined inadequate.
    (ii) Cost analysis, i.e., verifying the proposed cost data, the 
projections of the data, and the evaluation of the specific elements of 
costs and profits, is required.
    (iii) Grantees and subgrantees may be required to submit the 
proposed procurement to the awarding agency for pre-award review in 
accordance with paragraph (g) of this section.
    (e) Contracting with small and minority firms, women's business 
enterprise and labor surplus area firms. (1) The grantee and subgrantee 
will take all necessary affirmative steps to assure that minority firms, 
women's business enterprises, and labor surplus area firms are used when 
possible.
    (2) Affirmative steps shall include:
    (i) Placing qualified small and minority businesses and women's 
business enterprises on solicitation lists;
    (ii) Assuring that small and minority businesses, and women's 
business enterprises are solicited whenever they are potential sources;
    (iii) Dividing total requirements, when economically feasible, into 
smaller tasks or quantities to permit maximum participation by small and 
minority business, and women's business enterprises;
    (iv) Establishing delivery schedules, where the requirement permits, 
which encourage participation by small and minority business, and 
women's business enterprises;
    (v) Using the services and assistance of the Small Business 
Administration, and the Minority Business Development Agency of the 
Department of Commerce; and
    (vi) Requiring the prime contractor, if subcontracts are to be let, 
to take the affirmative steps listed in paragraphs (e)(2) (i) through 
(v) of this section.
    (f) Contract cost and price. (1) Grantees and subgrantees must 
perform a cost or price analysis in connection with every procurement 
action including contract modifications. The method and degree of 
analysis is dependent on the facts surrounding the particular 
procurement situation, but as a starting point, grantees must make 
independent estimates before receiving bids or proposals. A cost 
analysis must be performed when the offeror is required to submit the 
elements of his estimated cost, e.g., under professional, consulting, 
and architectural engineering services contracts. A cost analysis will 
be necessary when adequate price competition is lacking, and for sole 
source procurements, including contract modifications or change orders, 
unless price reasonableness can be established on the basis of a catalog 
or market price of a commercial product sold in substantial quantities 
to the general public or based on prices set by law or regulation. A 
price analysis will be used in all other instances to determine the 
reasonableness of the proposed contract price.
    (2) Grantees and subgrantees will negotiate profit as a separate 
element of

[[Page 290]]

the price for each contract in which there is no price competition and 
in all cases where cost analysis is performed. To establish a fair and 
reasonable profit, consideration will be given to the complexity of the 
work to be performed, the risk borne by the contractor, the contractor's 
investment, the amount of subcontracting, the quality of its record of 
past performance, and industry profit rates in the surrounding 
geographical area for similar work.
    (3) Costs or prices based on estimated costs for contracts under 
grants will be allowable only to the extent that costs incurred or cost 
estimates included in negotiated prices are consistent with Federal cost 
principles (see Sec. 1403.22). Grantees may reference their own cost 
principles that comply with the applicable Federal cost principles.
    (4) The cost plus a percentage of cost and percentage of 
constructing cost methods of contracting shall not be used.
    (g) Awarding agency review. (1) Grantees and subgrantees must make 
available, upon request of the awarding agency, technical specifications 
on proposed procurements where the awarding agency believes such review 
is needed to ensure that the item and/or service specified is the one 
being proposed for purchase. This review generally will take place prior 
to the time the specification is incorporated into a solicitation 
document. However, if the grantee or subgrantee desires to have the 
review accomplished after a solicitation has been developed, the 
awarding agency may still review the specifications, with such review 
usually limited to the technical aspects of the proposed purchase.
    (2) Grantees and subgrantees must on request make available for 
awarding agency pre-award review procurement documents, such as requests 
for proposals or invitations for bids, independent cost estimates, etc. 
when:
    (i) A grantee's or subgrantee's procurement procedures or operation 
fails to comply with the procurement standards in this section; or
    (ii) The procurement is expected to exceed the simplified 
acquisition threshold and is to be awarded without competition or only 
one bid or offer is received in response to a solicitation; or
    (iii) The procurement, which is expected to exceed the simplified 
acquisition threshold, specifies a ``brand name'' product; or
    (iv) The proposed award is more than the simplified acquisition 
threshold and is to be awarded to other than the apparent low bidder 
under a sealed bid procurement; or
    (v) A proposed contract modification changes the scope of a contract 
or increases the contract amount by more than the simplified acquisition 
threshold.
    (3) A grantee or subgrantee will be exempt from the pre-award review 
in paragraph (g)(2) of this section if the awarding agency determines 
that its procurement systems comply with the standards of this section.
    (i) A grantee or subgrantee may request that its procurement system 
be reviewed by the awarding agency to determine whether its system meets 
these standards in order for its system to be certified. Generally, 
these reviews shall occur where there is a continuous high-dollar 
funding, and third-party contracts are awarded on a regular basis.
    (ii) A grantee or subgrantee may self-certify its procurement 
system. Such self-certification shall not limit the awarding agency's 
right to survey the system. Under a self-certification procedure, 
awarding agencies may wish to rely on written assurances from the 
grantee or subgrantee that it is complying with these standards. A 
grantee or subgrantee will cite specific procedures, regulations, 
standards, etc., as being in compliance with these requirements and have 
its system available for review.
    (h) Bonding requirements. For construction or facility improvement 
contracts or subcontracts exceeding the simplified acquisition 
threshold, the awarding agency may accept the bonding policy and 
requirements of the grantee or subgrantee provided the awarding agency 
has made a determination that the awarding agency's interest is 
adequately protected. If such a determination has not been made, the 
minimum requirements shall be as follows:

[[Page 291]]

    (1) A bid guarantee from each bidder equivalent to five percent of 
the bid price. The ``bid guarantee'' shall consist of a firm commitment 
such as a bid bond, certified check, or other negotiable instrument 
accompanying a bid as assurance that the bidder will, upon acceptance of 
his bid, execute such contractual documents as may be required within 
the time specified.
    (2) A performance bond on the part of the contractor for 100 percent 
of the contract price. A ``performance bond'' is one executed in 
connection with a contract to secure fulfillment of all the contractor's 
obligations under such contract.
    (3) A payment bond on the part of the contractor for 100 percent of 
the contract price. A ``payment bond'' is one executed in connection 
with a contract to assure payment as required by law of all persons 
supplying labor and material in the execution of the work provided for 
in the contract.
    (i) Contract provisions. A grantee's and subgrantee's contracts must 
contain provisions in paragraph (i) of this section. Federal agencies 
are permitted to require changes, remedies, changed conditions, access 
and records retention, suspension of work, and other clauses approved by 
the Office of Federal Procurement Policy.
    (1) Administrative, contractual, or legal remedies in instances 
where contractors violate or breach contract terms, and provide for such 
sanctions and penalties as may be appropriate. (Contracts more than the 
simplified acquisition threshold)
    (2) Termination for cause and for convenience by the grantee or 
subgrantee including the manner by which it will be effected and the 
basis for settlement. (All contracts in excess of $10,000)
    (3) Compliance with Executive Order 11246 of September 24, 1965, 
entitled ``Equal Employment Opportunity,'' as amended by Executive Order 
11375 of October 13, 1967, and as supplemented in Department of Labor 
regulations (41 CFR chapter 60). (All construction contracts awarded in 
excess of $10,000 by grantees and their contractors or subgrantees)
    (4) Compliance with the Copeland ``Anti-Kickback'' Act (18 U.S.C. 
874) as supplemented in Department of Labor regulations (29 CFR Part 3). 
(All contracts and subgrants for construction or repair)
    (5) Compliance with the Davis-Bacon Act (40 U.S.C. 276a to 276a-7) 
as supplemented by Department of Labor regulations (29 CFR Part 5). 
(Construction contracts in excess of $2000 awarded by grantees and 
subgrantees when required by Federal grant program legislation)
    (6) Compliance with Sections 103 and 107 of the Contract Work Hours 
and Safety Standards Act (40 U.S.C. 327-330) as supplemented by 
Department of Labor regulations (29 CFR Part 5). (Construction contracts 
awarded by grantees and subgrantees in excess of $2000, and in excess of 
$2500 for other contracts which involve the employment of mechanics or 
laborers)
    (7) Notice of awarding agency requirements and regulations 
pertaining to reporting.
    (8) Notice of awarding agency requirements and regulations 
pertaining to patent rights with respect to any discovery or invention 
which arises or is developed in the course of or under such contract.
    (9) Awarding agency requirements and regulations pertaining to 
copyrights and rights in data.
    (10) Access by the grantee, the subgrantee, the Federal grantor 
agency, the Comptroller General of the United States, or any of their 
duly authorized representatives to any books, documents, papers, and 
records of the contractor which are directly pertinent to that specific 
contract for the purpose of making audit, examination, excerpts, and 
transcriptions.
    (11) Retention of all required records for three years after 
grantees or subgrantees make final payments and all other pending 
matters are closed.
    (12) Compliance with all applicable standards, orders, or 
requirements issued under section 306 of the Clean Air Act (42 U.S.C. 
1857(h)), section 508 of the Clean Water Act (33 U.S.C. 1368), Executive 
Order 11738, and Environmental Protection Agency regulations (40 CFR 
part 15). (Contracts, subcontracts, and subgrants of amounts in excess 
of $100,000).

[[Page 292]]

    (13) Mandatory standards and policies relating to energy efficiency 
which are contained in the state energy conservation plan issued in 
compliance with the Energy Policy and Conservation Act (Pub. L. 94-163, 
89 Stat. 871).

[57 FR 55092, Nov. 24, 1992, as amended at 60 FR 19639, 19642, Apr. 19, 
1995]



Sec. 1403.37  Subgrants.

    (a) States. States shall follow state law and procedures when 
awarding and administering subgrants (whether on a cost reimbursement or 
fixed amount basis) of financial assistance to local and Indian tribal 
governments. States shall:
    (1) Ensure that every subgrant includes any clauses required by 
Federal statute and executive orders and their implementing regulations;
    (2) Ensure that subgrantees are aware of requirements imposed upon 
them by Federal statute and regulation;
    (3) Ensure that a provision for compliance with Sec. 1403.42 is 
placed in every cost reimbursement subgrant; and
    (4) Conform any advances of grant funds to subgrantees substantially 
to the same standards of timing and amount that apply to cash advances 
by Federal agencies.
    (b) All other grantees. All other grantees shall follow the 
provisions of this part which are applicable to awarding agencies when 
awarding and administering subgrants (whether on a cost reimbursement or 
fixed amount basis) of financial assistance to local and Indian tribal 
governments. Grantees shall:
    (1) Ensure that every subgrant includes a provision for compliance 
with this part;
    (2) Ensure that every subgrant includes any clauses required by 
Federal statute and executive orders and their implementing regulations; 
and
    (3) Ensure that subgrantees are aware of requirements imposed upon 
them by Federal statutes and regulations.
    (c) Exceptions. By their own terms, certain provisions of this part 
do not apply to the award and administration of subgrants:
    (1) Section 1403.10;
    (2) Section 1403.11;
    (3) The letter-of-credit procedures specified in Treasury 
Regulations at 31 CFR part 205, cited in Sec. 1403.21; and
    (4) Section 1403.50.

              Reports, Records, Retention, and Enforcement



Sec. 1403.40  Monitoring and reporting program performance.

    (a) Monitoring by grantees. Grantees are responsible for managing 
the day-to-day operations of grant and subgrant supported activities. 
Grantees must monitor grant and subgrant supported activities to assure 
compliance with applicable Federal requirements and that performance 
goals are being achieved. Grantee monitoring must cover each program, 
function or activity.
    (b) Nonconstruction performance reports. The Federal agency may, if 
it decides that performance information available from subsequent 
applications contains sufficient information to meet its programmatic 
needs, require the grantee to submit a performance report only upon 
expiration or termination of grant support. Unless waived by the Federal 
agency this report will be due on the same date as the final Financial 
Status Report.
    (1) Grantees shall submit annual performance reports unless the 
awarding agency requires quarterly or semi-annual reports. However, 
performance reports will not be required more frequently than quarterly. 
Annual reports shall be due 90 days after the grant year, quarterly or 
semi-annual reports shall be due 30 days after the reporting period. The 
final performance report will be due 90 days after the expiration or 
termination of grant support. If a justified request is submitted by a 
grantee, the Federal agency may extend the due date for any performance 
report. Additionally, requirements for unnecessary performance reports 
may be waived by the Federal agency.
    (2) Performance reports will contain, for each grant, brief 
information on the following:
    (i) A comparison of actual accomplishments to the objectives 
established for the period. Where the output of the project can be 
quantified, a computation of the cost per unit of output

[[Page 293]]

may be required if that information will be useful.
    (ii) The reasons for slippage if established objectives were not 
met.
    (iii) Additional pertinent information including, when appropriate, 
analysis and explanation of cost overruns or high unit costs.
    (3) Grantees will not be required to submit more than the original 
and two copies of performance reports.
    (4) Grantees will adhere to the standards in this section in 
prescribing performance reporting requirements for subgrantees.
    (c) Construction performance reports. For the most part, on-site 
technical inspections and certified percentage-of-completion data are 
relied on heavily by Federal agencies to monitor progress under 
construction grants and subgrants. The Federal agency will require 
additional formal performance reports only when considered necessary, 
and never more frequently than quarterly.
    (d) Significant developments. Events may occur between the scheduled 
performance reporting dates which have significant impact upon the grant 
or subgrant supported activity. In such cases, the grantee must inform 
the Federal agency as soon as the following types of conditions become 
known:
    (1) Problems, delays, or adverse conditions which will materially 
impair the ability to meet the objective of the award. This disclosure 
must include a statement of the action taken, or contemplated, and any 
assistance needed to resolve the situation.
    (2) Favorable developments which enable meeting time schedules and 
objectives sooner or at less cost than anticipated or producing more 
beneficial results than originally planned.
    (e) Federal agencies may make site visits as warranted by program 
needs.
    (f) Waivers, extensions. (1) Federal agencies may waive any 
performance report required by this part if not needed.
    (2) The grantee may waive any performance report from a subgrantee 
when not needed. The grantee may extend the due date for any performance 
report from a subgrantee if the grantee will still be able to meet its 
performance reporting obligations to the Federal agency.



Sec. 1403.41  Financial reporting.

    (a) General. (1) Except as provided in paragraphs (a) (2) and (5) of 
this section, grantees will use only the forms specified in paragraphs 
(a) through (e) of this section, and such supplementary or other forms 
as may from time to time be authorized by OMB, for:
    (i) Submitting financial reports to Federal agencies, or
    (ii) Requesting advances or reimbursements when letters of credit 
are not used.
    (2) Grantees need not apply the forms prescribed in this section in 
dealing with their subgrantees. However, grantees shall not impose more 
burdensome requirements on subgrantees.
    (3) Grantees shall follow all applicable standard and supplemental 
Federal agency instructions approved by OMB to the extent required under 
the Paperwork Reduction Act of 1980 for use in connection with forms 
specified in paragraphs (b) through (e) of this section. Federal 
agencies may issue substantive supplementary instructions only with the 
approval of OMB. Federal agencies may shade out or instruct the grantee 
to disregard any line item that the Federal agency finds unnecessary for 
its decision making purposes.
    (4) Grantees will not be required to submit more than the original 
and two copies of forms required under this part.
    (5) Federal agencies may provide computer outputs to grantees to 
expedite or contribute to the accuracy of reporting. Federal agencies 
may accept the required information from grantees in machine usable 
format or computer printouts instead of prescribed forms.
    (6) Federal agencies may waive any report required by this section 
if not needed.
    (7) Federal agencies may extend the due date of any financial report 
upon receiving a justified request from a grantee.
    (b) Financial Status Report--(1) Form. Grantees will use Standard 
Form 269 or

[[Page 294]]

269A, Financial Status Report, to report the status of funds for all 
nonconstruction grants and for construction grants when required in 
accordance with paragraph Sec. 1403.41(e)(2)(iii) of this section.
    (2) Accounting basis. Each grantee will report program outlays and 
program income on a cash or accrual basis as prescribed by the awarding 
agency. If the Federal agency requires accrual information and the 
grantee's accounting records are not normally kept on the accrual basis, 
the grantee shall not be required to convert its accounting system but 
shall develop such accrual information through an analysis of the 
documentation on hand.
    (3) Frequency. The Federal agency may prescribe the frequency of the 
report for each project or program. However, the report will not be 
required more frequently than quarterly. If the Federal agency does not 
specify the frequency of the report, it will be submitted annually. A 
final report will be required upon expiration or termination of grant 
support.
    (4) Due date. When reports are required on a quarterly or semiannual 
basis, they will be due 30 days after the reporting period. When 
required on an annual basis, they will be due 90 days after the grant 
year. Final reports will be due 90 days after the expiration or 
termination of grant support.
    (c) Federal Cash Transactions Report--(1) Form. (i) For grants paid 
by letter of credit, Treasury check advances or electronic transfer of 
funds, the grantee will submit the Standard Form 272, Federal Cash 
Transactions Report, and when necessary, its continuation sheet, 
Standard Form 272a, unless the terms of the award exempt the grantee 
from this requirement.
    (ii) These reports will be used by the Federal agency to monitor 
cash advanced to grantees and to obtain disbursement or outlay 
information for each grant from grantees. The format of the report may 
be adapted as appropriate when reporting is to be accomplished with the 
assistance of automatic data processing equipment provided that the 
information to be submitted is not changed in substance.
    (2) Forecasts of Federal cash requirements. Forecasts of Federal 
cash requirements may be required in the ``Remarks'' section of the 
report.
    (3) Cash in hands of subgrantees. When considered necessary and 
feasible by the Federal agency, grantees may be required to report the 
amount of cash advances in excess of three days' needs in the hands of 
their subgrantees or contractors and to provide short narrative 
explanations of actions taken by the grantee to reduce the excess 
balances.
    (4) Frequency and due date. Grantees must submit the report no later 
than 15 working days following the end of each quarter. However, where 
an advance either by letter of credit or electronic transfer of funds is 
authorized at an annualized rate of one million dollars or more, the 
Federal agency may require the report to be submitted within 15 working 
days following the end of each month.
    (d) Request for advance or reimbursement--(1) Advance payments. 
Requests for Treasury check advance payments will be submitted on 
Standard Form 270, Request for Advance or Reimbursement. (This form will 
not be used for drawdowns under a letter of credit, electronic funds 
transfer or when Treasury check advance payments are made to the grantee 
automatically on a predetermined basis.)
    (2) Reimbursements. Requests for reimbursement under nonconstruction 
grants will also be submitted on Standard Form 270. (For reimbursement 
requests under construction grants, see paragraph (e)(1) of this 
section.)
    (3) The frequency for submitting payment requests is treated in 
Sec. 1403.41(b)(3).
    (e) Outlay report and request for reimbursement for construction 
programs--(1) Grants that support construction activities paid by 
reimbursement method. (i) Requests for reimbursement under construction 
grants will be submitted on Standard Form 271, Outlay Report and Request 
for Reimbursement for Construction Programs. Federal agencies may, 
however, prescribe the Request for Advance or Reimbursement form, 
specified in Sec. 1403.41(d), instead of this form.
    (ii) The frequency for submitting reimbursement requests is treated 
in Sec. 1403.41(b)(3).

[[Page 295]]

    (2) Grants that support construction activities paid by letter of 
credit, electronic funds transfer or Treasury check advance. (i) When a 
construction grant is paid by letter of credit, electronic funds 
transfer or Treasury check advances, the grantee will report its outlays 
to the Federal agency using Standard Form 271, Outlay Report and Request 
for Reimbursement for Construction Programs. The Federal agency will 
provide any necessary special instruction. However, frequency and due 
date shall be governed by Sec. 1403.41(b) (3) and (4).
    (ii) When a construction grant is paid by Treasury check advances 
based on periodic requests from the grantee, the advances will be 
requested on the form specified in Sec. 1403.41(d).
    (iii) The Federal agency may substitute the Financial Status Report 
specified in Sec. 1403.41(b) for the Outlay Report and Request for 
Reimbursement for Construction Programs.
    (3) Accounting basis. The accounting basis for the Outlay Report and 
Request for Reimbursement for Construction Programs shall be governed by 
Sec. 1403.41(b)(2).



Sec. 1403.42  Retention and access requirements for records.

    (a) Applicability. (1) This section applies to all financial and 
programmatic records, supporting documents, statistical records, and 
other records of grantees or subgrantees which are:
    (i) Required to be maintained by the terms of this Part, program 
regulations or the grant agreement, or
    (ii) Otherwise reasonably considered as pertinent to program 
regulations or the grant agreement.
    (2) This section does not apply to records maintained by contractors 
or subcontractors. For a requirement to place a provision concerning 
records in certain kinds of contracts, see Sec. 1403.36(i)(10).
    (b) Length of retention period. (1) Except as otherwise provided, 
records must be retained for three years from the starting date 
specified in paragraph (c) of this section.
    (2) If any litigation, claim, negotiation, audit or other action 
involving the records has been started before the expiration of the 3-
year period, the records must be retained until completion of the action 
and resolution of all issues which arise from it, or until the end of 
the regular 3-year period, whichever is later.
    (3) To avoid duplicate recordkeeping, awarding agencies may make 
special arrangements with grantees and subgrantees to retain any records 
which are continuously needed for joint use. The awarding agency will 
request transfer of records to its custody when it determines that the 
records possess long-term retention value. When the records are 
transferred to or maintained by the Federal agency, the 3-year retention 
requirement is not applicable to the grantee or subgrantees.
    (c) Starting date of retention period--(1) General. When grant 
support is continued or renewed at annual or other intervals, the 
retention period for the records of each funding period starts on the 
day the grantee or subgrantee submits to the awarding agency its single 
or last expenditure report for that period. However, if grant support is 
continued or renewed quarterly, the retention period for each year's 
records starts on the day the grantee submits its expenditure report for 
the last quarter of the Federal fiscal year. In all other cases, the 
retention period starts on the day the grantee submits its final 
expenditure report. If an expenditure report has been waived, the 
retention period starts on the day the report would have been due.
    (2) Real property and equipment records. The retention period for 
real property and equipment records starts from the date of the 
disposition or replacement or transfer at the direction of the awarding 
agency.
    (3) Records for income transactions after grant or subgrant support. 
In some cases grantees must report income after the period of grant 
support. Where there is such a requirement, the retention period for the 
records pertaining to the earning of the income starts from the end of 
the grantee's fiscal year in which the income is earned.
    (4) Indirect cost rate proposals, cost allocations plans, etc. This 
paragraph applies to the following types of documents, and their 
supporting records: indirect cost rate computations or proposals, cost 
allocation plans, and any

[[Page 296]]

similar accounting computations of the rate at which a particular group 
of costs is chargeable (such as computer usage chargeback rates or 
composite fringe benefit rates).
    (i) If submitted for negotiation. If the proposal, plan, or other 
computation is required to be submitted to the Federal Government (or to 
the grantee) to form the basis for negotiation of the rate, then the 3-
year retention period for its supporting records starts from the date of 
such submission.
    (ii) If not submitted for negotiation. If the proposal, plan, or 
other computation is not required to be submitted to the Federal 
Government (or to the grantee) for negotiation purposes, then the 3-year 
retention period for the proposal plan, or computation and its 
supporting records starts from end of the fiscal year (or other 
accounting period) covered by the proposal, plan, or other computation.
    (d) Substitution of microfilm. Copies made by microfilming, 
photocopying, or similar methods may be substituted for the original 
records.
    (e) Access to records--(1) Records of grantees and subgrantees. The 
awarding agency and the Comptroller General of the United States, or any 
of their authorized representatives, shall have the right of access to 
any pertinent books, documents, papers, or other records of grantees and 
subgrantees which are pertinent to the grant, in order to make audits, 
examinations, excerpts, and transcripts.
    (2) Expiration of right of access. The rights of access in this 
section must not be limited to the required retention period but shall 
last as long as the records are retained.
    (f) Restrictions on public access. The Federal Freedom of 
Information Act (5 U.S.C. 552) does not apply to records. Unless 
required by Federal, State, or local law, grantees and subgrantees are 
not required to permit public access to their records.



Sec. 1403.43  Enforcement.

