[Federal Register Volume 61, Number 30 (Tuesday, February 13, 1996)]
[Notices]
[Page 5571]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 96-3171]



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DEPARTMENT OF JUSTICE

Manufacturer of Controlled Substances; Notice of Application

    Pursuant to Section 1301.43(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on November 7, 1995, Orpharm, 
Inc., 728 West 19th Street, Houston, Texas 77008, made application to 
the Drug Enforcement Administration (DEA) for registration 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                         
------------------------------------------------------------------------

    The firm plans to manufacture methadone and methadone intermediate 
for the production of LAAM.
    Any other such applicant and any person who is presently registered 
with DEA to manufacture such substances may file comments or objections 
to the issuance of the above application.
    Any such comments or objections may be addressed, in quintuplicate, 
to the Deputy Assistance Administrator, Office of Diversion Control, 
Drug Enforcement Administration, United States Department of Justice, 
Washington, D.C. 20537, Attention: DEA Federal Register Representative 
(CCR), and must be filed no later than (60 days from publication).

    Dated: February 2, 1996.
Gene R. Haislip,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 96-3171 Filed 2-12-96; 8:45 am]
BILLING CODE 4410-09-M