Importer of Controlled Substances Application: Sigma Aldrich Co. LLC, 14291-14292 [2022-05318]
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14291
Federal Register / Vol. 87, No. 49 / Monday, March 14, 2022 / Notices
Morrissette Drive, Springfield, Virginia
22152; and (2) Drug Enforcement
Administration, Attn: DEA Federal
Register Representative/DPW, 8701
Morrissette Drive, Springfield, Virginia
22152. All requests for a hearing should
also be sent to: Drug Enforcement
Administration, Attn: Administrator,
8701 Morrissette Drive, Springfield,
Virginia 22152.
In
accordance with 21 CFR 1301.34(a), this
is notice that on February 2, 2022,
Meridian Medical Technologies, LLC,
2555 Hermelin Drive, Saint Louis,
Missouri 63144, applied to be registered
as an importer of the following basic
class(es) of controlled substance(s):
SUPPLEMENTARY INFORMATION:
Controlled substance
Morphine .........................
Drug
code
Schedule
9300
II
The company plans to import the
control substance for analytical and
research purposes. No other activity for
this drug code 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. 2022–05291 Filed 3–11–22; 8:45 am]
BILLING CODE 4410–09–P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–981]
Importer of Controlled Substances
Application: Sigma Aldrich Co. LLC
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
Sigma Aldrich Co. 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 submit
electronic comments on or objections to
the issuance of the proposed registration
on or before April 13, 2022. Such
persons may also file a written request
for a hearing on the application on or
before April 13, 2022.
ADDRESSES: DEA requires that all
comments be submitted electronically
through the Federal eRulemaking Portal,
SUMMARY:
which provides the ability to type short
comments directly into the comment
field on the web page or attach a file for
lengthier comments. Please go to
https://www.regulations.gov and follow
the online instructions at that site for
submitting comments. Upon submission
of your comment, you will receive a
Comment Tracking Number. Please be
aware that submitted comments are not
instantaneously available for public
view on https://www.regulations.gov. If
you have received a Comment Tracking
Number, your comment has been
successfully submitted and there is no
need to resubmit the same comment. All
requests for a hearing must 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. All requests for a hearing should
also be sent to: Drug Enforcement
Administration, Attn: Administrator,
8701 Morrissette Drive, Springfield,
Virginia 22152.
In
accordance with 21 CFR 1301.34(a), this
is notice that on January 21, 2022,
Sigma Aldrich Co. LLC, 3500 Dekalb
Street, Saint Louis, Missouri 63118–
4103, applied to be registered as an
importer of the following basic class(es)
of controlled substance(s):
SUPPLEMENTARY INFORMATION:
jspears on DSK121TN23PROD with NOTICES1
Controlled substance
Drug code
Cathinone ...............................................................................................................................................................................
Methcathinone ........................................................................................................................................................................
Mephedrone (4-Methyl-N-methylcathinone) ...........................................................................................................................
Gamma Hydroxybutyric Acid ..................................................................................................................................................
Tetrahydrocannabinols ...........................................................................................................................................................
4-Bromo-2,5-dimethoxyamphetamine ....................................................................................................................................
4-Bromo-2,5-dimethoxyphenethylamine .................................................................................................................................
2,5-Dimethoxyamphetamine ...................................................................................................................................................
3,4-Methylenedioxyamphetamine ...........................................................................................................................................
3,4-Methylenedioxy-N-ethylamphetamine ..............................................................................................................................
3,4-Methylenedioxymethamphetamine ...................................................................................................................................
4-Methoxyamphetamine .........................................................................................................................................................
Dimethyltryptamine .................................................................................................................................................................
N-Benzylpiperazine ................................................................................................................................................................
Heroin .....................................................................................................................................................................................
Normorphine ...........................................................................................................................................................................
Amobarbital ............................................................................................................................................................................
Secobarbital ............................................................................................................................................................................
Nabilone .................................................................................................................................................................................
Phencyclidine .........................................................................................................................................................................
Ecgonine .................................................................................................................................................................................
