Agency Information Collection Activities: Proposed Collection; Comments Requested, 48680-48681 [E7-16718]

Agencies

• Drug Enforcement Administration
• Department of Justice

[Federal Register Volume 72, Number 164 (Friday, August 24, 2007)]
[Notices]
[Pages 48680-48681]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-16718]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[OMB Number 1117-0006]


Agency Information Collection Activities: Proposed Collection; 
Comments Requested

ACTION: 30-day notice of information collection under review: 
Application for individual manufacturing quota for a basic class of 
controlled substance and for ephedrine, pseudoephedrine, and 
phenylpropanolamine DEA Form189.

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    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. The proposed 
information collection is published to obtain comments from the public 
and affected agencies. This proposed information collection was 
previously published in the Federal Register Volume 72, Number 117, 
page 33774 on June 19, 2007, allowing for a 60 day comment period.
    The purpose of this notice is to allow for an additional 30 days 
for public comment until September 24, 2007. This process is conducted 
in accordance with 5 CFR 1320.10. Written comments and/or suggestions 
regarding the items contained in this notice, especially the estimated 
public burden and associated response time, should be directed to the 
Office of Management and Budget, Office of Information and Regulatory 
Affairs, Attention Department of Justice Desk Officer, Washington, DC 
20503. Additionally, comments may be submitted to OMB via facsimile to 
(202) 395-5806.
    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 agencies estimate of the burden of the 
proposed collection of information, including the validity of the 
methodology and assumptions used;
--Enhance the quality, utility, and clarity of the information to be 
collected; and
--Minimize the burden of the collection of information on those who are 
to

[[Page 48681]]

respond, including through the use of appropriate automated, 
electronic, mechanical, or other technological collection techniques 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 an existing 
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.
    (3) Agency form number, if any and the applicable component of the 
Department sponsoring the collection:
    Form number: DEA Form 189.
    Component: Office of Diversion Control, Drug Enforcement 
Administration, U.S. Department of Justice.
    (4) Affected public who will be asked or required to respond, as 
well as a brief abstract:
    Primary: Business or other for-profit.
    Other: None.
    Abstract: 21 U.S.C. 826 and 21 CFR 1303.22 and 1315.22 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, pseudoephedrine, or 
phenylpropanolamine, must apply on DEA Form 189 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: DEA estimates 
that each form takes 0.5 hours (30 minutes) to complete. In total, 37 
firms submit 298 responses, with each response taking 0.5 hours (30 
minutes) to complete. This results in a total public burden of 149 
hours annually.
    (6) An estimate of the total public burden (in hours) associated 
with the collection: In total, 37 firms submit 298 responses, with each 
response taking 0.5 hours (30 minutes) to complete. This results in a 
total public burden of 149 hours annually.
    If additional information is required contact: Lynn Bryant, 
Department Clearance Officer, United States Department of Justice, 
Justice Management Division, Policy and Planning Staff, Patrick Henry 
Building, Suite 1600, 601 D Street, NW., Washington, DC 20530.

    Dated: August 20, 2007.
Lynn Bryant,
Department Clearance Officer, PRA, Department of Justice.
[FR Doc. E7-16718 Filed 8-23-07; 8:45 am]
BILLING CODE 4410-09-P