[Federal Register Volume 85, Number 57 (Tuesday, March 24, 2020)]
[Notices]
[Page 16654]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-06167]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-605]


Importer of Controlled Substances Application: Sharp (Bethlehem), 
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 April 23, 2020. 
Such persons may also file a written request for a hearing on the 
application on or before April 23, 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 
request 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 January 28, 2020, Sharp (Bethlehem), LLC, 2400 
Baglyos Circle, Bethlehem, Pennsylvania 18020-8024 applied to be 
registered as an importer of the following basic class(es) of 
controlled substances:

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                                           Drug
          Controlled substance             code          Schedule
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Gamma Hydroxybutyric Acid..............     2010  I
3,4-Methylenedioxymethamphetamine......     7405  I
Psilocybin.............................     7437  I
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    The company plans to import the listed controlled substances for 
clinical trials. Approval of permit applications will occur only when 
the registrant's activity is consistent with what is authorized under 
21 U.S.C. 952(a)(2). Authorization will not extend to the import of 
FDA-approved or non-approved finished dosage forms for commercial sale.

    Dated: March 12, 2020.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2020-06167 Filed 3-23-20; 8:45 am]
BILLING CODE 4410-09-P