Granting of Requests for Early Termination of the Waiting Period Under the Premerger Notification Rules, 40210-40211 [2021-15904]
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40210
Federal Register / Vol. 86, No. 141 / Tuesday, July 27, 2021 / Notices
DEPARTMENT OF JUSTICE
Bureau of Alcohol, Tobacco, Firearms
and Explosives
[OMB 1140–0067]
Agency Information Collection
Activities; Proposed eCollection of
eComments Requested; Revision of a
Currently Approved Collection;
Licensed Firearms Manufacturers
Records of Production, Disposition,
and Supporting Data
Bureau of Alcohol, Tobacco,
Firearms and Explosives, Department of
Justice.
ACTION: 60-Day notice.
AGENCY:
The Bureau of Alcohol,
Tobacco, Firearms and Explosives
(ATF), Department of Justice (DOJ), will
submit 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 collection OMB 1140–
0067 (Licensed Firearms Manufacturers
Records of Production, Disposition, and
Supporting Data) is being revised due to
an increase in respondents, although the
total responses and burden hours have
reduced since the last renewal in 2018.
This information collection is also being
published to obtain comments from the
public and affected agencies.
DATES: Comments are encouraged and
will be accepted for 60 days until
September 27, 2021.
FOR FURTHER INFORMATION CONTACT: If
you have additional comments
regarding 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:
Dawn Smith, ATF Firearms Industry
Programs Branch, either by mail at 244
Needy Road, Martinsburg, WV 25405,
by email at fipb-informationcollection@
atf.gov, or by telephone at 202–648–
0890.
SUMMARY:
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
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SUPPLEMENTARY INFORMATION:
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17:07 Jul 26, 2021
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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 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.
Overview of This Information
Collection
1. Type of Information Collection
(check justification or form 83):
Revision of a currently approved
collection.
2. The Title of the Form/Collection:
Licensed Firearms Manufacturers
Records of Production, Disposition, and
Supporting Data.
3. The agency form number, if any,
and the applicable component of the
Department sponsoring the collection:
Form number (if applicable): None.
Component: Bureau of Alcohol,
Tobacco, Firearms and Explosives, 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 (if applicable): None.
Abstract: Firearms manufacturers
must create and maintain permanent
records of all firearms manufactured
and disposed of. These records support
the Bureau of Alcohol, Tobacco,
Firearms and Explosives’ mission to
inquire into the disposition of any
firearm, during the course of during the
course a criminal investigation.
5. An estimate of the total number of
respondents and the amount of time
estimated for an average respondent to
respond: An estimated 10,513
respondents will respond 677.12822
times per year to this information
collection, and it will take each
respondent approximately 1.06 minutes
to complete a response.
6. An estimate of the total public
burden (in hours) associated with the
collection: The estimated annual public
burden associated with this collection is
123,801 hours, which is equal to 10,513
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Fmt 4703
Sfmt 4703
(# of respondents) * 677.12822 (# of
responses per respondent) * .0176728
(1.06 minutes).
7. An Explanation of the Change in
Estimates: The increase in total
respondents by 1,457, is due to more
firearms manufacturers responding to
this collection. However, the total
responses and burdens hours decreased
by 4,378,792 and 75,4040 hours
respectively, because less firearms were
produced since the last renewal of this
collection in 2018.
If additional information is required
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, Mail Stop
3E.405A, Washington, DC 20530.
Dated: July 22, 2021.
Melody Braswell,
Department Clearance Officer for PRA, U.S.
Department of Justice.
