[Federal Register: September 10, 2007 (Volume 72, Number 174)] [Notices] [Page 51664-51665] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr10se07-78] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Registration By Notice dated May 10, 2007, and published in the Federal Register on May 18, 2007, (72 FR 28073), Cody Laboratories, Inc., 601 Yellowstone Avenue, Cody, Wyoming 82414, 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 schedule I and II: ------------------------------------------------------------------------ Drug Schedule ------------------------------------------------------------------------ Dihydromorphine (9145)..................... I Amphetamine (1100)......................... II [[Page 51665]] Methamphetamine (1105)..................... II Amobarbital (2125)......................... II Pentobarbital (2270)....................... II Secobarbital (2315)........................ II Cocaine (9041)............................. II Oxycodone (9143)........................... II Hydromorphone (9150)....................... II Diphenoxylate (9170)....................... II Meperidine (9230).......................... II Oxymorphone (9652)......................... II Sufentanil (9740).......................... II Fentanyl (9801)............................ II ------------------------------------------------------------------------ The company plans on manufacturing the listed controlled substances in bulk for sale 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 Cody Laboratories, Inc. to manufacture the listed basic class of controlled substance is consistent with the public interest at this time. DEA has investigated Cody Laboratories, 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, 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: August 28, 2007. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. E7-17767 Filed 9-7-07; 8:45 am] BILLING CODE 4410-09-P
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