[Federal Register Volume 69, Number 102 (Wednesday, May 26, 2004)]
[Notices]
[Page 29979]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 04-11819]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration


Manufacturer of Controlled Substances; Notice of Application

     Pursuant to Sec.  1301.33(a) of Title 21 of the Code of Federal 
Regulations (CFR), this is notice that on February 24, 2004, Varian, 
Inc. Lake Forest, 25200 Commercentre Drive, Lake Forest, California 
92630-8810, made application by renewal 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
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 Phencyclidine (7471).......................................         II
 1-Piperidinocyclohexanecarbonitrile (8603).................         II
 Benzoylecgonine (9180).....................................         II
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     The firm plans to manufacture small quantities of controlled 
substances for use in diagnostic products. Any other such applicant and 
any person who is presently registered with DEA to manufacture such 
substance 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: Federal 
Register Representative, Office of Chief Counsel (CCD) and must be 
filed no later than June 25, 2004.

    Dated: May 5, 2004.
William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug 
Enforcement Administration.
[FR Doc. 04-11819 Filed 5-25-04; 8:45 am]
BILLING CODE 4410-09-M