Ethylmorphine .........................................................................................................................................................................
Levorphanol ............................................................................................................................................................................
Meperidine ..............................................................................................................................................................................
Thebaine .................................................................................................................................................................................
Opium, powdered ...................................................................................................................................................................
Levo-alphacetylmethadol ........................................................................................................................................................
VerDate Sep<11>2014
17:51 Mar 11, 2022
Jkt 256001
PO 00000
Frm 00055
Fmt 4703
Sfmt 4703
E:\FR\FM\14MRN1.SGM
14MRN1
1235
1237
1248
2010
7370
7391
7392
7396
7400
7404
7405
7411
7435
7493
9200
9313
2125
2315
7379
7471
9180
9190
9220
9230
9333
9639
9648
Schedule
I
I
I
I
I
I
I
I
I
I
I
I
I
I
I
I
II
II
II
II
II
II
II
II
II
II
II
14292
Federal Register / Vol. 87, No. 49 / Monday, March 14, 2022 / Notices
The company plans to import the
listed controlled substances for sale to
research facilities for drug testing and
analysis. In reference to drug code 7370
(Tetrahydrocannabinols) the company
plans to import synthetic
Tetrahydrocannabinols. No other
activity for this drug code 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. 2022–05318 Filed 3–11–22; 8:45 am]
BILLING CODE P
successfully submitted and there is no
need to resubmit the same comment. All
requests for a hearing must 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. All requests for a hearing should
also be sent to: Drug Enforcement
Administration, Attn: Administrator,
8701 Morrissette Drive, Springfield,
Virginia 22152.
SUPPLEMENTARY INFORMATION: In
accordance with 21 CFR 1301.34(a), this
is notice that on February 7, 2022,
Perkinelmer, Inc., 120 East Dedham
Street, Boston, Massachusetts 02118–
2852, applied to be registered as an
importer of the following basic class(es)
of controlled substance(s):
Controlled substance
DEPARTMENT OF JUSTICE
Lysergic Acid Diethylamide ......
Thebaine ...................................
Drug Enforcement Administration
[Docket No. DEA–977]
Importer of Controlled Substances
Application: Perkinelmer, Inc.
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
Perkinelmer, Inc. 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 submit
electronic comments on or objections to
the issuance of the proposed registration
on or before April 13, 2022. Such
persons may also file a written request
for a hearing on the application on or
before April 13, 2022.
ADDRESSES: The DEA requires that all
comments be submitted electronically
through the Federal eRulemaking Portal,
which provides the ability to type short
comments directly into the comment
field on the web page or attach a file for
lengthier comments. Please go to
https://www.regulations.gov and follow
the online instructions at that site for
submitting comments. Upon submission
of your comment, you will receive a
Comment Tracking Number. Please be
aware that submitted comments are not
instantaneously available for public
view on https://www.regulations.gov. If
you have received a Comment Tracking
Number, your comment has been
jspears on DSK121TN23PROD with NOTICES1
SUMMARY:
VerDate Sep<11>2014
17:51 Mar 11, 2022
Jkt 256001
Drug
code
Schedule
7315
9333
I
II
The company plans to import the
listed controlled substances for bulk
manufacturing into radioactive
formulations for sale to its customers for
research purposes. Drug code 9333
(Thebaine) will be used to import the
Thebaine derivative Diprenorphine. 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. 2022–05308 Filed 3–11–22; 8:45 am]
BILLING CODE P
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA–983]
Bulk Manufacturer of Controlled
Substances Application: Bulk
Manufacturer of Marihuana:
Agriculture Technology Institute, LLC
Drug Enforcement
Administration, Justice.
ACTION: Notice of application.
AGENCY:
The Drug Enforcement
Administration (DEA) is providing
SUMMARY:
PO 00000
Frm 00056
Fmt 4703
Sfmt 4703
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 therefore, may submit
electronic comments on or objections to
the issuance of the proposed registration
on or before May 13, 2022.