    (a) Remedies for noncompliance. If a grantee or subgrantee 
materially fails to comply with any term of an award, whether stated in 
a Federal statute or regulation, an assurance, in a State plan or 
application, a notice of award, or elsewhere, the awarding agency may 
take one or more of the following actions, as appropriate in the 
circumstances:
    (1) Temporarily withhold cash payments pending correction of the 
deficiency by the grantee or subgrantee or more severe enforcement 
action by the awarding agency,
    (2) Disallow (that is, deny both use of funds and matching credit 
for) all or part of the cost of the activity or action not in 
compliance,
    (3) Wholly or partly suspend or terminate the current award for the 
grantee's or subgrantee's program,
    (4) Withhold further awards for the program, or
    (5) Take other remedies that may be legally available.
    (b) Hearings, appeals. In taking an enforcement action, the awarding 
agency will provide the grantee or subgrantee an opportunity for such 
hearing, appeal, or other administrative proceeding to which the grantee 
or subgrantee is entitled under any statute or regulation applicable to 
the action involved.
    (c) Effects of suspension and termination. Costs of grantee or 
subgrantee resulting from obligations incurred by the grantee or 
subgrantee during a suspension or after termination of an award are not 
allowable unless the awarding agency expressly authorizes them in the 
notice of suspension or termination or subsequently. Other grantee or 
subgrantee costs during suspension or after termination which are 
necessary and not reasonably avoidable are allowable if:
    (1) The costs result from obligations which were properly incurred 
by the grantee or subgrantee before the effective date of suspension or 
termination, are not in anticipation of it, and, in the case of a 
termination, are noncancellable, and,
    (2) The costs would be allowable if the award were not suspended or 
expired normally at the end of the funding period in which the 
termination takes effect.
    (d) Relationship to Debarment and Suspension. The enforcement 
remedies identified in this section, including suspension and 
termination, do not preclude grantee or subgrantee from

[[Page 297]]

being subject to ``Debarment and Suspension'' under E.O. 12549 (see 
Sec. 1403.35).



Sec. 1403.44  Termination for convenience.

    Except as provided in Sec. 1403.43 awards may be terminated in whole 
or in part only as follows:
    (a) By the awarding agency with the consent of the grantee or 
subgrantee in which case the two parties shall agree upon the 
termination conditions, including the effective date and in the case of 
partial termination, the portion to be terminated, or
    (b) By the grantee or subgrantee upon written notification to the 
awarding agency, setting forth the reasons for such termination, the 
effective date, and in the case of partial termination, the portion to 
be terminated. However, if, in the case of a partial termination, the 
awarding agency determines that the remaining portion of the award will 
not accomplish the purposes for which the award was made, the awarding 
agency may terminate the award in its entirety under either Sec. 1403.43 
or paragraph (a) of this section.



                 Subpart D--After-The-Grant Requirements



Sec. 1403.50  Closeout.

    (a) General. The Federal agency will close out the award when it 
determines that all applicable administrative actions and all required 
work of the grant has been completed.
    (b) Reports. Within 90 days after the expiration or termination of 
the grant, the grantee must submit all financial, performance, and other 
reports required as a condition of the grant. Upon request by the 
grantee, Federal agencies may extend this time frame. These may include 
but are not limited to:
    (1) Final performance or progress report.
    (2) Financial Status Report (SF 269) or Outlay Report and Request 
for Reimbursement for Construction Programs (SF-271) (as applicable).
    (3) Final request for payment (SF-270) (if applicable).
    (4) Invention disclosure (if applicable).
    (5) Federally-owned property report: In accordance with 
Sec. 1403.32(f), a grantee must submit an inventory of all federally 
owned property (as distinct from property acquired with grant funds) for 
which it is accountable and request disposition instructions from the 
Federal agency of property no longer needed.
    (c) Cost adjustment. The Federal agency will, within 90 days after 
receipt of reports in paragraph (b) of this section, make upward or 
downward adjustments to the allowable costs.
    (d) Cash adjustments. (1) The Federal agency will make prompt 
payment to the grantee for allowable reimbursable costs.
    (2) The grantee must immediately refund to the Federal agency any 
balance of unobligated (unencumbered) cash advanced that is not 
authorized to be retained for use on other grants.



Sec. 1403.51  Later disallowances and adjustments.

    The closeout of a grant does not affect:
    (a) The Federal agency's right to disallow costs and recover funds 
on the basis of a later audit or other review;
    (b) The grantee's obligation to return any funds due as a result of 
later refunds, corrections, or other transactions;
    (c) Records retention as required in Sec. 1403.42;
    (d) Property management requirements in Sec. 1403.31 and 
Sec. 1403.32; and
    (e) Audit requirements in Sec. 1403.26.



Sec. 1403.52  Collection of amounts due.

    (a) Any funds paid to a grantee in excess of the amount to which the 
grantee is finally determined to be entitled under the terms of the 
award constitute a debt to the Federal Government. If not paid within a 
reasonable period after demand, the Federal agency may reduce the debt 
by:
    (1) Making an administrative offset against other requests for 
reimbursement,
    (2) Withholding advance payments otherwise due to the grantee, or
    (3) Other action permitted by law.
    (b) Except where otherwise provided by statutes or regulations, the 
Federal

[[Page 298]]

agency will charge interest on an overdue debt in accordance with the 
Federal Claims Collection Standards (4 CFR Ch. II). The date from which 
interest is computed is not extended by litigation or the filing of any 
form of appeal.



                   Subpart E--Entitlement  [Reserved]

Appendix A to Part 1403--OMB Circular A-128, ``Audits of State and Local 
                              Governments''

Circular No. A-128
April 12, 1985.

To the Heads of Executive Departments and Establishments
Subject: Audits of State and Local Governments.

    1. Purpose. This Circular is issued pursuant to the Single Audit Act 
of 1984, Pub. L. 98-502. It establishes audit requirements for State and 
local governments that receive Federal aid, and defines Federal 
responsibilities for implementing and monitoring those requirements.
    2. Supersession. The Circular supersedes Attachment P, ``Audit 
Requirements,'' of Circular A-102, ``Uniform requirements for grants to 
State and local governments.''
    3. Background. The Single Audit Act builds upon earlier efforts to 
improve audits of Federal aid programs. The Act requires State or local 
governments that receive $100,000 or more a year in Federal funds to 
have an audit made for that year. Section 7505 of the Act requires the 
Director of the Office of Management and Budget to prescribe policies, 
procedures and guidelines to implement the Act. It specifies that the 
Director shall designate ``cognizant'' Federal agencies, determine 
criteria for making appropriate charges to federal programs for the cost 
of audits, and provide procedures to assure that small firms or firms 
owned and controlled by disadvantaged individuals have the opportunity 
to participate in contracts for single audits.
    4. Policy. The Single Audit Act requires the following:
    a. State or local governments that receive $100,000 or more a year 
in Federal financial assistance shall have an audit made in accordance 
with this Circular.
    b. State or local governments that receive between $25,000 and 
$100,000 a year shall have an audit made in accordance with this 
Circular, or in accordance with Federal laws and regulations governing 
the programs they participate in.
    c. State or local governments that receive less than $25,000 a year 
shall be exempt from compliance with the Act and other Federal audit 
requirements. These State and local governments shall be governed by 
audit requirements prescribed by State or local law or regulation.
    d. Nothing in this paragraph exempts State or local governments from 
maintaining records of Federal financial assistance or from providing 
access to such records to Federal agencies, as provided for in Federal 
law or in Circular A-102, ``Uniform requirements for grants to state or 
local governments.''
    5. Definitions. For the purposes of this Circular the following 
definitions from the Single Audit Act apply:
    a. Cognizant agency means the Federal agency assigned by the Office 
of Management and Budget to carry out the responsibilities described in 
paragraph 11 of this Circular.
    b. Federal financial assistance means assistance provided by a 
Federal agency in the form of grants, contracts, cooperative agreements, 
loans, loan guarantees, property, interest subsidies, insurance, or 
direct appropriations, but does not include direct Federal cash 
assistance to individuals. It includes awards received directly from 
Federal agencies, or indirectly through other units of States and local 
governments.
    c. Federal agency has the same meaning as the term ``agency'' in 
section 551(1) of Title 5, United States Code.
    d. Generally accepted accounting principles has the meaning 
specified in the generally accepted government auditing standards.
    e. Generally accepted government auditing standards means the 
Standards For Audit of Government Organizations, Programs, Activities, 
and Functions, developed by the Comptroller General, dated February 27, 
1981.
    f. Independent auditor means:
    (1) A State or local government auditor who meets the independence 
standards specified in generally accepted government auditing standards; 
or
    (2) A public accountant who meets such independence standards.
    g. Internal controls means the plan of organization and methods and 
procedures adopted by management to ensure that:
    (1) Resource use is consistent with laws, regulations, and policies;
    (2) Resources are safeguarded against waste, loss, and misuse; and
    (3) Reliable data are obtained, maintained, and fairly disclosed in 
reports.
    h. Indian tribe means any Indian tribe, band, nations, or other 
organized group or community, including any Alaskan Native village or 
regional or village corporations (as defined in, or established under, 
the Alaskan Native Claims Settlement Act) that is recognized by the 
United States as eligible for the special programs and services provided 
by the United States to Indians because of their status as Indians.

[[Page 299]]

    i. Local government means any unit of local government within a 
State, including a county, a borough, municipality, city, town, 
township, parish, local public authority, special district, school 
district, intrastate district, council of government, and any other 
instrumentality of local government.
    j. Major Federal Assistance Program, as defined by Pub. L. 98-502, 
is described in the Attachment to this Circular.
    k. Public accountants means those individuals who meet the 
qualification standards included in generally accepted government 
auditing standards for personnel performing government audits.
    l. State means any State of the United States, the District of 
Columbia, the Commonwealth of Puerto Rico, the Virgin Islands, Guam, 
American Samoa, the Commonwealth of the Northern Mariana Islands, and 
the Trust Territory of the Pacific Islands, any instrumentality thereof, 
and any multi-State, regional, or interstate entity that has 
governmental functions and any Indian tribe.
    m. Subrecipient means any person or government department, agency, 
or establishment that receives Federal financial assistance to carry out 
a program through a State or local government, but does not include an 
individual that is a beneficiary of such a program. A subrecipient may 
also be a direct recipient of Federal financial assistance.
    6. Scope of audit. The Single Act provides that:
    a. The audit shall be made by an independent auditor in accordance 
with generally accepted government auditing standards covering financial 
and compliance audits.
    b. The audit shall cover the entire operations of a State or local 
government or, at the option of that government, it may cover 
departments, agencies or establishments that received, expended, or 
otherwise administered Federal financial assistance during the year. 
However, if a State or local government receives $25,000 or more in 
General Revenue Sharing Funds in a fiscal year, it shall have an audit 
of its entire operations. A series of audits of individual departments, 
agencies, and establishments for the same fiscal year may be considered 
a single audit.
    c. Public hospitals and public colleges and universities may be 
excluded from State and local audits and the requirements of this 
Circular. However, if such entities are excluded, audits of these 
entities shall be made in accordance with statutory requirements and the 
provisions of Circular A-110, ``Uniform requirements for grants to 
universities, hospitals, and other nonprofit organizations.''
    d. The auditor shall determine whether:
    (1) The financial statements of the government, department, agency 
or establishment present fairly its financial position and the results 
of its financial operations in accordance with generally accepted 
accounting principles;
    (2) The organization has internal accounting and other control 
systems to provide reasonable assurance that it is managing Federal 
financial assistance programs in compliance with applicable laws and 
regulations; and
    (3) The organization has complied with laws and regulations that may 
have material effect on its financial statements and on each major 
Federal assistance program.
    7. Frequency of audit. Audits shall be made annually unless the 
State or local government has, by January 1, 1987, a constitutional or 
statutory requirement for less frequent audits. For those governments, 
the cognizant agency shall permit biennial audits, covering both years, 
if the government so requests. It shall also honor requests for biennial 
audits by governments that have an administrative policy calling for 
audits less frequent than annual, but only for fiscal years beginning 
before January 1, 1987.
    8. Internal control and compliance reviews. The Single Audit Act 
requires that the independent auditor determine and report on whether 
the organization has internal control systems to provide reasonable 
assurance that it is managing Federal assistance programs in compliance 
with applicable laws and regulations.
    a. Internal control review. In order to provide this assurance the 
auditor must make a study and evaluation of internal control systems 
used in administering Federal assistance programs. The study and 
evaluation must be made whether or not the auditor intends to place 
reliance on such systems. As part of this review, the auditor shall:
    (1) Test whether these internal control systems are functioning in 
accordance with prescribed procedures.
    (2) Examine the recipient's system for monitoring subrecipients and 
obtaining and acting on subrecipient audit reports.
    b. Compliance review. The law also requires the auditor to determine 
whether the organization has complied with laws and regulations that may 
have a material effect on each major Federal assistance program.
    (1) In order to determine which major programs are to be tested for 
compliance, State and local governments shall identify in their accounts 
all Federal funds received and expended and the programs under which 
they were received. This shall include funds received directly from 
Federal agencies and through other State and local governments.
    (2) The review must include the selection and testing of a 
representative number of charges from each major Federal assistance 
program. The selection and testing of transactions shall be based on the 
auditor's professional judgment considering such factors as the amount 
of expenditures for the program and the individual awards; the newness

[[Page 300]]

of the program or changes in its conditions; prior experience with the 
program, particularly as revealed in audits and other evaluations (e.g., 
inspections program reviews); the extent to which the program is carried 
out through subrecipients; the extent to which the program contracts for 
goods or services; the level to which the program is already subject to 
program reviews or other forms of independent oversight; the adequacy of 
the controls for ensuring compliance; the exception of adherence or lack 
of adherence to the applicable laws and regulations; and the potential 
impact of adverse findings.
    (a) In making the test of transactions, the auditor shall determine 
whether:

--The amounts reported as expenditures were for allowable services, and
--The records show that those who received services or benefits were 
eligible to receive them.

    (b) In addition to transaction testing, the auditor shall determine 
whether:

--Matching requirements, levels of effort and earmarking limitations 
were met,
--Federal financial reports and claims for advances and reimbursements 
contain information that is supported by the books and records from 
which the basic financial statements have been prepared, and
--Amounts claimed or used for matching were determined in accordance 
with OMB Circular A-87, ``Cost principles for State and local 
governments,'' and Attachment F of Circular A-102, ``Uniform 
requirements for grants to State and local governments.''

    (c) The principal compliance requirements of the largest Federal aid 
programs may be ascertained by referring to the Compliance Supplement 
for Single Audits of State and Local Governments, issued by OMB and 
available from the Government Printing Office. For those programs not 
covered in the Compliance Supplement, the auditor may ascertain 
compliance requirements by researching the statutes, regulations, and 
agreements governing individual programs.
    (3) Transactions related to other Federal assistance programs that 
are selected in connection with examinations of financial statements and 
evaluations of internal controls shall be tested for compliance with 
Federal laws and regulations that apply to such transactions.
    9. Subrecipients. State or local governments that receive Federal 
financial assistance and provide $25,000 or more of it in a fiscal year 
to a subrecipient shall:
    a. Determine whether State or local subrecipients have met the audit 
requirements of this Circular and whether subrecipients covered by 
Circular A-110, ``Uniform requirements for grants to universities, 
hospitals, and other nonprofit organizations,'' have met that 
requirement;
    b. Determine whether the subrecipient spent Federal assistance funds 
provided in accordance with applicable laws and regulations. This may be 
accomplished by reviewing an audit of the subrecipient made in 
accordance with this Circular, Circular A-110, or through other means 
(e.g., program reviews) if the subrecipient has not yet had such an 
audit;
    c. Ensure that appropriate corrective action is taken within six 
months after receipt of the audit report in instances of noncompliance 
with Federal laws and regulations;
    d. Consider whether subrecipient audits necessitate adjustment of 
the recipient's own records; and
    e. Require each subrecipient to permit independent auditors to have 
access to the records and financial statements as necessary to comply 
with this Circular.
    10. Relation to other audit requirements. The Single Audit Act 
provides that an audit made in accordance with this Circular shall be in 
lieu of any financial or financial compliance audit required under 
individual Federal assistance programs. To the extent that a single 
audit provides Federal agencies with information and assurances they 
need to carry out their overall responsibilities, they shall rely upon 
and use such information. However, a Federal agency shall make any 
additional audits which are necessary to carry out its responsibilities 
under Federal law and regulation. Any additional Federal audit effort 
shall be planned and carried out in such a way as to avoid duplication.
    a. The provisions of this Circular do not limit the authority of 
Federal agencies to make, or contract for audits and evaluations of 
Federal financial assistance programs, nor do they limit the authority 
of any Federal agency Inspector General or other Federal audit official.
    b. The provisions of this Circular do not authorize any State or 
local government or subrecipient thereof to constrain Federal agencies, 
in any manner, from carrying out additional audits.
    c. A Federal agency that makes or contracts for audits in addition 
to the audits made by recipients pursuant to this Circular shall, 
consistent with other applicable laws and regulations, arrange for 
funding the cost of such additional audits. Such additional audits 
include economy and efficiency audits, program results audits, and 
program evaluations.
    11. Cognizant agency responsibilities. The Single Audit Act provides 
for cognizant Federal agencies to oversee the implementation of this 
Circular.
    a. The Office of Management and Budget will assign cognizant 
agencies for States and their subdivisions and larger local governments 
and their subdivisions. Other Federal agencies may participate with an 
assigned

[[Page 301]]

cognizant agency, in order to fulfill the cognizance responsibilities. 
Smaller governments not assigned a cognizant agency will be under the 
general oversight of the Federal agency that provides them the most 
funds whether directly or indirectly.
    b. A cognizant agency shall have the following responsibilities:
    (1) Ensure that audits are made and reports are received in a timely 
manner and in accordance with the requirements of this Circular.
    (2) Provide technical advice and liaison to State and local 
governments and independent auditors.
    (3) Obtain or make quality control reviews of selected audits made 
by non-Federal audit organizations, and provide the results, when 
appropriate, to other interested organizations.
    (4) Promptly inform other affected Federal agencies and appropriate 
Federal law enforcement officials of any reported illegal acts or 
irregularities. They should also inform State or local law enforcement 
and prosecuting authorities, if not advised by the recipient, of any 
violation of law within their jurisdiction.
    (5) Advise the recipient of audits that have been found not to have 
met the requirements set forth in this Circular. In such instances, the 
recipient will be expected to work with the auditor to take corrective 
action. If corrective action is not taken, the cognizant agency shall 
notify the recipient and Federal awarding agencies of the facts and make 
recommendations for followup action. Major inadequacies or repetitive 
substandard performance of independent auditors shall be referred to 
appropriate professional bodies for disciplinary action.
    (6) Coordinate, to the extent practicable, audits made by or for 
Federal agencies that are in addition to the audits made pursuant to 
this Circular; so that the additional audits build upon such audits.
    (7) Oversee the resolution of audit findings that affect the 
programs of more than one agency.
    12. Illegal acts or irregularities. If the auditor becomes aware of 
illegal acts or other irregularities, prompt notice shall be given to 
recipient management officials above the level of involvement. (See also 
paragraph 13(a)(3) below for the auditor's reporting responsibilities.) 
The recipient, in turn, shall promptly notify the cognizant agency of 
the illegal acts or irregularities and of proposed and actual actions, 
if any. Illegal acts and irregularities include such matters as 
conflicts of interest, falsification of records or reports, and 
misappropriations of funds or other assets.
    13. Audit reports. Audit reports must be prepared at the completion 
of the audit. Reports serve many needs of State and local governments as 
well as meeting the requirements of the Single Audit Act.
    a. The audit report shall state that the audit was made in 
accordance with the provisions of this Circular. The report shall be 
made up of at least:
    (1) The auditor's report on financial statements and on a schedule 
of Federal assistance; the financial statements; and a schedule of 
Federal assistance, showing the total expenditures for each Federal 
assistance program as identified in the Catalog of Federal Domestic 
Assistance. Federal programs or grants that have not been assigned a 
catalog number shall be identified under the caption ``other Federal 
assistance.''
    (2) The auditor's report on the study and evaluation of internal 
control systems must identify the organization's significant internal 
accounting controls, and those controls designed to provide reasonable 
assurance that Federal programs are being managed in compliance with 
laws and regulations. It must also identify the controls that were 
evaluated, the controls that were not evaluated, and the material 
weaknesses identified as a result of the evaluation.
    (3) The auditor's report on compliance containing:

--A statement of positive assurance with respect to those items tested 
for compliance, including compliance with law and regulations pertaining 
to financial reports and claims for advances and reimbursements;
--Negative assurance on those items not tested;
--A summary of all instances of noncompliance; and
--An identification of total amounts questioned, if any, for each 
Federal assistance award, as a result of noncompliance.

    b. The three parts of the audit report may be bound into a single 
report, or presented at the same time as separate documents.
    c. All fraud abuse, or illegal acts or indications of such acts, 
including all questioned costs found as the result of these acts that 
auditors become aware of, should normally be covered in a separate 
written report submitted in accordance with paragraph 13f.
    d. In addition to the audit report, the recipient shall provide 
comments on the findings and recommendations in the report, including a 
plan for corrective action taken or planned and comments on the status 
of corrective action taken on prior findings. If corrective action is 
not necessary, a statement describing the reason it is not should 
accompany the audit report.
    e. The reports shall be made available by the State or local 
government for public inspection within 30 days after the completion of 
the audit.
    f. In accordance with generally accepted government audit standards, 
reports shall be submitted by the auditor to the organization audited 
and to those requiring or arranging

[[Page 302]]

for the audit. In addition, the recipient shall submit copies of the 
reports to each Federal department or agency that provided Federal 
assistance funds to the recipient. Subrecipients shall submit copies to 
recipients that provided them Federal assistance funds. The reports 
shall be sent within 30 days after the completion of the audit, but no 
later than one year after the end of the audit period unless a longer 
period is agreed to with the cognizant agency.
    g. Recipients of more than $100,000 in Federal funds shall submit 
one copy of the audit report within 30 days after issuance to a central 
clearinghouse to be designated by the Office of Management and Budget. 
The clearinghouse will keep completed audits on file and follow up with 
State and local governments that have not submitted required audit 
reports.
    h. Recipients shall keep audit reports on file for three years from 
their issuance.
    14. Audit Resolution. As provided in paragraph 11, the cognizant 
agency shall be responsible for monitoring the resolution of audit 
findings that affect the programs of more than one Federal agency. 
Resolution of findings that relate to the programs of a single Federal 
agency will be the responsibility of the recipient and that agency. 
Alternate arrangements may be made on a case-by-case basis by agreement 
among the agencies concerned.
    Resolution shall be made within six months after receipt of the 
report by the Federal departments and agencies. Corrective action should 
proceed as rapidly as possible.
    15. Audit workpapers and reports. Workpapers and reports shall be 
retained for a minimum of three years from the date of the audit report, 
unless the auditor is notified in writing by the cognizant agency to 
extend the retention period. Audit workpapers shall be made available 
upon request to the cognizant agency or its designee or the General 
Accounting Office, at the completion of the audit.
    16. Audit Costs. The cost of audits made in accordance with the 
provisions of this Circular are allowable charges to Federal assistance 
programs.
    a. The charges may be considered a direct cost or an allocated 
indirect cost, determined in accordance with the provision of Circular 
A-87, ``Cost principles for State and local governments.''
    b. Generally, the percentage of costs charged to Federal assistance 
programs for a single audit shall not exceed the percentage that Federal 
funds expended represent of total funds expended by the recipient during 
the fiscal year. The percentage may be exceeded, however, if appropriate 
documentation demonstrates higher actual cost.
    17. Sanctions. The Single Audit Act provides that no cost may be 
charged to Federal assistance programs for audits required by the Act 
that are not made in accordance with this Circular. In cases of 
continued inability or unwillingness to have a proper audit, Federal 
agencies must consider other appropriate sanctions including:

--Withhodling a percentage of assistance payments until the audit is 
completed satisfactorily,
--Withholding or disallowing overhead costs, and
--Suspending the Federal assistance agreement until the audit is made.

    18. Auditor Selection. In arranging for audit services State and 
local governments shall follow the procurement standards prescribed by 
Attachment O of Circular A-102, ``Uniform requirements for grants to 
State and local governments.'' The standards provide that while 
recipients are encouraged to enter into intergovernmental agreements for 
audit and other services, analysis should be made to determine whether 
it would be more economical to purchase the services from private firms. 
In instances where use of such intergovernmental agreements are required 
by State statutes (e.g., audit services) these statutes will take 
precedence.
    19. Small and Minority Audit Firms. Small audit firms and audit 
firms owned and controlled by socially and economically disadvantaged 
individuals shall have the maximum practicable opportunity to 
participate in contracts awarded to fulfill the requirements of this 
Circular. Recipients of Federal assistance shall take the following 
steps to further this goal:
    a. Assure that small audit firms and audit firms owned and 
controlled by socially and economically disadvantaged individuals are 
used to the fullest extent practicable.
    b. Make information on forthcoming opportunities available and 
arrange time frames for the audit so as to encourage and facilitate 
participation by small audit firms and audit firms owned and controlled 
by socially and economically disadvantaged individuals.
    c. Consider in the contract process whether firms competing for 
larger audits intend to subcontract with small audit firms and audit 
firms owned and controlled by socially and economically disadvantaged 
individuals.
    d. Encourage contracting with small audit firms or audit firms owned 
and controlled by socially and economically disadvantaged individuals 
which have traditionally audited government programs and, in such cases 
where this is not possible, assure that these firms are given 
consideration for audit subcontracting opportunities.
    e. Encourage contracting with consortiums of small audit firms as 
described in paragraph (a) above when a contract is too large for an 
individual small audit firm or audit firm owned and controlled by 
socially and economically disadvantaged individuals.

