[Federal Register Volume 85, Number 63 (Wednesday, April 1, 2020)]
[Notices]
[Page 18277]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-06762]



[[Page 18277]]

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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-614]


Importer of Controlled Substances Application: Shertech 
Laboratories, LLC

ACTION: Notice of application.

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DATES: Registered bulk manufacturer 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 1, 2020. 
Such persons may also file a written request for a hearing on the 
application on or before May 1, 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 February 21, 2020, Shertech Laboratories, LLC, 1185 
Woods Chapel Road, Duncan, South Carolina 29334 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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Cocaine................................     9041  II
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    The company plans to import synthetic derivatives of the listed 
controlled substance in bulk form to conduct clinical trials. Approval 
of permit applications will occur only when the registrant's activity 
is consistent with what is authorized under to 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.

William T. McDermott,
Assistant Administrator.
[FR Doc. 2020-06762 Filed 3-31-20; 8:45 am]
 BILLING CODE 4410-09-P