Bulk Manufacturer of Controlled Substances Application: Kinetochem LLC, 69070-69071 [2021-26363]
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69070
Federal Register / Vol. 86, No. 231 / Monday, December 6, 2021 / Notices
Commission’s statement on adequacy,
and any individual Commissioner’s
statements will be available from the
Office of the Secretary and at the
Commission’s website.
Authority: These reviews are being
conducted under authority of title VII of
the Tariff Act of 1930; this notice is
published pursuant to § 207.62 of the
Commission’s rules.
By order of the Commission.
Issued: November 30, 2021.
Lisa Barton,
Secretary to the Commission.
[FR Doc. 2021–26341 Filed 12–3–21; 8:45 am]
BILLING CODE 7020–02–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–935]
Importer of Controlled Substances
Application: Johnson Matthey Inc.
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
Johnson Matthey Inc., 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 January 5, 2022. Such persons
may also file a written request for a
hearing on the application on or before
January 5, 2022.
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 November 2, 2021,
Johnson Matthey Inc., 2003 Nolte Drive,
khammond on DSKJM1Z7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
20:32 Dec 03, 2021
Jkt 256001
West Deptford, New Jersey 08066–0727,
applied to be registered as an importer
of the following basic class(es) of
controlled substance(s):
Controlled substance
Coca Leaves .............................
Thebaine ...................................
Opium, raw ...............................
Noroxymorphone ......................
Poppy Straw Concentrate .........
Fentanyl ....................................
Drug
code
Schedule
9040
9333
9600
9668
9670
9801
II
II
II
II
II
II
The company plans to import Coca
Leaves (9040), Opium raw (9600) and
Poppy Straw Concentrate (9670) in
order to bulk manufacture Active
Pharmaceutical Ingredients (API) for
distribution to its customers. The
company plans to also import Thebaine
(9333), Noroxymorphone (9668) and
Fentanyl (9801) to use as analytical
reference standards, both internally and
to be sold to their customers to support
testing of Johnson Matthey Inc.’s API’s
only.
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 the Food and Drug
Administration-approved or nonapproved finished dosage forms for
commercial sale.
Brian S. Besser,
Acting Assistant Administrator.
[FR Doc. 2021–26361 Filed 12–3–21; 8:45 am]
BILLING CODE P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–936]
Importer of Controlled Substances
Application: Fisher Clinical Services,
Inc.
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 August 25, 2021, Fisher
Clinical Services, Inc., 700A–C Nestle
Way, Breinigsville, Pennsylvania
18031–1522, applied to be registered as
an importer of the following basic
class(es) of controlled substance(s):
ADDRESSES:
Controlled substance
Marihuana Extract .....................
Psilocybin ..................................
Methylphenidate ........................
Levorphanol ..............................
Noroxymorphone ......................
Tapentadol ................................
Drug
code
Schedule
7350
7437
1724
9220
9668
9780
I
I
II
II
II
II
The company plans to import the
listed controlled substances for use in
clinical trials only. 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.
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
Brian S. Besser,
Acting Assistant Administrator.
Fisher Clinical Services, Inc.,
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 January 5, 2022. Such persons
may also file a written request for a
hearing on the application on or before
January 5, 2022.
BILLING CODE 4410–09–P
AGENCY:
SUMMARY:
PO 00000
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Fmt 4703
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[FR Doc. 2021–26364 Filed 12–3–21; 8:45 am]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–934]
Bulk Manufacturer of Controlled
Substances Application: Kinetochem
LLC
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
E:\FR\FM\06DEN1.SGM
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Federal Register / Vol. 86, No. 231 / Monday, December 6, 2021 / Notices
Kinetochem 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 February 4, 2022. Such
persons may also file a written request
for a hearing on the application on or
before February 4, 2022.
ADDRESSES: Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia
22152.
SUMMARY:
In
accordance with 21 CFR 1301.33(a), this
is notice that on November 8, 2021,
Kinetochem LLC, 96 Market Street,
Suite 102, Georgetown, Texas 78626–
3618, applied to be registered as a bulk
manufacturer of the following basic
class(es) of controlled substance(s):
SUPPLEMENTARY INFORMATION:
Controlled Substance
Drug
code
Schedule
7360
7370
I
I
Marihuana .................................
Tetrahydrocannabinols .............
The company plans to bulk
manufacture the listed controlled
substances for the internal use
intermediates or for sale to its
customers. In reference to drug codes
7360 (Marihuana) and 7370
(Tetrahydrocannabinols), the company
plans to synthetically manufacture in
bulk for distribution and sale to its
customers. No other activities for these
drug codes are authorized for this
registration.
Brian S. Besser,
Acting Assistant Administrator.
[FR Doc. 2021–26363 Filed 12–3–21; 8:45 am]
BILLING CODE P
DEPARTMENT OF JUSTICE
U.S. Marshals Service
khammond on DSKJM1Z7X2PROD with NOTICES
Agency Information Collection
Activities; Proposed eCollection
eComments Requested; Extension
With Change, of a Previously
Approved Collection; Sequestered
Juror Information Form
U.S. Marshals Service,
Department of Justice.