[[Page 303]]

    f. Use the services and assistance, as appropriate, of such 
organizations as the Small Business Administration in the solicitation 
and utilization of small audit firms or audit firms owned and controlled 
by socially and economically disadvantaged individuals.
    20. Reporting. Each Federal agency will report to the Director of 
OMB on or before March 1, 1987, and annually thereafter on the 
effectiveness of State and local governments in carrying out the 
provisions of this Circular. The report must identify each State or 
local government or Indian tribe that, in the opinion of the agency, is 
failing to comply with Circular.
    21. Regulations. Each Federal agency shall include the provisions of 
this Circular in its regulations implementing the Single Audit Act.
    22. Effective date. This Circular is effective upon publication and 
shall apply to fiscal years of State and local governments that begin 
after December 31, 1984. Earlier implementation is encouraged. However, 
until it is implemented, the audit provisions of Attachment P to 
Circular A-102 shall continue to be observed.
    23. Inquiries. All questions or inquiries should be addressed to 
Financial Management Division, Office of Management and Budget, 
telephone number (202) 395-3993.
    24. Sunset review date. This Circular shall have an independent 
policy review to ascertain its effectiveness three years from the date 
of issuance.

David A. Stockman,
    Director.

                        Circular A-128 Attachment

        Definition of Major Program as Provided in Pub. L. 98-502

    ``Major Federal Assistance Program,'' for State and local 
governments having Federal assistance expenditures between $100,000 and 
$100,000,000. means any program for which Federal expenditures during 
the applicable year exceed the larger of $300,000, or 3 percent of such 
total expenditures.
    Where total expenditures of Federal assistance exceed $100,000,000, 
the following criteria apply:

------------------------------------------------------------------------
     Total expenditures of Federal financial           Major Federal    
           assistance for all programs              assistance program  
------------------------------------------------- means any program that
       More than              But less than               exceeds       
------------------------------------------------------------------------
$100 million             1 billion                $3 million            
    1 billion            2 billion                4 million             
    2 billion            3 billion                7 million             
    3 billion            4 billion                10 million            
    4 billion            5 billion                13 million            
    5 billion            6 billion                16 million            
    6 billion            7 billion                19 million            
Over 7 billion           .......................  20 million            
------------------------------------------------------------------------


[57 FR 55092, Nov. 24, 1992; 58 FR 26185, Apr. 30, 1993]



PART 1404--GOVERNMENTWIDE DEBARMENT AND SUSPENSION (NONPROCUREMENT) AND GOVERNMENTWIDE REQUIREMENTS FOR DRUG-FREE WORKPLACE (GRANTS)--Table of Contents




                           Subpart A--General

Sec.
1404.100  Purpose.
1404.105  Definitions.
1404.110  Coverage.
1404.115  Policy.

                       Subpart B--Effect of Action

1404.200  Debarment or suspension.
1404.205  Ineligible persons.
1404.210  Voluntary exclusion.
1404.215  Exception provision.
1404.220  Continuation of covered transactions.
1404.225  Failure to adhere to restrictions.

                          Subpart C--Debarment

1401.300  General.
1404.305  Causes for debarment.
1404.310  Procedures.
1404.311  Investigation and referral.
1404.312  Notice of proposed debarment.
1404.313  Opportunity to contest proposed debarment.
1404.314  Debarring official's decision.
1404.315  Settlement and voluntary exclusion.
1404.320  Period of debarment.
1404.325  Scope of debarment.

                          Subpart D--Suspension

1404.400  General.
1404.405  Causes for suspension.
1404.410  Procedures.
1404.411  Notice of suspension.
1404.412  Opportunity to contest suspension.
1404.413  Suspending official's decision.
1404.415  Period of suspension.
1404.420  Scope of suspension.

       Subpart E--Responsibilities of GSA, Agency and Participants

1404.500  GSA responsibilities.
1404.505  ONDCP responsibilities.
1404.510  Participants' responsibilities.

          Subpart F--Drug-Free Workplace Requirements (Grants)

1404.600  Purpose.

[[Page 304]]

1404.605  Definitions.
1404.610  Coverage.
1404.615  Grounds for suspension of payments, suspension or termination 
          of grants, or suspension or debarment.
1404.620  Effect of violation.
1404.625  Exception provision.
1404.630  Certification requirements and procedures.
1404.635  Reporting of and employee sanctions for convictions of 
          criminal drug offenses.

Appendix A to Part 1404--Certification Regarding Debarment, Suspension, 
          and Other Responsibility Matters--Primary Covered Transactions
Appendix B to Part 1404--Certification Regarding Debarment, Suspension, 
          Ineligibility and Voluntary Exclusion--Lower Tier Covered 
          Transactions
Appendix C to Part 1404--Certification Regarding Drug-Free Workplace 
          Requirements

    Authority: Executive Order 12549, 3 CFR, 1986 Comp., p. 189; 5 
U.S.C. 301; Sec. 5151-5160 of the Drug-Free Workplace Act of 1988 (Pub. 
L. 100-690, Title V, Subtitle D, 102 stat. 4304; 41 U.S.C. 701 et seq.).

    Source: 57 FR 56263, Nov. 27, 1992, unless otherwise noted.



                           Subpart A--General



Sec. 1404.100  Purpose.

    (a) Executive Order (E.O.) 12549 provides that, to the extent 
permitted by law, Executive departments and agencies shall participate 
in a governmentwide system for nonprocurement debarment and suspension. 
A person who is debarred or suspended shall be excluded from Federal 
financial and nonfinancial assistance and benefits under Federal 
programs and activities. Debarment or suspension of a participant in a 
program by one agency shall have governmentwide effect.
    (b) These regulations implement section 3 of E.O. 12549 and the 
guidelines promulgated by the Office of Management and Budget under 
section 6 of the E.O. by:
    (1) Prescribing the programs and activities that are covered by the 
governmentwide system;
    (2) Prescribing the governmentwide criteria and governmentwide 
minimum due process procedures that each agency shall use;
    (3) Providing for the listing of debarred and suspended 
participants, participants declared ineligible (see definition of 
``ineligible'' in Sec. 1404.105), and participants who have voluntarily 
excluded themselves from participation in covered transactions;
    (4) Setting forth the consequences of a debarment, suspension, 
determination of ineligibility, or voluntary exclusion; and
    (5) Offering such other guidance as necessary for the effective 
implementation and administration of the governmentwide system.
    (c) These regulations also implement Executive Order 12689 (3 CFR, 
1989 Comp., p. 235) and 31 U.S.C. 6101 note (Public Law 103-355, sec. 
2455, 108 Stat. 3327) by--
    (1) Providing for the inclusion in the List of Parties Excluded from 
Federal Procurement and Nonprocurement Programs all persons proposed for 
debarment, debarred or suspended under the Federal Acquisition 
Regulation, 48 CFR Part 9, subpart 9.4; persons against which 
governmentwide exclusions have been entered under this part; and persons 
determined to be ineligible; and
    (2) Setting forth the consequences of a debarment, suspension, 
determination of ineligibility, or voluntary exclusion.
    (d) Although these regulations cover the listing of ineligible 
participants and the effect of such listing, they do not prescribe 
policies and procedures governing declarations of ineligibility.

[60 FR 33040, 33045, June 26, 1995]



Sec. 1404.105  Definitions.

    The following definitions apply to this part:
     Adequate evidence. Information sufficient to support the reasonable 
belief that a particular act or omission has occurred.
    Affiliate. Persons are affiliates of each other if, directly or 
indirectly, either one controls or has the power to control the other, 
or, a third person controls or has the power to control both. Indicia of 
control include, but are not limited to: interlocking management or 
ownership, identity of interests among family members, shared facilities 
and equipment, common use of employees, or a business entity organized 
following the suspension or debarment of a person which has the

[[Page 305]]

same or similar management, ownership, or principal employees as the 
suspended, debarred, ineligible, or voluntarily excluded person.
     Agency. Any executive department, military department or defense 
agency or other agency of the executive branch, excluding the 
independent regulatory agencies.
     Civil judgment. The disposition of a civil action by any court of 
competent jurisdiction, whether entered by verdict, decision, 
settlement, stipulation, or otherwise creating a civil liability for the 
wrongful acts complained of; or a final determination of liability under 
the Program Fraud Civil Remedies Act of 1988 (31 U.S.C. 3801-12).
    Conviction. A judgment or conviction of a criminal offense by any 
court of competent jurisdiction, whether entered upon a verdict or a 
plea, including a plea of nolo contendere.
     Debarment. An action taken by a debarring official in accordance 
with these regulations to exclude a person from participating in covered 
transactions. A person so excluded is ``debarred.''
     Debarring official. An official authorized to impose debarment. The 
debarring official is either:
    (1) The agency head, or
    (2) An official designated by the agency head.
     Indictment. Indictment for a criminal offense. An information or 
other filing by competent authority charging a criminal offense shall be 
given the same effect as an indictment.
     Ineligible. Excluded from participation in Federal nonprocurement 
programs pursuant to a determination of ineligibility under statutory, 
executive order, or regulatory authority, other than Executive Order 
12549 and its agency implementing regulations; for example, excluded 
pursuant to the Davis-Bacon Act and its implementing regulations, the 
equal employment opportunity acts and executive orders, or the 
environmental protection acts and executive orders. A person is 
ineligible where the determination of ineligibility affects such 
person's eligibility to participate in more than one covered 
transaction.
    Legal proceedings. Any criminal proceeding or any civil judicial 
proceeding to which the Federal Government or a State or local 
government or quasi-governmental authority is a party. The term includes 
appeals from such proceedings.
    List of Parties Excluded from Federal Procurement and Nonprocurement 
Programs. A list compiled, maintained and distributed by the General 
Services Administration (GSA) containing the names and other information 
about persons who have been debarred, suspended, or voluntarily excluded 
under Executive Orders 12549 and 12689 and these regulations or 48 CFR 
part 9, subpart 9.4, persons who have been proposed for debarment under 
48 CFR part 9, subpart 9.4, and those persons who have been determined 
to be ineligible.
     Notice. A written communication served in person or sent by 
certified mail, return receipt requested, or its equivalent, to the last 
known address of a party, its identified counsel, its agent for service 
of process, or any partner, officer, director, owner, or joint venturer 
of the party. Notice, if undeliverable, shall be considered to have been 
received by the addressee five days after being properly sent to the 
last address known by the agency.
     Participant. Any person who submits a proposal for, enters into, or 
reasonably may be expected to enter into a covered transaction. This 
term also includes any person who acts on behalf of or is authorized to 
commit a participant in a covered transaction as an agent or 
representative of another participant.
     Person. Any individual, corporation, partnership, association, unit 
of government or legal entity, however organized, except: Foreign 
governments or foreign governmental entities, public international 
organizations, foreign government owned (in whole or in part) or 
controlled entities, and entities consisting wholly or partially of 
foreign governments or foreign governmental entities.
     Preponderance of the evidence. Proof by information that, compared 
with that opposing it, leads to the conclusion that the fact at issue is 
more probably true than not.
     Principal. Officer, director, owner, partner, key employee, or 
other person within a participant with primary

[[Page 306]]

management or supervisory responsibilities; or a person who has a 
critical influence on or substantive control over a covered transaction, 
whether or not employed by the participant. Persons who have a critical 
influence on or substantive control over a covered transaction are:
    (1) Principal investigators.
     Proposal. A solicited or unsolicited bid, application, request, 
invitation to consider or similar communication by or on behalf of a 
person seeking to participate or to receive a benefit, directly or 
indirectly, in or under a covered transaction.
     Respondent. A person against whom a debarment or suspension action 
has been initiated.
     State. Any of the States of the United States, the District of 
Columbia, the Commonwealth of Puerto Rico, any territory or possession 
of the United States, or any agency of a State, exclusive of 
institutions of higher education, hospitals, and units of local 
government. A State instrumentality will be considered part of the State 
government if it has a written determination from a State government 
that such State considers that instrumentality to be an agency of the 
State government.
     Suspending official. An official authorized to impose suspension. 
The suspending official is either:
    (1) The agency head, or
    (2) An official designated by the agency head.
     Suspension. An action taken by a suspending official in accordance 
with these regulations that immediately excludes a person from 
participating in covered transactions for a temporary period, pending 
completion of an investigation and such legal, debarment, or Program 
Fraud Civil Remedies Act proceedings as may ensue. A person so excluded 
is ``suspended.''
     Voluntary exclusion or voluntarily excluded. A status of 
nonparticipation or limited participation in covered transactions 
assumed by a person pursuant to the terms of a settlement.

[57 FR 56263, Nov. 27, 1992, as amended at 60 FR 33041, 33045, June 26, 
1995]



Sec. 1404.110  Coverage.

    (a) These regulations apply to all persons who have participated, 
are currently participating or may reasonably be expected to participate 
in transactions under Federal nonprocurement programs. For purposes of 
these regulations such transactions will be referred to as ``covered 
transactions.''
    (1) Covered transaction. For purposes of these regulations, a 
covered transaction is a primary covered transaction or a lower tier 
covered transaction. Covered transactions at any tier need not involve 
the transfer of Federal funds.
    (i) Primary covered transaction. Except as noted in paragraph (a)(2) 
of this section, a primary covered transaction is any nonprocurement 
transaction between an agency and a person, regardless of type, 
including: Grants, cooperative agreements, scholarships, fellowships, 
contracts of assistance, loans, loan guarantees, subsidies, insurance, 
payments for specified use, donation agreements and any other 
nonprocurement transactions between a Federal agency and a person. 
Primary covered transactions also include those transactions specially 
designated by the U.S. Department of Housing and Urban Development in 
such agency's regulations governing debarment and suspension.
    (ii) Lower tier covered transaction. A lower tier covered 
transaction is:
    (A) Any transaction between a participant and a person other than a 
procurement contract for goods or services, regardless of type, under a 
primary covered transaction.
    (B) Any procurement contract for goods or services between a 
participant and a person, regardless of type, expected to equal or 
exceed the Federal procurement small purchase threshold fixed at 10 
U.S.C. 2304(g) and 41 U.S.C. 253(g) (currently $25,000) under a primary 
covered transaction.
    (C) Any procurement contract for goods or services between a 
participant and a person under a covered transaction, regardless of 
amount, under which that person will have a critical influence on or 
substantive control over that covered transaction. Such persons are:
    (1) Principal investigators.

[[Page 307]]

    (2) Providers of federally-required audit services.
    (2) Exceptions. The following transactions are not covered:
    (i) Statutory entitlements or mandatory awards (but not subtier 
awards thereunder which are not themselves mandatory), including 
deposited funds insured by the Federal Government;
    (ii) Direct awards to foreign governments or public international 
organizations, or transactions with foreign governments or foreign 
governmental entities, public international organizations, foreign 
government owned (in whole or in part) or controlled entities, entities 
consisting wholly or partially of foreign governments or foreign 
governmental entities;
    (iii) Benefits to an individual as a personal entitlement without 
regard to the individual's present responsibility (but benefits received 
in an individual's business capacity are not excepted);
    (iv) Federal employment;
    (v) Transactions pursuant to national or agency-recognized 
emergencies or disasters;
    (vi) Incidental benefits derived from ordinary governmental 
operations; and
    (vii) Other transactions where the application of these regulations 
would be prohibited by law.
    (b) Relationship to other sections. This section describes the types 
of transactions to which a debarment or suspension under the regulations 
will apply. Subpart B, ``Effect of Action,'' Sec. 1404.200, ``Debarment 
or suspension,'' sets forth the consequences of a debarment or 
suspension. Those consequences would obtain only with respect to 
participants and principals in the covered transactions and activities 
described in Sec. 1404.110(a). Sections Sec. 1404.325, ``Scope of 
debarment,'' and Sec. 1404.420, ``Scope of suspension,'' govern the 
extent to which a specific participant or organizational elements of a 
participant would be automatically included within a debarment or 
suspension action, and the conditions under which affiliates or persons 
associated with a participant may also be brought within the scope of 
the action.
    (c) Relationship to Federal procurement activities. In accordance 
with E.O. 12689 and section 2455 of Public Law 103-355, any debarment, 
suspension, proposed debarment or other governmentwide exclusion 
initiated under the Federal Acquisition Regulation (FAR) on or after 
August 25, 1995 shall be recognized by and effective for Executive 
Branch agencies and participants as an exclusion under this regulation. 
Similarly, any debarment, suspension or other governmentwide exclusion 
initiated under this regulation on or after August 25, 1995 shall be 
recognized by and effective for those agencies as a debarment or 
suspension under the FAR.

[57 FR 56263, Nov. 27, 1992, as amended at 60 FR 33041, 33045, June 26, 
1995]



Sec. 1404.115  Policy.

    (a) In order to protect the public interest, it is the policy of the 
Federal Government to conduct business only with responsible persons. 
Debarment and suspension are discretionary actions that, taken in 
accordance with Executive Order 12549 and these regulations, are 
appropriate means to implement this policy.
    (b) Debarment and suspension are serious actions which shall be used 
only in the public interest and for the Federal Government's protection 
and not for purposes of punishment. Agencies may impose debarment or 
suspension for the causes and in accordance with the procedures set 
forth in these regulations.
    (c) When more than one agency has an interest in the proposed 
debarment or suspension of a person, consideration shall be given to 
designating one agency as the lead agency for making the decision. 
Agencies are encouraged to establish methods and procedures for 
coordinating their debarment or suspension actions.



                       Subpart B--Effect of Action



Sec. 1404.200  Debarment or suspension.

    (a) Primary covered transactions. Except to the extent prohibited by 
law, persons who are debarred or suspended shall be excluded from 
primary covered transactions as either participants or principals 
throughout the Executive Branch of the Federal Government for the period 
of their debarment, suspension, or the period they are proposed for 
debarment under 48 CFR part 9,

[[Page 308]]

subpart 9.4. Accordingly, no agency shall enter into primary covered 
transactions with such excluded persons during such period, except as 
permitted pursuant to Sec. 1404.215.
    (b) Lower tier covered transactions. Except to the extent prohibited 
by law, persons who have been proposed for debarment under 48 CFR part 
9, subpart 9.4, debarred or suspended shall be excluded from 
participating as either participants or principals in all lower tier 
covered transactions (see Sec. 1404.110(a)(1)(ii)) for the period of 
their exclusion.
    (c) Exceptions. Debarment or suspension does not affect a person's 
eligibility for--
    (1) Statutory entitlements or mandatory awards (but not subtier 
awards thereunder which are not themselves mandatory), including 
deposited funds insured by the Federal Government;
    (2) Direct awards to foreign governments or public international 
organizations, or transactions with foreign governments or foreign 
governmental entities, public international organizations, foreign 
government owned (in whole or in part) or controlled entities, and 
entities consisting wholly or partially of foreign governments or 
foreign governmental entities;
    (3) Benefits to an individual as a personal entitlement without 
regard to the individual's present responsibility (but benefits received 
in an individual's business capacity are not excepted);
    (4) Federal employment;
    (5) Transactions pursuant to national or agency-recognized 
emergencies or disasters;
    (6) Incidental benefits derived from ordinary governmental 
operations; and
    (7) Other transactions where the application of these regulations 
would be prohibited by law.

[60 FR 33041, 33045, June 26, 1995]



Sec. 1404.205  Ineligible persons.

    Persons who are ineligible, as defined in Sec. 1404.105(i), are 
excluded in accordance with the applicable statutory, executive order, 
or regulatory authority.



Sec. 1404.210  Voluntary exclusion.

    Persons who accept voluntary exclusions under Sec. 1404.315 are 
excluded in accordance with the terms of their settlements. The Office 
of National Drug Control Policy (ONDCP) shall, and participants may, 
contact the original action agency to ascertain the extent of the 
exclusion.



Sec. 1404.215  Exception provision.

    [Agency] may grant an exception permitting a debarred, suspended, or 
voluntarily excluded person, or a person proposed for debarment under 48 
CFR part 9, subpart 9.4, to participate in a particular covered 
transaction upon a written determination by the agency head or an 
authorized designee stating the reason(s) for deviating from the 
Presidential policy established by Executive Order 12549 and 
Sec. 1404.200. However, in accordance with the President's stated 
intention in the Executive Order, exceptions shall be granted only 
infrequently. Exceptions shall be reported in accordance with 
Sec. 1404.505(a).

[60 FR 33041, 33045, June 26, 1995]



Sec. 1404.220  Continuation of covered transactions.

    (a) Notwithstanding the debarment, suspension, proposed debarment 
under 48 CFR part 9, subpart 9.4, determination of ineligibility, or 
voluntary exclusion of any person by an agency, agencies and 
participants may continue covered transactions in existence at the time 
the person was debarred, suspended, proposed for debarment under 48 CFR 
part 9, subpart 9.4, declared ineligible, or voluntarily excluded. A 
decision as to the type of termination action, if any, to be taken 
should be made only after thorough review to ensure the propriety of the 
proposed action.
    (b) Agencies and participants shall not renew or extend covered 
transactions (other than no-cost time extensions) with any person who is 
debarred, suspended, proposed for debarment under 48 CFR part 9, subpart 
9.4, ineligible or voluntary excluded, except as provided in 
Sec. 1404.215.

[60 FR 33041, 33045, June 26, 1995]



Sec. 1404.225  Failure to adhere to restrictions.

    (a) Except as permitted under Sec. 1404.215 or Sec. 1404.220, a 
participant

[[Page 309]]

shall not knowingly do business under a covered transaction with a 
person who is--
    (1) Debarred or suspended;
    (2) Proposed for debarment under 48 CFR part 9, subpart 9.4; or
    (3) Ineligible for or voluntarily excluded from the covered 
transaction.
    (b) Violation of the restriction under paragraph (a) of this section 
may result in disallowance of costs, annulment or termination of award, 
issuance of a stop work order, debarment or suspension, or other 
remedies as appropriate.
    (c) A participant may rely upon the certification of a prospective 
participant in a lower tier covered transaction that it and its 
principals are not debarred, suspended, proposed for debarment under 48 
CFR part 9, subpart 9.4, ineligible, or voluntarily excluded from the 
covered transaction (See appendix B of these regulations), unless it 
knows that the certification is erroneous. An agency has the burden of 
proof that a participant did knowingly do business with a person that 
filed an erroneous certification.

[60 FR 33041, 33045, June 26, 1995]



                          Subpart C--Debarment



Sec. 1404.300  General.

    The debarring official may debar a person for any of the causes in 
Sec. 1404.305, using procedures established in Sec. 1404.310 through 
Sec. 1404.314. The existence of a cause for debarment, however, does not 
necessarily require that the person be debarred; the seriousness of the 
person's acts or omissions and any mitigating factors shall be 
considered in making any debarment decision.



Sec. 1404.305  Causes for debarment.

    Debarment may be imposed in accordance with the provisions of 
Sec. 1404.300 through Sec. 1404.314 for:
    (a) Conviction of or civil judgment for:
    (1) Commission of fraud or a criminal offense in connection with 
obtaining, attempting to obtain, or performing a public or private 
agreement or transaction;
    (2) Violation of Federal or State antitrust statutes, including 
those proscribing price fixing between competitors, allocation of 
customers between competitors, and bid rigging;
    (3) Commission of embezzlement, theft, forgery, bribery, 
falsification or destruction of records, making false statements, 
receiving stolen property, making false claims, or obstruction of 
justice; or
    (4) Commission of any other offense indicating a lack of business 
integrity or business honesty that seriously and directly affects the 
present responsibility of a person.
    (b) Violation of the terms of a public agreement or transaction so 
serious as to affect the integrity of an agency program, such as:
    (1) A willful failure to perform in accordance with the terms of one 
or more public agreements or transactions;
    (2) A history of failure to perform or of unsatisfactory performance 
of one or more public agreements or transactions; or
    (3) A willful violation of a statutory or regulatory provision or 
requirement applicable to a public agreement or transaction.
    (c) Any of the following causes:
    (1) A nonprocurement debarment by any Federal agency taken before 
October 1, 1988, or a procurement debarment by any Federal agency taken 
pursuant to 48 CFR subpart 9.4;
    (2) Knowingly doing business with a debarred, suspended, ineligible, 
or voluntarily excluded person, in connection with a covered 
transaction, except as permitted in Sec. 1404.215 or Sec. 1404.220;
    (3) Failure to pay a single substantial debt, or a number of 
outstanding debts (including disallowed costs and overpayments, but not 
including sums owed the Federal Government under the Internal Revenue 
Code) owed to any Federal agency or instrumentality, provided the debt 
is uncontested by the debtor or, if contested, provided that the 
debtor's legal and administrative remedies have been exhausted;
    (4) Violation of a material provision of a voluntary exclusion 
agreement entered into under Sec. 1404.315 or of any settlement of a 
debarment or suspension action; or

[[Page 310]]

    (5) Violation of any requirement of Subpart F of this part relating 
to providing a drug-free workplace, as set forth in Sec. 1404.615 of 
this part.
    (d) Any other cause of so serious or compelling a nature that it 
affects the present responsibility of a person.



Sec. 1404.310  Procedures.

    ONDCP shall process debarment actions as informally as practicable, 
consistent with the principles of fundamental fairness, using the 
procedures in Sec. 1404.311 through Sec. 1404.314.



Sec. 1404.311  Investigation and referral.

    Information concerning the existence of a cause for debarment from 
any source shall be promptly reported, investigated, and referred, when 
appropriate, to the debarring official for consideration. After 
consideration, the debarring official may issue a notice of proposed 
debarment.



