[Federal Register Volume 88, Number 152 (Wednesday, August 9, 2023)]
[Notices]
[Pages 53922-53923]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-17030]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-1231]


Bulk Manufacturer of Controlled Substances Application: Cambrex 
High Point, Inc.

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

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SUMMARY: Cambrex High Point, 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 
October 10, 2023. Such persons may also file a written request for a 
hearing on the application on or before October 10, 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

[[Page 53923]]

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 June 14, 2023, Cambrex High Point, Inc., 4180 
Mendenhall Oaks Parkway, High Point, North Carolina 27265-8017, applied 
to be registered as a bulk manufacturer of the following basic 
class(es) of controlled substance(s):

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         Controlled substance           Drug code         Schedule
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Oxymorphone...........................       9652  II
Noroxymorphone........................       9668  II
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    The company plans to manufacture the above listed controlled 
substances in bulk for use as internal intermediates and distribution 
to its customers. No other activities for these drug codes are 
authorized for this registration.

Claude Redd,
Acting Deputy Assistant Administrator.
[FR Doc. 2023-17030 Filed 8-8-23; 8:45 am]
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