[Federal Register: December 27, 2007 (Volume 72, Number 247)]
[Notices]
[Page 73369-73370]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr27de07-88]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated September 21, 2007, and published in the Federal
Register on September 27, 2007, (72 FR 54931), 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 schedule II:
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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 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 classes 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 classes of controlled substances listed.
[[Page 73370]]
Dated: December 17, 2007.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E7-25050 Filed 12-26-07; 8:45 am]
BILLING CODE 4410-09-P