[Federal Register Volume 76, Number 76 (Wednesday, April 20, 2011)] [Notices] [Pages 22146-22147] From the Federal Register Online via the Government Publishing Office [www.gpo.gov] [FR Doc No: 2011-9611] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Registration By Notice dated June 17, 2010, and published in the Federal Register on June 28, 2010, 75 FR 36679, Lin Zhi International Inc., 670 Almanor Avenue, Sunnyvale, California 94085, 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 ------------------------------------------------------------------------ Tetrahydrocannabinols (7370)............... I 3,4-Methylenedioxymethamphetamine (MDMA) I (7405). Cocaine (9041)............................. II Oxycodone (9143)........................... II Hydrocodone (9193)......................... II Methadone (9250)........................... II Dextropropoxyphene, bulk (non-dosage forms) II (9273). Morphine (9300)............................ II ------------------------------------------------------------------------ The company plans to manufacture the listed controlled substances as bulk reagents for use in drug abuse testing. [[Page 22147]] 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 Lin Zhi International Inc., to manufacture the listed basic classes of controlled substances is consistent with the public interest at this time. DEA has investigated Lin Zhi International 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: April 13, 2011. Joseph T. Rannazzisi, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 2011-9611 Filed 4-19-11; 8:45 am] BILLING CODE 4410-09-P