Sec. 1404.312  Notice of proposed debarment.

    A debarment proceeding shall be initiated by notice to the 
respondent advising:
    (a) That debarment is being considered;
    (b) Of the reasons for the proposed debarment in terms sufficient to 
put the respondent on notice of the conduct or transaction(s) upon which 
it is based;
    (c) Of the cause(s) relied upon under Sec. 1404.305 for proposing 
debarment;
    (d) Of the provisions of Sec. 1404.311 through Sec. 1404.314, and 
any other ONDCP procedures, if applicable, governing debarment decision 
making; and
    (e) Of the potential effect of a debarment.



Sec. 1404.313  Opportunity to contest proposed debarment.

    (a) Submission in opposition. Within 30 days after receipt of the 
notice of proposed debarment, the respondent may submit, in person, in 
writing, or through a representative, information and argument in 
opposition to the proposed debarment.
    (b) Additional proceedings as to disputed material facts. (1) In 
actions not based upon a conviction or civil judgment, if the debarring 
official finds that the respondent's submission in opposition raises a 
genuine dispute over facts material to the proposed debarment, 
respondent(s) shall be afforded an opportunity to appear with a 
representative, submit documentary evidence, present witnesses, and 
confront any witness the agency presents.
    (2) A transcribed record of any additional proceedings shall be made 
available at cost to the respondent, upon request, unless the respondent 
and the agency, by mutual agreement, waive the requirement for a 
transcript.



Sec. 1404.314  Debarring official's decision.

    (a) No additional proceedings necessary. In actions based upon a 
conviction or civil judgment, or in which there is no genuine dispute 
over material facts, the debarring official shall make a decision on the 
basis of all the information in the administrative record, including any 
submission made by the respondent. The decision shall be made within 45 
days after receipt of any information and argument submitted by the 
respondent, unless the debarring official extends this period for good 
cause.
    (b) Additional proceedings necessary. (1) In actions in which 
additional proceedings are necessary to determine disputed material 
facts, written findings of fact shall be prepared. The debarring 
official shall base the decision on the facts as found, together with 
any information and argument submitted by the respondent and any other 
information in the administrative record.
    (2) The debarring official may refer disputed material facts to 
another official for findings of fact. The debarring official may reject 
any such findings, in whole or in part, only after specifically 
determining them to be arbitrary and capricious or clearly erroneous.
    (3) The debarring official's decision shall be made after the 
conclusion of the proceedings with respect to disputed facts.
    (c) (1) Standard of proof. In any debarment action, the cause for 
debarment must be established by a preponderance of the evidence. Where 
the proposed debarment is based upon a conviction or civil judgment, the 
standard shall be deemed to have been met.

[[Page 311]]

    (2) Burden of proof. The burden of proof is on the agency proposing 
debarment.
    (d) Notice of debarring official's decision. (1) If the debarring 
official decides to impose debarment, the respondent shall be given 
prompt notice:
    (i) Referring to the notice of proposed debarment;
    (ii) Specifying the reasons for debarment;
    (iii) Stating the period of debarment, including effective dates; 
and
    (iv) Advising that the debarment is effective for covered 
transactions throughout the executive branch of the Federal Government 
unless an agency head or an authorized designee makes the determination 
referred to in Sec. 1404.215.
    (2) If the debarring official decides not to impose debarment, the 
respondent shall be given prompt notice of that decision. A decision not 
to impose debarment shall be without prejudice to a subsequent 
imposition of debarment by any other agency.



Sec. 1404.315  Settlement and voluntary exclusion.

    (a) When in the best interest of the Government, ONDCP may, at any 
time, settle a debarment or suspension action.
    (b) If a participant and the agency agree to a voluntary exclusion 
of the participant, such voluntary exclusion shall be entered on the 
Nonprocurement List (see Subpart E of this part).



Sec. 1404.320  Period of debarment.

    (a) Debarment shall be for a period commensurate with the 
seriousness of the causes(s). If a suspension precedes a debarment, the 
suspension period shall be considered in determining the debarment 
period.
    (1) Debarment for causes other than those related to a violation of 
the requirements of Subpart F of this part generally should not exceed 
three years. When circumstances warrant, a longer period of debarment 
may be imposed.
    (2) In the case of a debarment for a violation of the requirement of 
Subpart F of this part (see Sec. 1404.305.(c)(5)), the period of 
debarment shall not exceed five years.
    (b) The debarring official may extend an existing debarment for an 
additional period, if that official determines that an extension is 
necessary to protect the public interest. However, a debarment may not 
be extended solely on the basis of the facts and circumstances upon 
which the initial debarment action was based. If debarment for an 
additional period is determined to be necessary, the procedures of 
Sec. 1404.311 through Sec. 1404.314 shall be followed to extend the 
debarment.
    (c) The respondent may request the debarring official to reverse the 
debarment decision or to reduce the period or scope of debarment. Such a 
request shall be in writing and supported by documentation. The 
debarring official may grant such a request for reasons including, but 
not limited to:
    (1) Newly discovered material evidence;
    (2) Reversal of the conviction or civil judgment upon which the 
debarment was based;
    (3) Bona fide change in ownership or management;
    (4) Elimination of other causes for which the debarment was imposed; 
or
    (5) Other reasons the debarring official deems appropriate.



Sec. 1404.325  Scope of debarment.

    (a) Scope in general. (1) Debarment of a person under these 
regulations constitutes debarment of all its divisions and other 
organizational elements from all covered transactions, unless the 
debarment decision is limited by its terms to one or more specifically 
identified individuals, divisions or other organizational elements or to 
specific types of transactions.
    (2) The debarment action may include any affiliate of the 
participant that is specifically named and given notice of the proposed 
debarment and an opportunity to respond (see Sec. 1404.311 through 
Sec. 1404.314).
    (b) Imputing conduct. For purposes of determining the scope of 
debarment, conduct may be imputed as follows:
    (1) Conduct imputed to participant. The fraudulent, criminal or 
other seriously improper conduct of any officer, director, shareholder, 
partner, employee, or

[[Page 312]]

other individual associated with a participant may be imputed to the 
participant when the conduct occurred in connection with the 
individual's performance of duties for or on behalf of the participant, 
or with the participant's knowledge, approval, or acquiescence. The 
participant's acceptance of the benefits derived from the conduct shall 
be evidence of such knowledge, approval, or acquiescence.
    (2) Conduct imputed to individuals associated with participant. The 
fraudulent, criminal, or other seriously improper conduct of a 
participant may be imputed to any officer, director, shareholder, 
partner, employee, or other individual associated with the participant 
who participated in, knew of, or had reason to know of the participant's 
conduct.
    (3) Conduct of one participant imputed to other participants in a 
joint venture. The fraudulent, criminal, or other seriously improper 
conduct of one participant in a joint venture, grant pursuant to a joint 
application, or similar arrangement may be imputed to other participants 
if the conduct occurred for or on behalf of the joint venture, grant 
pursuant to a joint application, or similar arrangement may be imputed 
to other participants if the conduct occurred for or on behalf of the 
joint venture, grant pursuant to a joint application, or similar 
arrangement or with the knowledge, approval, or acquiescence of these 
participants. Acceptance of the benefits derived from the conduct shall 
be evidence of such knowledge, approval, or acquiescence.



                          Subpart D--Suspension



Sec. 1404.400  General.

    (a) The suspending official may suspend a person for any of the 
causes in Sec. 1404.405 using procedures established in Sec. 1404.410 
through Sec. 1404.413.
    (b) Suspension is a serious action to be imposed only when:
    (1) There exists adequate evidence of one or more of the causes set 
out in Sec. 1404.405, and
    (2) Immediate action is necessary to protect the public interest.
    (c) In assessing the adequacy of the evidence, the agency should 
consider how much information is available, how credible it is given the 
circumstances, whether or not important allegations are corroborated, 
and what inferences can reasonably be drawn as a result. This assessment 
should include an examination of basic documents such as grants, 
cooperative agreements, loan authorizations, and contracts.



Sec. 1404.405  Causes for suspension.

    (a) Suspension may be imposed in accordance with the provisions of 
Sec. 1404.400 through Sec. 1404.413 upon adequate evidence:
    (1) To suspect the commission of an offense listed in 
Sec. 1404.305(a); or
    (2) That a cause for debarment under Sec. 1404.305 may exist.
    (b) Indictment shall constitute adequate evidence for purposes of 
suspension actions.



Sec. 1404.410  Procedures.

    (a) Investigation and referral. Information concerning the existence 
of a cause for suspension from any source shall be promptly reported, 
investigated, and referred, when appropriate, to the suspending official 
for consideration. After consideration, the suspending official may 
issue a notice of suspension.
    (b) Decision making process. ONDCP shall process suspension actions 
as informally as practicable, consistent with principles of fundamental 
fairness, using the procedures in Sec. 1404.411 through Sec. 1404.413.



Sec. 1404.411  Notice of suspension.

    When a respondent is suspended, notice shall immediately be given:
    (a) That suspension has been imposed;
    (b) That the suspension is based on an indictment, conviction, or 
other adequate evidence that the respondent has committed irregularities 
seriously reflecting on the propriety of further Federal Government 
dealings with the respondent;
    (c) Describing any such irregularities in terms sufficient to put 
the respondent on notice without disclosing the Federal Government's 
evidence;
    (d) Of the cause(s) relied upon under Sec. 1404.405 for imposing 
suspension;

[[Page 313]]

    (e) That the suspension is for a temporary period pending the 
completion of an investigation or ensuing legal, debarment, or Program 
Fraud Civil Remedies Act proceedings;
    (f) Of the provisions of Sec. 1404.411 through Sec. 1404.413 and any 
other ONDCP procedures, if applicable, governing suspension decision 
making; and
    (g) Of the effect of the suspension.



Sec. 1404.412  Opportunity to contest suspension.

    (a) Submission in opposition. Within 30 days after receipt of the 
notice of suspension, the respondent may submit, in person, in writing, 
or through a representative, information and argument in opposition to 
the suspension.
    (b) Additional proceedings as to disputed material facts. (1) If the 
suspending official finds that the respondent's submission in opposition 
raises a genuine dispute over facts material to the suspension, 
respondent(s) shall be afforded an opportunity to appear with a 
representative, submit documentary evidence, present witnesses, and 
confront any witness the agency presents, unless:
    (i) The action is based on an indictment, conviction or civil 
judgment, or
    (ii) A determination is made, on the basis of Department of Justice 
advice, that the substantial interests of the Federal Government in 
pending or contemplated legal proceedings based on the same facts as the 
suspension would be prejudiced.
    (2) A transcribed record of any additional proceedings shall be 
prepared and made available at cost to the respondent, upon request, 
unless the respondent and the agency, by mutual agreement, waive the 
requirement for a transcript.



Sec. 1404.413  Suspending official's decision.

    The suspending official may modify or terminate the suspension (for 
example, see Sec. 1404.320(c) for reasons for reducing the period or 
scope of debarment) or may leave it in force. However, a decision to 
modify or terminate the suspension shall be without prejudice to the 
subsequent imposition of suspension by any other agency or debarment by 
any agency. The decision shall be rendered in accordance with the 
following provisions:
    (a) No additional proceedings necessary. In actions: based on an 
indictment, conviction, or civil judgment; in which there is no genuine 
dispute over material facts; or in which additional proceedings to 
determine disputed material facts have been denied on the basis of 
Department of Justice advice, the suspending official shall make a 
decision on the basis of all the information in the administrative 
record, including any submission made by the respondent. The decision 
shall be made within 45 days after receipt of any information and 
argument submitted by the respondent, unless the suspending official 
extends this period for good cause.
    (b) Additoinal proceedings necessary. (1) In actions in which 
additional proceedings are necessary to determine disputed material 
facts, written findings of fact shall be prepared. The suspending 
official shall base the decision on the facts as found, together with 
any information and argument submitted by the respondent and any other 
information in the administrative record.
    (2) The suspending official may refer matters involving disputed 
material facts to another official for findings of fact. The suspending 
official may reject any such findings, in whole or in part, only after 
specifically determining them to be arbitrary or capricious or clearly 
erroneous.
    (c) Notice of suspending official's decision. Prompt written notice 
of the suspending official's decision shall be sent to the respondent.



Sec. 1404.415  Period of suspension.

    (a) Suspension shall be for a temporary period pending the 
completion of an investigation or ensuing legal, debarment, or Program 
Fraud Civil Remedies Act proceedings, unless terminated sooner by the 
suspending official or as provided in paragraph (b) of this section.
    (b) If legal or administrative proceedings are not initiated within 
12 months after the date of the suspension notice, the suspension shall 
be terminated unless an Assistant Attorney General or United States 
Attorney requests its extension in writing, in which case it may be 
extended for an additional six

[[Page 314]]

months. In no event may a suspension extend beyond 18 months, unless 
such proceedings have been initiated within that period.
    (c) The suspending official shall notify the Department of Justice 
of an impending termination of a suspension, at least 30 days before the 
12-month period expires, to give that Department an opportunity to 
request an extension.



Sec. 1404.420  Scope of suspension.

    The scope of a suspension is the same as the scope of a debarment 
(see Sec. 1404.325), except that the procedures of Sec. 1404.410 through 
Sec. 1404.413 shall be used in imposing a suspension.



       Subpart E--Responsibilities of GSA, Agency and Participants



Sec. 1404.500  GSA responsibilities.

    (a) In accordance with the OMB guidelines, GSA shall compile, 
maintain, and distribute a list of all persons who have been debarred, 
suspended, or voluntarily excluded by agencies under Executive Order 
12549 and these regulations, and those who have been determined to be 
ineligible.
    (b) At a minimum, this list shall indicate:
    (1) The names and addresses of all debarred, suspended, ineligible, 
and voluntarily excluded persons, in alphabetical order, with cross-
references when more than one name is involved in a single action;
    (2) The type of action;
    (3) The cause for the action;
    (4) The scope of the action;
    (5) Any termination date for each listing; and
    (6) The agency and name and telephone number of the agency point of 
contact for the action.



Sec. 1404.505  ONDCP responsibilities.

    (a) The agency shall provide GSA with current information concerning 
debarments, suspension, determinations of ineligibility, and voluntary 
exclusions it has taken.
    (b) Unless an alternative schedule is agreed to by GSA, the agency 
shall advise GSA of the information set forth in Sec. 1404.500(b) and of 
the exceptions granted under Sec. 1404.215 within five working days 
after taking such actions.
    (c) The agency shall direct inquiries concerning listed persons to 
the agency that took the action.
    (d) Agency officials shall check the Nonprocurement List before 
entering covered transactions to determine whether a participant in a 
primary transaction is debarred, suspended, ineligible, or voluntarily 
excluded (Tel. ).
    (e) Agency officials shall check the Nonprocurement List before 
approving principals or lower tier participants where agency approval of 
the principal or lower tier participant is required under the terms of 
the transaction, to determine whether such principals or participants 
are debarred, suspended, ineligible, or voluntarily excluded.



Sec. 1404.510  Participants' responsibilities.

    (a) Certification by participants in primary covered transactions. 
Each participant shall submit the certification in Appendix A to this 
Part for it and its principals at the time the participant submits its 
proposal in connection with a primary covered transaction, except that 
States need only complete such certification as to their principals. 
Participants may decide the method and frequency by which they determine 
the eligibility of their principals. In addition, each participant may, 
but is not required to, check the Nonprocurement List for its 
principals. Adverse information on the certification will not 
necessarily result in denial of participation. However, the 
certification, and any additional information pertaining to the 
certification submitted by the participant, shall be considered in the 
administration of covered transactions.
    (b) Certification by participants in lower tier covered 
transactions. (1) Each participant shall require participants in lower 
tier covered transactions to include the certification in Appendix B to 
this Part for it and its principals in any proposal submitted in 
connection with such lower tier covered transactions.

[[Page 315]]

    (2) A participant may rely upon the certification of a prospective 
participant in a lower tier covered transaction that it and its 
principals are not debarred, suspended, ineligible, or voluntarily 
excluded from the covered transaction by any Federal agency, unless it 
knows that the certification is erroneous. Participants may decide the 
method and frequency by which they determine the eligibility of their 
principals. In addition, a participant may, but is not required to, 
check the Nonprocurement List for its principals and for participants.
    (c) Changed circumstances regarding certification. A participant 
shall provide immediate written notice to ONDCP if at any time the 
participant learns that its certification was erroneous when submitted 
or has become erroneous by reason of changed circumstances. Participants 
in lower tier covered transactions shall provide the same updated notice 
to the participant to which it submitted its proposals.



          Subpart F--Drug-Free Workplace Requirements (Grants)



Sec. 1404.600  Purpose.

    (a) The purpose of this subpart is to carry out the Drug-Free 
Workplace Act of 1988 by requiring that--
    (1) A grantee, other than an individual, shall certify to the agency 
that it will provide a drug-free workplace;
    (2) A grantee who is an individual shall certify to the agency that, 
as a condition of the grant, he or she will not engage in the unlawful 
manufacture, distribution, dispensing, possession or use of a controlled 
substance in conducting any activity with the grant.
    (b) Requirements implementing the Drug-Free Workplace Act of 1988 
for contractors with the agency are found at 48 CFR subparts 9.4, 23.5, 
and 52.2.



Sec. 1404.605  Definitions.

    (a) Except as amended in this section, the definitions of 
Sec. 1404.105 apply to this subpart.
    (b) For purposes of this subpart--
    (1) Controlled substance means a controlled substance in schedules I 
through V of the Controlled Substances Act (21 U.S.C. 812), and as 
further defined by regulation at 21 CFR 1308.11 through 1308.15;
    (2) Conviction means a finding of guilt (including a plea of nolo 
contendere) or imposition of sentence, or both, by any judicial body 
charged with the responsibility to determine violations of the Federal 
or State criminal drug statutes;
    (3) Criminal drug statute means a Federal or non-Federal criminal 
statute involving the manufacture, distribution, dispensing, use, or 
possession of any controlled substance;
    (4) Drug-free workplace means a site for the performance of work 
done in connection with a specific grant at which employees of the 
grantee are prohibited from engaging in the unlawful manufacture, 
distribution, dispensing, possession, or use of a controlled substance;
    (5) Employee means the employee of a grantee directly engaged in the 
performance of work under the grant, including:
    (i) All direct charge employees;
    (ii) All indirect charge employees, unless their impact or 
involvement is insignificant to the performance of the grant; and,
    (iii) Temporary personnel and consultants who are directly engaged 
in the performance of work under the grant and who are on the grantee's 
payroll. This definition does not include workers not on the payroll of 
the grantee (e.g., volunteers, even if used to meet a matching 
requirement; consultants or independent contractors not on the payroll; 
or employees of subrecipients or subcontractors in covered workplaces);
    (6) Federal agency or agency means any United States executive 
department, military department, government corporation, government 
controlled corporation, any other establishment in the executive branch 
(including the Executive Office of the President), or any independent 
regulatory agency;
    (7) Grant means an award of financial assistance, including a 
cooperative agreement, in the form of money, or property in lieu of 
money, by a Federal agency directly to a grantee. The term grant 
includes block grant and entitlement grant programs, whether or not

[[Page 316]]

exempted from coverage under the grants management government 
government-wide common rule on uniform administrative requirements for 
grants and cooperative agreements. The term does not include technical 
assistance that provides services instead of money, or other assistance 
in the form of loans, loan guarantees, interest subsidies, insurance, or 
direct appropriations; or any veterans' benefits to individuals, i.e., 
any benefit to veterans, their families, or survivors by virtue of the 
service of a veteran in the Armed Forces of the United States;
    (8) Grantee means a person who applies for or receives a grant 
directly from a Federal agency (except another Federal agency);
    (9) Individual means a natural person;
    (10) State means any of the States of the United States, the 
District of Columbia, the Commonwealth of Puerto Rico, any territory or 
possession of the United States, or any agency of a State, exclusive of 
institutions of higher education, hospitals, and units of local 
government. A State instrumentality will be considered part of the State 
government if it has a written determination from a State government 
that such State considers the instrumentality to be an agency of the 
State government.



Sec. 1404.610  Coverage.

    (a) This subpart applies to any grantee of the agency.
    (b) This subpart applies to any grant, except where application of 
this subpart would be inconsistent with the international obligations of 
the United States or the laws or regulations of a foreign government. A 
determination of such inconsistency may be made only by the agency head 
or his/her designee.
    (c) The provisions of subparts A, B, C, D and E of this part apply 
to matters covered by this subpart, except where specifically modified 
by this subpart. In the event of any conflict between provisions of this 
subpart and other provisions of this part, the provisions of this 
subpart are deemed to control with respect to the implementation of 
drug-free workplace requirements concerning grants.



Sec. 1404.615  Grounds for suspension of payments, suspension or termination of grants, or suspension or debarment.

    A grantee shall be deemed in violation of the requirements of this 
subpart if the agency head or his or her official designee determines, 
in writing, that--
    (a) The grantee has made a false certification under Sec. 1404.630;
    (b) With respect to a grantee other than an individual--
    (1) The grantee has violated the certification by failing to carry 
out the requirements of subparagraphs (A)(a)-(g) and/or (B) of the 
certification (Alternate I to Appendix C); or
    (2) Such a member of employees of the grantee have been convicted of 
violations of criminal drug statutes for violations occurring in the 
workplace as to indicate that the grantee has failed to make a good 
faith effort to provide a drug-free workplace.
    (c) With respect to a grantee who is an individual--
    (1) The grantee has violated the certification by failing to carry 
out its requirements (Alternate II to Appendix C); or
    (2) The grantee is convicted of a criminal drug offense resulting 
from a violation occurring during the conduct of any grant activity.



Sec. 1404.620  Effect of violation.

    (a) In the event of a violation of this subpart as provided in 
Sec. 1404.615, and in accordance with applicable law, the grantee shall 
be subject to one or more of the following actions:
    (1) Suspension of payments under the grant;
    (2) Suspension or termination of the grant; and
    (3) Suspension or debarment of the grantee under the provisions of 
this part.
    (b) Upon issuance of any final decision under this part requiring 
debarment of a grantee, the debarred grantee shall be ineligible for 
award of any grant from any Federal agency for a period specified in the 
decision, not to exceed five years (see Sec. 1404.320(a)(2) of this 
part).

[[Page 317]]



Sec. 1404.625  Exception provision.

    The agency head may waive with respect to a particular grant, in 
writing, a suspension of payments under a grant, suspension or 
termination of a grant, or suspension or debarment of a grantee if the 
agency head determines that such a waiver would be in the public 
interest. This exception authority cannot be delegated to any other 
official.



Sec. 1404.630  Certification requirements and procedures.

    (a)(1) As a prior condition of being awarded a grant, each grantee 
shall make the appropriate certification to the Federal agency providing 
the grant, as provided in Appendix C to this part.
    (2) Grantees are not required to make a certification in order to 
continue receiving funds under a grant awarded before March 18, 1989, or 
under a no-cost time extension of such a grant. However, the grantee 
shall make a one-time drug-free workplace certification for a non-
automatic continuation of such a grant made on or after March 18, 1989.
    (b) Except as provided in this section, all grantees shall make the 
required certification for each grant. For mandatory formula grants and 
entitlements that have no application process, grantees shall submit a 
one-time certification in order to continue receiving awards.
    (c) A grantee that is a State may elect to make one certification in 
each Federal fiscal year. States that previously submitted an annual 
certification are not required to make a certification for Fiscal Year 
1990 until June 30, 1990. Except as provided in paragraph (d) of this 
section, this certification shall cover all grants to all State agencies 
from any Federal agency. The State shall retain the original of this 
statewide certification in its Governor's office and, prior to grant 
award, shall ensure that a copy is submitted individually with respect 
to each grant, unless the Federal agency had designated a central 
location for submission.
    (d)(1) The Governor of a State may exclude certain State agencies 
from the statewide certification and authorize these agencies to submit 
their own certifications to Federal agencies. The statewide 
certification shall name any State agencies so excluded.
    (2) A State agency to which the statewide certification does not 
apply, or a State agency in a State that does not have a statewide 
certification, may elect to make one certification in each Federal 
fiscal year. State agencies that previously submitted a State agency 
certification are not required to make a certification for Fiscal Year 
1990 until June 30, 1990. The State agency shall retain the original of 
this State agency-wide certification in its central office and, prior to 
grant award, shall ensure that a copy is submitted individually with 
respect to each grant, unless the Federal agency designates a central 
location for submission.
    (3) When the work of a grant is done by more than one State agency, 
the certification of the State agency directly receiving the grant shall 
be deemed to certify compliance for all workplaces, including those 
located in other State agencies.
    (e)(1) For a grant of less than 30 days performance duration, 
grantees shall have this policy statement and program in place as soon 
as possible, but in any case by a date prior to the date on which 
performance is expected to be completed.
    (2) For a grant of 30 days or more performance duration, grantees 
shall have this policy statement and program in place within 30 days 
after award.
    (3) Where extraordinary circumstances warrant for a specific grant, 
the grant officer may determine a different date on which the policy 
statement and program shall be in place.



Sec. 1404.635  Reporting of and employee sanctions for convictions of criminal drug offenses.

