Importer of Controlled Substances Application: Noramco Coventry LLC, 10389 [2022-03902]
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10389
Federal Register / Vol. 87, No. 37 / Thursday, February 24, 2022 / Notices
The company plans to bulk
manufacture the listed controlled
substances for the internal use
intermediates or for sale to its
customers. The company plans to
manufacture the above-listed controlled
substances in bulk to produce finished
dosage forms and conduct research to
develop new drug products and for
clinical studies. In reference to drug
code 7370 (Tetrahydrocannabinols), the
company plans to bulk manufacture this
drug as a synthetic. No other activities
for these drug codes are authorized for
this registration.
Matthew J. Strait,
Deputy Assistant Administrator.
[FR Doc. 2022–03897 Filed 2–23–22; 8:45 am]
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DEPARTMENT OF JUSTICE
Controlled substance
Amphetamine ..................
Methylphenidate ..............
Nabilone ..........................
Hydrocodone ...................
Levorphanol .....................
Thebaine ..........................
Alfentanil ..........................
Remifentanil .....................
Sufentanil .........................
Drug
code
Schedule
1100
1724
7379
9193
9220
9333
9737
9739
9740
II
II
II
II
II
II
II
II
II
The company plans to support its
other manufacturing facilities located in
West Deptford, New Jersey and
Conshohocken, Pennsylvania with
manufacturing and analytical testing. In
reference to drug code 9333 as bulk, the
company plans to manufacture a
Thebaine derivative for distribution to
its customers. No other activities for
these drug codes are authorized for this
registration.
Drug Enforcement Administration
Matthew J. Strait,
Deputy Assistant Administrator.
[Docket No. DEA–956]
[FR Doc. 2022–03901 Filed 2–23–22; 8:45 am]
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Bulk Manufacturer of Controlled
Substances Application: Johnson
Matthey Pharmaceutical Materials Inc.
Drug Enforcement Administration
Drug Enforcement
Administration, Justice.
AGENCY:
ACTION:
[Docket No. DEA–958]
Notice of application.
Johnson Matthey
Pharmaceutical Materials Inc. 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.
SUMMARY:
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 April 25, 2022. Such persons
may also file a written request for a
hearing on the application on or before
April 25, 2022.
DATES:
Written comments should
be sent to: Drug Enforcement
Administration, Attention: DEA Federal
Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia
22152.
ADDRESSES:
In
accordance with 21 CFR 1301.33(a), this
is notice that on November 5, 2021,
Johnson Matthey Pharmaceutical
Materials Inc., 25 Patton Road, Devens,
Massachusetts 01434, applied to be
registered as a bulk manufacturer of the
following basic class(es) of controlled
substance(s):
jspears on DSK121TN23PROD with NOTICES1
SUPPLEMENTARY INFORMATION:
VerDate Sep<11>2014
16:46 Feb 23, 2022
DEPARTMENT OF JUSTICE
Jkt 256001
Importer of Controlled Substances
Application: Noramco Coventry LLC
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
Noramco Coventry LLC 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 March 28, 2022. Such persons
may also file a written request for a
hearing on the application on or before
March 28, 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:
SUMMARY:
PO 00000
Frm 00058
Fmt 4703
Sfmt 9990
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.
In
accordance with 21 CFR 1301.34(a), this
is notice that on September 29, 2021,
Noramco Coventry LLC, 498
Washington Street, Coventry, Rhode
Island 02816, applied to be registered as
an importer of the following basic
class(es) of controlled substance(s):
SUPPLEMENTARY INFORMATION:
Controlled substance
Tetrahydrocannabinols ....
Methylphenidate ..............
Oxycodone ......................
Hydromorphone ...............
Hydrocodone ...................
Morphine ..........................
Opium, raw ......................
Oxymorphone ..................
Poppy Straw Concentrate
Drug
code
Schedule
7370
1724
9143
9150
9193
9300
9600
9652
9670
I
II
II
II
II
II
II
II
II
The company plans to import Opium,
raw (9600), and Poppy Straw
Concentrate (9670) in order to bulk
manufacture-controlled substances in
Active Pharmaceutical Ingredient (API)
form. The company will use the
imported narcotic raw materials in
ancillary activities including process
development and analytical studies.
Noramco does not anticipate
redistributing the imported narcotic raw
materials domestically to other
registered bulk manufacturers. The
company plans to import the other
listed controlled substances for internal
reference standards use 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.
Matthew J. Strait,
Deputy Assistant Administrator.
[FR Doc. 2022–03902 Filed 2–23–22; 8:45 am]
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E:\FR\FM\24FEN1.SGM
24FEN1
]]>Agencies
[Federal Register Volume 87, Number 37 (Thursday, February 24, 2022)]
[Notices]
[Page 10389]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-03902]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-958]
Importer of Controlled Substances Application: Noramco Coventry
LLC
AGENCY: Drug Enforcement Administration, Justice.
ACTION: Notice of application.
-----------------------------------------------------------------------
SUMMARY: Noramco Coventry LLC 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 March 28, 2022.
Such persons may also file a written request for a hearing on the
application on or before March 28, 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 September 29, 2021, Noramco Coventry LLC, 498
Washington Street, Coventry, Rhode Island 02816, applied to be
registered as an importer of the following basic class(es) of
controlled substance(s):
------------------------------------------------------------------------
Drug
Controlled substance code Schedule
------------------------------------------------------------------------
Tetrahydrocannabinols................... 7370 I
Methylphenidate......................... 1724 II
Oxycodone............................... 9143 II
Hydromorphone........................... 9150 II
Hydrocodone............................. 9193 II
Morphine................................ 9300 II
Opium, raw.............................. 9600 II
Oxymorphone............................. 9652 II
Poppy Straw Concentrate................. 9670 II
------------------------------------------------------------------------
The company plans to import Opium, raw (9600), and Poppy Straw
Concentrate (9670) in order to bulk manufacture-controlled substances
in Active Pharmaceutical Ingredient (API) form. The company will use
the imported narcotic raw materials in ancillary activities including
process development and analytical studies. Noramco does not anticipate
redistributing the imported narcotic raw materials domestically to
other registered bulk manufacturers. The company plans to import the
other listed controlled substances for internal reference standards use
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 non-approved finished
dosage forms for commercial sale.
Matthew J. Strait,
Deputy Assistant Administrator.
[FR Doc. 2022-03902 Filed 2-23-22; 8:45 am]
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