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GE Healthcare
FR Doc E8-6389[Federal Register: March 28, 2008 (Volume 73, Number 61)]
[Notices] [Page 16713] From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr28mr08-114]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated December 17, 2007, and published in the Federal Register on
December 27, 2007, (72 FR 73358), GE Healthcare, 3350 North Ridge Avenue,
Arlington Heights, Illinois 60004-1412, made application to the Drug Enforcement
Administration (DEA) to be registered as a bulk manufacturer of Cocaine (9041),
a basic class of controlled substance listed in schedule II.
The company plans to manufacture a radioactive product used in diagnostic
imaging in the diagnosis of Parkinson's Disease and for manufacture in bulk for
investigational new drug (IND) submission and clinical trials.
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 GE Healthcare to
manufacture the listed basic class of controlled substance is consistent with
the public interest at this time. DEA has investigated GE Healthcare 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 substance listed.
Dated: March 19, 2008.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E8-6389 Filed 3-27-08; 8:45 am]
BILLING CODE 4410-09-P
NOTICE: This is an
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