[Federal Register Volume 84, Number 226 (Friday, November 22, 2019)]
[Notices]
[Page 64563]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-25401]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-529]


Bulk Manufacturer of Controlled Substances Application: Patheon 
API Manufacturing, Inc.

ACTION: Notice of application.

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DATES: Registered bulk manufacturers of the affected basic classes, and 
applicants therefore, may file written comments on or objections to the 
issuance of the proposed registration on or before January 21, 2020.

ADDRESSES:  Written comments should be sent to: Drug Enforcement 
Administration, Attention: DEA Federal Register Representative/DPW, 
8701 Morrissette Drive, Springfield, Virginia 22152.

SUPPLEMENTARY INFORMATION:  In accordance with 21 CFR 1301.33(a), this 
is notice that on March 15, 2019, Patheon API Manufacturing, Inc., 309 
Delaware Street, Greenville, South Carolina 29605 applied to be 
registered as a bulk manufacturer of the following basic classes of 
controlled substances:

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          Controlled substance               Drug code       Schedule
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Thebaine................................            9333              II
Noroxymorphone..........................            9668              II
Gamma Hydroxybutyric Acid...............            2010               I
Alpha-methyltryptamine..................            7432               I
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    The company plans to bulk manufacture the listed controlled 
substances as an Active Pharmaceutical Ingredient for supply to its 
customers.

    Dated: November 5, 2019.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2019-25401 Filed 11-21-19; 8:45 am]
BILLING CODE 4410-09-P