[Federal Register: April 6, 2005 (Volume 70, Number 65)]
[Notices]
[Page 17474-17475]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr06ap05-122]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Application
Pursuant to Section 1301.33(a) of Title 21 of the Code of Federal
Regulations (CFR), this is notice that on February 16, 2005, Varian,
Inc., Lake Forest, 25200 Commercentre Drive, Lake Forest, California
92630-8810, made application by renewal to the Drug Enforcement
Administration (DEA) to be registered as a bulk manufacturer of the
basic classes of controlled substances listed in Schedules II:
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Drug Schedule
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Phencyclidine (7471)....................... II
1-Piperidinocyclohexane-carbonitrile (8603) II
Benzoylecgonine (9180)..................... II
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The company plans to manufacture small quantities of the listed
controlled substances for use in diagnostic products.
Any other such applicant and any person who is presently registered
with DEA to manufacture such a substance may file comments or
objections to the issuance of the proposed registration pursuant to 21
CFR 1301.33(a).
Any such written comments or objections being sent via regular mail
may be addressed, in quintuplicate, to the Deputy Assistant
Administrator, Office of Diversion Control, Drug Enforcement
Administration, Washington, DC 20537, Attention: DEA
[[Page 17475]]
Federal Register Representative, Liaison and Policy Section (ODL); or
any being sent via express mail should be sent to DEA Headquarters,
Attention: DEA Federal Register Representative/ODL, 2401 Jefferson-
Davis Highway, Alexandria, Virginia 22301; and must be filed no later
than (60 days from publication).
Dated: March 29, 2005.
William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 05-6796 Filed 4-5-05; 8:45 am]
BILLING CODE 4410-09-P