96-11254. Manufacturer of Controlled Substances; Notice of Registration

[Federal Register Volume 61, Number 88 (Monday, May 6, 1996)]
[Notices]
[Page 20275]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 96-11254]



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DEPARTMENT OF JUSTICE
Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Registration

    By Notice dated February 2, 1996, and published in the Federal 
Register on February 13, 1996, (61 FR 5571), Orpharm Inc., 728 West 
19th Street, Houston, Texas 77008, made application to the Drug 
Enforcement Administration (DEA) to be registered as a bulk 
manufacturer of the basic classes of controlled substances listed 
below:

------------------------------------------------------------------------
                    Drug                               Schedule         
------------------------------------------------------------------------
Methadone (9250)...........................  II.                        
Methadone-intermediate (9254)..............  II.                        
Levo-alphacetylmethadol (9648).............  II.                        
------------------------------------------------------------------------

    No comments or objections have been received. DEA has considered 
the factors in 21 U.S.C. Sec. 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 C.F.R. Secs. 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: April 29, 1996.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 96-11254 Filed 5-3-96; 8:45 am]
BILLING CODE 4410-09-M