    (a) When a grantee other than an individual is notified that an 
employee has been convicted for a violation of a criminal drug statute 
occurring in the workplace, it shall take the following actions:
    (1) Within 10 calendar days of receiving notice of the conviction, 
the grantee shall provide written notice, including the convicted 
employee's position

[[Page 318]]

title, to every grant officer, or other designee on whose grant activity 
the convicted employee was working, unless a Federal agency has 
designated a central point for the receipt of such notifications. 
Notification shall include the identification number(s) for each of the 
Federal agency's affected grants.
    (2) Within 30 calendar days of receiving notice of the conviction, 
the grantee shall do the following with respect to the employee who was 
convicted:
    (i) Take appropriate personnel action against the employee, up to 
and including termination, consistent with requirements of the 
Rehabilitation Act of 1973, as amended; or
    (ii) Require the employee to participate satisfactorily in a drug 
abuse assistance or rehabilitation program approved for such purposes by 
a Federal, State, or local health, law enforcement, or other appropriate 
agency.
    (b) A grantee who is an individual who is convicted for a violation 
of a criminal drug statute occurring during the conduct of any grant 
activity shall report the conviction, in writing, within 10 calendar 
days, to his or her Federal agency grant officer, or other designee, 
unless the Federal agency has designated a central point for the receipt 
of such notices. Notification shall include the identification number(s) 
for each of the Federal agency's affected grants.

Appendix A to Part 1404--Certification Regarding Debarment, Suspension, 
     and Other Responsibility Matters--Primary Covered Transactions

                     Instructions for Certification

    1. By signing and submitting this proposal, the prospective primary 
participant is providing the certification set out below.
    2. The inability of a person to provide the certification required 
below will not necessarily result in denial of participation in this 
covered transaction. The prospective participant shall submit an 
explanation of why it cannot provide the certification set out below. 
The certification or explanation will be considered in connection with 
the department or agency's determination whether to enter into this 
transaction. However, failure of the prospective primary participant to 
furnish a certification or an explanation shall disqualify such person 
from participation in this transaction.
    3. The certification in this clause is a material representation of 
fact upon which reliance was placed when the department or agency 
determined to enter into this transaction. If it is later determined 
that the prospective primary participant knowingly rendered an erroneous 
certification, in addition to other remedies available to the Federal 
Government, the department or agency may terminate this transaction for 
cause or default.
    4. The prospective primary participant shall provide immediate 
written notice to the department or agency to which this proposal is 
submitted if at any time the prospective primary participant learns that 
its certification was erroneous when submitted or has become erroneous 
by reason of changed circumstances.
    5. The terms covered transaction, debarred, suspended, ineligible, 
lower tier covered transaction, participant, person, primary covered 
transaction, principal, proposal, and voluntarily excluded, as used in 
this clause, have the meanings set out in the Definitions and Coverage 
sections of the rules implementing Executive Order 12549. You may 
contact the department or agency to which this proposal is being 
submitted for assistance in obtaining a copy of those regulations.
    6. The prospective primary participant agrees by submitting this 
proposal that, should the proposed covered transaction be entered into, 
it shall not knowingly enter into any lower tier covered transaction 
with a person who is proposed for debarment under 48 CFR part 9, subpart 
9.4, debarred, suspended, declared ineligible, or voluntarily excluded 
from participation in this covered transaction, unless authorized by the 
department or agency entering into this transaction.
    7. The prospective primary participant further agrees by submitting 
this proposal that it will include the clause titled ``Certification 
Regarding Debarment, Suspension, Ineligibility and Voluntary Exclusion-
Lower Tier Covered Transaction,'' provided by the department or agency 
entering into this covered transaction, without modification, in all 
lower tier covered transactions and in all solicitations for lower tier 
covered transactions.
    8. A participant in a covered transaction may rely upon a 
certification of a prospective participant in a lower tier covered 
transaction that it is not proposed for debarment under 48 CFR part 9, 
subpart 9.4, debarred, suspended, ineligible, or voluntarily excluded 
from the covered transaction, unless it knows that the certification is 
erroneous. A participant may decide the method and frequency by which it 
determines the eligibility of its principals. Each participant may, but 
is not required to, check the List of Parties Excluded from Federal 
Procurement and Nonprocurement Programs.

[[Page 319]]

    9. Nothing contained in the foregoing shall be construed to require 
establishment of a system of records in order to render in good faith 
the certification required by this clause. The knowledge and information 
of a participant is not required to exceed that which is normally 
possessed by a prudent person in the ordinary course of business 
dealings.
    10. Except for transactions authorized under paragraph 6 of these 
instructions, if a participant in a covered transaction knowingly enters 
into a lower tier covered transaction with a person who is proposed for 
debarment under 48 CFR part 9, subpart 9.4, suspended, debarred, 
ineligible, or voluntarily excluded from participation in this 
transaction, in addition to other remedies available to the Federal 
Government, the department or agency may terminate this transaction for 
cause or default.

Certification Regarding Debarment, Suspension, and Other Responsibility 
                  Matters--Primary Covered Transactions

    (1) The prospective primary participant certifies to the best of its 
knowledge and belief, that it and its principals:
    (a) Are not presently debarred, suspended, proposed for debarment, 
declared ineligible, or voluntarily excluded by any Federal department 
or agency;
    (b) Have not within a three-year period preceding this proposal been 
convicted of or had a civil judgment rendered against them for 
commission of fraud or a criminal offense in connection with obtaining, 
attempting to obtain, or performing a public (Federal, State or local) 
transaction or contract under a public transaction; violation of Federal 
or State antitrust statutes or commission of embezzlement, theft, 
forgery, bribery, falsification or destruction of records, making false 
statements, or receiving stolen property;
    (c) Are not presently indicted for or otherwise criminally or 
civilly charged by a governmental entity (Federal, State or local) with 
commission of any of the offenses enumerated in paragraph (1)(b) of this 
certification; and
    (d) Have not within a three-year period preceding this application/
proposal had one or more public transactions (Federal, State or local) 
terminated for cause or default.
    (2) Where the prospective primary participant is unable to certify 
to any of the statements in this certification, such prospective 
participant shall attach an explanation to this proposal.

[60 FR 33042, 33045, June 26, 1995]

Appendix B to Part 1404--Certification Regarding Debarment, Suspension, 
 Ineligibility and Voluntary Exclusion--Lower Tier Covered Transactions

                     Instructions for Certification

    1. By signing and submitting this proposal, the prospective lower 
tier participant is providing the certification set out below.
    2. The certification in this clause is a material representation of 
fact upon which reliance was placed when this transaction was entered 
into. If it is later determined that the prospective lower tier 
participant knowingly rendered an erroneous certification, in addition 
to other remedies available to the Federal Government the department or 
agency with which this transaction originated may pursue available 
remedies, including suspension and/or debarment.
    3. The prospective lower tier participant shall provide immediate 
written notice to the person to which this proposal is submitted if at 
any time the prospective lower tier participant learns that its 
certification was erroneous when submitted or had become erroneous by 
reason of changed circumstances.
    4. The terms covered transaction, debarred, suspended, ineligible, 
lower tier covered transaction, participant, person, primary covered 
transaction, principal, proposal, and voluntarily excluded, as used in 
this clause, have the meaning set out in the Definitions and Coverage 
sections of rules implementing Executive Order 12549. You may contact 
the person to which this proposal is submitted for assistance in 
obtaining a copy of those regulations.
    5. The prospective lower tier participant agrees by submitting this 
proposal that, should the proposed covered transaction be entered into, 
it shall not knowingly enter into any lower tier covered transaction 
with a person who is proposed for debarment under 48 CFR part 9, subpart 
9.4, debarred, suspended, declared ineligible, or voluntarily excluded 
from participation in this covered transaction, unless authorized by the 
department or agency with which this transaction originated.
    6. The prospective lower tier participant further agrees by 
submitting this proposal that it will include this clause titled 
``Certification Regarding Debarment, Suspension, Ineligibility and 
Voluntary Exclusion-Lower Tier Covered Transaction,'' without 
modification, in all lower tier covered transactions and in all 
solicitations for lower tier covered transactions.
    7. A participant in a covered transaction may rely upon a 
certification of a prospective participant in a lower tier covered 
transaction that it is not proposed for debarment under 48 CFR part 9, 
subpart 9.4, debarred, suspended, ineligible, or voluntarily excluded 
from covered transactions,

[[Page 320]]

unless it knows that the certification is erroneous. A participant may 
decide the method and frequency by which it determines the eligibility 
of its principals. Each participant may, but is not required to, check 
the List of Parties Excluded from Federal Procurement and Nonprocurement 
Programs.
    8. Nothing contained in the foregoing shall be construed to require 
establishment of a system of records in order to render in good faith 
the certification required by this clause. The knowledge and information 
of a participant is not required to exceed that which is normally 
possessed by a prudent person in the ordinary course of business 
dealings.
    9. Except for transactions authorized under paragraph 5 of these 
instructions, if a participant in a covered transaction knowingly enters 
into a lower tier covered transaction with a person who is proposed for 
debarment under 48 CFR part 9, subpart 9.4, suspended, debarred, 
ineligible, or voluntarily excluded from participation in this 
transaction, in addition to other remedies available to the Federal 
Government, the department or agency with which this transaction 
originated may pursue available remedies, including suspension and/or 
debarment.

    Certification Regarding Debarment, Suspension, Ineligibility an 
          Voluntary Exclusion--Lower Tier Covered Transactions

    (1) The prospective lower tier participant certifies, by submission 
of this proposal, that neither it nor its principals is presently 
debarred, suspended, proposed for debarment, declared ineligible, or 
voluntarily excluded from participation in this transaction by any 
Federal department or agency.
    (2) Where the prospective lower tier participant is unable to 
certify to any of the statements in this certification, such prospective 
participant shall attach an explanation to this proposal.

[60 FR 33042, 33045, June 26, 1995]

  Appendix C to Part 1404--Certification Regarding Drug-Free Workplace 
                              Requirements

                     Instructions for Certification

    1. By signing and/or submitting this application or grant agreement, 
the grantee is providing the certification set out below.
    2. The certification set out below is a material representation of 
fact upon which reliance is placed when the agency awards the grant. If 
it is later determined that the grantee knowingly rendered a false 
certification, or otherwise violates the requirements of the Drug-Free 
Workplace Act, the agency, in addition to any other remedies available 
to the Federal Government, may take action authorized under the Drug-
Free Workplace Act.
    3. For grantees other than individuals, Alternate I applies.
    4. For grantees who are individuals, Alternate II applies.
    5. Workplaces under grants, for grantees other than individuals, 
need not be identified on the certification. If known, they may be 
identified in the grant application. If the grantee does not identify 
the workplaces at the time of application, or upon award, if there is no 
application, the grantee must keep the identity of the workplace(s) on 
file in its office and make the information available for Federal 
inspection. Failure to identify all known workplaces constitutes a 
violation of the grantee's drug-free workplace requirements.
    6. Workplace identifications must include the actual address of 
buildings (or parts of buildings) or other sites where work under the 
grant takes place. Categorical descriptions may be used (e.g., all 
vehicles of a mass transit authority or State highway department while 
in operation, State employees in each local unemployment office, 
performers in concert halls or radio studios).
    7. If the workplace identified to the agency changes during the 
performance of the grant, the grantee shall inform the agency of the 
change(s), if it previously identified the workplaces in question (see 
paragraph five).
    8. Definitions of terms in the Nonprocurement Suspension and 
Debarment common rule and Drug-Free Workplace common rule apply to this 
certification. Grantees' attention is called, in particular, to the 
following definitions from these rules:
    Controlled substance means a controlled substance in Schedules I 
through V of the Controlled Substances Act (21 U.S.C. 812) and as 
further defined by regulation (21 CFR 1308.11 through 1308.15);
    Conviction means a finding of guilt (including a plea of nolo 
contendere) or imposition of sentence, or both, by any judicial body 
charged with the responsibility to determine violations of the Federal 
or State criminal drug statutes;
    Criminal drug statute means a Federal or non-Federal criminal 
statute involving the manufacture, distribution, dispensing, use, or 
possession of any controlled substance;
    Employee means the employee of a grantee directly engaged in the 
performance of work under a grant, including: (i) All ``direct charge'' 
employees; (ii) all ``indirect charge'' employees unless their impact or 
involvement is insignificant to the performance of the grant; and, (iii) 
temporary personnel and consultants who are directly engaged in the 
performance of work under the grant and who are on the grantee's 
payroll. This definition does not include workers not on the payroll of 
the grantee (e.g., volunteers,

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even if used to meet a matching requirement; consultants or independent 
contractors not on the grantee's payroll; or employees of subrecipients 
or subcontractors in covered workplaces).

        Certification Regarding Drug-Free Workplace Requirements

Alternate I. (Grantees Other Than Individuals)
    A. The grantee certifies that it will or will continue to provide a 
drug-free workplace by:
    (a) Publishing a statement notifying employees that the unlawful 
manufacture, distribution, dispensing, possession, or use of a 
controlled substance is prohibited in the grantee's workplace and 
specifying the actions that will be taken against employees for 
violation of such prohibition;
    (b) Establishing an ongoing drug-free awareness program to inform 
employees about--
    (1) The dangers of drug abuse in the workplace;
    (2) The grantee's policy of maintaining a drug-free workplace;
    (3) Any available drug counseling, rehabilitation, and employee 
assistance programs; and
    (4) The penalties that may be imposed upon employees for drug abuse 
violations occurring in the workplace;
    (c) Making it a requirement that each employee to be engaged in the 
performance of the grant be given a copy of the statement required by 
paragraph (a);
    (d) Notifying the employee in the statement required by paragraph 
(a) that, as a condition of employment under the grant, the employee 
will--
    (1) Abide by the terms of the statement; and
    (2) Notify the employer in writing of his or her conviction for a 
violation of a criminal drug statute occurring in the workplace no later 
than five calendar days after such conviction;
    (e) Notifying the agency in writing, within ten calendar days after 
receiving notice under subparagraph (d)(2) from an employee or otherwise 
receiving actual notice of such conviction. Employers of convicted 
employees must provide notice, including position title, to every grant 
officer or other designee on whose grant activity the convicted employee 
was working, unless the Federal agency has designated a central point 
for the receipt of such notices. Notice shall include the identification 
number(s) of each affected grant;
    (f) Taking one of the following actions, within 30 calendar days of 
receiving notice under subparagraph (d)(2), with respect to any employee 
who is so convicted--
    (1) Taking appropriate personnel action against such an employee, up 
to and including termination, consistent with the requirements of the 
Rehabilitation Act of 1973, as amended; or
    (2) Requiring such employee to participate satisfactorily in a drug 
abuse assistance or rehabilitation program approved for such purposes by 
a Federal, State, or local health, law enforcement, or other appropriate 
agency;
    (g) Making a good faith effort to continue to maintain a drug-free 
workplace through implementation of paragraphs (a), (b), (c), (d), (e) 
and (f).
    B. The grantee may insert in the space provided below the site(s) 
for the performance of work done in connection with the specific grant:
Place of Performance (Street address, city, county, state, zip code)
_______________________________________________________________________
_______________________________________________________________________
_______________________________________________________________________
Check {time}  if there are workplaces on file that are not identified 
here.
Alternate II. (Grantees Who Are Individuals)
    (a) The grantee certifies that, as a condition of the grant, he or 
she will not engage in the unlawful manufacture, distribution, 
dispensing, possession, or use of a controlled substance in conducting 
any activity with the grant;
    (b) If convicted of a criminal drug offense resulting from a 
violation occurring during the conduct of any grant activity, he or she 
will report the conviction, in writing, within 10 calendar days of the 
conviction, to every grant officer or other designee, unless the Federal 
agency designates a central point for the receipt of such notices. When 
notice is made to such a central point, it shall include the 
identification number(s) of each affected grant.



PARTS 1405--1499  [RESERVED]--Table of Contents




[[Page 323]]



                              FINDING AIDS




  --------------------------------------------------------------------

  A list of CFR titles, subtitles, chapters, subchapters and parts and 
an alphabetical list of agencies publishing in the CFR are included in 
the CFR Index and Finding Aids volume to the Code of Federal Regulations 
which is published separately and revised annually.

  Table of CFR Titles and Chapters
  Alphabetical List of Agencies Appearing in the CFR
  List of CFR Sections Affected


                                                                    Chap.

[[Page 325]]



                    Table of CFR Titles and Chapters



                     (Revised as of March 29, 1996)

                      Title 1--General Provisions

         I  Administrative Committee of the Federal Register 
                (Parts 1--49)
        II  Office of the Federal Register (Parts 50--299)
        IV  Miscellaneous Agencies (Parts 400--500)

                          Title 2--[Reserved]

                        Title 3--The President

         I  Executive Office of the President (Parts 100--199)

                           Title 4--Accounts

         I  General Accounting Office (Parts 1--99)
        II  Federal Claims Collection Standards (General 
                Accounting Office--Department of Justice) (Parts 
                100--299)

                   Title 5--Administrative Personnel

         I  Office of Personnel Management (Parts 1--1199)
        II  Merit Systems Protection Board (Parts 1200--1299)
       III  Office of Management and Budget (Parts 1300--1399)
        IV  Advisory Committee on Federal Pay (Parts 1400--1499)
         V  The International Organizations Employees Loyalty 
                Board (Parts 1500--1599)
        VI  Federal Retirement Thrift Investment Board (Parts 
                1600--1699)
       VII  Advisory Commission on Intergovernmental Relations 
                (Parts 1700--1799)
      VIII  Office of Special Counsel (Parts 1800--1899)
        IX  Appalachian Regional Commission (Parts 1900--1999)
        XI  Armed Forces Retirement Home (Part 2100)
       XIV  Federal Labor Relations Authority, General Counsel of 
                the Federal Labor Relations Authority and Federal 
                Service Impasses Panel (Parts 2400--2499)
        XV  Office of Administration, Executive Office of the 
                President (Parts 2500--2599)
       XVI  Office of Government Ethics (Parts 2600--2699)
       XXI  Department of the Treasury (Parts 3100--3199)
      XXII  Federal Deposit Insurance Corporation (Part 3202)
      XXVI  Department of Defense (Part 3601)

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       XXX  Farm Credit System Insurance Corporation (Parts 4000--
                4099)
      XXXI  Farm Credit Administration (Parts 4100--4199)
    XXXIII  Overseas Private Investment Corporation (Part 4301)
        XL  Interstate Commerce Commission (Part 5001)
       XLI  Commodity Futures Trading Commission (Part 5101)
      XLVI  Postal Rate Commission (Part 5601)
     XLVII  Federal Trade Commission (Part 5701)
    XLVIII  Nuclear Regulatory Commission (Part 5801)
       LII  Export-Import Bank of the United States (Part 6201)
      LIII  Department of Education (Parts 6300--6399)
       LIX  National Aeronautics and Space Administration (Part 
                6901)
        LX  United States Postal Service (Part 7001)
      LXII  Equal Employment Opportunity Commission (Part 7201)
     LXIII  Inter-American Foundation (Part 7301)
     LXXVI  Federal Retirement Thrift Investment Board (Part 8601)
    LXXVII  Office of Management and Budget (Part 8701)

                          Title 6--[Reserved]

                         Title 7--Agriculture

            Subtitle A--Office of the Secretary of Agriculture 
                (Parts 0--26)
            Subtitle B--Regulations of the Department of 
                Agriculture
         I  Agricultural Marketing Service (Standards, 
                Inspections, Marketing Practices), Department of 
                Agriculture (Parts 27--209)
        II  Food and Consumer Service, Department of Agriculture 
                (Parts 210--299)
       III  Animal and Plant Health Inspection Service, Department 
                of Agriculture (Parts 300--399)
        IV  Federal Crop Insurance Corporation, Department of 
                Agriculture (Parts 400--499)
         V  Agricultural Research Service, Department of 
                Agriculture (Parts 500--599)
        VI  Natural Resources Conservation Service, Department of 
                Agriculture (Parts 600--699)
       VII  Farm Service Agency, Department of Agriculture (Parts 
                700--799)
      VIII  Grain Inspection, Packers and Stockyards 
                Administration (Federal Grain Inspection Service), 
                Department of Agriculture (Parts 800--899)
        IX  Agricultural Marketing Service (Marketing Agreements 
                and Orders; Fruits, Vegetables, Nuts), Department 
                of Agriculture (Parts 900--999)
         X  Agricultural Marketing Service (Marketing Agreements 
                and Orders; Milk), Department of Agriculture 
                (Parts 1000--1199)

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        XI  Agricultural Marketing Service (Marketing Agreements 
                and Orders; Miscellaneous Commodities), Department 
                of Agriculture (Parts 1200--1299)
       XIV  Commodity Credit Corporation, Department of 
                Agriculture (Parts 1400--1499)
        XV  Foreign Agricultural Service, Department of 
                Agriculture (Parts 1500--1599)
       XVI  Rural Telephone Bank, Department of Agriculture (Parts 
                1600--1699)
      XVII  Rural Utilities Service, Department of Agriculture 
                (Parts 1700--1799)
     XVIII  Rural Housing Service, Rural Business-Cooperative 
                Service, Rural Utilities Service, and Farm Service 
                Agency, Department of Agriculture (Parts 1800--
                2099)
       XXI  Foreign Economic Development Service, Department of 
                Agriculture (Parts 2100--2199)
      XXII  Office of International Cooperation and Development, 
                Department of Agriculture (Parts 2200--2299)
       XXV  Office of the General Sales Manager, Department of 
                Agriculture (Parts 2500--2599)
      XXVI  Office of Inspector General, Department of Agriculture 
                (Parts 2600--2699)
     XXVII  Office of Information Resources Management, Department 
                of Agriculture (Parts 2700--2799)
    XXVIII  Office of Operations, Department of Agriculture (Parts 
                2800--2899)
      XXIX  Office of Energy, Department of Agriculture (Parts 
                2900--2999)
       XXX  Office of Finance and Management, Department of 
                Agriculture (Parts 3000--3099)
      XXXI  Office of Environmental Quality, Department of 
                Agriculture (Parts 3100--3199)
     XXXII  [Reserved]
    XXXIII  Office of Transportation, Department of Agriculture 
                (Parts 3300--3399)
     XXXIV  Cooperative State Research, Education, and Extension 
                Service, Department of Agriculture (Parts 3400--
                3499)
     XXXVI  National Agricultural Statistics Service, Department 
                of Agriculture (Parts 3600--3699)
    XXXVII  Economic Research Service, Department of Agriculture 
                (Parts 3700--3799)
   XXXVIII  World Agricultural Outlook Board, Department of 
                Agriculture (Parts 3800--3899)
     XXXIX  Economic Analysis Staff, Department of Agriculture 
                (Parts 3900--3999)
        XL  Economics Management Staff, Department of Agriculture 
                (Parts 4000--4099)
       XLI  [Reserved]
      XLII  Rural Business-Cooperative Service and Rural Utilities 
                Service, Department of Agriculture (Parts 4200--
                4299)

[[Page 328]]

                    Title 8--Aliens and Nationality

         I  Immigration and Naturalization Service, Department of 
                Justice (Parts 1--499)

                 Title 9--Animals and Animal Products

         I  Animal and Plant Health Inspection Service, Department 
                of Agriculture (Parts 1--199)
        II  Grain Inspection, Packers and Stockyards 
                Administration (Packers and Stockyards Programs), 
                Department of Agriculture (Parts 200--299)
       III  Food Safety and Inspection Service, Meat and Poultry 
                Inspection, Department of Agriculture (Parts 300--
                399)

                           Title 10--Energy

         I  Nuclear Regulatory Commission (Parts 0--199)
        II  Department of Energy (Parts 200--699)
       III  Department of Energy (Parts 700--999)
         X  Department of Energy (General Provisions) (Parts 
                1000--1099)
        XI  United States Enrichment Corporation (Parts 1100--
                1199)
        XV  Office of the Federal Inspector for the Alaska Natural 
                Gas Transportation System (Parts 1500--1599)
      XVII  Defense Nuclear Facilities Safety Board (Parts 1700--
                1799)

                      Title 11--Federal Elections

         I  Federal Election Commission (Parts 1--9099)

                      Title 12--Banks and Banking

         I  Comptroller of the Currency, Department of the 
                Treasury (Parts 1--199)
        II  Federal Reserve System (Parts 200--299)
       III  Federal Deposit Insurance Corporation (Parts 300--399)
        IV  Export-Import Bank of the United States (Parts 400--
                499)
         V  Office of Thrift Supervision, Department of the 
                Treasury (Parts 500--599)
        VI  Farm Credit Administration (Parts 600--699)
       VII  National Credit Union Administration (Parts 700--799)
      VIII  Federal Financing Bank (Parts 800--899)
        IX  Federal Housing Finance Board (Parts 900--999)
        XI  Federal Financial Institutions Examination Council 
                (Parts 1100--1199)
       XIV  Farm Credit System Insurance Corporation (Parts 1400--
                1499)
        XV  Thrift Depositor Protection Oversight Board (Parts 
                1500--1599)
      XVII  Office of Federal Housing Enterprise Oversight, 
                Department of Housing and Urban Development (Parts 
                1700-1799)
     XVIII  Community Development Financial Institutions Fund, 
                Department of the Treasury (Parts 1800--1899)

