[Federal Register Volume 90, Number 57 (Wednesday, March 26, 2025)]
[Notices]
[Page 13782]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2025-05055]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-1512]
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
May 27, 2025. Such persons may also file a written request for a
hearing on the application on or before May 27, 2025.
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 February 11, 2025, 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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Dimethyltryptamine.................... 7435 I
Oxymorphone........................... 9652 II
Noroxymorphone........................ 9668 II
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The company plans to bulk manufacture the listed controlled
substances to produce material for clinical trials. No other activities
for these drug codes are authorized for this registration.
Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2025-05055 Filed 3-25-25; 8:45 am]
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