[Federal Register Volume 88, Number 215 (Wednesday, November 8, 2023)]
[Notices]
[Page 77109]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-24615]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-1291]


Bulk Manufacturer of Controlled Substances Application: Curia 
Missouri, Inc.

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

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SUMMARY: Curia Missouri Inc. 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 
January 8, 2024. Such persons may also file a written request for a 
hearing on the application on or before January 8, 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 August 3, 2023, Curia Missouri Inc., 2460 West 
Bennett Street, Springfield, Missouri 65807-1229, 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
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Gamma Hydroxybutyric Acid..............    2010  I
Amphetamine............................    1100  II
Lisdexamfetamine.......................    1205  II
Methylphenidate........................    1724  II
Phenylacetone..........................    8501  II
Tapentadol.............................    9780  II
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    The company plans to bulk manufacture the listed controlled 
substances for internal use intermediates or for sale to its customers. 
No other activities for these drug codes are authorized for this 
registration.

Claude Redd,
Acting Deputy Assistant Administrator.
[FR Doc. 2023-24615 Filed 11-7-23; 8:45 am]
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