[Federal Register: August 6, 2008 (Volume 73, Number 152)]
[Notices]
[Page 45788-45789]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr06au08-105]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated March 11, 2008 and published in the Federal
Register on March 19, 2008 (73 FR 14841), 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-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.
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
[[Page 45789]]
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.
Dated: July 30, 2008.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E8-18042 Filed 8-5-08; 8:45 am]
BILLING CODE 4410-09-P