Federal
Register Notices >
Notices of Application - 2003 > Siegfried (USA) Inc.
FR Doc 03-8582
[Federal Register: April 9, 2003 (Volume 68, Number 68)]
[Notices]
[Page 17408]
From the Federal Register Online via GPO Access [wais.access.gpo.gov]
[DOCID:fr09ap03-89]
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 March 29, 2002, Siegfried (USA) Inc., made application
by renewal to the Drug Enforcement Administration for registration as a
bulk manufacturer of the basic classes of controlled substance listed
below:
Drug |
Schedule |
Amphetamine (1100) |
II |
Methylphenidate (1724) |
II |
Amobarbital (2125) |
II |
Pentobarbital (2270) |
II |
Secobarbital (2315) |
II |
Glutethimide (2550) |
II |
Codeine (9050) |
II |
Hydrocodone (9193) |
II |
Morphine (9300) |
II |
Oxycodone (9143) |
II |
Methadone (9250) |
II |
Methadone-intermediate (9254) |
II |
Dextropropoxyphene, bulk (non
dosage forms) (9273). |
II |
Any other such applicant and any person who is
presently registered with DEA to manufacture such substance 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: DEA Federal Register
Representative (CCR), and must be filed no later than 60 days from
publication.
Dated: March 21, 2003.
Laura M. Nagel,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 03-8582 Filed 4-8-03; 8:45 am]
BILLING CODE 4410-09-M
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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