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> Archimica, Inc.
FR Doc E8-14588[Federal Register: June 27, 2008 (Volume 73, Number 125)]
[Notices] [Page 36573] From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr27jn08-97]
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 May 7, 2008, Archimica, Inc., 2460 W. Bennett Street,
Springfield, Missouri 65807-1229, made application by renewal 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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Methylphenidate (1724)
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II
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Phenylacetone (8501)
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II
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Methadone Intermediate (9254)
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II
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The company plans to manufacture the listed controlled substances in bulk for
research purposes, and sale 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 Drug Enforcement Administration, Office of
Diversion Control, Federal Register Representative (ODL), Washington, DC 20537,
or any being sent via express mail should be sent to Drug Enforcement
Administration, Office of Diversion Control, Federal Register Representative (ODL),
8701 Morrissette Drive, Springfield, Virginia 22152; and must be filed no later
than August 26, 2008.
Dated: June 20, 2008.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion
Control, Drug Enforcement Administration.
[FR Doc. E8-14588 Filed 6-26-08; 8:45 am]
BILLING CODE 4410-09-P
NOTICE: This is an
unofficial version. An official version of these publications may be obtained
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