Federal
Register Notices >
Notices of Application - 2003 > Rhodes Technologies
FR Doc 03-7827
[Federal Register: April 2, 2003 (Volume 68, Number 63)]
[Notices]
[Page 16091-16092]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr02ap03-138]
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 January 9, 2003, Rhodes Technologies, 498 Washington
Street, Coventry, Rhode Island 02816, made application by renewal and by
letters dated January 28, 2003 and
February 26, 2003, to the Drug Enforcement Administration (DEA) for
registration as a bulk manufacturer of the basic class of Schedule I and
II controlled substances listed below:
Drug |
Schedule |
Codeine (9050) |
II |
Oxycodone (9143) |
II |
Thebaine (9333) |
II |
Methylphenidate (1724) |
II |
Tetrahydrocannabinols (7370) |
II |
Hydromorphone (9150) |
II |
Hydrocodone (9193) |
II |
Fentanyl (9801) |
II |
Noroxymorphone (9668) |
II |
Dihydrocodeine (9120) |
II |
The firm plans to produce bulk products for
conversion and distribution to its customers.
Any other such applicant and any person who is
presently registered with
[[Page 16092]]
DEA to manufacture such substances may file comments
or objections to the issuance of the proposed registration.
Any such comments or objections may be addressed, in
quintuplicate, to the Deputy Assistant Administrator, Office of Diversion
Control, Drug Enforcement Administration, United States Department of
Justice, Washington, DC 20537, Attention: Drug Operations Section,
Domestic Drug Unit (ODOD) and must be filed no later than 60 days from
publication.
Dated: March 14, 2003.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 03-7827 Filed 4-1-03; 8:45 am]
BILLING CODE 4410-09-M
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