[Federal Register Volume 89, Number 88 (Monday, May 6, 2024)]
[Notices]
[Pages 37260-37261]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-09805]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-1357]


Bulk Manufacturer of Controlled Substances Application: Pharmaron 
Manufacturing Services (US) LLC

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

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SUMMARY: Pharmaron Manufacturing Services (US) 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 
July 5, 2024. Such persons may also file a written request for a 
hearing on the application on or before July 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

[[Page 37261]]

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 March 25, 2024, Pharmaron Manufacturing Services (US) 
LLC, 498 Washington Street, Coventry, Rhode Island 02816, 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 bulk manufacture the listed controlled 
substances for the purpose of producing material for clinical trials. 
No other activities for these drug codes are authorized for this 
registration.

Marsha Ikner,
Acting Deputy Assistant Administrator.
[FR Doc. 2024-09805 Filed 5-3-24; 8:45 am]
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