[[Page 329]]

               Title 13--Business Credit and Assistance

         I  Small Business Administration (Parts 1--199)
       III  Economic Development Administration, Department of 
                Commerce (Parts 300--399)

                    Title 14--Aeronautics and Space

         I  Federal Aviation Administration, Department of 
                Transportation (Parts 1--199)
        II  Office of the Secretary, Department of Transportation 
                (Aviation Proceedings) (Parts 200--399)
       III  Office of Commercial Space Transportation, Department 
                of Transportation (Parts 400--499)
         V  National Aeronautics and Space Administration (Parts 
                1200--1299)

                 Title 15--Commerce and Foreign Trade

            Subtitle A--Office of the Secretary of Commerce (Parts 
                0--29)
            Subtitle B--Regulations Relating to Commerce and 
                Foreign Trade
         I  Bureau of the Census, Department of Commerce (Parts 
                30--199)
        II  National Institute of Standards and Technology, 
                Department of Commerce (Parts 200--299)
       III  International Trade Administration, Department of 
                Commerce (Parts 300--399)
        IV  Foreign-Trade Zones Board, Department of Commerce 
                (Parts 400--499)
       VII  Bureau of Export Administration, Department of 
                Commerce (Parts 700--799)
      VIII  Bureau of Economic Analysis, Department of Commerce 
                (Parts 800--899)
        IX  National Oceanic and Atmospheric Administration, 
                Department of Commerce (Parts 900--999)
        XI  Technology Administration, Department of Commerce 
                (Parts 1100--1199)
       XII  United States Travel and Tourism Administration, 
                Department of Commerce (Parts 1200--1299)
      XIII  East-West Foreign Trade Board (Parts 1300--1399)
       XIV  Minority Business Development Agency (Parts 1400--
                1499)
            Subtitle C--Regulations Relating to Foreign Trade 
                Agreements
        XX  Office of the United States Trade Representative 
                (Parts 2000--2099)
            Subtitle D--Regulations Relating to Telecommunications 
                and Information
     XXIII  National Telecommunications and Information 
                Administration, Department of Commerce (Parts 
                2300--2399)

[[Page 330]]

                    Title 16--Commercial Practices

         I  Federal Trade Commission (Parts 0--999)
        II  Consumer Product Safety Commission (Parts 1000--1799)

             Title 17--Commodity and Securities Exchanges

         I  Commodity Futures Trading Commission (Parts 1--199)
        II  Securities and Exchange Commission (Parts 200--399)
        IV  Department of the Treasury (Parts 400--499)

          Title 18--Conservation of Power and Water Resources

         I  Federal Energy Regulatory Commission, Department of 
                Energy (Parts 1--399)
       III  Delaware River Basin Commission (Parts 400--499)
        VI  Water Resources Council (Parts 700--799)
      VIII  Susquehanna River Basin Commission (Parts 800--899)
      XIII  Tennessee Valley Authority (Parts 1300--1399)

                       Title 19--Customs Duties

         I  United States Customs Service, Department of the 
                Treasury (Parts 1--199)
        II  United States International Trade Commission (Parts 
                200--299)
       III  International Trade Administration, Department of 
                Commerce (Parts 300--399)

                     Title 20--Employees' Benefits

         I  Office of Workers' Compensation Programs, Department 
                of Labor (Parts 1--199)
        II  Railroad Retirement Board (Parts 200--399)
       III  Social Security Administration (Parts 400--499)
        IV  Employees' Compensation Appeals Board, Department of 
                Labor (Parts 500--599)
         V  Employment and Training Administration, Department of 
                Labor (Parts 600--699)
        VI  Employment Standards Administration, Department of 
                Labor (Parts 700--799)
       VII  Benefits Review Board, Department of Labor (Parts 
                800--899)
      VIII  Joint Board for the Enrollment of Actuaries (Parts 
                900--999)
        IX  Office of the Assistant Secretary for Veterans' 
                Employment and Training, Department of Labor 
                (Parts 1000--1099)

                       Title 21--Food and Drugs

         I  Food and Drug Administration, Department of Health and 
                Human Services (Parts 1--1299)
        II  Drug Enforcement Administration, Department of Justice 
                (Parts 1300--1399)
       III  Office of National Drug Control Policy (Parts 1400--
                1499)

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                      Title 22--Foreign Relations

         I  Department of State (Parts 1--199)
        II  Agency for International Development, International 
                Development Cooperation Agency (Parts 200--299)
       III  Peace Corps (Parts 300--399)
        IV  International Joint Commission, United States and 
                Canada (Parts 400--499)
         V  United States Information Agency (Parts 500--599)
        VI  United States Arms Control and Disarmament Agency 
                (Parts 600--699)
       VII  Overseas Private Investment Corporation, International 
                Development Cooperation Agency (Parts 700--799)
        IX  Foreign Service Grievance Board Regulations (Parts 
                900--999)
         X  Inter-American Foundation (Parts 1000--1099)
        XI  International Boundary and Water Commission, United 
                States and Mexico, United States Section (Parts 
                1100--1199)
       XII  United States International Development Cooperation 
                Agency (Parts 1200--1299)
      XIII  Board for International Broadcasting (Parts 1300--
                1399)
       XIV  Foreign Service Labor Relations Board; Federal Labor 
                Relations Authority; General Counsel of the 
                Federal Labor Relations Authority; and the Foreign 
                Service Impasse Disputes Panel (Parts 1400--1499)
        XV  African Development Foundation (Parts 1500--1599)
       XVI  Japan-United States Friendship Commission (Parts 
                1600--1699)
      XVII  United States Institute of Peace (Parts 1700--1799)

                          Title 23--Highways

         I  Federal Highway Administration, Department of 
                Transportation (Parts 1--999)
        II  National Highway Traffic Safety Administration and 
                Federal Highway Administration, Department of 
                Transportation (Parts 1200--1299)
       III  National Highway Traffic Safety Administration, 
                Department of Transportation (Parts 1300--1399)

                Title 24--Housing and Urban Development

            Subtitle A--Office of the Secretary, Department of 
                Housing and Urban Development (Parts 0--99)
            Subtitle B--Regulations Relating to Housing and Urban 
                Development
         I  Office of Assistant Secretary for Equal Opportunity, 
                Department of Housing and Urban Development (Parts 
                100--199)
        II  Office of Assistant Secretary for Housing-Federal 
                Housing Commissioner, Department of Housing and 
                Urban Development (Parts 200--299)
       III  Government National Mortgage Association, Department 
                of Housing and Urban Development (Parts 300--399)

[[Page 332]]

         V  Office of Assistant Secretary for Community Planning 
                and Development, Department of Housing and Urban 
                Development (Parts 500--599)
        VI  Office of Assistant Secretary for Community Planning 
                and Development, Department of Housing and Urban 
                Development (Parts 600--699) [Reserved]
       VII  Office of the Secretary, Department of Housing and 
                Urban Development (Housing Assistance Programs and 
                Public and Indian Housing Programs) (Parts 700--
                799)
      VIII  Office of the Assistant Secretary for Housing--Federal 
                Housing Commissioner, Department of Housing and 
                Urban Development (Section 8 Housing Assistance 
                Programs and Section 202 Direct Loan Program) 
                (Parts 800--899)
        IX  Office of Assistant Secretary for Public and Indian 
                Housing, Department of Housing and Urban 
                Development (Parts 900--999)
         X  Office of Assistant Secretary for Housing--Federal 
                Housing Commissioner, Department of Housing and 
                Urban Development (Interstate Land Sales 
                Registration Program) (Parts 1700--1799)
       XII  Office of Inspector General, Department of Housing and 
                Urban Development (Parts 2000--2099)
        XX  Office of Assistant Secretary for Housing--Federal 
                Housing Commissioner, Department of Housing and 
                Urban Development (Parts 3200--3699)
       XXV  Neighborhood Reinvestment Corporation (Parts 4100--
                4199)

                           Title 25--Indians

         I  Bureau of Indian Affairs, Department of the Interior 
                (Parts 1--299)
        II  Indian Arts and Crafts Board, Department of the 
                Interior (Parts 300--399)
       III  National Indian Gaming Commission, Department of the 
                Interior (Parts 500--599)
        IV  Office of Navajo and Hopi Indian Relocation (Parts 
                700--799)
        VI  Office of the Assistant Secretary-Indian Affairs, 
                Department of the Interior (Part 1001)

                      Title 26--Internal Revenue

         I  Internal Revenue Service, Department of the Treasury 
                (Parts 1--799)

           Title 27--Alcohol, Tobacco Products and Firearms

         I  Bureau of Alcohol, Tobacco and Firearms, Department of 
                the Treasury (Parts 1--299)

                   Title 28--Judicial Administration

         I  Department of Justice (Parts 0--199)

[[Page 333]]

       III  Federal Prison Industries, Inc., Department of Justice 
                (Parts 300--399)
         V  Bureau of Prisons, Department of Justice (Parts 500--
                599)
        VI  Offices of Independent Counsel, Department of Justice 
                (Parts 600--699)
       VII  Office of Independent Counsel (Parts 700--799)

                            Title 29--Labor

            Subtitle A--Office of the Secretary of Labor (Parts 
                0--99)
            Subtitle B--Regulations Relating to Labor
         I  National Labor Relations Board (Parts 100--199)
        II  Office of Labor-Management Programs, Department of 
                Labor (Parts 200--299)
       III  National Railroad Adjustment Board (Parts 300--399)
        IV  Office of Labor-Management Standards, Department of 
                Labor (Parts 400--499)
         V  Wage and Hour Division, Department of Labor (Parts 
                500--899)
        IX  Construction Industry Collective Bargaining Commission 
                (Parts 900--999)
         X  National Mediation Board (Parts 1200--1299)
       XII  Federal Mediation and Conciliation Service (Parts 
                1400--1499)
       XIV  Equal Employment Opportunity Commission (Parts 1600--
                1699)
      XVII  Occupational Safety and Health Administration, 
                Department of Labor (Parts 1900--1999)
        XX  Occupational Safety and Health Review Commission 
                (Parts 2200--2499)
       XXV  Pension and Welfare Benefits Administration, 
                Department of Labor (Parts 2500--2599)
      XXVI  Pension Benefit Guaranty Corporation (Parts 2600--
                2699)
     XXVII  Federal Mine Safety and Health Review Commission 
                (Parts 2700--2799)

                      Title 30--Mineral Resources

         I  Mine Safety and Health Administration, Department of 
                Labor (Parts 1--199)
        II  Minerals Management Service, Department of the 
                Interior (Parts 200--299)
       III  Board of Surface Mining and Reclamation Appeals, 
                Department of the Interior (Parts 300--399)
        IV  Geological Survey, Department of the Interior (Parts 
                400--499)
        VI  Bureau of Mines, Department of the Interior (Parts 
                600--699)
       VII  Office of Surface Mining Reclamation and Enforcement, 
                Department of the Interior (Parts 700--999)

[[Page 334]]

                 Title 31--Money and Finance: Treasury

            Subtitle A--Office of the Secretary of the Treasury 
                (Parts 0--50)
            Subtitle B--Regulations Relating to Money and Finance
         I  Monetary Offices, Department of the Treasury (Parts 
                51--199)
        II  Fiscal Service, Department of the Treasury (Parts 
                200--399)
        IV  Secret Service, Department of the Treasury (Parts 
                400--499)
         V  Office of Foreign Assets Control, Department of the 
                Treasury (Parts 500--599)
        VI  Bureau of Engraving and Printing, Department of the 
                Treasury (Parts 600--699)
       VII  Federal Law Enforcement Training Center, Department of 
                the Treasury (Parts 700--799)
      VIII  Office of International Investment, Department of the 
                Treasury (Parts 800--899)

                      Title 32--National Defense

            Subtitle A--Department of Defense
         I  Office of the Secretary of Defense (Parts 1--399)
         V  Department of the Army (Parts 400--699)
        VI  Department of the Navy (Parts 700--799)
       VII  Department of the Air Force (Parts 800--1099)
            Subtitle B--Other Regulations Relating to National 
                Defense
       XII  Defense Logistics Agency (Parts 1200--1299)
       XVI  Selective Service System (Parts 1600--1699)
       XIX  Central Intelligence Agency (Parts 1900--1999)
        XX  Information Security Oversight Office, National 
                Archives and Records Administration (Parts 2000--
                2099)
       XXI  National Security Council (Parts 2100--2199)
      XXIV  Office of Science and Technology Policy (Parts 2400--
                2499)
     XXVII  Office for Micronesian Status Negotiations (Parts 
                2700--2799)
    XXVIII  Office of the Vice President of the United States 
                (Parts 2800--2899)
      XXIX  Presidential Commission on the Assignment of Women in 
                the Armed Forces (Part 2900)

               Title 33--Navigation and Navigable Waters

         I  Coast Guard, Department of Transportation (Parts 1--
                199)
        II  Corps of Engineers, Department of the Army (Parts 
                200--399)
        IV  Saint Lawrence Seaway Development Corporation, 
                Department of Transportation (Parts 400--499)

                          Title 34--Education

            Subtitle A--Office of the Secretary, Department of 
                Education (Parts 1--99)

[[Page 335]]

            Subtitle B--Regulations of the Offices of the 
                Department of Education
         I  Office for Civil Rights, Department of Education 
                (Parts 100--199)
        II  Office of Elementary and Secondary Education, 
                Department of Education (Parts 200--299)
       III  Office of Special Education and Rehabilitative 
                Services, Department of Education (Parts 300--399)
        IV  Office of Vocational and Adult Education, Department 
                of Education (Parts 400--499)
         V  Office of Bilingual Education and Minority Languages 
                Affairs, Department of Education (Parts 500--599)
        VI  Office of Postsecondary Education, Department of 
                Education (Parts 600--699)
       VII  Office of Educational Research and Improvement, 
                Department of Education (Parts 700--799)
        XI  National Institute for Literacy (Parts 1100-1199)
            Subtitle C--Regulations Relating to Education
       XII  National Council on Disability (Parts 1200--1299)

                        Title 35--Panama Canal

         I  Panama Canal Regulations (Parts 1--299)

             Title 36--Parks, Forests, and Public Property

         I  National Park Service, Department of the Interior 
                (Parts 1--199)
        II  Forest Service, Department of Agriculture (Parts 200--
                299)
       III  Corps of Engineers, Department of the Army (Parts 
                300--399)
        IV  American Battle Monuments Commission (Parts 400--499)
         V  Smithsonian Institution (Parts 500--599)
       VII  Library of Congress (Parts 700--799)
      VIII  Advisory Council on Historic Preservation (Parts 800--
                899)
        IX  Pennsylvania Avenue Development Corporation (Parts 
                900--999)
        XI  Architectural and Transportation Barriers Compliance 
                Board (Parts 1100--1199)
       XII  National Archives and Records Administration (Parts 
                1200--1299)
       XIV  Assassination Records Review Board (Parts 1400-1499)

             Title 37--Patents, Trademarks, and Copyrights

         I  Patent and Trademark Office, Department of Commerce 
                (Parts 1--199)
        II  Copyright Office, Library of Congress (Parts 200--299)
        IV  Assistant Secretary for Technology Policy, Department 
                of Commerce (Parts 400--499)
         V  Under Secretary for Technology, Department of Commerce 
                (Parts 500--599)

[[Page 336]]

           Title 38--Pensions, Bonuses, and Veterans' Relief

         I  Department of Veterans Affairs (Parts 0--99)

                       Title 39--Postal Service

         I  United States Postal Service (Parts 1--999)
       III  Postal Rate Commission (Parts 3000--3099)

                  Title 40--Protection of Environment

         I  Environmental Protection Agency (Parts 1--799)
         V  Council on Environmental Quality (Parts 1500--1599)

          Title 41--Public Contracts and Property Management

            Subtitle B--Other Provisions Relating to Public 
                Contracts
        50  Public Contracts, Department of Labor (Parts 50-1--50-
                999)
        51  Committee for Purchase From People Who Are Blind or 
                Severely Disabled (Parts 51-1--51-99)
        60  Office of Federal Contract Compliance Programs, Equal 
                Employment Opportunity, Department of Labor (Parts 
                60-1--60-999)
        61  Office of the Assistant Secretary for Veterans 
                Employment and Training, Department of Labor 
                (Parts 61-1--61-999)
            Subtitle C--Federal Property Management Regulations 
                System
       101  Federal Property Management Regulations (Parts 101-1--
                101-99)
       105  General Services Administration (Parts 105-1--105-999)
       109  Department of Energy Property Management Regulations 
                (Parts 109-1--109-99)
       114  Department of the Interior (Parts 114-1--114-99)
       115  Environmental Protection Agency (Parts 115-1--115-99)
       128  Department of Justice (Parts 128-1--128-99)
            Subtitle D--Other Provisions Relating to Property 
                Management [Reserved]
            Subtitle E--Federal Information Resources Management 
                Regulations System
       201  Federal Information Resources Management Regulation 
                (Parts 201-1--201-99)
            Subtitle F--Federal Travel Regulation System
       301  Travel Allowances (Parts 301-1--301-99)
       302  Relocation Allowances (Parts 302-1--302-99)
       303  Payment of Expenses Connected with the Death of 
                Certain Employees (Parts 303-1--303-2)
       304  Payment from a Non-Federal Source for Travel Expenses 
                (Parts 304-1--304-99)

                        Title 42--Public Health

         I  Public Health Service, Department of Health and Human 
                Services (Parts 1--199)

[[Page 337]]

        IV  Health Care Financing Administration, Department of 
                Health and Human Services (Parts 400--499)
         V  Office of Inspector General-Health Care, Department of 
                Health and Human Services (Parts 1000--1999)

                   Title 43--Public Lands: Interior

            Subtitle A--Office of the Secretary of the Interior 
                (Parts 1--199)
            Subtitle B--Regulations Relating to Public Lands
         I  Bureau of Reclamation, Department of the Interior 
                (Parts 200--499)
        II  Bureau of Land Management, Department of the Interior 
                (Parts 1000--9999)
       III  Utah Reclamation Mitigation and Conservation 
                Commission (Parts 10000--10005)

             Title 44--Emergency Management and Assistance

         I  Federal Emergency Management Agency (Parts 0--399)
        IV  Department of Commerce and Department of 
                Transportation (Parts 400--499)

                       Title 45--Public Welfare

            Subtitle A--Department of Health and Human Services, 
                General Administration (Parts 1--199)
            Subtitle B--Regulations Relating to Public Welfare
        II  Office of Family Assistance (Assistance Programs), 
                Administration for Children and Families, 
                Department of Health and Human Services (Parts 
                200--299)
       III  Office of Child Support Enforcement (Child Support 
                Enforcement Program), Administration for Children 
                and Families, Department of Health and Human 
                Services (Parts 300--399)
        IV  Office of Refugee Resettlement, Administration for 
                Children and Families Department of Health and 
                Human Services (Parts 400--499)
         V  Foreign Claims Settlement Commission of the United 
                States, Department of Justice (Parts 500--599)
        VI  National Science Foundation (Parts 600--699)
       VII  Commission on Civil Rights (Parts 700--799)
      VIII  Office of Personnel Management (Parts 800--899)
         X  Office of Community Services, Administration for 
                Children and Families, Department of Health and 
                Human Services (Parts 1000--1099)
        XI  National Foundation on the Arts and the Humanities 
                (Parts 1100--1199)
       XII  ACTION (Parts 1200--1299)

[[Page 338]]

      XIII  Office of Human Development Services, Department of 
                Health and Human Services (Parts 1300--1399)
       XVI  Legal Services Corporation (Parts 1600--1699)
      XVII  National Commission on Libraries and Information 
                Science (Parts 1700--1799)
     XVIII  Harry S. Truman Scholarship Foundation (Parts 1800--
                1899)
       XXI  Commission on Fine Arts (Parts 2100--2199)
      XXII  Christopher Columbus Quincentenary Jubilee Commission 
                (Parts 2200--2299)
     XXIII  Arctic Research Commission (Part 2301)
      XXIV  James Madison Memorial Fellowship Foundation (Parts 
                2400--2499)
       XXV  Corporation for National and Community Service (Parts 
                2500--2599)

                          Title 46--Shipping

         I  Coast Guard, Department of Transportation (Parts 1--
                199)
        II  Maritime Administration, Department of Transportation 
                (Parts 200--399)
       III  Saint Lawrence Seaway Development Corporation (Great 
                Lakes Pilotage), Department of Transportation 
                (Parts 400--499)
        IV  Federal Maritime Commission (Parts 500--599)

                      Title 47--Telecommunication

         I  Federal Communications Commission (Parts 0--199)
        II  Office of Science and Technology Policy and National 
                Security Council (Parts 200--299)
       III  National Telecommunications and Information 
                Administration, Department of Commerce (Parts 
                300--399)

           Title 48--Federal Acquisition Regulations System

         1  Federal Acquisition Regulation (Parts 1--99)
         2  Department of Defense (Parts 200--299)
         3  Department of Health and Human Services (Parts 300--
                399)
         4  Department of Agriculture (Parts 400--499)
         5  General Services Administration (Parts 500--599)
         6  Department of State (Parts 600--699)
         7  Agency for International Development (Parts 700--799)
         8  Department of Veterans Affairs (Parts 800--899)
         9  Department of Energy (Parts 900--999)
        10  Department of the Treasury (Parts 1000--1099)
        12  Department of Transportation (Parts 1200--1299)
        13  Department of Commerce (Parts 1300--1399)
        14  Department of the Interior (Parts 1400--1499)

[[Page 339]]

        15  Environmental Protection Agency (Parts 1500--1599)
        16  Office of Personnel Management Federal Employees 
                Health Benefits Acquisition Regulation (Parts 
                1600--1699)
        17  Office of Personnel Management (Parts 1700--1799)
        18  National Aeronautics and Space Administration (Parts 
                1800--1899)
        19  United States Information Agency (Parts 1900--1999)
        20  Nuclear Regulatory Commission (Parts 2000--2099)
        21  Office of Personnel Management, Federal Employees 
                Group Life Insurance Federal Acquisition 
                Regulation (Parts 2100--2199)
        22  Small Business Administration (Parts 2200--2299)
        24  Department of Housing and Urban Development (Parts 
                2400--2499)
        25  National Science Foundation (Parts 2500--2599)
        28  Department of Justice (Parts 2800--2899)
        29  Department of Labor (Parts 2900--2999)
        34  Department of Education Acquisition Regulation (Parts 
                3400--3499)
        35  Panama Canal Commission (Parts 3500--3599)
        44  Federal Emergency Management Agency (Parts 4400--4499)
        51  Department of the Army Acquisition Regulations (Parts 
                5100--5199)
        52  Department of the Navy Acquisition Regulations (Parts 
                5200--5299)
        53  Department of the Air Force Federal Acquisition 
                Regulation Supplement (Parts 5300--5399)
        54  Defense Logistics Agency, Department of Defense (Part 
                5452)
        57  African Development Foundation (Parts 5700--5799)
        61  General Services Administration Board of Contract 
                Appeals (Parts 6100--6199)
        63  Department of Transportation Board of Contract Appeals 
                (Parts 6300--6399)
        99  Cost Accounting Standards Board, Office of Federal 
                Procurement Policy, Office of Management and 
                Budget (Parts 9900--9999)

                       Title 49--Transportation

            Subtitle A--Office of the Secretary of Transportation 
                (Parts 1--99)
            Subtitle B--Other Regulations Relating to 
                Transportation
         I  Research and Special Programs Administration, 
                Department of Transportation (Parts 100--199)
        II  Federal Railroad Administration, Department of 
                Transportation (Parts 200--299)
       III  Federal Highway Administration, Department of 
                Transportation (Parts 300--399)

[[Page 340]]

        IV  Coast Guard, Department of Transportation (Parts 400--
                499)
         V  National Highway Traffic Safety Administration, 
                Department of Transportation (Parts 500--599)
        VI  Federal Transit Administration, Department of 
                Transportation (Parts 600--699)
       VII  National Railroad Passenger Corporation (AMTRAK) 
                (Parts 700--799)
      VIII  National Transportation Safety Board (Parts 800--999)
         X  Surface Transportation Board, Department of 
                Transportation (Parts 1000--1399)

                   Title 50--Wildlife and Fisheries

         I  United States Fish and Wildlife Service, Department of 
                the Interior (Parts 1--199)
        II  National Marine Fisheries Service, National Oceanic 
                and Atmospheric Administration, Department of 
                Commerce (Parts 200--299)
       III  International Regulatory Agencies (Fishing and 
                Whaling) (Parts 300--399)
        IV  Joint Regulations (United States Fish and Wildlife 
                Service, Department of the Interior and National 
                Marine Fisheries Service, National Oceanic and 
                Atmospheric Administration, Department of 
                Commerce); Endangered Species Committee 
                Regulations (Parts 400--499)
         V  Marine Mammal Commission (Parts 500--599)
        VI  Fishery Conservation and Management, National Oceanic 
                and Atmospheric Administration, Department of 
                Commerce (Parts 600--699)

