[Federal Register: May 26, 2004 (Volume 69, Number 102)]
[Notices]
[Page 29979]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr26my04-95]
-----------------------------------------------------------------------
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.
------------------------------------------------------------------------
Drug Schedule
------------------------------------------------------------------------
Phencyclidine (7471)....................................... II
1-Piperidinocyclohexanecarbonitrile (8603)................. II
Benzoylecgonine (9180)..................................... II
------------------------------------------------------------------------
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