94-11998. Manufacturer of Controlled Substances; Registration
[Federal Register Volume 59, Number 95 (Wednesday, May 18, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-11998]
[[Page Unknown]]
[Federal Register: May 18, 1994]
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DEPARTMENT OF JUSTICE
Manufacturer of Controlled Substances; Registration
By Notice dated March 21, 1994, and published in the Federal
Register on April 1, 1994, (59 FR 15459), MD Pharmaceutical, Inc. 3501
West Garry Avenue, Santa Ana, California 92704, made application to the
Drug Enforcement Administration (DEA) to be registered as a bulk
manufacturer of the basic classes of controlled substances listed
below:
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Drug Schedule
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Methylphenidate (1724)................................... II
Diphenoxylate (9170)..................................... II
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No comments or objections have been received. Therefore, pursuant
to Section 303 of the Comprehensive Drug Abuse Prevention and Control
Act of 1970 and Title 21, Code of Federal Regulations, Section
1301.54(e), the Deputy Assistant Administrator, Office of Diversion
Control, hereby orders that the application submitted by the above firm
for registration as a bulk manufacturer of the basic classes of
controlled substances listed above is granted.
Dated: May 11, 1994.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 94-11998 Filed 5-17-94; 8:45 am]
BILLING CODE 4410-09-M
Document Information
- Published:
- 05/18/1994
- Department:
- Justice Department
- Entry Type:
- Uncategorized Document
- Document Number:
- 94-11998
- Pages:
- 0-0 (1 pages)
- Docket Numbers:
- Federal Register: May 18, 1994