[Federal Register Volume 84, Number 127 (Tuesday, July 2, 2019)]
[Notices]
[Page 31622]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-14028]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-392]


Bulk Manufacturer of Controlled Substances Application: Pisgah 
Laboratories, 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 September 3, 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 5, 2019, Pisgah Laboratories, Inc., 3222 Old 
Hendersonville Highway, Pisgah Forest, North Carolina 28768 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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Difenoxin..........................            9168  I
Diphenoxylate......................            9170  II
Levorphanol........................            9220  II
Meperidine intermediate-B..........            9233  II
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    The company plans to manufacture the listed controlled substances 
in bulk for distribution to its customers.

    Dated: June 19, 2019.
John J. Martin,
Assistant Administrator.
[FR Doc. 2019-14028 Filed 7-1-19; 8:45 am]
 BILLING CODE 4410-09-P