Manufacturer of Controlled Substances; Notice of Application

[Federal Register Volume 64, Number 23 (Thursday, February 4, 1999)]
[Notices]
[Page 5679]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 99-2684]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Application

    Pursuant to Section 1301.33(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on December 10, 1998, Orpharm 
Inc., 4815 Dacoma, Houston, Texas 77092, made application by renewal to 
the Drug Enforcement Administration (DEA) for registration as a bulk 
manufacture 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.
    Any other such applicant and any person who is presently registered 
with DEA to manufacturer such substances may file comments or 
objections to the issuance of the proposed registration.
    Any such comments or objections may be addressed, in quintuplicate, 
to the Deputy Assistant 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 April 5, 1999.

    Dated: January 27, 1999.
John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 99-2684 Filed 2-3-99; 8:45 am]
BILLING CODE 4410-09-M