ADDRESSES: DEA requires that all
comments be submitted electronically
through the Federal eRulemaking Portal,
which provides the ability to type short
comments directly into the comment
field on the web page or attach a file for
lengthier comments. Please go to
https://www.regulations.gov and follow
the online instructions at that site for
submitting comments. Upon submission
of your comment, you will receive a
Comment Tracking Number. Please be
aware that submitted comments are not
instantaneously available for public
view on https://www.regulations.gov. If
you have received a Comment Tracking
Number, your comment has been
successfully submitted and there is no
need to resubmit the same comment.’’
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
submit electronic 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
E:\FR\FM\14MRN1.SGM
14MRN1
]]>Agencies
[Federal Register Volume 87, Number 49 (Monday, March 14, 2022)]
[Notices]
[Pages 14291-14292]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-05318]
-----------------------------------------------------------------------
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-981]
Importer of Controlled Substances Application: Sigma Aldrich Co.
LLC
AGENCY: Drug Enforcement Administration, Justice.
ACTION: Notice of application.
-----------------------------------------------------------------------
SUMMARY: Sigma Aldrich Co. 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 submit electronic comments on or
objections to the issuance of the proposed registration on or before
April 13, 2022. Such persons may also file a written request for a
hearing on the application on or before April 13, 2022.
ADDRESSES: DEA requires that all comments be submitted electronically
through the Federal eRulemaking Portal, which provides the ability to
type short comments directly into the comment field on the web page or
attach a file for lengthier comments. Please go to https://www.regulations.gov and follow the online instructions at that site for
submitting comments. Upon submission of your comment, you will receive
a Comment Tracking Number. Please be aware that submitted comments are
not instantaneously available for public view on https://www.regulations.gov. If you have received a Comment Tracking Number,
your comment has been successfully submitted and there is no need to
resubmit the same comment. All requests for a hearing must 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. All requests
for a hearing should also be sent to: Drug Enforcement Administration,
Attn: Administrator, 8701 Morrissette Drive, Springfield, Virginia
22152.
SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.34(a), this
is notice that on January 21, 2022, Sigma Aldrich Co. LLC, 3500 Dekalb
Street, Saint Louis, Missouri 63118-4103, applied to be registered as
an importer of the following basic class(es) of controlled
substance(s):
------------------------------------------------------------------------
Controlled substance Drug code Schedule
------------------------------------------------------------------------
Cathinone............................. 1235 I
Methcathinone......................... 1237 I
Mephedrone (4-Methyl-N- 1248 I
methylcathinone).
Gamma Hydroxybutyric Acid............. 2010 I
Tetrahydrocannabinols................. 7370 I
4-Bromo-2,5-dimethoxyamphetamine...... 7391 I
4-Bromo-2,5-dimethoxyphenethylamine... 7392 I
2,5-Dimethoxyamphetamine.............. 7396 I
3,4-Methylenedioxyamphetamine......... 7400 I
3,4-Methylenedioxy-N-ethylamphetamine. 7404 I
3,4-Methylenedioxymethamphetamine..... 7405 I
4-Methoxyamphetamine.................. 7411 I
Dimethyltryptamine.................... 7435 I
N-Benzylpiperazine.................... 7493 I
Heroin................................ 9200 I
Normorphine........................... 9313 I
Amobarbital........................... 2125 II
Secobarbital.......................... 2315 II
Nabilone.............................. 7379 II
Phencyclidine......................... 7471 II
Ecgonine.............................. 9180 II
Ethylmorphine......................... 9190 II
Levorphanol........................... 9220 II
Meperidine............................ 9230 II
Thebaine.............................. 9333 II
Opium, powdered....................... 9639 II
Levo-alphacetylmethadol............... 9648 II
------------------------------------------------------------------------
[[Page 14292]]
The company plans to import the listed controlled substances for
sale to research facilities for drug testing and analysis. In reference
to drug code 7370 (Tetrahydrocannabinols) the company plans to import
synthetic Tetrahydrocannabinols. No other activity for this drug code
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. 2022-05318 Filed 3-11-22; 8:45 am]
BILLING CODE P
