97-11923. Manufacturer of Controlled Substances; Notice of Registration
[Federal Register Volume 62, Number 89 (Thursday, May 8, 1997)]
[Notices]
[Page 25210]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 97-11923]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated December 31, 1996, and published in the Federal
Register on January 9, 1997 (62 FR 1342), MD Pharmaceutical, Inc., 3501
West Garry Avenue, Santa Ana, California 92704, made application by
renewal 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. DEA has considered
the factors in Title 21, United States Code, Section 823(a) and
determined that the registration of MD Pharmaceutical, Inc. to
manufacture the listed controlled substances is consistent with the
public interest at this time. Therefore, pursuant to 21 U.S.C. Sec. 823
and 28 CFR 0.100 and 0.104, the Acting 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: April 24, 1997.
Terrance W. Woodworth,
Acting Deputy Assistant Administrator, Office of Diversion Control,
Drug Enforcement Administration.
[FR Doc. 97-11923 Filed 5-7-97; 8:45 am]
BILLING CODE 4410-09-M
Document Information
- Published:
- 05/08/1997
- Department:
- Drug Enforcement Administration
- Entry Type:
- Notice
- Document Number:
- 97-11923
- Pages:
- 25210-25210 (1 pages)
- PDF File:
-
97-11923.pdf