98-24295. Manufacturer of Controlled Substances Notice of Registration
[Federal Register Volume 63, Number 175 (Thursday, September 10, 1998)]
[Notices]
[Page 48523]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 98-24295]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances Notice of Registration
By Notice dated January 21, 1998, and published in the Federal
Register on February 12, 1998, (63 FR 7182), 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
------------------------------------------------------------------------
The firm plans to manufacture methadone and methadone-intermediate
for production of LAAM.
DEA has considered the factors in 21 U.S.C. 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. 823 and 28 C.F.R. 0.100 and
0.104, 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: August 21, 1998.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 98-24295 Filed 9-9-98; 8:45 am]
BILLING CODE 4410-09-M
Document Information
- Published:
- 09/10/1998
- Department:
- Drug Enforcement Administration
- Entry Type:
- Notice
- Document Number:
- 98-24295
- Pages:
- 48523-48523 (1 pages)
- PDF File:
-
98-24295.pdf