                      CFR Index and Finding Aids

            Subject/Agency Index
            List of Agency Prepared Indexes
            Parallel Tables of Statutory Authorities and Rules
            List of CFR Titles, Chapters, Subchapters, and Parts
            Alphabetical List of Agencies Appearing in the CFR



[[Page 341]]





           Alphabetical List of Agencies Appearing in the CFR



                     (Revised as of March 29, 1996)

                                                  CFR Title, Subtitle or
                     Agency                               Chapter

ACTION                                            45, XII
Administrative Committee of the Federal Register  1, I
Advanced Research Projects Agency                 32, I
Advisory Commission on Intergovernmental          5, VII
     Relations
Advisory Committee on Federal Pay                 5, IV
Advisory Council on Historic Preservation         36, VIII
African Development Foundation                    22, XV
  Federal Acquisition Regulation                  48, 57
Agency for International Development              22, II
  Federal Acquisition Regulation                  48, 7
Agricultural Marketing Service                    7, I, IX, X, XI
Agricultural Research Service                     7, V
Agriculture Department
  Agricultural Marketing Service                  7, I, IX, X, XI
  Agricultural Research Service                   7, V
  Animal and Plant Health Inspection Service      7, III; 9, I
  Commodity Credit Corporation                    7, XIV
  Cooperative State Research, Education, and      7, XXXIV
       Extension Service
  Economic Analysis Staff                         7, XXXIX
  Economic Research Service                       7, XXXVII
  Economics Management Staff                      7, XL
  Energy, Office of                               7, XXIX
  Environmental Quality, Office of                7, XXXI
  Farm Service Agency                             7, VII, XVIII
  Federal Acquisition Regulation                  48, 4
  Federal Crop Insurance Corporation              7, IV
  Finance and Management, Office of               7, XXX
  Food and Consumer Service                       7, II
  Food Safety and Inspection Service              9, III
  Foreign Agricultural Service                    7, XV
  Forest Service                                  36, II
  Grain Inspection, Packers and Stockyards        7, VIII; 9, II
       Administration
  Information Resources Management, Office of     7, XXVII
  Inspector General, Office of                    7, XXVI
  National Agricultural Library                   7, XLI
  National Agricultural Statistics Service        7, XXXVI
  Natural Resources Conservation Service          7, VI
  Operations, Office of                           7, XXVIII
  Rural Business-Cooperative Service              7, XVIII, XLII
  Rural Development Administration                7, XLII
  Rural Housing Service                           7, XVIII
  Rural Telephone Bank                            7, XVI
  Rural Utilities Service                         7, XVII, XVIII, XLII
  Secretary of Agriculture, Office of             7, Subtitle A
  Transportation, Office of                       7, XXXIII
  World Agricultural Outlook Board                7, XXXVIII
Air Force Department                              32, VII
  Federal Acquisition Regulation Supplement       48, 53
Alaska Natural Gas Transportation System, Office  10, XV
     of the Federal Inspector
Alcohol, Tobacco and Firearms, Bureau of          27, I
AMTRAK                                            49, VII

[[Page 342]]

American Battle Monuments Commission              36, IV
Animal and Plant Health Inspection Service        7, III; 9, I
Appalachian Regional Commission                   5, IX
Architectural and Transportation Barriers         36, XI
     Compliance Board
Arctic Research Commission                        45, XXIII
Arms Control and Disarmament Agency, United       22, VI
     States
Army Department                                   32, V
  Engineers, Corps of                             33, II; 36, III
  Federal Acquisition Regulation                  48, 51
Assassination Records Review Board                36, XIV
Benefits Review Board                             20, VII
Bilingual Education and Minority Languages        34, V
     Affairs, Office of
Blind or Severely Disabled, Committee for         41, 51
     Purchase From People Who Are
Board for International Broadcasting              22, XIII
Census Bureau                                     15, I
Central Intelligence Agency                       32, XIX
Child Support Enforcement, Office of              45, III
Children and Families, Administration for         45, II, III, IV, X
Christopher Columbus Quincentenary Jubilee        45, XXII
     Commission
Civil Rights, Commission on                       45, VII
Civil Rights, Office for                          34, I
Coast Guard                                       33, I; 46, I; 49, IV
Commerce Department                               44, IV
  Census Bureau                                   15, I`
  Economic Affairs, Under Secretary               37, V
  Economic Analysis, Bureau of                    15, VIII
  Economic Development Administration             13, III
  Emergency Management and Assistance             44, IV
  Export Administration, Bureau of                15, VII
  Federal Acquisition Regulation                  48, 13
  Fishery Conservation and Management             50, VI
  Foreign-Trade Zones Board                       15, IV
  International Trade Administration              15, III; 19, III
  National Institute of Standards and Technology  15, II
  National Marine Fisheries Service               50, II, IV
  National Oceanic and Atmospheric                15, IX; 50, II, III, IV, 
       Administration                             VI
  National Telecommunications and Information     15, XXIII; 47, III
       Administration
  National Weather Service                        15, IX
  Patent and Trademark Office                     37, I
  Productivity, Technology and Innovation,        37, IV
       Assistant Secretary for
  Secretary of Commerce, Office of                15, Subtitle A
  Technology, Under Secretary for                 37, V
  Technology Administration                       15, XI
  Technology Policy, Assistant Secretary for      37, IV
  Travel and Tourism Administration, United       15, XII
       States
Commercial Space Transportation, Office of        14, III
Commodity Credit Corporation                      7, XIV
Commodity Futures Trading Commission              5, XLI; 17, I
Community Planning and Development, Office of     24, V, VI
     Assistant Secretary for
Community Services, Office of                     45, X
Comptroller of the Currency                       12, I
Construction Industry Collective Bargaining       29, IX
     Commission
Consumer Product Safety Commission                16, II
Cooperative State Research, Education, and        7, XXXIV
     Extension Service
Copyright Office                                  37, II
Cost Accounting Standards Board                   48, 99
Council on Environmental Quality                  40, V
Customs Service, United States                    19, I
Defense Contract Audit Agency                     32, I
Defense Department                                5, XXVI; 32, Subtitle A
  Advanced Research Projects Agency               32, I
  Air Force Department                            32, VII

[[Page 343]]

  Army Department                                 32, V; 33, II; 36, III, 
                                                  48, 51
  Defense Intelligence Agency                     32, I
  Defense Logistics Agency                        32, I, XII; 48, 54
  Defense Mapping Agency                          32, I
  Engineers, Corps of                             33, II; 36, III
  Federal Acquisition Regulation                  48, 2
  Navy Department                                 32, VI; 48, 52
  Secretary of Defense, Office of                 32, I
Defense Contract Audit Agency                     32, I
Defense Intelligence Agency                       32, I
Defense Logistics Agency                          32, XII; 48, 54
Defense Mapping Agency                            32, I
Defense Nuclear Facilities Safety Board           10, XVII
Delaware River Basin Commission                   18, III
Drug Enforcement Administration                   21, II
East-West Foreign Trade Board                     15, XIII
Economic Affairs, Under Secretary                 37, V
Economic Analysis, Bureau of                      15, VIII
Economic Analysis Staff                           7, XXXIX
Economic Development Administration               13, III
Economics Management Staff                        7, XL
Economic Research Service                         7, XXXVII
Education, Department of                          5, LIII
  Bilingual Education and Minority Languages      34, V
       Affairs, Office of
  Civil Rights, Office for                        34, I
  Educational Research and Improvement, Office    34, VII
       of
  Elementary and Secondary Education, Office of   34, II
  Federal Acquisition Regulation                  48, 34
  Postsecondary Education, Office of              34, VI
  Secretary of Education, Office of               34, Subtitle A
  Special Education and Rehabilitative Services,  34, III
       Office of
  Vocational and Adult Education, Office of       34, IV
Educational Research and Improvement, Office of   34, VII
Elementary and Secondary Education, Office of     34, II
Employees' Compensation Appeals Board             20, IV
Employees Loyalty Board                           5, V
Employment and Training Administration            20, V
Employment Standards Administration               20, VI
Endangered Species Committee                      50, IV
Energy, Department of                             10, II, III, X
  Federal Acquisition Regulation                  48, 9
  Federal Energy Regulatory Commission            18, I
  Property Management Regulations                 41, 109
Energy, Office of                                 7, XXIX
Engineers, Corps of                               33, II; 36, III
Engraving and Printing, Bureau of                 31, VI
Enrichment Corporation, United States             10, XI
Environmental Protection Agency                   40, I
  Federal Acquisition Regulation                  48, 15
  Property Management Regulations                 41, 115
Environmental Quality, Office of                  7, XXXI
Equal Employment Opportunity Commission           5, LXII; 29, XIV
Equal Opportunity, Office of Assistant Secretary  24, I
     for
Executive Office of the President                 3, I
  Administration, Office of                       5, XV
  Environmental Quality, Council on               40, V
  Management and Budget, Office of                25, III, LXXVII; 48, 99
  National Drug Control Policy, Office of         21, III
  National Security Council                       32, XXI; 47, 2
  Presidential Documents                          3
  Science and Technology Policy, Office of        32, XXIV; 47, II
  Trade Representative, Office of the United      15, XX
       States
Export Administration, Bureau of                  15, VII
Export-Import Bank of the United States           5, LII; 12, IV
Family Assistance, Office of                      45, II

[[Page 344]]

Farm Credit Administration                        5, XXXI; 12, VI
Farm Credit System Insurance Corporation          5, XXX; 12, XIV
Farm Service Agency                               7, VII, XVIII
Farmers Home Administration                       7, XVIII
Federal Acquisition Regulation                    48, 1
Federal Aviation Administration                   14, I
Federal Claims Collection Standards               4, II
Federal Communications Commission                 47, I
Federal Contract Compliance Programs, Office of   41, 60
Federal Crop Insurance Corporation                7, IV
Federal Deposit Insurance Corporation             5, XXII; 12, III
Federal Election Commission                       11, I
Federal Emergency Management Agency               44, I
  Federal Acquisition Regulation                  48, 44
Federal Employees Group Life Insurance Federal    48, 21
     Acquisition Regulation
Federal Employees Health Benefits Acquisition     48, 16
     Regulation
Federal Energy Regulatory Commission              18, I
Federal Financial Institutions Examination        12, XI
     Council
Federal Financing Bank                            12, VIII
Federal Highway Administration                    23, I, II; 49, III
Federal Home Loan Mortgage Corporation            1, IV
Federal Housing Enterprise Oversight Office       12, XVII
Federal Housing Finance Board                     12, IX
Federal Information Resources Management          41, Subtitle E, Ch. 201
     Regulations
Federal Inspector for the Alaska Natural Gas      10, XV
     Transportation System, Office of
Federal Labor Relations Authority, and General    5, XIV; 22, XIV
     Counsel of the Federal Labor Relations 
     Authority
Federal Law Enforcement Training Center           31, VII
Federal Maritime Commission                       46, IV
Federal Mediation and Conciliation Service        29, XII
Federal Mine Safety and Health Review Commission  29, XXVII
Federal Pay, Advisory Committee on                5, IV
Federal Prison Industries, Inc.                   28, III
Federal Procurement Policy Office                 48, 99
Federal Property Management Regulations           41, 101
Federal Property Management Regulations System    41, Subtitle C
Federal Railroad Administration                   49, II
Federal Register, Administrative Committee of     1, I
Federal Register, Office of                       1, II
Federal Reserve System                            12, II
Federal Retirement Thrift Investment Board        5, VI, LXXVI
Federal Service Impasses Panel                    5, XIV
Federal Trade Commission                          5, XLVII; 16, I
Federal Transit Administration                    49, VI
Federal Travel Regulation System                  41, Subtitle F
Finance and Management, Office of                 7, XXX
Fine Arts, Commission on                          45, XXI
Fiscal Service                                    31, II
Fish and Wildlife Service, United States          50, I, IV
Fishery Conservation and Management               50, VI
Fishing and Whaling, International Regulatory     50, III
     Agencies
Food and Drug Administration                      21, I
Food and Consumer Service                         7, II
Food Safety and Inspection Service                9, III
Foreign Agricultural Service                      7, XV
Foreign Assets Control, Office of                 31, V
Foreign Claims Settlement Commission of the       45, V
     United States
Foreign Service Grievance Board                   22, IX
Foreign Service Impasse Disputes Panel            22, XIV
Foreign Service Labor Relations Board             22, XIV
Foreign-Trade Zones Board                         15, IV
Forest Service                                    36, II
General Accounting Office                         4, I, II
General Services Administration
  Contract Appeals, Board of                      48, 61

[[Page 345]]

  Federal Acquisition Regulation                  48, 5
  Federal Information Resources Management        41, Subtitle E, Ch. 201
       Regulations
  Federal Property Management Regulations System  41, 101, 105
  Federal Travel Regulation System                41, Subtitle F
  Payment From a Non-Federal Source for Travel    41, 304
       Expenses
  Payment of Expenses Connected With the Death    41, 303
       of Certain Employees
  Relocation Allowances                           41, 302
  Travel Allowances                               41, 301
Geological Survey                                 30, IV
Government Ethics, Office of                      5, XVI
Government National Mortgage Association          24, III
Grain Inspection, Packers and Stockyards          7, VIII; 9, II
     Administration
Great Lakes Pilotage                              46, III
Harry S. Truman Scholarship Foundation            45, XVIII
Health and Human Services, Department of          45, Subtitle A
  Child Support Enforcement, Office of            45, III
  Children and Families, Administration for       45, II, III, IV, X
  Community Services, Office of                   45, X
  Family Assistance, Office of                    45, II
  Federal Acquisition Regulation                  48, 3
  Food and Drug Administration                    21, I
  Health Care Financing Administration            42, IV
  Human Development Services, Office of           45, XIII
  Inspector General (Health Care), Office of      42, V
  Public Health Service                           42, I
  Refugee Resettlement, Office of                 45, IV
Health Care Financing Administration              42, IV
Housing and Urban Development, Department of      24, Subtitle B
  Community Planning and Development, Office of   24, V, VI
       Assistant Secretary for
  Equal Opportunity, Office of Assistant          24, I
       Secretary for
  Federal Acquisition Regulation                  48, 24
  Federal Housing Enterprise Oversight, Office    12, XVII
       of
  Government National Mortgage Association        24, III
  Housing--Federal Housing Commissioner, Office   24, II, VIII, X, XX
       of Assistant Secretary for
  Inspector General, Office of                    24, XII
  Public and Indian Housing, Office of Assistant  24, IX
       Secretary for
  Secretary, Office of                            24, Subtitle A, VII
Housing--Federal Housing Commissioner, Office of  24, II, VIII, X, XX
     Assistant Secretary for
Human Development Services, Office of             45, XIII
Immigration and Naturalization Service            8, I
Independent Counsel, Office of                    28, VII
Indian Affairs, Bureau of                         25, I
Indian Affairs, Office of the Assistant           25, VI
     Secretary
Indian Arts and Crafts Board                      25, II
Information Agency, United States                 22, V
  Federal Acquisition Regulation                  48, 19
Information Resources Management, Office of       7, XXVII
Information Security Oversight Office, National   32, XX
     Archives and Records Administration
Inspector General
  Agriculture Department                          7, XXVI
  Health and Human Services Department            42, V
  Housing and Urban Development Department        24, XII
Institute of Peace, United States                 22, XVII
Inter-American Foundation                         5, LXIII; 22, X
Intergovernmental Relations, Advisory Commission  5, VII
     on
Interior Department
  Endangered Species Committee                    50, IV
  Federal Acquisition Regulation                  48, 14
  Federal Property Management Regulations System  41, 114
  Fish and Wildlife Service, United States        50, I, IV
  Geological Survey                               30, IV
  Indian Affairs, Bureau of                       25, I

[[Page 346]]

  Indian Affairs, Office of the Assistant         25, VI
       Secretary
  Indian Arts and Crafts Board                    25, II
  Land Management, Bureau of                      43, II
  Minerals Management Service                     30, II
  Mines, Bureau of                                30, VI
  National Indian Gaming Commission               25, III
  National Park Service                           36, I
  Reclamation, Bureau of                          43, I
  Secretary of the Interior, Office of            43, Subtitle A
  Surface Mining and Reclamation Appeals, Board   30, III
       of
  Surface Mining Reclamation and Enforcement,     30, VII
       Office of
Internal Revenue Service                          26, I
International Boundary and Water Commission,      22, XI
     United States and Mexico, United States 
     Section
International Development, Agency for             22, II
  Federal Acquisition Regulation                  48, 7
International Development Cooperation Agency,     22, XII
     United States
  International Development, Agency for           22, II; 48, 7
  Overseas Private Investment Corporation         5, XXXIII; 22, VII
International Investment, Office of               31, VIII
International Joint Commission, United States     22, IV
     and Canada
International Organizations Employees Loyalty     5, V
     Board
International Regulatory Agencies (Fishing and    50, III
     Whaling)
International Trade Administration                15, III; 19, III
International Trade Commission, United States     19, II
Interstate Commerce Commission                    5, XL
James Madison Memorial Fellowship Foundation      45, XXIV
Japan-United States Friendship Commission         22, XVI
Joint Board for the Enrollment of Actuaries       20, VIII
Justice Department                                28, I
  Drug Enforcement Administration                 21, II
  Federal Acquisition Regulation                  48, 28
  Federal Claims Collection Standards             4, II
  Federal Prison Industries, Inc.                 28, III
  Foreign Claims Settlement Commission of the     45, V
       United States
  Immigration and Naturalization Service          8, I
  Offices of Independent Counsel                  28, VI
  Prisons, Bureau of                              28, V
  Property Management Regulations                 41, 128
Labor Department
  Benefits Review Board                           20, VII
  Employees' Compensation Appeals Board           20, IV
  Employment and Training Administration          20, V
  Employment Standards Administration             20, VI
  Federal Acquisition Regulation                  48, 29
  Federal Contract Compliance Programs, Office    41, 60
       of
  Federal Procurement Regulations System          41, 50
  Labor-Management Relations and Cooperative      29, II
       Programs, Bureau of
  Labor-Management Programs, Office of            29, IV
  Mine Safety and Health Administration           30, I
  Occupational Safety and Health Administration   29, XVII
  Pension and Welfare Benefits Administration     29, XXV
  Public Contracts                                41, 50
  Secretary of Labor, Office of                   29, Subtitle A
  Veterans' Employment and Training, Office of    41, 61; 20, IX
       the Assistant Secretary for
  Wage and Hour Division                          29, V
  Workers' Compensation Programs, Office of       20, I
Labor-Management Relations and Cooperative        29, II
     Programs, Bureau of
Labor-Management Programs, Office of              29, IV
Land Management, Bureau of                        43, II
Legal Services Corporation                        45, XVI
Library of Congress                               36, VII

[[Page 347]]

  Copyright Office                                37, II
Management and Budget, Office of                  5, III, LXXVII; 48, 99
Marine Mammal Commission                          50, V
Maritime Administration                           46, II
Merit Systems Protection Board                    5, II
Micronesian Status Negotiations, Office for       32, XXVII
Mine Safety and Health Administration             30, I
Minerals Management Service                       30, II
Mines, Bureau of                                  30, VI
Minority Business Development Agency              15, XIV
Miscellaneous Agencies                            1, IV
Monetary Offices                                  31, I
National Aeronautics and Space Administration     5, LIX; 14, V
  Federal Acquisition Regulation                  48, 18
National Agricultural Library                     7, XLI
National Agricultural Statistics Service          7, XXXVI
National Archives and Records Administration      36, XII
  Information Security Oversight Office           32, XX
National Bureau of Standards                      15, II
National Capital Planning Commission              1, IV
National Commission for Employment Policy         1, IV
National Commission on Libraries and Information  45, XVII
     Science
National and Community Service, Corporation for   45, XXV
National Council on Disability                    34, XII
National Credit Union Administration              12, VII
National Drug Control Policy, Office of           21, III
National Foundation on the Arts and the           45, XI
     Humanities
National Highway Traffic Safety Administration    23, II, III; 49, V
National Indian Gaming Commission                 25, III
National Institute for Literacy                   34, XI
National Institute of Standards and Technology    15, II
National Labor Relations Board                    29, I
National Marine Fisheries Service                 50, II, IV
National Mediation Board                          29, X
National Oceanic and Atmospheric Administration   15, IX; 50, II, III, IV, 
                                                  VI
National Park Service                             36, I
National Railroad Adjustment Board                29, III
National Railroad Passenger Corporation (AMTRAK)  49, VII
National Science Foundation                       45, VI
  Federal Acquisition Regulation                  48, 25
National Security Council                         32, XXI
National Security Council and Office of Science   47, II
     and Technology Policy
National Telecommunications and Information       15, XXIII; 47, III
     Administration
National Transportation Safety Board              49, VIII
National Weather Service                          15, IX
Natural Resources Conservation Service            7, VI
Navajo and Hopi Indian Relocation, Office of      25, IV
Navy Department                                   32, VI
  Federal Acquisition Regulation                  48, 52
Neighborhood Reinvestment Corporation             24, XXV
Nuclear Regulatory Commission                     5, XLVIII; 10, I
  Federal Acquisition Regulation                  48, 20
Occupational Safety and Health Administration     29, XVII
Occupational Safety and Health Review Commission  29, XX
Offices of Independent Counsel                    28, VI
Operations Office                                 7, XXVIII
Overseas Private Investment Corporation           5, XXXIII; 22, VII
Panama Canal Commission                           48, 35
Panama Canal Regulations                          35, I
Patent and Trademark Office                       37, I
Payment From a Non-Federal Source for Travel      41, 304
     Expenses
Payment of Expenses Connected With the Death of   41, 303
     Certain Employees
Peace Corps                                       22, III
Pennsylvania Avenue Development Corporation       36, IX

[[Page 348]]

Pension and Welfare Benefits Administration       29, XXV
Pension Benefit Guaranty Corporation              29, XXVI
Personnel Management, Office of                   5, I; 45, VIII
  Federal Acquisition Regulation                  48, 17
  Federal Employees Group Life Insurance Federal  48, 21
       Acquisition Regulation
  Federal Employees Health Benefits Acquisition   48, 16
       Regulation
Postal Rate Commission                            5, XLVI; 39, III
Postal Service, United States                     5, LX; 39, I
Postsecondary Education, Office of                34, VI
President's Commission on White House             1, IV
     Fellowships
Presidential Commission on the Assignment of      32, XXIX
     Women in the Armed Forces
Presidential Documents                            3
Prisons, Bureau of                                28, V
Productivity, Technology and Innovation,          37, IV
     Assistant Secretary
Public Contracts, Department of Labor             41, 50
Public and Indian Housing, Office of Assistant    24, IX
     Secretary for
Public Health Service                             42, I
Railroad Retirement Board                         20, II
Reclamation, Bureau of                            43, I
Refugee Resettlement, Office of                   45, IV
Regional Action Planning Commissions              13, V
Relocation Allowances                             41, 302
Research and Special Programs Administration      49, I
Rural Business-Cooperative Service                7, XVIII, XLII
Rural Development Administration                  7, XLII
Rural Housing Service                             7, XVIII
Rural Telephone Bank                              7, XVI
Rural Utilities Service                           7, XVII, XVIII, XLII
Saint Lawrence Seaway Development Corporation     33, IV; 46, III
Science and Technology Policy, Office of          32, XXIV
Science and Technology Policy, Office of, and     47, II
     National Security Council
Secret Service                                    31, IV
Securities and Exchange Commission                17, II
Selective Service System                          32, XVI
Small Business Administration                     13, I
  Federal Acquisition Regulation                  48, 22
Smithsonian Institution                           36, V
Social Security Administration                    20, III
Soldiers' and Airmen's Home, United States        5, XI
Special Counsel, Office of                        5, VIII
Special Education and Rehabilitative Services,    34, III
     Office of
State Department                                  22, I
  Federal Acquisition Regulation                  48, 6
Surface Mining and Reclamation Appeals, Board of  30, III
Surface Mining Reclamation and Enforcement,       30, VII
     Office of
Surface Transportation Board                      49, X
Susquehanna River Basin Commission                18, VIII
Technology Administration                         15, XI
Technology Policy, Assistant Secretary for        37, IV
Technology, Under Secretary for                   37, V
Tennessee Valley Authority                        18, XIII
Thrift Depositor Protection Oversight Board       12, XV
Thrift Supervision Office, Department of the      12, V
     Treasury
Trade Representative, United States, Office of    15, XX
Transportation, Department of
  Coast Guard                                     33, I; 46, I; 49, IV
  Commercial Space Transportation, Office of      14, III
  Contract Appeals, Board of                      48, 63
  Emergency Management and Assistance             44, IV
  Federal Acquisition Regulation                  48, 12
  Federal Aviation Administration                 14, I
  Federal Highway Administration                  23, I, II; 49, III
  Federal Railroad Administration                 49, II

[[Page 349]]

  Federal Transit Administration                  49, VI
  Maritime Administration                         46, II
  National Highway Traffic Safety Administration  23, II, III; 49, V
  Research and Special Programs Administration    49, I
  Saint Lawrence Seaway Development Corporation   33, IV; 46, III
  Secretary of Transportation, Office of          14, II; 49, Subtitle A
  Surface Transportation Board                    49, X
Transportation, Office of                         7, XXXIII
Travel Allowances                                 41, 301
Travel and Tourism Administration, United States  15, XII
Treasury Department                               5, XXI; 17, IV
  Alcohol, Tobacco and Firearms, Bureau of        27, I
  Community Development Financial Institutions    12, XVIII
       Fund
  Comptroller of the Currency                     12, I
  Customs Service, United States                  19, I
  Engraving and Printing, Bureau of               31, VI
  Federal Acquisition Regulation                  48, 10
  Federal Law Enforcement Training Center         31, VII
  Fiscal Service                                  31, II
  Foreign Assets Control, Office of               31, V
  Internal Revenue Service                        26, I
  International Investment, Office of             31, VIII
  Monetary Offices                                31, I
  Secret Service                                  31, IV
  Secretary of the Treasury, Office of            31, Subtitle A
  Thrift Supervision, Office of                   12, V
Truman, Harry S. Scholarship Foundation           45, XVIII
United States and Canada, International Joint     22, IV
     Commission
United States and Mexico, International Boundary  22, XI
     and Water Commission, United States Section
United States Enrichment Corporation              10, XI
Utah Reclamation Mitigation and Conservation      43, III
     Commission
Veterans Affairs Department                       38, I
  Federal Acquisition Regulation                  48, 8
Veterans' Employment and Training, Office of the  41, 61; 20, IX
     Assistant Secretary for
Vice President of the United States, Office of    32, XXVIII
Vocational and Adult Education, Office of         34, IV
Wage and Hour Division                            29, V
Water Resources Council                           18, VI
Workers' Compensation Programs, Office of         20, I
World Agricultural Outlook Board                  7, XXXVIII

[[Page 351]]





List of CFR Sections Affected


All changes in this volume of the Code of Federal Regulations which were 
made by documents published in the Federal Register since January 1, 
1986, are enumerated in the following list. Entries indicate the nature 
of the changes effected. Page numbers refer to Federal Register pages. 
The user should consult the entries for chapters and parts as well as 
sections for revisions.

