[Federal Register Volume 88, Number 37 (Friday, February 24, 2023)]
[Notices]
[Pages 11955-11956]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-03827]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-1151]


Bulk Manufacturer of Controlled Substances Application: S&B 
Pharma LLC

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

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[[Page 11956]]

SUMMARY: S&B Pharma 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 
April 25, 2023. Such persons may also file a written request for a 
hearing on the application on or before April 25, 2023.

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.

SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.33(a), this 
is notice that on January 10, 2023, S&B Pharma LLC, 405 South Motor 
Avenue, Azusa, California 91702, applied to be registered as a bulk 
manufacturer of the following basic class(es) of controlled 
substance(s):

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                                           Drug
          Controlled substance             code          Schedule
------------------------------------------------------------------------
Marihuana..............................     7360  I
Tetrahydrocannabinols..................     7370  I
Amphetamine............................     1100  II
Methamphetamine........................     1105  II
Lisdexamfetamine.......................     1205  II
Methylphenidate........................     1724  II
Pentobarbital..........................     2270  II
4-Anilino-N-Phenethyl-4-Piperidine          8333  II
 (ANPP).
Tapentadol.............................     9780  II
Fentanyl...............................     9801  II
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    The company plans to bulk manufacture the listed controlled 
substances for the internal use intermediates for formulation and 
analytical development purposes or for sale to its customers. In 
reference to drug codes 7360 (Marihuana), and 7370 
(Tetrahydrocannabinols), the company plans to bulk manufacture these 
drugs as synthetic. No other activities for these drug codes are 
authorized for this registration.

Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2023-03827 Filed 2-23-23; 8:45 am]
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