[Federal Register Volume 61, Number 88 (Monday, May 6, 1996)] [Notices] [Page 20275] From the Federal Register Online via the Government Publishing Office [www.gpo.gov] [FR Doc No: 96-11254] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Registration By Notice dated February 2, 1996, and published in the Federal Register on February 13, 1996, (61 FR 5571), Orpharm Inc., 728 West 19th Street, Houston, Texas 77008, made application to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled substances listed below: ------------------------------------------------------------------------ Drug Schedule ------------------------------------------------------------------------ Methadone (9250)........................... II. Methadone-intermediate (9254).............. II. Levo-alphacetylmethadol (9648)............. II. ------------------------------------------------------------------------ No comments or objections have been received. DEA has considered the factors in 21 U.S.C. Sec. 823(a) and determined that the registration of Orpharm Inc. to manufacture the listed controlled substances is consistent with the public interest at this time. Therefore, pursuant to 21 U.S.C. Sec. 823 and 28 C.F.R. Secs. 0.100 and 0.104, the Deputy Assistant Administrator, Office of Diversion Control, hereby orders that the application submitted by the above firm for registration as a bulk manufacturer of the basic classes of controlled substances listed above is granted. Dated: April 29, 1996. Gene R. Haislip, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 96-11254 Filed 5-3-96; 8:45 am] BILLING CODE 4410-09-M