81 FR 1219 - Agency Information Collection Activities; Proposed eCollection, eComments Requested; Extension Without Change of a Previously Approved Collection Application for Procurement Quota for a Controlled Substance and for Ephedrine, Pseudoephedrine, and Phenylpropanolamine DEA Form 250

DEPARTMENT OF JUSTICE

Federal Register Volume 81, Issue 6 (January 11, 2016)

Page Range		1219-1219
FR Document		2016-00234

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.

Federal Register, Volume 81 Issue 6 (Monday, January 11, 2016)

[Federal Register Volume 81, Number 6 (Monday, January 11, 2016)]
[Notices]
[Page 1219]
From the Federal Register Online  [www.thefederalregister.org]
[FR Doc No: 2016-00234]


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DEPARTMENT OF JUSTICE

[OMB Number 1117-0008]


Agency Information Collection Activities; Proposed eCollection, 
eComments Requested; Extension Without Change of a Previously Approved 
Collection Application for Procurement Quota for a Controlled Substance 
and for Ephedrine, Pseudoephedrine, and Phenylpropanolamine DEA Form 
250

AGENCY: Drug Enforcement Administration, Department of Justice.

ACTION: 60-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.

DATES: Comments are encouraged and will be accepted for 60 days until 
March 11, 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.

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 Procurement Quota 
for Controlled Substance and for Ephedrine, Pseudoephedrine, and 
Phenylpropanolamine (DEA Form 250).
    3. The agency form number, if any, and the applicable component of 
the Department sponsoring the collection: Form Number: DEA Form 250. 
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: Any United States companies that desire to use any basic 
class of controlled substances listed in schedule I or II or the List I 
chemicals ephedrine, pseudoephedrine, or phenylpropanolamine for 
purposes of manufacturing during the next calendar year shall apply on 
DEA Form 250 for a procurement quota for such class.
    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, 417 respondents 
submit 2,960 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 1,480 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: January 5, 2016.
Jerri Murray,
Department Clearance Officer for PRA, U.S. Department of Justice.
[FR Doc. 2016-00234 Filed 1-8-16; 8:45 am]
BILLING CODE 4410-09-P

Document Created: 2016-01-16 01:06:30
Document Modified: 2016-01-16 01:06:30

Category		Regulatory Information
Collection		Federal Register
sudoc Class		AE 2.7: GS 4.107: AE 2.106:
Publisher		Office of the Federal Register, National Archives and Records Administration
Section		Notices
Action		60-Day notice.
Dates		Comments are encouraged and will be accepted for 60 days until March 11, 2016.
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
FR Citation		81 FR 1219