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Start Preamble
Pursuant to section 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on October 3, 2002, Varian, Inc., Lake Forest, 25200 Commercentre Drive, Lake Forest, California 92630-8810, made application to the Drug Enforcement Administration (DEA) for registration as a bulk manufacturer of the basic classes of controlled substances listed below:
Drug Schedule Phencyclidine (7470) II 1-Piperidincyclohexane- carbonitrille (8603) II Benzoylecgoonine (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 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 (CCD) and must be filed no later than August 11, 2003.
Start SignatureStart Printed Page 35007End Signature End PreambleDated: May 16, 2003.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.
[FR Doc. 03-14736 Filed 6-10-03; 8:45 am]
BILLING CODE 4410-09-M
Document Information
- Published:
- 06/11/2003
- Department:
- Drug Enforcement Administration
- Entry Type:
- Notice
- Document Number:
- 03-14736
- Pages:
- 35006-35007 (2 pages)
- PDF File:
- 03-14736.pdf