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Federal
Register Notices > Manufacturers
2009 > Rhodes
Technologies
FR Doc E9-9806[Federal Register: April 29, 2009 (Volume 74, Number 81)]
[Notices] [Page 19597] From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr29ap09-122]
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 February 25, 2009, Rhodes Technologies, 498 Washington Street,
Coventry, Rhode Island 02816, 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 schedules I and II:
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Drug
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Schedule
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Tetrahydrocannabinols (7370)
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I
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Methylphenidate (1724)
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II
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Codeine (9050)
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II
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Dihydrocodeine (9120)
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II
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Oxycodone (9143)
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II
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Hydromorphone (9150)
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II
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Hydrocodone (9193)
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II
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Oripavine (9330)
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II
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Thebaine (9333)
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II
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Oxymorphone (9652)
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II
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Noroxymorphone (9668)
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II
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Fentanyl (9801)
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II
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The company plans to manufacture the listed controlled substances in bulk for
conversion and sale to dosage form manufacturers.
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 should be addressed, in quintuplicate,
to the Drug Enforcement Administration, Office of Diversion Control, Federal
Register Representative (ODL), 8701 Morrissette Drive, Springfield, Virginia
22152; and must be filed no later than June 29, 2009.
Dated: April 17, 2009.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. E9-9806 Filed 4-28-09; 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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