[FR Doc. 2021–15946 Filed 7–26–21; 8:45 am]
BILLING CODE 4410–FY–P
DEPARTMENT OF JUSTICE
Antitrust Division
Granting of Requests for Early
Termination of the Waiting Period
Under the Premerger Notification
Rules
Section 7A of the Clayton Act, 15
U.S.C. 18a, as added by Title II of the
Hart-Scott-Rodino Antitrust
Improvements Act of 1976, requires
persons contemplating certain mergers
or acquisitions to give the Federal Trade
Commission and the Assistant Attorney
General advance notice and to wait
designated periods before
consummation of such plans. Section
7A(b)(2) of the Act permits the agencies,
in individual cases, to terminate this
waiting period prior to its expiration
and requires that notice of this action be
published in the Federal Register. The
following transaction was granted early
termination—on the date indicated—of
the waiting period provided by law and
the premerger notification rules. The
listing includes the transaction number
and the parties to the transaction. The
Federal Trade Commission and the
Assistant Attorney General for the
Antitrust Division of the Department of
Justice made the grants. Neither agency
intends to take any action with respect
to these proposed acquisitions during
the applicable waiting period.
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40211
Federal Register / Vol. 86, No. 141 / Tuesday, July 27, 2021 / Notices
EARLY TERMINATION GRANTED
[07/21/2021]
20211736 ........
G
Green Dot Corporation; Republic Bancorp, Inc.; Republic Bank & Trust Company.
Suzanne Morris,
Chief, Premerger and Division Statistics,
Antitrust Division, Department of Justice.
Controlled substance
Gamma Hydroxybutyric Acid ....
Lysergic Acid Diethylamide ......
[FR Doc. 2021–15904 Filed 7–26–21; 8:45 am]
Drug
code
Schedule
2010
7315
I
I
BILLING CODE 4410–11–P
The company plans to import the
above controlled substances as finished
dosage unit products for clinical trials,
research, and analytical activities. No
other activity for these drug codes is
authorized for this registration.
Approval of permit applications will
occur only when the registrant’s
business activity is consistent with what
is authorized under 21 U.S.C. 952(a)(2).
Authorization will not extend to the
import of Food and Drug
Administration-approved or nonapproved finished dosage forms for
commercial sale.
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–866]
Importer of Controlled Substances
Application: Catalent Pharma
Solutions, LLC.
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
Catalent Pharma Solutions,
LLC. has applied to be registered as an
importer of basic class(es) of controlled
substance(s). Refer to SUPPLEMENTARY
INFORMATION listed below for further
drug information.
DATES: Registered bulk manufacturers of
the affected basic class(es), and
applicants therefore, may file written
comments on or objections to the
issuance of the proposed registration on
or before August 26, 2021. Such persons
may also file a written request for a
hearing on the application on or before
August 26, 2021.
ADDRESSES: Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia
22152. All requests for a hearing must
be sent to: Drug Enforcement
Administration, Attn: Administrator,
8701 Morrissette Drive, Springfield,
Virginia 22152. All request for a hearing
should also be sent to: (1) Drug
Enforcement Administration, Attn:
Hearing Clerk/OALJ, 8701 Morrissette
Drive, Springfield, Virginia 22152; and
(2) Drug Enforcement Administration,
Attn: DEA Federal Register
Representative/DPW, 8701 Morrissette
Drive, Springfield, Virginia 22152.
SUPPLEMENTARY INFORMATION: In
accordance with 21 CFR 1301.34(a), this
is notice that on June 2, 2021, Catalent
Pharma Solutions, LLC., 3031 Red Lion
Road, Philadelphia, Pennsylvania
19114, applied to be registered as an
importer of the following basic class(es)
of controlled substance(s):
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SUMMARY:
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Brian S. Besser,
Acting Assistant Administrator.
[FR Doc. 2021–15919 Filed 7–26–21; 8:45 am]
BILLING CODE P
In
accordance with 21 CFR 1301.33(a), this
is notice that on June 17, 2021,
Novitium Pharma, LLC., 70 Lake Drive,
East Windsor, New Jersey 08520,
applied to be registered as a bulk
manufacturer of the following basic
class(es) of controlled substance(s):
SUPPLEMENTARY INFORMATION:
Controlled substance
Psilocybin ..................................
