97-11924. 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: 97-11924]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated December 17, 1996, and published in the Federal
Register on January 8, 1997, (62 FR 1134), Orpharm, Inc., 728 West 19th
Street, Houston, Texas 77008, 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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Methadone (9250)............................ II
Methadone-intermediate (9254)............... II
levo-alphacetylmethadol (9648).............. 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 Orpharm, 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: March 21, 1997.
Terrance W. Woodworth,
Acting Deputy Assistant Administrator, Office of Diversion Control,
Drug Enforcement Administration.
[FR Doc. 97-11924 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:
- 97-11924
- Pages:
- 25210-25210 (1 pages)
- PDF File:
-
97-11924.pdf