[Federal Register Volume 85, Number 108 (Thursday, June 4, 2020)]
[Notices]
[Pages 34465-34466]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-12080]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-653]


Importer of Controlled Substances Application: Akorn, Inc.

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 July 6, 2020. 
Such persons may also file a written request for a hearing on the 
application on or before July 6, 2020.

ADDRESSES: Written comments should be sent to: Drug Enforcement 
Administration, Attention: DEA Federal Register Representative/DPW, 
8701 Morrissette Drive, Springfield, Virginia 22152. All requests for a 
hearing must be sent to: Drug Enforcement Administration, Attn: 
Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152. All 
requests for a hearing should also be sent to: (1) Drug Enforcement 
Administration, Attn: Hearing Clerk/OALJ, 8701 Morrissette Drive, 
Springfield, Virginia 22152; and (2) Drug Enforcement Administration, 
Attn: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, 
Springfield, Virginia 22152.

SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.34(a), this 
is notice that on May 14, 2020, Akorn, Inc., 1222 West Grand Avenue, 
Decatur, Illinois 62522-1412, applied to be registered as an importer 
of the following basic class(es) of a controlled substance:

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                                          Drug
         Controlled substance             code           Schedule
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Remifentanil..........................     9739   II
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[[Page 34466]]

    The company plans to import the listed controlled substance for 
research purposes.

William T. McDermott,
Assistant Administrator.
[FR Doc. 2020-12080 Filed 6-3-20; 8:45 am]
BILLING CODE 4410-09-P