[Federal Register Volume 89, Number 37 (Friday, February 23, 2024)]
[Notices]
[Page 13746]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-03686]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-1319]


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 
April 23, 2024. Such persons may also file a written request for a 
hearing on the application on or before April 23, 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 December 21, 2023, 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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                                           Drug
          Controlled substance             code          Schedule
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Dimethyltryptamine.....................     7435  I
Psilocybin.............................     7437  I
Psilocyn...............................     7438  I
Amphetamine............................     1100  II
Methadone..............................     9250  II
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    The company plans to bulk manufacture the above controlled 
substances to support customers' clinical trials. No other activities 
for these drug codes are authorized for this registration.

Marsha Ikner,
Acting Deputy Assistant Administrator.
[FR Doc. 2024-03686 Filed 2-22-24; 8:45 am]
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