[Federal Register Volume 84, Number 146 (Tuesday, July 30, 2019)]
[Notices]
[Page 36947]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-16177]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-392]


Bulk Manufacturer of Controlled Substances Application: AMPAC 
Fine Chemicals LLC

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 September 30, 2019.

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 
18, 2019, AMPAC Fine Chemicals LLC, Highway 50 and Hazel Avenue, 
Building 05001, Rancho Cordova, California 95670 applied to be 
registered as 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
Levomethorphan...................                9210  II
Levorphanol......................                9220  II
Thebaine.........................                9333  II
Tapentadol.......................                9780  II
Remifentanil.....................                9739  II
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    The company plans to manufacture the listed controlled substances 
for distribution to its customers.

    Dated: July 16, 2019.
John J. Martin,
Assistant Administrator.
[FR Doc. 2019-16177 Filed 7-29-19; 8:45 am]
 BILLING CODE 4410-09-P