[Federal Register Volume 85, Number 47 (Tuesday, March 10, 2020)]
[Notices]
[Page 13927]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-04834]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-599]
Importer of Controlled Substances Application: SpecGx 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 9, 2020.
Such persons may also file a written request for a hearing on the
application on or before April 9, 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 December 30, 2019, SpecGx LLC, 3600 North Second
Street, Saint Louis, Missouri 63147 applied to be registered as an
importer of the following basic class(es) of controlled substances:
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Controlled substance Drug code Schedule
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Marihuana.......................... 7360 I
Phenylacetone...................... 8501 II
Coca Leaves........................ 9040 II
Thebaine........................... 9333 II
Opium, raw......................... 9600 II
Poppy Straw Concentrate............ 9670 II
Tapentadol......................... 9780 II
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The company plans to import the listed controlled substances for
bulk manufacture into Active Pharmaceutical Ingredients (API) for
distribution to its customers. In reference to drug code 7360
(marihuana), the company plans to import synthetic cannabinol. No other
activity for this drug is authorized for this registration. Placement
of these codes onto the company's registration does not translate into
automatic approval of subsequent permit applications to import
controlled substances.
Approval of permit applications will occur only when the
registrant's business activity is consistent with what is authorized
under 21 U.S.C. 952(a)(2).
Authorization will not extend the import of FDA approved or non-
approved finished forms for commercial sale.
Dated: February 27, 2020.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2020-04834 Filed 3-9-20; 8:45 am]
BILLING CODE 4410-09-P