Diversion Control Division, US Department of Justice, Drug Enforcement Administration

Manufacturers Notice of Application - 2012

[Federal Register, Volume 77, Number 81 (Thursday, April 26, 2012)]
[Notices]
[Pages 24986-24987]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-10054]


DEPARTMENT OF JUSTICE

Drug Enforcement Administration

Manufacturer of Controlled Substances; Notice of Application Rhodes Technologies

Pursuant to Sec. 1301.33(a), Title 21 of the Code of Federal Regulations (CFR), this is notice that on February 24, 2012, 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 following basic classes of controlled substances:

Drug Schedule
Tetrahydrocannabinols (7370) I
Methylphenidate (1724) II
Codeine (9050) II
Dihydrocodeine (9120) II
Oxycodone (9143) II
Hydromorphone (9150) II
Hydrocodone (9193) II
Oripavine (9330) II
Thebaine (9333) II
Oxymorphone (9652) II
Noroxymorphone (9668) II
Fentanyl (9801) II

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

[[Page 24987]]

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 25, 2012.

Dated: April 17, 2012.

Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.

[FR Doc. 2012-10054 Filed 4-25-12; 8:45 am]

BILLING CODE 4410-09-P

 

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