[Federal Register Volume 81, Number 50 (Tuesday, March 15, 2016)]
[Notices]
[Pages 13828-13829]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-05791]


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DEPARTMENT OF JUSTICE

[OMB Number 1117-0006]


Agency Information Collection Activities; Proposed eCollection, 
eComments Requested; Extension Without Change of a Previously Approved 
Collection Application for Individual Manufacturing Quota for a Basic 
Class of Controlled Substance and for Ephedrine, Pseudoephedrine, and 
Phenylpropanolamine DEA Form 189

AGENCY: Drug Enforcement Administration, Department of Justice.

ACTION: 30-Day notice.

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SUMMARY: The Department of Justice (DOJ), Drug Enforcement 
Administration (DEA), will be submitting the following information 
collection request to the Office of Management and Budget (OMB) for 
review and approval in accordance with the Paperwork Reduction Act of 
1995. This proposed information collection was previously published in 
the Federal Register at 81 FR 1219, on January 11, 2016, allowing for a 
60 day comment period.

DATES: Comments are encouraged and will be accepted for an additional 
30 days until April 14, 2016.

FOR FURTHER INFORMATION CONTACT: If you have comments on the estimated 
public burden or associated response time, suggestions, or need a copy 
of the proposed information collection instrument with instructions or 
additional information, please contact Barbara J. Boockholdt, Office of 
Diversion Control, Drug Enforcement Administration; Mailing Address: 
8701 Morrissette Drive, Springfield, Virginia 22152; Telephone: (202) 
598-6812. Written comments and/or suggestions can also be directed to 
the Office of Management and Budget, Office of Information and 
Regulatory Affairs, Attention Department of Justice Desk Officer, 
Washington, DC 20503 or sent to [email protected].

SUPPLEMENTARY INFORMATION: Written comments and suggestions from the 
public and affected agencies concerning the proposed collection of 
information are encouraged. Your comments should address one or more of 
the following four points:

--Evaluate whether the proposed collection of information is necessary 
for the proper performance of the functions of the agency, including 
whether the information will have practical utility;
--Evaluate the accuracy of the agency's estimate of the burden of the 
proposed collection of information, including the validity of the 
methodology and assumptions used;
--Evaluate whether and if so how the quality, utility, and clarity of 
the information proposed to be collected can be enhanced; and
--Minimize the burden of the collection of information on those who are 
to respond, including through the use of appropriate automated, 
electronic, mechanical, or other forms of information technology, e.g., 
permitting electronic submission of responses.

Overview of This Information Collection

    1. Type of Information Collection: Extension of a currently 
approved collection.
    2. Title of the Form/Collection: Application for Individual 
Manufacturing Quota for a Basic Class of Controlled Substance and for 
Ephedrine, Pseudoephedrine, and Phenylpropanolamine (DEA Form 189).
    3. The agency form number, if any, and the applicable component of 
the Department sponsoring the collection: Form Number: DEA Form 189. 
The applicable component within the Department of Justice is the Drug 
Enforcement Administration, Office of Diversion Control.
    4. Affected public who will be asked or required to respond, as 
well as a brief abstract:
    Affected public (Primary): Business or other for-profit.
    Affected public (Other): None.
    Abstract: The Controlled Substance Act (CSA) require that any 
person who is registered to manufacture any basic class of controlled 
substances listed in Schedule I or II and who desires to manufacture a 
quantity of such class; or who desires to manufacture using the List I 
chemicals ephedrine,

[[Page 13829]]

pseudoephedrine, or phenylpropanolamine, must complete the DEA Form 189 
online, for a manufacturing quota for such quantity of such class or 
List I chemical.
    5. An estimate of the total number of respondents and the amount of 
time estimated for an average respondent to respond: The DEA estimates 
that each form takes 0.5 hours to complete. In total, 34 respondents 
submit 660 responses, with each response taking 0.5 hours to complete.
    6. An estimate of the total public burden (in hours) associated 
with the proposed collection: The DEA estimates that this collection 
takes 330 annual burden hours.

If additional information is required please contact: Jerri Murray, 
Department Clearance Officer, United States Department of Justice, 
Justice Management Division, Policy and Planning Staff, Two 
Constitution Square, 145 N Street NE., Suite 3E.405B, Washington, DC 
20530.

    Dated: March 10, 2016.
Jerri Murray,
Department Clearance Officer for PRA, U.S. Department of Justice.
[FR Doc. 2016-05791 Filed 3-14-16; 8:45 am]
BILLING CODE 4410-09-P