[Federal Register Volume 85, Number 77 (Tuesday, April 21, 2020)]
[Notices]
[Page 22178]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-08352]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-596]
Bulk Manufacturer of Controlled Substances Application: Cedarburg
Pharmaceuticals
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 June 22, 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 3, 2018, Cedarburg Pharmaceuticals, 870
Badger Circle, Grafton, Wisconsin 53024-0000 applied to be registered
as a bulk manufacturer of the following basic class(es) of controlled
substances:
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Drug
Controlled substance code Schedule
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Tetrahydrocannabinols.................. 7370 I
Methylphenidate........................ 1724 II
Nabilone............................... 7379 II
4-Anilino-N-phenethyl-4-piperidine 8333 II
(ANPP).
Fentanyl............................... 9801 II
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The company plans to manufacture bulk active pharmaceutical
ingredients (API) for distribution to its customers. In reference to
drug code 7370 (Tetrahydrocannabinols) the company plans to bulk
manufacture as synthetic. No other activity for this drug code is
authorized for this registration.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2020-08352 Filed 4-20-20; 8:45 am]
BILLING CODE 4410-09-P