97-15844. Manufacturer of Controlled Substances; Notice of Application
[Federal Register Volume 62, Number 116 (Tuesday, June 17, 1997)]
[Notices]
[Page 32824]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 97-15844]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Application
Pursuant to Section 1301.33 of Title 21 of the Code of Federal
Regulations (CFR), this is notice that on May 16, 1997, Dupont
Pharmaceuticals, The Dupont Merck Pharmaceutical Co., 1000 Steward
Avenue, Garden City, New York 11530, 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
------------------------------------------------------------------------
Oxycodone (9143)........................... II
Hydrocodone (9193)......................... II
Oxymorphone (9652)......................... II
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The firm plans to manufacture the listed controlled substances to
make finished products.
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, D.C. 20537, Attention: DEA Federal Register Representative
(CCR), and must be filed no later than August 18, 1997.
Dated: June 9, 1997.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 97-15844 Filed 6-16-97; 8:45 am]
BILLING CODE 4410-09-M
Document Information
- Published:
- 06/17/1997
- Department:
- Drug Enforcement Administration
- Entry Type:
- Notice
- Document Number:
- 97-15844
- Pages:
- 32824-32824 (1 pages)
- PDF File:
-
97-15844.pdf