[Federal Register Volume 59, Number 90 (Wednesday, May 11, 1994)]
[Unknown Section]
[Page 0]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 94-11331]


[[Page Unknown]]

[Federal Register: May 11, 1994]


-----------------------------------------------------------------------

DEPARTMENT OF JUSTICE
Drug Enforcement Administration

 

Manufacturer of Controlled Substances Notice of Registration

    By Notice dated December 21, 1993, and published in the Federal 
Register on December 28, 1993, (58 FR 68664), Orpharm, Inc., 728 West 
19th Street, Houston, Texas 77008, made application to the Drug 
Enforcment Administration to be registered as a bulk manufacturer of 
Methadone (9250), a basic class of controlled substance listed in 
Schedule II.
    Comments were received, however, no written request for a hearing 
exists if the DEA can determine that Orpharm will manufacture methadone 
to process LAAM. The DEA has determined that this is the case. 
Therefore, pursuant to section 303 of the Comprehensive Drug Abuse 
Prevention and Control Act of 1970 and title 21, Code of Federal 
Regulations, Sec. 1301.54(e), the Deputy Assistant Administrator hereby 
orders that the application submitted by the above firm for 
registration as a bulk manufacturer of the basic class of controlled 
substance listed above is approved.

    Dated: May 4, 1994.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 94-11331 Filed 5-10-94; 8:45 am]
BILLING CODE 4410-09-M