Agency Information Collection Activities: Proposed Collection; Comments Requested; Application for Import Quota for Ephedrine, Pseudoephedrine, and Phenylpropanolamine (DEA Form 488), 54653 [2010-22384]
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Federal Register / Vol. 75, No. 173 / Wednesday, September 8, 2010 / Notices
Chelmsford, MA; Manufacturing
Techniques, Inc., Kilmarnock, VA;
QorTek, Inc., Williamsport, PA;
Resodyn Acoustic Mixers, Butte, MT;
Rockwell Collins, Cedar Rapids, IA;
Sabre Consulting and Training, LLC,
Wharton, NJ; and UTRON, Inc.,
Manassas, VA, have been added as a
party to this venture.
No other changes have been made in
either the membership or planned
activity of the group research project.
Membership in this group research
project remains open, and NWEC
intends to file additional written
notifications disclosing all changes in
membership.
On June 29, 2000, NWEC filed its
original notification pursuant to Section
6(a) of the Act. The Department of
Justice published a notice in the Federal
Register pursuant to section 6(b) of the
Act on June 30, 2000 (65 FR 40693).
The last notification was filed with
the Department on April 16, 2009. A
notice was published in the Federal
Register pursuant to section 6(b) of the
Act on May 22, 2009 (74 FR 24035).
Patricia A. Brink,
Deputy Director of Operations, Antitrust
Division.
[FR Doc. 2010–22221 Filed 9–7–10; 8:45 am]
BILLING CODE 4410–11–M
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[OMB Number 1117–0047]
Agency Information Collection
Activities: Proposed Collection;
Comments Requested; Application for
Import Quota for Ephedrine,
Pseudoephedrine, and
Phenylpropanolamine (DEA Form 488)
30-Day Notice of Information
Collection Under Review.
jlentini on DSKJ8SOYB1PROD with NOTICES
ACTION:
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 75, Number 128, Page
38834 on July 6, 2010, allowing for a 60
day comment period.
The purpose of this notice is to allow
for an additional 30 days for public
comment until October 8, 2010. This
VerDate Mar<15>2010
16:41 Sep 07, 2010
Jkt 220001
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
agency’s 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 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 Information Collection
1117–0013
(1) Type of Information Collection:
Extension of a currently approved
collection.
(2) Title of the Form/Collection:
Application for Import Quota for
Ephedrine, Pseudoephedrine, and
Phenylpropanolamine (DEA Form 488).
(3) Agency form number, if any, and
the applicable component of the
Department sponsoring the collection:
Form number: DEA Form 488, Office of
Diversion Control, Drug Enforcement
Administration, 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. 952 and 21 CFR
1315.34 require that persons who desire
to import the List I chemicals
ephedrine, pseudoephedrine, and
phenylpropanolamine during the next
PO 00000
Frm 00068
Fmt 4703
Sfmt 4703
54653
calendar year shall apply on DEA Form
488 for import quota for such List I
chemicals.
(5) An estimate of the total number of
respondents and the amount of time
estimated for an average respondent to
respond: DEA estimates that fifty-seven
(57) individual respondents will submit
eighty (80) individual import quota
applications. DEA estimates that each
response will take one hour.
(6) An estimate of the total public
burden (in hours) associated with the
collection: DEA estimates that this
collection will involve eighty (80)
annual public burden hours.
IF ADDITIONAL INFORMATION IS REQUIRED
CONTACT: Lynn Murray, Department
Clearance Officer, United States
Department of Justice, Justice
Management Division, Policy and
Planning Staff, Two Constitution
Square, 145 N Street, NE., Suite 2E–502,
Washington, DC 20530.
Dated: August 2, 2010.
Lynn Murray,
Department Clearance Officer, PRA, United
States Department of Justice.
[FR Doc. 2010–22384 Filed 9–7–10; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[OMB Number 1117–0013]
Agency Information Collection
Activities: Proposed Collection;
Comments Requested; Application for
Permit To Import Controlled
Substances for Domestic and/or
Scientific Purposes Pursuant to 21
U.S.C. 952; DEA Form 357
30-Day Notice of Information
Collection Under Review.
ACTION:
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 75, Number 128, page
38835 on July 6, 2010, allowing for a 60
day comment period.
The purpose of this notice is to allow
for an additional 30 days for public
comment until October 8, 2010. This
process is conducted in accordance with
5 CFR 1320.10.
E:\FR\FM\08SEN1.SGM
08SEN1
]]>Agencies
[Federal Register Volume 75, Number 173 (Wednesday, September 8, 2010)]
[Notices]
[Page 54653]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-22384]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[OMB Number 1117-0047]
Agency Information Collection Activities: Proposed Collection;
Comments Requested; Application for Import Quota for Ephedrine,
Pseudoephedrine, and Phenylpropanolamine (DEA Form 488)
ACTION: 30-Day Notice of Information Collection Under Review.
-----------------------------------------------------------------------
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 75, Number 128,
Page 38834 on July 6, 2010, allowing for a 60 day comment period.
The purpose of this notice is to allow for an additional 30 days
for public comment until October 8, 2010. 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 agency's 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 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 Information Collection 1117-0013
(1) Type of Information Collection: Extension of a currently
approved collection.
(2) Title of the Form/Collection: Application for Import Quota for
Ephedrine, Pseudoephedrine, and Phenylpropanolamine (DEA Form 488).
(3) Agency form number, if any, and the applicable component of the
Department sponsoring the collection: Form number: DEA Form 488, Office
of Diversion Control, Drug Enforcement Administration, 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. 952 and 21 CFR 1315.34 require that persons who
desire to import the List I chemicals ephedrine, pseudoephedrine, and
phenylpropanolamine during the next calendar year shall apply on DEA
Form 488 for import quota for such List I chemicals.
(5) An estimate of the total number of respondents and the amount
of time estimated for an average respondent to respond: DEA estimates
that fifty-seven (57) individual respondents will submit eighty (80)
individual import quota applications. DEA estimates that each response
will take one hour.
(6) An estimate of the total public burden (in hours) associated
with the collection: DEA estimates that this collection will involve
eighty (80) annual public burden hours.
IF ADDITIONAL INFORMATION IS REQUIRED CONTACT: Lynn Murray, Department
Clearance Officer, United States Department of Justice, Justice
Management Division, Policy and Planning Staff, Two Constitution
Square, 145 N Street, NE., Suite 2E-502, Washington, DC 20530.
Dated: August 2, 2010.
Lynn Murray,
Department Clearance Officer, PRA, United States Department of Justice.
[FR Doc. 2010-22384 Filed 9-7-10; 8:45 am]
BILLING CODE 4410-09-P
