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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