Importer of Controlled Substances Application: Sigma Aldrich Company LLC, 16030 [2024-04756]

Download as PDF 16030 Federal Register / Vol. 89, No. 45 / Wednesday, March 6, 2024 / Notices to be registered as an importer of the following basic class(es) of controlled substance(s): Controlled substance Dimethyltryptamine .......... Cocaine ........................... Methadone ...................... I Drug code Schedule 7435 9041 9250 I II II I The company plans to import the listed controlled substances for clinical trials. No other activities for these drug codes are 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. Marsha L. Ikner, Acting Deputy Assistant Administrator. [FR Doc. 2024–04753 Filed 3–5–24; 8:45 am] BILLING CODE P DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 February 7, 2024, Sigma Aldrich Company 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: Controlled substance [Docket No. DEA–1332] Importer of Controlled Substances Application: Sigma Aldrich Company LLC Drug Enforcement Administration, Justice. ACTION: Notice of application. AGENCY: Sigma Aldrich Company 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 submit electronic comments on or objections to the issuance of the proposed registration on or before April 5, 2024. Such persons may also file a written request for a hearing on the application on or before April 5, 2024. ADDRESSES: The Drug Enforcement Administration 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 ddrumheller on DSK120RN23PROD with NOTICES1 SUMMARY: VerDate Sep<11>2014 16:57 Mar 05, 2024 Jkt 262001 Cathinone ........................ Methcathinone ................. Mephedrone (4-Methyl-Nmethylcathinone). Gamma Hydroxybutyric Acid. Tetrahydrocannabinols .... 4-Bromo-2,5dimethoxyamphetamine. 4-Bromo-2,5dimethoxyphenethylamine. 2,5Dimethoxyamphetamine. 3,4Methylenedioxyamphetamine. 3,4-Methylenedioxy-Nethylamphetamine. 3,4Methylenedioxymethamphetamine. 4-Methoxyamphetamine .. Dimethyltryptamine .......... N-Benzylpiperazine ......... Heroin .............................. Normorphine .................... Amobarbital ..................... Secobarbital ..................... Nabilone .......................... Phencyclidine .................. Ecgonine .......................... Ethylmorphine .................. Levorphanol ..................... Meperidine ....................... Thebaine .......................... Opium, powdered ............ PO 00000 Frm 00062 Fmt 4703 Drug code Schedule 1235 1237 1248 I I I 2010 I 7370 7391 I I 7392 I 7396 I 7400 I 7404 I 7405 I 7411 7435 7493 9200 9313 2125 2315 7379 7471 9180 9190 9220 9230 9333 9639 I I I I I II II II II II II II II II II Sfmt 4703 Controlled substance Levo-alphacetylmethadol Drug code Schedule I 9648 III 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 activities for these drug codes are 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. Marsha Ikner, Acting Deputy Assistant Administrator. [FR Doc. 2024–04756 Filed 3–5–24; 8:45 am] BILLING CODE P DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–1328] Bulk Manufacturer of Controlled Substances Application: Sterling Pharma USA LLC Drug Enforcement Administration, Justice. ACTION: Notice of application. AGENCY: Sterling Pharma USA 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 submit electronic comments on or objections to the issuance of the proposed registration on or before May 6, 2024. Such persons may also file a written request for a hearing on the application on or before May 6, 2024. ADDRESSES: The Drug Enforcement Administration 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 SUMMARY: E:\FR\FM\06MRN1.SGM 06MRN1

Agencies

[Federal Register Volume 89, Number 45 (Wednesday, March 6, 2024)]
[Notices]
[Page 16030]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-04756]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-1332]


Importer of Controlled Substances Application: Sigma Aldrich 
Company LLC

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

-----------------------------------------------------------------------

SUMMARY: Sigma Aldrich Company 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 submit electronic comments on or 
objections to the issuance of the proposed registration on or before 
April 5, 2024. Such persons may also file a written request for a 
hearing on the application on or before April 5, 2024.

ADDRESSES: The Drug Enforcement Administration 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 February 7, 2024, Sigma Aldrich Company 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):

------------------------------------------------------------------------
                                           Drug
          Controlled substance             code          Schedule
------------------------------------------------------------------------
Cathinone...............................    1235  I
Methcathinone...........................    1237  I
Mephedrone (4-Methyl-N-methylcathinone).    1248  I
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
------------------------------------------------------------------------

    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 activities for these drug 
codes are 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.

Marsha Ikner,
Acting Deputy Assistant Administrator.
[FR Doc. 2024-04756 Filed 3-5-24; 8:45 am]
BILLING CODE P
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