[Federal Register Volume 61, Number 170 (Friday, August 30, 1996)]
[Notices]
[Page 45986]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 96-22218]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Application
Pursuant to Section 1301.43(a) of Title 21 of the Code of Federal
Regulations (CFR), this is notice that on July 15, 1995, Celgene
Corporation, 7 Powder Horn Drive, Warren, NJ 07059, made application 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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2,5-Dimethoxyamphetamine (7396)............................... I
Amphetamine (1100)............................................ II
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The firm plans to manufacture small quantities of 2,5-
dimethoxyamphetamine using biocatalysis to develop, manufacture and
sell high value added compounds to pharmaceutical and agrochemical
industries and amphetamine for distribution of the bulk active
substances 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 above application.
Any such comments or objections may be addressed, in quintuplicate,
to the Deputy Assistant Administrator, Office of Diversion Control,
Drug Enforcement Administration, U.S. Department of Justice,
Washington, DC 20537, Attention: DEA Federal Register Representative
(CCR), and must be filed no later than October 29, 1996.
Dated: August 21, 1996.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 96-22218 Filed 8-29-96; 8:45 am]
BILLING CODE 4410-09-M