AGENCY:
20:32 Dec 03, 2021
60-Day notice.
The Department of Justice
(DOJ), U.S. Marshals Service (USMS),
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.
DATES: Comments are encouraged and
will be accepted for 60 days until
February 4, 2022.
FOR FURTHER INFORMATION CONTACT: If
you have additional comments,
particularly with respect to the
estimated public burden or associated
response time, have suggestions, need a
copy of the proposed information
collection instrument with instructions,
or desire any additional information,
please contact Nicole Timmons either
by mail at CG–3, 10th Floor,
Washington, DC 20530–0001, by email
at Nicole.Timmons@usdoj.gov, or by
telephone at 202–236–2646.
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 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.
SUMMARY:
Jkt 256001
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Fmt 4703
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Dated: December 1, 2021.
Melody Braswell,
Department Clearance Officer for PRA, U.S.
Department of Justice.
[FR Doc. 2021–26372 Filed 12–3–21; 8:45 am]
BILLING CODE 4410–04–P
DEPARTMENT OF LABOR
Bureau of Labor Statistics
Technical Advisory Committee;
Request for Nominations
AGENCY:
Bureau of Labor Statistics
Request for nominations for
membership on the BLS Technical
Advisory Committee.
ACTION:
(1) Type of Information Collection
(check justification or form 83):
Extension with change of a currently
approved collection.
(2) The Title of the Form/Collection:
Sequestered Juror Information Form.
(3) The agency form number, if any,
and the applicable component of the
Department sponsoring the collection:
PO 00000
Form number (if applicable): Form
USM–523A.
Component: United States Marshals
Service, U.S. Department of Justice.
(4) Affected public who will be asked
or required to respond, as well as a brief
abstract: Primary: Households/
individuals.
Abstract: The United States Marshals
Service is responsible for ensuring the
security of federal courthouses,
courtrooms, and federal jurist. This
information assists Marshals Service
personnel in the planning of, and
response to, potential security needs of
the court and jurors during the course
of proceedings. The authority for
collecting the information on this form
is 28 U.S.C. 509, 510 and 561 et seq.
(5) An estimate of the total number of
respondents and the amount of time
estimated for an average respondent to
respond: An estimated 14 respondents
will utilize the form, and it will take
each respondent approximately 4
minutes to complete the form.
(6) An estimate of the total public
burden (in hours) associated with the
collection: The estimated annual public
burden associated with this collection is
1 hour, which is equal to (14 (total # of
annual responses) * 4 minutes = 56
minutes or 1 hour).
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, 3E.405A,
Washington, DC 20530.
(BLS).
Overview of This Information
Collection
[OMB Number 1105–0096]
VerDate Sep<11>2014
ACTION:
69071
The BLS is soliciting new
members for the Technical Advisory
Committee (TAC) to address six member
terms expiring on April 11, 2022, and
any vacancy that may occur on the TAC
between the date of publication of this
notice and April 11, 2022.
SUMMARY:
E:\FR\FM\06DEN1.SGM
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]]>Agencies
[Federal Register Volume 86, Number 231 (Monday, December 6, 2021)]
[Notices]
[Pages 69070-69071]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-26363]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-934]
Bulk Manufacturer of Controlled Substances Application:
Kinetochem LLC
AGENCY: Drug Enforcement Administration, Justice.
ACTION: Notice of application.
-----------------------------------------------------------------------
[[Page 69071]]
SUMMARY: Kinetochem 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 February 4,
2022. Such persons may also file a written request for a hearing on the
application on or before February 4, 2022.
ADDRESSES: Written comments should be sent to: Drug Enforcement
Administration, Attention: DEA Federal Register Representative/DPW,
8701 Morrissette Drive, Springfield, Virginia 22152.
SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.33(a), this
is notice that on November 8, 2021, Kinetochem LLC, 96 Market Street,
Suite 102, Georgetown, Texas 78626-3618, applied to be registered as a
bulk manufacturer of the following basic class(es) of controlled
substance(s):
------------------------------------------------------------------------
Drug
Controlled Substance code Schedule
------------------------------------------------------------------------
Marihuana............................... 7360 I
Tetrahydrocannabinols................... 7370 I
------------------------------------------------------------------------
The company plans to bulk manufacture the listed controlled
substances for the internal use intermediates or for sale to its
customers. In reference to drug codes 7360 (Marihuana) and 7370
(Tetrahydrocannabinols), the company plans to synthetically manufacture
in bulk for distribution and sale to its customers. No other activities
for these drug codes are authorized for this registration.
Brian S. Besser,
Acting Assistant Administrator.
[FR Doc. 2021-26363 Filed 12-3-21; 8:45 am]
BILLING CODE P
