97-4346. Manufacturer of Controlled Substances; Application
[Federal Register Volume 62, Number 35 (Friday, February 21, 1997)]
[Notices]
[Page 8041]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 97-4346]
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DEPARTMENT OF JUSTICE
Manufacturer of Controlled Substances; Application
Pursuant to Sec. 1301.43(a) of Title 21 of the Code of Federal
Regulations (CFR), this is notice that on January 13, 1997, Noramco of
Delaware, Inc., Division of McNeilab, Inc., 500 Old Swedes Landing
Road, Wilmington, Delaware 19801, 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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Morphine (9300)............................ II
Codeine (9050)............................. II
Thebaine (9333)............................ II
Hydrocodone (9193)......................... II
Oxycodone (9143)........................... II
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The firm plans to manufacture the listed controlled substances for
distribution to its customers as bulk product.
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, United States Department of Justice,
Washington, DC. 20537, Attention: DEA Federal Register Representative
(CCR), and must be filed no later than April 22, 1997.
Dated: February 6, 1997.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 97-4346 Filed 2-20-97; 8:45 am]
BILLING CODE 4410-09-M
Document Information
- Published:
- 02/21/1997
- Department:
- Justice Department
- Entry Type:
- Notice
- Document Number:
- 97-4346
- Pages:
- 8041-8041 (1 pages)
- PDF File:
-
97-4346.pdf