83 FR 64369 - 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

DEPARTMENT OF JUSTICE

Federal Register Volume 83, Issue 240 (December 14, 2018)

Page Range		64369-64370
FR Document		2018-27057

The Department of Justice, Drug Enforcement Administration (DEA), will be submitting the following information collection request to the Office of Management and Budget for review and approval in accordance with the Paperwork Reduction Act of 1995.

Federal Register, Volume 83 Issue 240 (Friday, December 14, 2018)

[Federal Register Volume 83, Number 240 (Friday, December 14, 2018)]
[Notices]
[Pages 64369-64370]
From the Federal Register Online  [www.thefederalregister.org]
[FR Doc No: 2018-27057]


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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: 60-Day notice.

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SUMMARY: The Department of Justice, Drug Enforcement Administration 
(DEA), will be submitting the following information collection request 
to the Office of Management and Budget 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 
February 12, 2019.

FOR FURTHER INFORMATION CONTACT: If you have comments, especially 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 Kathy L. 
Federico, Diversion Control Division, 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 technological collection techniques or 
other forms of information technology, e.g., permitting electronic 
submission of responses.

[[Page 64370]]

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.
    3. The agency form number, if any, and the applicable component of 
the Department sponsoring the collection: DEA Form 189. The applicable 
component within the Department of Justice is the Drug Enforcement 
Administration, Diversion Control Division.
    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: Pursuant to 21 U.S.C. 826(c) and 21 CFR 1303.22 and 
1315.22, any person who is registered to manufacture any basic class of 
controlled substances listed in Schedule I or II, or the List I 
chemicals ephedrine, pseudoephedrine, or phenylpropanolamine, and who 
desires to manufacture a quantity of such class or such List I 
chemical, 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: The DEA estimates 
33 respondents complete 859 DEA Form 189 applications annually, and 
that each form takes 0.5 hours to complete.
    6. An estimate of the total public burden (in hours) associated 
with the proposed collection: The DEA estimates this collection takes a 
total of 430 annual burden hours.
    If additional information is required, please contact: Melody 
Braswell, 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: December 10, 2018.
Melody Braswell,
Department Clearance Officer for PRA, U.S. Department of Justice.
[FR Doc. 2018-27057 Filed 12-13-18; 8:45 am]
BILLING CODE 4410-09-P

Federal Register / Vol. 83, No. 240 / Friday, December 14, 2018 / Notices 64369

Evaluate whether and if so how the Act of 1993; Renewal Application for registration for that purpose. The DEA
quality, utility, and clarity of the Registration under Domestic Chemical will be revising the proposed
information proposed to be collected Diversion Control Act of 1993. information collection instruments
can be enhanced; and 3. The agency form number, if any, concerning the liability questions on the
Minimize the burden of the and the applicable component of the Application for Registration under
collection of information on those who Department sponsoring the collection: Domestic Chemical Diversion Control
are to respond, including through the DEA Forms: 510, 510A. The applicable Act of 1993; and Renewal Application
use of appropriate automated, component within the Department of for Registration under Domestic
electronic, mechanical, or other Justice is the Drug Enforcement Chemical Diversion Control Act of 1993.
technological collection techniques or Over the years, many applicants have
Administration, Diversion Control
other forms of information technology, answered some of the liability questions
Division.
e.g., permitting electronic submission of incorrectly. These changes will avoid
responses. 4. Affected public who will be asked
or required to respond, as well as a brief confusion to the applicant by separating
Overview of this information
abstract: Affected public (Primary): compound questions into multiple parts
collection:
1. Type of Information Collection: Business or other for-profit. Affected that will require the applicant to answer
Revision of a currently approved public (Other): None. Abstract: The DEA them individually.
collection. implements the Controlled Substances 5. An estimate of the total number of
2. Title of the Form/Collection: Act (CSA) which requires that every respondents and the amount of time
Application for Registration under person who manufactures or distributes estimated for an average respondent to
Domestic Chemical Diversion Control a list I chemical shall annually obtain a respond:

Number of Total annual
annual Average time per response burden hours
respondents

DEA–510 (paper) .......................................................... 6 0.20 hours (12 minutes) ............................................... 1.20
DEA–510 (electronic) ................................................... 88 0.17 hours (8 minutes) ................................................. 11.73
DEA–510A (paper) ....................................................... 28 0.2 hours (10 minutes) ................................................. 4.67
DEA–510A (electronic) ................................................. 874 0.07 hours (4 minutes) ................................................. 58.27

Total ....................................................................... 996 ....................................................................................... 76.87

6. An estimate of the total public DEPARTMENT OF JUSTICE Control Division, Drug Enforcement
burden (in hours) associated with the Administration; Mailing Address: 8701
[OMB Number 1117–0006]
proposed collection: The DEA estimates Morrissette Drive, Springfield, Virginia
that this collection takes 76.87 annual Agency Information Collection 22152; Telephone: (202) 598–6812.
burden hours. Activities; Proposed eCollection, SUPPLEMENTARY INFORMATION: Written
If additional information is required eComments Requested; Extension comments and suggestions from the
please contact: Melody Braswell, Without Change of a Previously public and affected agencies concerning
Department Clearance Officer, United Approved Collection; Application for the proposed collection of information
States Department of Justice, Justice Individual Manufacturing Quota for a are encouraged. Your comments should
Management Division, Policy and Basic Class of Controlled Substance address one or more of the following
Planning Staff, Two Constitution and for Ephedrine, Pseudoephedrine, four points:
and Phenylpropanolamine; DEA Form —Evaluate whether the proposed
Square, 145 N Street NE, Suite 3E.405B,
189 collection of information is necessary
Washington, DC 20530.
AGENCY: Drug Enforcement for the proper performance of the
Dated: December 10, 2018. functions of the agency, including
Administration, Department of Justice.
Melody Braswell, whether the information will have
ACTION: 60-Day notice.
Department Clearance Officer for PRA, U.S. practical utility;
Department of Justice. SUMMARY: The Department of Justice, —Evaluate the accuracy of the agency’s
[FR Doc. 2018–27060 Filed 12–13–18; 8:45 am] Drug Enforcement Administration estimate of the burden of the
BILLING CODE 4410–09–P (DEA), will be submitting the following proposed collection of information,
information collection request to the including the validity of the
Office of Management and Budget for methodology and assumptions used;
review and approval in accordance with —Evaluate whether and if so how the
the Paperwork Reduction Act of 1995. quality, utility, and clarity of the
DATES: Comments are encouraged and information proposed to be collected
will be accepted for 60 days until can be enhanced; and
February 12, 2019. —Minimize the burden of the collection
FOR FURTHER INFORMATION CONTACT: If of information on those who are to
amozie on DSK3GDR082PROD with NOTICES1

you have comments, especially on the respond, including through the use of
estimated public burden or associated appropriate automated, electronic,
response time, suggestions, or need a mechanical, or other technological
copy of the proposed information collection techniques or other forms
collection instrument with instructions of information technology, e.g.,
or additional information, please permitting electronic submission of
contact Kathy L. Federico, Diversion responses.

VerDate Sep<11>2014 16:57 Dec 13, 2018 Jkt 247001 PO 00000 Frm 00059 Fmt 4703 Sfmt 4703 E:\FR\FM\14DEN1.SGM 14DEN1

Document Created: 2018-12-14 03:50:38
Document Modified: 2018-12-14 03:50:38

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 February 12, 2019.
Contact		If you have comments, especially 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 Kathy L. Federico, Diversion Control Division, Drug Enforcement Administration;
FR Citation		83 FR 64369