Bulk Manufacturer of Controlled Substances Application: Bulk Manufacturer of Marihuana: Natural Fulfillment LLC, 2458-2459 [2021-00327]
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2458
Federal Register / Vol. 86, No. 7 / Tuesday, January 12, 2021 / Notices
Controlled substance
Drug code
Morphine ..........................................................................................................................................................................
The company plans to synthesize the
above listed control substances for
distribution to its customers. In
reference to drug codes 7360
(Marihuana) and 7370
(Tetrahydrocannabinol), the company
plans to bulk manufacture these drugs
as synthetics. No other activity for these
drug codes are authorized for this
registration.
William T. McDermott,
Assistant Administrator.
In
accordance with 21 CFR 1301.34(a), this
is notice that on August 25, 2020, S&B
Pharma LLC, dba: Norac Pharma, 405
South Motor Avenue, Azusa, California
91702, applied to be registered as an
importer of the following basic class(es)
of controlled substance(s):
SUPPLEMENTARY INFORMATION:
Drug
code
Controlled substance
4-Anilino-N-phenethyl-4piperidine (ANPP).
Tapentadol ....................
[FR Doc. 2021–00356 Filed 1–11–21; 8:45 am]
Schedule
8333
II
9780
II
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–762]
Importer of Controlled Substances
Application: S&B Pharma LLC dba
Norac Pharma
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
S&B Pharma LLC, dba: Norac
Pharma has applied to be registered as
an importer of basic class(es) of
controlled substance(s). Refer to
Supplemental 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 11, 2021. Such
persons may also file a written request
for a hearing on the application on or
before February 11, 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 requests 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.
khammond on DSKJM1Z7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:09 Jan 11, 2021
Jkt 253001
The company plans to import the
listed controlled substances in bulk for
the manufacture of controlled
substances for distribution to its
customers. 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.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2021–00326 Filed 1–11–21; 8:45 am]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–764]
Bulk Manufacturer of Controlled
Substances Application: Siegfried
USA, LLC
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
9300
Schedule
II
hearing on the application on or before
March 15, 2021.
ADDRESSES: Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia
22152.
In
accordance with 21 CFR 1301.33(a), this
is notice that on December 9, 2020,
Siegfried USA, LLC, 33 Industrial Park
Road, Pennsville, New Jersey 08070–
3244, applied to be registered as an bulk
manufacturer of the following basic
class(es) of controlled substance(s):
SUPPLEMENTARY INFORMATION:
Controlled substance
Gamma Hydroxybutyric
Acid.
Amphetamine ...............
Methylphenidate ...........
Amobarbital ..................
Pentobarbital ................
Secobarbital ..................
Codeine ........................
Oxycodone ...................
Hydromorphone ............
Hydrocodone ................
Methadone ....................
Methadone intermediate
Morphine .......................
Oripavine ......................
Thebaine .......................
Opium tincture ..............
Oxymorphone ...............
Tapentadol ....................
Drug
code
Schedule
2010
I
1100
1724
2125
2270
2315
9050
9143
9150
9193
9250
9254
9300
9330
9333
9630
9652
9780
II
II
II
II
II
II
II
II
II
II
II
II
II
II
II
II
II
The company plans to bulk
manufacture the listed controlled
substances in bulk for sale to its
customers. No other activities for these
drug codes are authorized for this
registration.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2021–00354 Filed 1–11–21; 8:45 am]
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Siegfried USA, LLC has
applied to be registered as a bulk
manufacturer of basic class(es) of
controlled substance(s). Refer to
Supplemental 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 March 15, 2021. Such persons
may also file a written request for a
SUMMARY:
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Frm 00079
Fmt 4703
Sfmt 4703
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–760]
Bulk Manufacturer of Controlled
Substances Application: Bulk
Manufacturer of Marihuana: Natural
Fulfillment LLC
Drug Enforcement
Administration, Justice.
AGENCY:
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Federal Register / Vol. 86, No. 7 / Tuesday, January 12, 2021 / Notices
ACTION:
Notice of application.
The Drug Enforcement
Administration (DEA) is providing
notice of an application it has received
from an entity applying to be registered
to manufacture in bulk basic class(es) of
controlled substances listed in schedule
I. DEA intends to evaluate this and other
pending applications according to its
regulations governing the program of
growing marihuana for scientific and
medical research under DEA
registration.
DATES: Registered bulk manufacturers of
the affected basic class(es), and
applicants therefor, may file written
comments on or objections to the
issuance of the proposed registration on
or before March 15, 2021.
