[Federal Register: April 29, 2004 (Volume 69, Number 83)]
[Notices]               
[Page 23538]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr29ap04-73]                         

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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

 
Manufacturer of Controlled Substances; Notice of Withdrawal of 
Application

    By notice dated February 4, 2004, and published in the Federal 
Register on February 18, 2004 (68 FR 7656), IRIX Pharmaceuticals, Inc., 
101 Technology Place, Florence, South Carolina 29501, made application 
by renewal to the Drug Enforcement Administration (DEA) for 
registration as a bulk manufacturer of methylphenidate (1724), a basic 
class of controlled substance listed in Schedule II.
    The firm planned to manufacture methylphenidate for sale to its 
customers.
    By letter dated February 18, 2004, IRIX Pharmaceuticals, Inc., 
requested that its registration as a Schedule II bulk manufacturer be 
retired. Therefore, IRIX Pharmaceuticals, Inc's renewal application to 
import the above listed controlled substance is hereby withdrawn.

    Dated: March 29, 2004.
William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 04-9660 Filed 4-28-04; 8:45 am]

BILLING CODE 4410-09-M