[Federal Register Volume 62, Number 26 (Friday, February 7, 1997)] [Notices] [Page 5845] From the Federal Register Online via the Government Publishing Office [www.gpo.gov] [FR Doc No: 97-3083] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Manufacturer of Controlled Substances; Notice of Registration By Notice dated July 25, 1996, and published in the Federal Register on July 31, 1996, (61 FR 39986), Guilford Pharmaceuticals, Inc., Attn: Ross S. Laderman, 6611 Tributary Street, Baltimore, Maryland 21224, made application to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of cocaine (9041), a basic class of controlled substance listed in Schedule 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 Guilford Pharmaceuticals, Inc. to manufacture cocaine is consistent with the public interest at this time. Therefore, pursuant to 21 U.S.C. Sec. 823 and 28 CFR 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 class of controlled substance listed above is granted. Dated: January 9, 1997. Gene R. Haislip, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 97-3083 Filed 2-6-97; 8:45 am] BILLING CODE 4410-09-M