[Federal Register Volume 88, Number 229 (Thursday, November 30, 2023)]
[Notices]
[Pages 83577-83578]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-26343]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-1299]


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.

[[Page 83578]]


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 29, 2024. Such persons may also file a written request for a 
hearing on the application on or before January 29, 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 October 23, 2023, 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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                                           Drug
          Controlled substance             code          Schedule
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Dimethyltryptamine.....................     7435  I
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    The company plans to bulk manufacture the listed controlled 
substance for the purpose of producing material for clinical trials. No 
other activities for this drug code are authorized for this 
registration.

Claude Redd,
Acting Deputy Assistant Administrator.
[FR Doc. 2023-26343 Filed 11-29-23; 8:45 am]
BILLING CODE 4410-09-P