[Federal Register: April 2, 2003 (Volume 68, Number 63)] [Notices] [Page 16089-16090] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr02ap03-132] ----------------------------------------------------------------------- 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 14, 2003, Mallinckrodt, Inc., Mallinckrodt & Second Streets, St. Louis, Missouri 63147, made application by renewal to the Drug Enforcement Administration (DEA) for registration as a bulk manufacturer of the basic classes of controlled substance listed below: ------------------------------------------------------------------------ Drug Schedule ------------------------------------------------------------------------ Amphetamine (1100)......................... II Methamphetamine (1105)..................... II Methylphenidate (1724)..................... II Codeine (9050)............................. II Codeine-N-oxide (9053)..................... I Diprenorphine (9058)....................... II [[Page 16090]] Etorphine HCl (9059)....................... II Dihydrocodeine (9120)...................... II Oxycodone (9160)........................... II Dihydromorphine (9145)..................... I Hydromorphone (9150)....................... II Difenoxin (9168)........................... I Diphenoxylate (9170)....................... II Benzoylecgonine (9180)..................... II Ecgonine (9180)............................ II Hydrocodone (9193)......................... II Heroin (9200).............................. I Levorphanol (9220)......................... II Meperidine (9230).......................... II Methadone (9250)........................... II Methadone intermediate (9254).............. II Metopon (9260)............................. II Dextropropoxyphene, bulk (9273)............ II Morphine (9300)............................ II Morphine-N-oxide (9307).................... I Nicomorphine (9312)........................ I Normorphine (9313)......................... I Thebaine (9333)............................ II Opium extracts (9610)...................... II Opium fluid extract (9620)................. II Norlevorphanol (9634)...................... I Opium tincture (9630)...................... II Opium, powdered (9639)..................... II Opium, granulated (9640)................... II Levo-alphacetylmethadol (9648)............. II Oxymorphone (9652)......................... II Alfentanil (9737).......................... II Sufentanil (9740).......................... II Fentanyl (9801)............................ II Tetrahydrocannabinols (7370)............... I ------------------------------------------------------------------------ The firm plans to manufacture the controlled substances as analytical reference standards to be used internally and for sale to other companies. Any other such applicant and any person who is presently registered with 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. 03-7826 Filed 4-1-03; 8:45 am] BILLING CODE 4410-09-M