95-13990. Manufacturer of Controlled Substances; Notice of Application
[Federal Register Volume 60, Number 110 (Thursday, June 8, 1995)]
[Notices]
[Page 30320]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-13990]
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DEPARTMENT OF JUSTICE
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 March 16, 1995, Johnson &
Johnson Pharmaceutical Partners, HC02 State Road 933, KMO.1 Mamey Ward,
HC-02 Box 19250, Gurabo, Puerto Rico 00778-9629, 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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Alfentanil (9737).................... II
Sufentanil (9740).................... II
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The firm plans to manufacture the listed controlled substances for
bulk 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 above application and may also file a written
request for a hearing thereon in accordance with 21 CFR 1301.54 and in
the form prescribed by 21 CFR 1316.47.
Any such comments, objections, or requests for a hearing may be
addressed 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 July 10, 1995.
Dated: May 30, 1995.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 95-13990 Filed 6-7-95; 8:45 am]
BILLING CODE 4410-09-M
Document Information
- Published:
- 06/08/1995
- Department:
- Justice Department
- Entry Type:
- Notice
- Document Number:
- 95-13990
- Pages:
- 30320-30320 (1 pages)
- PDF File:
-
95-13990.pdf