[Federal Register: August 22, 2005 (Volume 70, Number 161)]
[Notices]
[Page 48980-48981]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr22au05-110]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By notice dated March 29, 2005, and published in the Federal
Register on April 6, 2005, (70 FR 17474-17475), 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 class of
controlled substances listed in Schedule 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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[[Page 48981]]
The company plans to manufacture small quantities of the listed
controlled substances for use in diagnostic products.
No comments or objections have been received. DEA has considered
the factors in 21 U.S.C. 823(a) and determined that the registration of
Varian, Inc. to manufacture the listed basic class of controlled
substances is consistent with the public interest at this time. DEA has
investigated Varian, Inc. to ensure that the company's registration is
consistent with the public interest. The investigation has included
inspection and testing of the company's physical security systems,
verification of the company's compliance with state and local laws, and
a review of the company's background and history. Therefore, pursuant
to 21 U.S.C. 823, and in accordance with 21 CFR 1301.33, the above
named company is granted registration as a bulk manufacturer of the
basic class of controlled substances listed.
Dated: August 15, 2005.
William J. Walker,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 05-16565 Filed 8-19-05; 8:45 am]
BILLING CODE 4410-09-P