[Federal Register Volume 85, Number 54 (Thursday, March 19, 2020)]
[Notices]
[Pages 15799-15800]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-05750]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-602]


Bulk Manufacturer of Controlled Substances Application: Navinta 
LLC

ACTION: Notice of application.

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DATES: Registered bulk manufacturers of the affected basic class(es), 
and applicants therefore, may file written comments on or objections to 
the issuance of the proposed registration on or before May 18, 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 September 23, 2019, Navinta LLC, 1499 Lower Ferry 
Road, Ewing, New Jersey 08618-1414 registered as a bulk manufacturer of 
the following basic class(es), of controlled substances:

[[Page 15800]]



------------------------------------------------------------------------
        Controlled substance            Drug code          Schedule
------------------------------------------------------------------------
4-Anilino-N-phenethyl-4-piperidine             8333  II
 (ANPP).
Levomethorphan.....................            9210  II
Levorphanol........................            9220  II
Remifentanil.......................            9739  II
Fentanyl...........................            9801  II
------------------------------------------------------------------------

    The company plans to bulk manufacture API quantities of the listed 
controlled substances for validation purposes and FDA approval.

    Dated: March 5, 2020.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2020-05750 Filed 3-18-20; 8:45 am]
 BILLING CODE 4410-09-P