[Federal Register: November 7, 2006 (Volume 71, Number 215)]
[Notices]
[Page 65135]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr07no06-71]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Application
Pursuant to Sec. 1301.33(a), Title 21 of the Code of Federal
Regulations (CFR), this is notice that on June 26, 2006, and August 17,
2006, Siegfried (USA), Inc., Industrial Park Road, Pennsville, New
Jersey 08070, made application by letter to the Drug Enforcement
Administration (DEA) to be registered as a bulk manufacturer of the
basic classes of controlled substances listed in schedules I and II:
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Drug Schedule
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Dihydromorphine (9145)..................... I
Oxymorphone (9652)......................... II
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The company plans to manufacture the listed controlled substances
in bulk for distribution to its customers.
Any other such applicant and any person who is presently registered
with DEA to manufacture such substances may file comments or objections
to the issuance of the proposed registration pursuant to 21 CFR
1301.33(a).
Any such written comments or objections being sent via regular mail
should be addressed, in quintuplicate, to the Deputy Assistant
Administrator, Office of Diversion Control, Drug Enforcement
Administration, Washington, DC 20537, Attention: DEA Federal Register
Representative/ODL; or any being sent via express mail should be sent
to DEA Headquarters, Attention: DEA Federal Register Representative/
ODL, 2401 Jefferson-Davis Highway, Alexandria, Virginia 22301; and must
be filed no later than January 8, 2007.
Dated: October 31, 2006.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E6-18714 Filed 11-6-06; 8:45 am]
BILLING CODE 4410-09-P