Diversion Control Homepage Diversion Control Homepage Privacy Policy Contact Us What's New Hot Items Site Map Search Diversion SiteDEA Diversion Control Program Logo and Banner

 

Federal Register Notices > Notice of Application 2006 > Mallinckrodt Inc.

Notices of Application - 2006


FR Doc E6-8917 [Federal Register: June 8, 2006 (Volume 71, Number 110)] [Notices] [Page 33315] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr08jn06-75]


DEPARTMENT OF JUSTICE

Drug Enforcement Administration

Manufacturer of Controlled Substances; Notice of Application

Pursuant to section 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on December 12, 2005, Mallinckrodt Inc., 3600 North Second Street, St. Louis, Missouri 63147, 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:

Drug  Schedule
Codeine-N-oxide (9053)  I
Difenoxin (9168)  I
Dihydromorphine (9145)  I
Morphine-N-oxide (9307)  I
Norlevorphanol (9634)  I
Normorphine (9313)  I
Tetrahydrocannabinols (7370)  I
Alfentanil (9737)  II
Amphetamine (1100)  II
Ecgonine (9180)  II
Codeine (9050)  II
Dextropropoxyphene, bulk (9273)  II
Dihydrocodeine (9120)  II
Diphenoxylate (9170)  II
Diprenorphine (9058)  II
Etorphine HCL (9059)  II
Fentanyl (9801)  II
Hydrocodone (9193)  II
Hydromorphone (9150)  II
Levo-alphacetylmethadol (9648)  II
Levorphanol (9220)  II
Meperidine (9230)  II
Methadone (9250)  II
Methadone intermediate (9254)  II
Methamphetamine (1105)  II
Methylphenidate (1724)  II
Metopon (9260)  II
Morphine (9300)  II
Nabilone (7379)  II
Opium extracts (9610)  II
Opium fluid extract (9620)  II
Opium tincture (9630)  II
Opium, granulated (9640)  II
Opium, powdered (9639)  II
Oxycodone (9143)  II
Oxymorphone (9652)  II
Phenazocine (9715)  II
Remifentanil (9739)  II
Sufentanil (9740)  II
Thebaine (9333)  II

The firm plans to manufacture the listed controlled substances for internal use and for sale to other companies.

Any other such applicant and any person who is presently registered with DEA to manufacture such a substance 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 being sent via regular mail may be addressed, in quintuplicate, to the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, Washington, DC 20537, Attention: DEA Federal Register Representative, Liaison and Policy Section (ODL); or any being sent via express mail should be sent to DEA Headquarters, Attention: DEA Federal Register Representative/ODL, 2401 Jefferson-Davis Highway, Alexandria, Virginia 22301; and must be filed no later than August 7, 2006.

Dated: June 1, 2006.

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

[FR Doc. E6-8917 Filed 6-7-06; 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).


     HOME

CONTACT US

SEARCH

BACK TO TOP