Notice2025-06707

Bulk Manufacturer of Controlled Substances Application: Patheon API Services Inc.

Primary source

Metadata and text below are from the Federal Register, a public-domain U.S. government work. Always verify the official published version before relying on it for any legal matter.

Published
April 18, 2025

Issuing agencies

Justice DepartmentDrug Enforcement Administration

Abstract

Patheon API Services 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.

Full Text

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<title>Federal Register, Volume 90 Issue 74 (Friday, April 18, 2025)</title>
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[Federal Register Volume 90, Number 74 (Friday, April 18, 2025)]
[Notices]
[Pages 16554-16555]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2025-06707]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-1529]


Bulk Manufacturer of Controlled Substances Application: Patheon 
API Services Inc.

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

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SUMMARY: Patheon API Services 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 
June 17, 2025. Such persons may also file a written request for a 
hearing on the application on or before June 17, 2025.

ADDRESSES: The Drug Enforcement Administration requires that all

[[Page 16555]]

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 <a href="https://www.regulations.gov">https://www.regulations.gov</a> 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 <a href="https://www.regulations.gov">https://www.regulations.gov</a>. 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 5, 2025, Patheon API Services Inc., 101 
Technology Place, Florence, South Carolina 29501, 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
Psilocybin...........................         7437  I
Psilocyn.............................         7438  I
Amphetamine..........................         1100  II
Methadone............................         9250  II
------------------------------------------------------------------------

    The company plans to bulk manufacture the listed controlled 
substances to support the clinical trials of their customers. No other 
activities for these drug codes are authorized for this registration.

Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2025-06707 Filed 4-17-25; 8:45 am]
BILLING CODE P


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Indexed from Federal Register on April 18, 2025.

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