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Federal
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Siegfried (USA), Inc.
FR Doc E7-9628 [Federal Register: May 18, 2007 (Volume 72, Number 96)]
[Notices] [Page 28078] From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr18my07-108]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Registration
By Notice dated July 26, 2006, and published in the Federal Register on
August 2, 2006, (71 FR 43814-43815), Siegfried (USA) Inc., 33 Industrial Park
Road, Pennsville, New Jersey 08070, made application by renewal to the Drug
Enforcement Administration (DEA) to be registered as a bulk manufacturer of
Hydromorphone (9150), a basic class of controlled substance listed in schedule
II.
The company plans to manufacture in bulk for distribution to its customers.
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 Siegfried (USA), Inc. to manufacture the
listed basic class of controlled substance is consistent with the public
interest at this time. DEA has investigated Siegfried (USA), 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 substance listed.
Dated: May 10, 2007.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E7-9628 Filed 5-17-07; 8:45 am]
BILLING CODE 4410-09-P
NOTICE: This is an
unofficial version. An official version of these publications may be obtained
directly from the Government Printing Office (GPO).
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