[Federal Register Volume 68, Number 112 (Wednesday, June 11, 2003)]
[Notices]
[Page 35006]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 03-14737]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Pending 
Registration

    By Notice dated January 27, 2003, and published in the Federal 
Register on February 6, 2003, (68 FR 6183), Houba, Inc., 16235 State 
Road 17, Culver, Indiana 46511, made application by renewal to the Drug 
Enforcement Administration (DEA) for registration as a bulk 
manufacturer of the basic classes of Schedule II controlled substances 
Oxycodone (9143) and Hydrocodone (9193). The firm plans to bulk 
manufacture the controlled substances for sale to its customers for the 
production of finished dosage form products.
    Comments and Objections have been filed with the Drug Enforcement 
Administration and are currently under review. A final decision 
regarding the firm's renewal application as a bulk manufacturer is 
hereby being held pending investigation and resolution of issues 
raised.
    Houba, Inc. is authorized to continue operating under the 
manufacturer registration issued pursuant to the Notice of Registration 
published June 13, 2002 (67 FR 40752) pending final approval or denial 
of the renewal application.

    Dated: May 23, 2003.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 03-14737 Filed 6-10-03; 8:45 am]
BILLING CODE 4410-09-M