ADDRESSES: Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/DPW 8701
Morrissette Drive, Springfield, Virginia
22152. To ensure proper handling of
comments, please reference Docket
No—DEA–760 in all correspondence,
including attachments.
SUPPLEMENTARY INFORMATION: The
Controlled Substances Act (CSA)
prohibits the cultivation and
distribution of marihuana except by
persons who are registered under the
CSA to do so for lawful purposes. In
accordance with the purposes specified
in 21 CFR 1301.33(a), DEA is providing
notice that the entity identified below
has applied for registration as a bulk
manufacturer of schedule I controlled
substances. In response, registered bulk
manufacturers of the affected basic
class(es), and applicants therefor, may
file written comments on or objections
of the requested registration, as
provided in this notice. This notice does
not constitute any evaluation or
determination of the merits of the
application submitted.
The applicant plans to manufacture
bulk active pharmaceutical ingredients
(APIs) for product development and
distribution to DEA registered
researchers. If the application for
registration is granted, the registrant
would not be authorized to conduct
other activity under this registration
aside from those coincident activities
specifically authorized by DEA
regulations. DEA will evaluate the
application for registration as a bulk
manufacturer for compliance with all
applicable laws, treaties, and
regulations and to ensure adequate
safeguards against diversion are in
place.
As this applicant has applied to
become registered as a bulk
khammond on DSKJM1Z7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
17:09 Jan 11, 2021
Jkt 253001
manufacturer of marihuana, the
application will be evaluated under the
criteria of 21 U.S.C. 823(a). DEA will
conduct this evaluation in the manner
described in the rule published at 85 FR
82333 on December 18, 2020, and
reflected in DEA regulations at 21 CFR
part 1318.
In accordance with 21 CFR
1301.33(a), DEA is providing notice that
on December 1, 2020, Natural
Fulfillment LLC, 5495 North Academy
Boulevard, Colorado Springs, Colorado
80918, applied to be registered as a bulk
manufacturer of the following basic
class(es) of controlled substances:
Controlled
substance
Drug
code
Marihuana .................
7360
Schedule
I
William T. McDermott,
Assistant Administrator.
[FR Doc. 2021–00327 Filed 1–11–21; 8:45 am]
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NATIONAL SCIENCE FOUNDATION
Notice of Open to the Public Meetings
of the Networking and Information
Technology Research and
Development (NITRD) Program
Networking and Information
Technology Research and Development
(NITRD) National Coordination Office
(NCO), National Science Foundation.
ACTION: Notice of public meetings.
AGENCY:
The NITRD Program holds
meetings that are open to the public to
attend. The Joint Engineering Team
(JET) and Middleware And Grid
Interagency Coordination (MAGIC)
Team provide an opportunity for the
public to engage and participate in
information sharing with Federal
agencies. The JET and MAGIC Teams
report to the NITRD Large Scale
Networking (LSN) Interagency Working
Group (IWG).
DATES: January 2021–December 2021.
FOR FURTHER INFORMATION CONTACT:
NITRD NCO at admin@nitrd.gov.
Individuals who use a
telecommunications device for the deaf
(TDD) may call the Federal Information
Relay Service (FIRS) at 1–800–877–8339
between 8 a.m. and 8 p.m., Eastern time,
Monday through Friday.
SUPPLEMENTARY INFORMATION: The Joint
Engineering Team (JET), established in
1997, provides an opportunity for
information sharing among Federal
agencies and non-Federal participants
who have an interest in highSUMMARY:
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Fmt 4703
Sfmt 4703
2459
performance research and engineering
or research and education (REN)
networking and networking to support
science applications.
The MAGIC Team, established in
2002, provides for information sharing
among Federal agencies and nonFederal participants with interests and
responsibility for middleware, Grid, and
cloud projects; individuals involved in
middleware, Grid, and cloud research
and infrastructure; individuals involved
in implementing or operating Grids and
clouds; and users of Grids, clouds and
middleware. The JET and MAGIC Team
meetings are hosted by the NITRD NCO
with WebEx and/or teleconference
participation available for each meeting.
Public Meetings Website: The JET and
MAGIC Team meetings are scheduled
30 days in advance of the meeting date.
Please reference the NITRD Public
Meetings web page (https://
www.nitrd.gov/meetings/public/) for
each Team’s upcoming meeting dates
and times, in addition to the agendas,
minutes, and other meeting materials
and information.
