[Federal Register Volume 60, Number 134 (Thursday, July 13, 1995)]
[Notices]
[Pages 36164-36165]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-17119]



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DEPARTMENT OF JUSTICE

Importation of Controlled Substances; Notice of Application

    Pursuant to Section 1008 of the Controlled Substances Import and 
Export Act (21 U.S.C. 958(i)), the Attorney General shall, prior to 
issuing a registration under this Section to a bulk manufacturer of a 
controlled substance in Schedule I or II and prior to issuing a 
regulation under Section 1002(a) authorizing the importation of such a 
substance, provide manufacturers holding registrations for the bulk 
manufacture of the substance an opportunity for a hearing.
    Therefore, in accordance with Sec. 1311.42 of Title 21, Code of 
Federal Regulations (CFR), notice is hereby given that on May 18, 1995, 
Applied Science Labs, Division of Alltech Associates, Inc., 2701 
Carolean Industrial Drive, P.O. Box 440, State College, Pennsylvania 
16801, made application to the Drug Enforcement Administration to be 
registered as an importer of the basic classes of controlled substances 
listed below:

------------------------------------------------------------------------
                           Drug                               Schedule  
------------------------------------------------------------------------
Heroin (9200).............................................  I           
Morphine (9300)...........................................  II          
------------------------------------------------------------------------

    The firm plans to import these controlled substances for the 
manufacture of reference standards.
    Any manufacturer holding, or applying for, registration as a bulk 
manufacturer of these basic classes of controlled substances may file 
written comments on or objections to the application described above 
and may, at the same time, file a written request for a hearing on such 
application in accordance with 21 CFR 1301.54 in such form as 
prescribed in 21 CFR 1316.47.
    Any such comments, objections, or requests for a hearing may be 
addressed to the Deputy Assistant Administrator, Office of Diversion 
Control, Drug Enforcement Administration, United States Department of 
Justice, Washington, D.C. 20537, Attention: DEA Federal Register 
Representative (CCR), and must be filed no later than August 14, 1995.
    This procedure is to be conducted simultaneously with and 
independent of the procedures described in 21 CFR 

[[Page 36165]]
1311.42(b), (c), (d), (e), and (f). As noted in a previous notice at 40 
FR 43745-46 (September 23, 1975), all applicants for registration to 
import basic classes of any controlled substances in Schedule I or II 
are and will continue to be required to demonstrate to the Deputy 
Assistant Administrator, Office of Diversion Control, Drug Enforcement 
Administration that the requirements for such registration pursuant to 
21 U.S.C. 958(a), 21 U.S.C. 823(a), and 21 CFR 1311.42(a), (b), (c), 
(d), (e), and (f) are satisfied.

    Dated: July 5, 1995.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 95-17119 Filed 7-12-95; 8:45 am]
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