[Federal Register Volume 78, Number 17 (Friday, January 25, 2013)] [Notices] [Pages 5500-5501] From the Federal Register Online via the Government Publishing Office [www.gpo.gov] [FR Doc No: 2013-01600] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Registration; Noramco, Inc. By Notice dated October 9, 2012, and published in the Federal Register on October 18, 2012, 77 FR 64143, Noramco, Inc., 500 Swedes Landing Road, Wilmington, Delaware 19801-4417, 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 ------------------------------------------------------------------------ Codeine-N-oxide (9053)..................... I Dihydromorphine (9145)..................... I Morphine-N-oxide (9307).................... I Amphetamine (1100)......................... II Methylphenidate (1724)..................... II Phenylacetone (8501)....................... II Codeine (9050)............................. II Dihydrocodeine (9120)...................... II Oxycodone (9143)........................... II [[Page 5501]] Hydromorphone (9150)....................... II Hydrocodone (9193)......................... II Morphine (9300)............................ II Oripavine (9330)........................... II Thebaine (9333)............................ II Opium extracts (9610)...................... II Opium fluid extract (9620)................. II Opium tincture (9630)...................... II Opium, powdered (9639)..................... II Opium, granulated (9640)................... II Oxymorphone (9652)......................... II Noroxymorphone (9668)...................... II Tapentadol (9780).......................... II ------------------------------------------------------------------------ The company plans to manufacture the listed controlled substances in bulk for distribution to its customers. No comments or objections have been received. DEA has considered the factors in 21 U.S.C. 823(a) and determined that the registration of Noramco, Inc., to manufacture the listed basic classes of controlled substances is consistent with the public interest at this time. DEA has investigated Noramco, Inc., to ensure that the company's registration is consistent with the public interest. The investigation has included inspection and testing of the company's physical security systems, verification of the company's compliance with state and local laws, and a review of the company's background and history. Therefore, pursuant to 21 U.S.C. 823(a), and in accordance with 21 CFR 1301.33, the above named company is granted registration as a bulk manufacturer of the basic classes of controlled substances listed. Dated: January 15, 2013. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 2013-01600 Filed 1-24-13; 8:45 am] BILLING CODE 4410-09-P