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Johnson Matthey, Inc.
FR Doc E6-18844 [Federal Register: November 8, 2006 (Volume 71, Number 216)]
[Notices] [Page 65544] From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr08no06-110]
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 August 21, 2006 and August 24, 2006, Johnson Matthey, Inc.,
Custom Pharmaceuticals Department, 2003 Nolte Drive, West Deptford, New Jersey
08066, 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 schedule II:
Drug
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Schedule
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Nabilone (7379)
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II
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Noroxymorphone (9668)
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II
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The company plans to manufacture the listed controlled substances in bulk for
sales 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: November 2, 2006.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E6-18844 Filed 11-7-06; 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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