[Federal Register Volume 89, Number 130 (Monday, July 8, 2024)]
[Notices]
[Pages 55985-55986]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-14910]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-1385]


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

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

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SUMMARY: S&B Pharma LLC DBA Norac Pharma 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 
September 6, 2024. Such persons may also file a written request for a 
hearing on the application on or before September 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 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 April 30, 2024, S&B Pharma LLC DBA Norac Pharma, 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):

[[Page 55986]]



 
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        Controlled substance             Drug code         Schedule
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Gamma Hydroxybutyric Acid...........            2010  I
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    The company plans to manufacture the above listed controlled 
substance for internal research and for development purposes as part of 
the process in seeking Food and Drug Administration approval prior to 
distribution to customers. No other activity for this drug code is 
authorized for this registration.

Marsha L. Ikner,
Acting Deputy Assistant Administrator.
[FR Doc. 2024-14910 Filed 7-5-24; 8:45 am]
BILLING CODE P