[Federal Register Volume 63, Number 29 (Thursday, February 12, 1998)] [Notices] [Page 7182] From the Federal Register Online via the Government Publishing Office [www.gpo.gov] [FR Doc No: 98-3613] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Application Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that by letter dated October 2, 1997, which was received for processing on October 26, 1997, Nycomed, Inc., 33 Riverside Avenue, Rensselaer, New York 12144, made application to the Drug Enforcement Administration (DEA) for registration as a bulk manufacturer of methylphenidate (1724) a basic class of controlled substance listed in Schedule II. This bulk manufacture of methylphenidate is being conducted in conjunction and coordination with another bulk manufacturer. Any other such applicant and any person who is presently registered with DEA to manufacture such substances may file comments or objections to the issuance of the proposed registration. Any such comments or objections may be addressed, in quintuplicate, to the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, United States Department of Justice, Washington, DC 20537, Attention: DEA Federal Register Representative (CCR), and must be filed no later than April 13, 1998. Dated: January 8, 1998. John H. King, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 98-3613 Filed 2-11-98; 8:45 am] BILLING CODE 4410-09-M