Public Meetings Mailing Lists:
Members of the public may be added to
the mailing lists by sending their full
name and email address to jet-signup@
nitrd.gov for JET and magic-signup@
nitrd.gov for MAGIC, with the subject
line: ‘‘Add to JET’’ and/or ‘‘Add to
MAGIC.’’ Meeting notifications and
information are shared via the mailing
lists.
Public Comments: The government
seeks individual input; attendees/
participants may provide individual
advice only. Members of the public are
welcome to submit their comments for
JET to jet-comments@nitrd.gov and for
MAGIC to magic-comments@nitrd.gov.
Please note that under the provisions of
the Federal Advisory Committee Act
(FACA), all public comments and/or
presentations will be treated as public
documents and may be made available
to the public via the JET and MAGIC
web pages.
Reference Website: NITRD website at:
https://www.nitrd.gov/.
Submitted by the National Science
Foundation in support of the
Networking and Information
Technology Research and Development
(NITRD) National Coordination Office
(NCO) on January 6, 2021.
Suzanne H. Plimpton,
Reports Clearance Officer, National Science
Foundation.
[FR Doc. 2021–00365 Filed 1–11–21; 8:45 am]
BILLING CODE 7555–01–P
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Agencies
[Federal Register Volume 86, Number 7 (Tuesday, January 12, 2021)]
[Notices]
[Pages 2458-2459]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-00327]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-760]
Bulk Manufacturer of Controlled Substances Application: Bulk
Manufacturer of Marihuana: Natural Fulfillment LLC
AGENCY: Drug Enforcement Administration, Justice.
[[Page 2459]]
ACTION: Notice of application.
-----------------------------------------------------------------------
SUMMARY: The Drug Enforcement Administration (DEA) is providing notice
of an application it has received from an entity applying to be
registered to manufacture in bulk basic class(es) of controlled
substances listed in schedule I. DEA intends to evaluate this and other
pending applications according to its regulations governing the program
of growing marihuana for scientific and medical research under DEA
registration.
DATES: Registered bulk manufacturers of the affected basic class(es),
and applicants therefor, may file written comments on or objections to
the issuance of the proposed registration on or before March 15, 2021.
ADDRESSES: Written comments should be sent to: Drug Enforcement
Administration, Attention: DEA Federal Register Representative/DPW 8701
Morrissette Drive, Springfield, Virginia 22152. To ensure proper
handling of comments, please reference Docket No--DEA-760 in all
correspondence, including attachments.
SUPPLEMENTARY INFORMATION: The Controlled Substances Act (CSA)
prohibits the cultivation and distribution of marihuana except by
persons who are registered under the CSA to do so for lawful purposes.
In accordance with the purposes specified in 21 CFR 1301.33(a), DEA is
providing notice that the entity identified below has applied for
registration as a bulk manufacturer of schedule I controlled
substances. In response, registered bulk manufacturers of the affected
basic class(es), and applicants therefor, may file written comments on
or objections of the requested registration, as provided in this
notice. This notice does not constitute any evaluation or determination
of the merits of the application submitted.
The applicant plans to manufacture bulk active pharmaceutical
ingredients (APIs) for product development and distribution to DEA
registered researchers. If the application for registration is granted,
the registrant would not be authorized to conduct other activity under
this registration aside from those coincident activities specifically
authorized by DEA regulations. DEA will evaluate the application for
registration as a bulk manufacturer for compliance with all applicable
laws, treaties, and regulations and to ensure adequate safeguards
against diversion are in place.
As this applicant has applied to become registered as a bulk
manufacturer of marihuana, the application will be evaluated under the
criteria of 21 U.S.C. 823(a). DEA will conduct this evaluation in the
manner described in the rule published at 85 FR 82333 on December 18,
2020, and reflected in DEA regulations at 21 CFR part 1318.
In accordance with 21 CFR 1301.33(a), DEA is providing notice that
on December 1, 2020, Natural Fulfillment LLC, 5495 North Academy
Boulevard, Colorado Springs, Colorado 80918, applied to be registered
as a bulk manufacturer of the following basic class(es) of controlled
substances:
------------------------------------------------------------------------
Controlled substance Drug code Schedule
------------------------------------------------------------------------
Marihuana............................. 7360 I
------------------------------------------------------------------------
William T. McDermott,
Assistant Administrator.
[FR Doc. 2021-00327 Filed 1-11-21; 8:45 am]
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