Psilocyn .....................................
Drug
code
Schedule
7347
7348
I
I
The company plans to bulk
manufacture the above controlled
substances to produce Active
Pharmaceutical Ingredient (API) and
finished dosage forms for clinical trial
purposes. No other activities for these
drug codes are authorized for this
registration.
Brian S. Besser,
Acting Assistant Administrator.
[FR Doc. 2021–15920 Filed 7–26–21; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
DEPARTMENT OF JUSTICE
[Docket No. DEA–867]
Notice of Lodging of Proposed
Consent Decree Under the Clean Water
Act
Bulk Manufacturer of Controlled
Substances Application: Novitium
Pharma, LLC
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
Novitium Pharma, LLC has
applied to be registered as a bulk
manufacturer of basic class(es) of
controlled substance(s). Refer to
SUPPLEMENTARY INFORMATION listed
below for further drug information.
DATES: Registered bulk manufacturers of
the affected basic class(es), and
applicants therefore, may file written
comments on or objections to the
issuance of the proposed registration on
or before September 27, 2021. Such
persons may also file a written request
for a hearing on the application on or
before September 27, 2021.
ADDRESS: Written comments should be
sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia
22152.
SUMMARY:
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Fmt 4703
Sfmt 4703
On July 16, 2021, the U.S. Department
of Justice (DOJ) lodged a proposed
Amendment to Consent Decree with the
United States District Court for the
Northern District of Indiana in United
States and State of Indiana v. City of
Elkhart, Indiana, Civil Action No.
2:11CV328. The lodging of the proposed
Amendment to Consent Decree, by the
United States on behalf of the U.S.
Environmental Protection Agency, with
the concurrence of the State of Indiana
on behalf of the Indiana Department of
Environmental Management, modifies
the Consent Decree in this action that
was entered by the Court on November
30, 2011.
The 2011 Consent Decree resolved
claims for civil penalties as well as
injunctive relief in the form of a Long
Term Control Plan (LTCP) for violations
of the Clean Water Act and related State
law claims in connection with the City
of Elkhart’s operation of its municipal
wastewater and sewer system. The
proposed Amendment to Consent
Decree modifies the LTCP by allowing
the City to change the technology
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]]>Agencies
[Federal Register Volume 86, Number 141 (Tuesday, July 27, 2021)]
[Notices]
[Pages 40210-40211]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-15904]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Antitrust Division
Granting of Requests for Early Termination of the Waiting Period
Under the Premerger Notification Rules
Section 7A of the Clayton Act, 15 U.S.C. 18a, as added by Title II
of the Hart-Scott-Rodino Antitrust Improvements Act of 1976, requires
persons contemplating certain mergers or acquisitions to give the
Federal Trade Commission and the Assistant Attorney General advance
notice and to wait designated periods before consummation of such
plans. Section 7A(b)(2) of the Act permits the agencies, in individual
cases, to terminate this waiting period prior to its expiration and
requires that notice of this action be published in the Federal
Register. The following transaction was granted early termination--on
the date indicated--of the waiting period provided by law and the
premerger notification rules. The listing includes the transaction
number and the parties to the transaction. The Federal Trade Commission
and the Assistant Attorney General for the Antitrust Division of the
Department of Justice made the grants. Neither agency intends to take
any action with respect to these proposed acquisitions during the
applicable waiting period.
[[Page 40211]]
Early Termination Granted
[07/21/2021]
------------------------------------------------------------------------
------------------------------------------------------------------------
20211736................... G Green Dot Corporation;
Republic Bancorp, Inc.;
Republic Bank & Trust
Company.
------------------------------------------------------------------------
Suzanne Morris,
Chief, Premerger and Division Statistics, Antitrust Division,
Department of Justice.
[FR Doc. 2021-15904 Filed 7-26-21; 8:45 am]
BILLING CODE 4410-11-P
