[Federal Register: December 1, 2006 (Volume 71, Number 231)]
[Notices]
[Page 69592]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr01de06-109]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Application
Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal
Regulations (CFR), this is notice that on September 28, 2006, and
October 25, 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 I and II:
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Drug Schedule
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Methadone (9250)........................... II
Methadone Intermediate (9254).............. II
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The company plans to use the Methadone Intermediate to produce the
Methadone HCL for sale to its customers who are final dosage
manufacturers.
Any other such applicant and any person who is presently registered
with DEA to manufacture such a substance 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 30, 2007.
Dated: November 21, 2006.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E6-20343 Filed 11-30-06; 8:45 am]
BILLING CODE 4410-09-P