For the period before January 1, 1986, see the ``List of CFR Sections 
Affected, 1949-1963, 1964-1972, and 1973-1985'' published in seven 
separate volumes.

                                  1986

21 CFR
                                                                   51 FR
                                                                    Page
Chapter II
1301.03  Amended....................................................5319
1301.24  (b) amended................................................5319
1301.26  (e) amended................................................5319
1301.32  (a)(7), (c) and (f) amended................................5319
1301.33  (c) amended................................................5319
1301.34  (a) amended................................................5319
1301.61  Amended....................................................5319
1301.64  Removed....................................................5319
1301.71  (d) amended................................................5319
1302  Authtority citation revised...................................5319
1303  Authority citation revised....................................5319
1303.12  (b) and (d) amended........................................5319
1303.22  Amended....................................................5319
1303.27  Amended....................................................5319
1304.03  (d) amended................................................5319
    (b) corrected..................................................26154
1304.04  (f) and (g) amended........................................5320
1304.31  Removed; new 1304.31 redesignated from 1304.33.............5319
    (a) amended.....................................................5320
1304.32  Removed; new 1304.32 redesignated from 1304.34.............5319
    (a) amended.....................................................5320
1304.33  Redesignated as 1304.31; new 1304.33 redesignated from 
        1304.35.....................................................5319
1304.34  Redesignated as 1304.32....................................5319
    Redesignated from 1304.37 and amended...........................5320
    (c) redesignated from 1304.36(c)................................5320
1304.35  Redesignated as 1304.33 and (a) amended....................5319
    Redesignated from 1304.38.......................................5320
1304.36  (a) and (b) removed........................................5319
    (c) redesignated as 1304.34(c)..................................5320
    Redesignated from 1304.39.......................................5320
1304.37  Redesignated as 1304.34 and amended; new 1304.37 
        redesignated from 1304.40...................................5320
1304.38  Redesignated as 1304.35; new 1304.38 redesignated from 
        1304.41.....................................................5320
1304.39  Redesignated as 1304.36....................................5320
1304.40  Redesignated as 1304.37....................................5320
1304.41  (a) amended................................................5319
    Redesignated as 1304.38.........................................5320
1305.03  (c) amended................................................5320
1305.05  (b) and (d) amended........................................5319
1305.12  (b) amended................................................5319
1306  Authority citation revised....................................5319
1306.15  Amended....................................................5320
1306.23  Amended....................................................5320
1306.25  Amended....................................................5320
1306.31  (a) amended................................................5320
1307.14  (a) amended................................................5319
1308.02  (c) revised; (e) and (f) redesignated as (f) and (g); new 
        (e) added..................................................15317
1308.03  (a) revised...............................................15318
1308.04  (a) amended................................................5320

[[Page 352]]

1308.11  (g)(13) added..............................................4723
    (b)(17) amended.................................................5320
    (b)(17) correctly designated....................................9440
1308.11  (g)(1) effective date extended............................15474
    (g)(2) effective date extended.................................21912
    (g)(3) and (4) effective date extended.........................28695
    (g)(1) removed; (b)(31) through (46) and (g)(2) through (13) 
redesignated as (b)(32) through (47) and (g)(1) through (12); new 
(b)(31) added......................................................33593
    (d)(7) through (24) redesignated as (d)(8) through (25); new 
(d)(7) added; (g)(1) removed; (g)(2) through (12) redesignated as 
(g)(1) through (11)................................................36560
    (g)(5) through (12) addition at 50 FR 43700 effective date 
extended...........................................................42834
1308.12  (b)(4) revised............................................15318
    (f) redesignated as (g); new (f) added.........................17478
1308.13  (e)(3) and (4) amended.....................................5320
1308.14  (c)(3) table revised......................................10191
1308.24  Amended....................................................5319
1308.52  Added.....................................................15318
1311  Authority citation revised....................................5319
1311.03  Amended....................................................5319
1311.32  (c) and (f) amended........................................5319
    (b) and (c) amended.............................................5320
1311.61  Amended....................................................5319
1311.64  Removed....................................................5320
1312  Authority citation revised....................................5319
1312.02  (a) amended................................................5320
1312.12  (a) amended..........................................5319, 5320
1312.14  (a) amended................................................5319
1312.16  (b) amended................................................5319
1312.18  (b) amended................................................5319
1312.19  (a) and (b) amended........................................5319
1312.22  (a) amended................................................5319
1312.24  (a) amended................................................5319
1312.25  Amended....................................................5319
1312.27  (a) amended................................................5319
1312.28  (c) and (d) amended........................................5319
1312.31  (b) amended................................................5319
1312.32  (a) amended................................................5319
1316  Authority citation revised....................................5319
1316.03  (d) amended................................................5319

                                  1987

21 CFR
                                                                   52 FR
                                                                    Page
Chapter II
1301.11  (c) and (d) revised.......................................20598
1301.12  Revised...................................................20599
1301.22  (a)(10) revised...........................................17287
1301.31  (c) revised; (d) added....................................20599
1306.22  (a) revised..........................................1904, 3605
    Technical correction...........................................13430
1308.11  (g) (1) and (2) removed; (b) (33) through (47) and (g) 
        (3) through (11) redesignated as (b) (34) through (37) and 
        (b) (39) through (49) and (g) (1) through (9); (b) (33) 
        and (38) added..............................................2516
    (b)(2) removed; (b) (3) through (49) redesignated as (b) (2) 
through (48)........................................................2517
    (g) designations corrected......................................6546
    (g) temporary placement extended................................7270
    (b) introductory text revised; (b) (1) through (48) 
redesignated as (b) (2) through (7), (9) and (10), (12) through 
(33), (35) through (40), (42) through (51), (53) and (54); new (b) 
(1), (8), (11), (34), (41), and (52) added; (g) (1), (2), (4), 
(6), (8), and (9) removed; (g) (3), (5), and (7) redesignated as 
(g) (1), (2), and (3)..............................................20072
    Technical correction...........................................27198
    (g) (4) through (6) added......................................38226
1308.12  (c) (1) through (23) redesignated as (c) (2) through 
        (24); new (c)(1) added......................................2517
    (f)(2) added...................................................11043
    (f)(2) corrected...............................................12285
1308.13  (c)(12) added..............................................2222
    (c)(1)(i), (ii), and (iii) and (2)(i), (ii), and (iii) revised
                                                                    5952
1308.14  (b)(1) and (2) revised.....................................5952
1308.15  (c)(6) revised.............................................5952
1308.24  (i) table revised; interim.................................9807
1308.31--1308.32  Undesignated center heading revised; interim......9803
1308.31  Heading, (a), (b) introductory text, and (d) revised; (c) 
        amended; interim............................................9803
1308.32  Revised; interim...........................................9803
1311.02  (d) revised...............................................17288
1311.21  Revised...................................................17288
1311.26  Revised...................................................17288

[[Page 353]]

1311.32  (d) revised; (e) and (f) redesignated as (f) and (g); new 
        (e) added..................................................17288
1311.42  (a), (b)(6) (i) and (iv) revised..........................17288
1311.44  (a) and (b) revised; (c) through (e) redesignated as (e) 
        through (g); new (c) and (d) added; new (f) (1) and (2) 
        and (g) (1) and (2) revised................................17288
1311.47  Revised...................................................17289
1311.53  Revised...................................................17289
1311.61  Revised...................................................17289
1312  Authority citation revised...................................17289
1312.11  (a) and (b) revised.......................................17289
1312.12  (a) introductory text revised.............................17289
1312.13  (a)(1) revised; (b) through (e) redesignated as (d) 
        through (g); new (b) and (c) added.........................17289
1312.18  (a), (b), and (c)(2) revised..............................17290
1312.21  (a) and (b) revised.......................................17290
1312.22  (a) revised...............................................17290
1312.23  (b) through (d) redesignated as (d) through (f); new (b) 
        and (c) added .......... 17290
1312.27  (a), (b) (2) and (4) revised; (b)(5) added................17290
1312.28  (d) revised...............................................17291
1312.30  Added.....................................................17291
1316.71-1316.81 (Subpart E)  Authority citation revised............24446
    1316.74  Amended...............................................41418
1316.75  (b)(3) amended............................................24446

                                  1988

21 CFR
                                                                   53 FR
                                                                    Page
Chapter II
1301.11  (a) through (f) amended....................................4963
1301.12  Amended....................................................4963
1301.13  (a) through (c) amended....................................4963
1301.22  (a)(4) and (b) (5) and (6) amended.........................4963
1301.32  (a) (1) through (6) and (8), (b) (1) through (9) and (c) 
        amended.....................................................4963
1301.32  (d) revised; (e) and (f) redesignated as (f) and (g); new 
        (e) added..................................................21813
1301.44  (a) and (b) amended........................................4963
1301.61  Amended....................................................4963
1303.12  (f) amended................................................4963
1305.03  Introductory text amended..................................4963
1305.05  (a) revised; (b) amended...................................4963
1305.06  (a) and (b) amended........................................4963
1306.11  (d) introductory text amended..............................4964
1308.11  (g)(2) removed; (b) (12) through (54) and (g) (3) through 
        (6) redesignated as (b) (13) through (55) and (g) (2) 
        through (5); new (b)(12) added...............................501
    (d)(7) rdmoved; (d)(8) through (25) redesignated as (d)(7) 
through (24)........................................................2226
    (b)(12) correctly revised.......................................3744
    (d) (7) through (24) redesignated as (d) (8) through (25); new 
(d)(7) added........................................................5158
1308.11  (g)(6) added..............................................29233
    (g) temporary scheduling extended..............................40061
1308.12  (f)(2) corrected; CFR correction..........................31837
    (c) (6) through (24) redesignated as (c) (7) through (25); new 
(c)(6) added.......................................................43685
1308.14  (e) (1) through (6) redesignated as (e) (2), (5), and (7) 
        through (10); new (e) (1), (3), (4), and (6) added.........17460
1308.15  (d) added.................................................10870
1308.24  (i) table revised..................................10835, 36152
1308.32  Table revised.............................................10861
1311.11  (a) and (b) amended........................................4963
1311.12  Revised....................................................4963
1311.32  (a), (b) and (c) amended...................................4963
1311.43  (a) and (b) amended........................................4963
1312.14  (a) amended...............................................48244
1312.16  (b) amended...............................................48244
1312.19  (a) and (b) amended.......................................48244
1312.24  (a) amended...............................................48244
1312.25  Amended...................................................48244
1312.28  (c) amended...............................................48244
1312.31  (b) amended...............................................48244
1312.32  (a) amended...............................................48244

                                  1989

21 CFR
                                                                   54 FR
                                                                    Page
Chapter II
1301.74  (g) amended...............................................33674

[[Page 354]]

1301.75  (d) amended...............................................33674
1306.06  (b) amended...............................................33674
1306.13  (d) amended...............................................33674
1305.16  (a) and (b)(1) amended....................................33674
1308.11  (g) (3) and (4) removed; (d) (8) through (25) and (g) (5) 
        and (6) redesignated as (d) (10) through (27) and (g) (3) 
        and (4); (d) (8) and (9) added.............................14798
    (g)(3) removed; (f)(2) and (g)(4) redesignated as (f)(3) and 
(g)(3); new (f)(2) added...........................................14800
    (d)(28) added..................................................28415
    (g) temporary scheduling extended..............................31815
1308.22  Table amended..............................................2100
    Table revised..................................................12162
1308.24  (i) table revised; interim................................10633
1308.32  Table revised; interim....................................11520
1310  Revised......................................................31662
1313  Added........................................................31665
    Policy statement...............................................49750
1316  Authority citation revised...................................37610
1316.21--1316.22 (Subpart B)  Authority citation revised...........31670
1316.21  Redesignated as 1316.23; new 1316.21 added................31670
1316.22  Redesignated as 1316.24; new 1316.22 added................31670
1316.23  Redesignated from 1316.21.................................31670
1316.24  Redesignated from 1316.22.................................31670
1316.90--1316.99 (Subpart F)  Added................................37610

                                  1990

21 CFR
                                                                   55 FR
                                                                    Page
Chapter II
1308.11  (f)(3) added; (g)(3) removed...............................3588
    (f)(4) correctly added..........................................9117
1308.22  table revised.............................................12162
1308.24  (i) table revised; interim; eff. 4-9-90....................8915
1308.32  Table revised; interim.....................................9114
1316.03  (a) revised...............................................50827
1316.45  Amended...................................................27464

                                  1991

21 CFR
                                                                   56 FR
                                                                    Page
Chapter II
1301.02  (e) revised...............................................36726
1301.76  (a) revised...............................................36728
1302  Labeling deadlines extension.................................42231
1306.05  (a) revised...............................................25026
1306.13  (b), (c) introductory text and (1) revised................25027
1308  Technical correction.........................................13854
1308.02  (b) through (g) redesignated as (c) through (h); new (b) 
        added.......................................................5754
1308.12  (e)(2) through (4) redesignated as (e)(3) through (5); 
        new (e)(2) added...........................................11932
1308.13  (f) added..................................................5754
    (c)(5) removed; (c)(6) through (12) redesignated as (c)(5) 
through (11).......................................................11932
1308.15  (d)(1) removed; (d)(2) redesignated as (d)(1).............61372
1308.24  (i) table revised; interim.................................9133
1308.25--1308.26  Undesignated center heading added................42936
1308.25  Added.....................................................42936
1308.26  Added.....................................................42936
1308.33--1308.34  Undesignated center heading added................42936
1308.33  Added.....................................................42936
1308.34  Added.....................................................42937
1310.02  (a)(13) through (24) added; (b)(5) removed; (b)(6), (7) 
        and (8) redesignated as (b)(5), (6) and (7)................48733
1310.03  Amended....................................................8277
1310.04  (f)(1)(xii) revised; (f)(1)(xiii) through (xxiv) added; 
        (f)(2)(i)(E), and (ii)(E) removed; (f)(2)(i)(F), (G), (H), 
        (ii)(F), (G) and (H) redesignated as (f)(2)(i)(E), (F), 
        (G), (ii)(E), (F) and (G)..................................48733
1313  Policy statement.............................................19269
1313.15  (d) redesignated as (e); new (d) added....................55076
1313.24  (d) redesignated as (e); new (d) added....................55077
1316.75  (a) and (b) amended........................................8686
1316.76  (a) amended................................................8686
1316.77  (a) amended................................................8686
1316.78  Amended....................................................8686
1316.79  (a) amended................................................8686
1316.81  Amended....................................................8686

[[Page 355]]

                                  1992

21 CFR
                                                                   57 FR
                                                                    Page
Chapter II
1302  Labeling deadlines extension..................................5817
1308.11  (g)(3) added..............................................18825
    (g)(4) added...................................................43401
1308.12  (b)(1) introductory text revised..........................31126
1308.24  (i) table revised; interim.................................5818
    Regulation at 57 FR 5818 confirmed.............................36371
1308.26  (a) table revised; interim................................19534
    Regulation at 57 FR 19534 confirmed............................36372
1308.32  Introductory text revised.................................23301
1308.33  (c)(10)(a) and (b) correctly designated as (c)(10)(i) and 
        (ii).......................................................10815
1308.34  Table revised......................................32423, 55091
1310.02  (b)(8) and (9) added......................................43615
1310.04  (f)(2)(iv) added..........................................43615
1310.05  (c) added..................................................2461
1310.06  (c) revised; (e), (f) and (g) added........................2462
1310.08  Added.....................................................43615

Chapter III
Chapter III  Chapter established...................................55089
1401  Added........................................................59803
1402  Added........................................................55089
1403  Added........................................................55092
1404  Added........................................................56263

                                  1993

21 CFR
                                                                   58 FR
                                                                    Page
Chapter II
1301  Effective date paragraph at 58 FR 31172 corrected............31907
1301.11  Revised...................................................15274
1301.22  (b)(6) revised............................................31175
1301.24  (b) and (c) introductory text revised.....................31175
1304  Effective date paragraph at 58 FR 31172 corrected............31907
1304.02  (f) through (i) redesignated as (g) through (j); new (f) 
        added......................................................31175
1304.03  (e) through (g) redesignated as (f) through (h); new (e) 
        added; new (h) revised.....................................31175
1308.11  (d)(3) through (28) redesignated as (d)(4) through (29); 
        new (d)(3) added............................................4317
    (f)(1) through (4) redesignated as (f)(2) through (5); new 
(f)(1) added........................................................4318
    (g)(5) added...................................................13534
    Regulation at 57 FR 18824 eff. date extended to 11-1-93........25934
    (b)(4) revised.................................................43796
    Regulation at 57 FR 43401 eff. date extended to 3-21-94........44611
    (g)(3) removed; (f)(3), (4), (5), (g)(4) and (5) redesignated 
as (f)(4), (5), (6), (g)(3) and (4); new (f)(3) added..............53406
1308.12  (c)(11) through (25) redesignated as (c)(12) through 
        (26); new (c)(11) added....................................43796
1308.14  (c)(48) added..............................................7187
1308.24  (i) table revised.........................................17107
1308.26  (a) table amended.........................................15088
1308.34  Table amended; interim....................................16773
    Table amended; interim.........................................34708
    Regulation at 58 FR 16773 confirmed............................34709
    Regulation at 58 FR 34708 confirmed............................49924
1311.11  Revised...................................................15274
Chapter III
1403  appendix A corrected.........................................26185

                                  1994

21 CFR
                                                                   59 FR
                                                                    Page
Chapter II
1301.13  (a) and (b) revised........................................8859
1306.02  (h) redesignated as (i); new (h) added....................26111
1306.11  (a) revised; (e) and (f) added............................26111
    (a) and (f) corrected..........................................30832
1306.21  (a) and (c) revised.......................................26112
1306.31  (c) revised...............................................26112
    (c) corrected..................................................30832
1308.11  (g)(5)  added...............................................673
    Regulation at 58 FR 13534 eff. date extended to 9-12-94........10720
    (f)(1) through (6) redesignated as (f)(2) through (7); new 
(f)(1) added.......................................................12829

[[Page 356]]

    (g)(3) removed; (g)(4) and (5) redesignated as (g)(3) and (4) 
                                                                   12830
    (g)(3) removed; (d)(1) through (29) and (g)(4) redesignated as 
(d)(2) through (30) and (g)(3); new (d)(1) added...................46759
    Regulation at 59 FR 673 eff. date extended.....................65710
1308.24  (i)  table revised........................................15053
    Regulation at 59 FR 15053 confirmed............................52905
1310  Technical correction.........................................52588
1310.04  (f) introductory text revised; (f)(1)(iii) removed; 
        (f)(1)(iv) through (xxiv) redesignated as (f)(1)(iii) 
        through (xxiii); (g) added.................................51367
1310.06  (b) revised; interim......................................51364
1310.09  Added; interim............................................13882
1313  Technical correction.........................................52588
1313.12  (a) introductory text revised.............................51367
1313.21  (a) introductory text revised.............................51367

                                  1995

21 CFR
                                                                   60 FR
                                                                    Page
Chapter II
1301  Policy statement.............................................55310
1301.24  (b), (c) introductory text and (5) revised................36641
1308.24  (i) table amendeded.......................................15956
1301.37  (a) revised...............................................32101
1301.43  (a) revised...............................................32101
1301.44  (b) redesignated as (c); new (b) added....................32101
1301.54  (a) through (d) revised...................................32101
1301.55  (a) revised...............................................32102
1306.05  (b) revised...............................................36641
1307.03  Revised...................................................32454
1308.11  (d)(3) through (30) redesignated as (d)(4) through (31); 
        new (d)(3) added; (g)(3) removed...........................28719
1309  Added........................................................32454
1309.02  (f), (g) and (h) correctly redesignated as (e), (f) and 
        (g)........................................................42436
1309.12  (b) corrected......................................35264, 36334
1310  Technical correction.........................................54409
1310.01  (b) through (e), (f)(1) and (g) revised; (k) redesignated 
        as (m); new (k) and (l) added..............................32459
1310.02  (b)(10) added.............................................19510
    Introductory text, (a) and (b) revised.........................32460
1310.04  (f)(2)(v) added...........................................19510
    (a), (b), (f)(1) and (2) introductory text revised; 
(f)(1)(xiv), (xx) and (xxii) removed; (f)(1)(xv) through (xix), 
(xxi), and (xxiii) redesignated as (f)(1)(xiv) through (xviii), 
(xix) and (xx); new (f)(1)(xxi) and (xxii) added...................32460
    1310.04  (f)(1)(xxii) and (xxiii) correctly redesignated as 
(f)(1)(xxi) and (xxii).............................................42436
1310.06  Regulation at 59 FR 51364 confirmed.......................17628
    (a) introductory text, (1), (c) and (d) revised................32461
1310.07  (a) and (b) revised.......................................32461
1310.08  (c), (d) and (e) added....................................19510
    (b) introductory text revised..................................32461
1310.09  Revised; interim..........................................53122
1310.10  Added.....................................................32461
1310.11  Added.....................................................32462
1310.14  Added.....................................................32462
1310.15  Added.....................................................32463
1313.01  Amended...................................................32465
1313.02  (c), (d) introductory text, (1), (h) and (i) revised; (m) 
        redesignated as (o); new (m) and (n) added.................32463
1313.12--1313.15  Undesignated center heading amended..............32465
1313.12  (c) revised; (d), (e) and (f) added.......................32464
1313.13  (a) amended...............................................32465
1313.14  Introductory text and (a) amended.........................32465
1313.15  Revised...................................................32464
1313.21--1313.25  Undesignated center heading amended..............32465
1313.21  (d) redesignated as (g); (c) and new (g) revised; new 
        (d), (e) and (f) added.....................................32464
1313.22  (a) amended...............................................32465
1313.23  Introductory text and (a) amended.........................32465
1313.31  Undesignated center heading added.........................32465

[[Page 357]]

1313.32  Added.....................................................32465
1313.33  Added.....................................................32465
1313.34  Added.....................................................32465
    (a) corrected...........................................35264, 36334
1316  Authority citation revised...................................32465
1316.02  (c)(2) revised............................................32465
    (c)(2) corrected........................................35264, 36334
1316.03  (b) through (e) revised...................................32465
1316.09  (a)(3) revised............................................32466
Chapter III
1403.36  (d), (g), (h) and (i) revised......................19639, 19642
1404.100  Revised...........................................33040, 33045
1404.105  Amended...........................................33041, 33045
1404.110  (c) revised.......................................33041, 33045
1404.200  Revised...........................................33041, 33045
1404.215  Revised...........................................33041, 33045
1404.220  Revised...........................................33041, 33045
1404.225  Revised...........................................33041, 33045
1404  Appendixes A and B revised............................33042, 33045

                                  1996

   (Regulations published from January 1, 1996, through April 1, 1996)

21 CFR
                                                                   61 FR
                                                                    Page
Chapter II
1308.24  (i) table revised.........................................13690
1310.03  Existing text designated as (a); (b) added; eff. 4-29-96 
                                                                   14023
1310.05  (d) added; eff. 4-29-96...................................14024
1310.06  (h) added; eff. 4-29-96...................................14024
1313  Policy statement.............................................13759