[Federal Register: July 13, 2004 (Volume 69, Number 133)]
[Notices]
[Page 42067-42068]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr13jy04-76]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Application
Pursuant to section 1301.33(a) of Title 21 of the Code of Federal
Regulations (CFR), this is notice that on April 29, 2004, Cedarburg
Pharmaceuticals, Inc.,
[[Page 42068]]
870 Badger Circle, Grafton, Wisconsin 53024, made application by
renewal to the Drug Enforcement Administration (DEA) for registration
as a bulk manufacturer of the basic classes of controlled substances
listed below:
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Drug Schedule
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Tetrahydrocannabinols (7370)............... I
Dihydromorphine (9145)..................... I
Hydromorphone (9150)....................... II
Fentanyl (9801)............................ II
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The firm plans to manufacture the listed controlled substances for
distribution to its customers.
Any other such applicant and any person who is presently registered
with DEA to manufacture such substances may file comments or objections
to the issuance of the proposed registration.
Any such comments or objections may be addressed, in quintuplicate,
to the Deputy Assistant Administrator, Office of Diversion Control,
Drug Enforcement Administration, United States Department of Justice,
Washington, DC 20537, Attention: Federal Register Representative,
Office of Chief Counsel (CCD) and must be filed no later than September
13, 2004.
Dated: June 28, 2004.
William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 04-15771 Filed 7-12-04; 8:45 am]
BILLING CODE 4410-09-M