[Federal Register Volume 84, Number 248 (Friday, December 27, 2019)]
[Notices]
[Page 71474]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-27952]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-566]


Bulk Manufacturer of Controlled Substances Application: Janssen 
Pharmaceuticals 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 February 25, 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 October 9, 2019, Janssen Pharmaceuticals Inc., 
Buildings 1-5 & 7-14, 1440 Olympic Drive, Athens, Georgia 30601 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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Methylphenidate.......................       1724  II
Hydromorphone.........................       9150  II
Hydrocodone...........................       9193  II
Oripavine.............................       9330  II
Thebaine..............................       9333  II
Tapentadol............................       9780  II
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    The company plans to manufacture the above-listed controlled 
substances in bulk for distribution to its customers.

    Dated: December 10, 2019.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2019-27952 Filed 12-26-19; 8:45 am]
BILLING CODE 4410-09-P