[Federal Register Volume 66, Number 173 (Thursday, September 6, 2001)]
[Notices]
[Page 46654]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 01-22325]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substance; Notice of Application

    Pursuant to Section 1301.33(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on February 6, 2001, Houba Inc., 
P.O. Box 190, 16235 State Road 17, Culver, Indiana 46511, made 
application by letter to the Drug Enforcement Administration (DEA) for 
registration as a bulk manufacturer of the basic classes of controlled 
substances listed below:

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                   Drug                               Schedule
------------------------------------------------------------------------
Codeine (9050)............................  II
Oxycodone (9143)..........................  II
Hydrocodone (9193)........................  II
------------------------------------------------------------------------

    The firm plans to bulk manufacture the controlled substances for 
the production of finished dosage form products.
    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 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, DC 20537, Attention: DEA Federal Register Representative 
(CCR), and must be filed no later than (60 days from publication).

    Dated: August 23, 2001.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 01-22325 Filed 9-5-01; 8:45 am]
BILLING CODE 4410-09-M