[Federal Register Volume 60, Number 249 (Thursday, December 28, 1995)] [Notices] [Pages 67140-67141] From the Federal Register Online via the Government Publishing Office [www.gpo.gov] [FR Doc No: 95-31389] ======================================================================= ----------------------------------------------------------------------- [[Page 67141]] DEPARTMENT OF JUSTICE Drug Enforcement Administration Importation of Controlled Substances; Notice of Application Pursuant to Section 1008 of the Controlled Substances Import and Export Act (21 U.S.C. 958(i)), the Attorney General shall, prior to issuing a registration under this Section to a bulk manufacturer of a controlled substance in Schedule I or II and prior to issuing a regulation under Section 1002(a) authorizing the importation of such a substance, provide manufacturers holding registrations for the bulk manufacture of the substance an opportunity for a hearing. Therefore, in accordance with Section 1311.42 of Title 21, Code of Federal Regulations (CFR), notice is hereby given that on October 11, 1995, The Binding Site, Inc., 5889 Oberlin Drive, Suite 101, San Diego, California 92121, made application to the Drug Enforcement Administration to be registered as an importer of the basic classes of controlled substances listed below: ------------------------------------------------------------------------ Drug Schedule ------------------------------------------------------------------------ Methaqualone (2565)........................ I Lysergic acid diethylamide (7315).......... I Tetrahydrocannabinols (7370)............... I Normorphine (9313)......................... I Methamphetamine (1105)..................... II Amobarbital (2125)......................... II Secobarbital (2315)........................ II Ecgonine (9130)............................ II Ethylmorphine (9190)....................... II Meperidine intermediate-C (9234)........... II ------------------------------------------------------------------------ The firm plans to import the above listed substances in milligrams quantities for labelling with enzymes, fluorophores and radioisotopes for immunoassays. Any manufacturer holding, or applying for, registration as a bulk manufacturer of this basic class of controlled substance may file written comments on or objections to the application described above and may, at the same time, file a written request for a hearing on such application in accordance with 21 CFR 1301.54 in such form as prescribed by 21 CFR 1316.47. Any such comments, objections, or requests for a hearing may be addressed to the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, United States Department of Justice, Washington, D.C. 20537, Attention: DEA Federal Register Representative (CCR), and must be filed no later than January 29, 1996. This procedure is to be conducted simultaneously with and independent of the procedures described in 21 CFR 1311.42(b), (c), (d), (e), and (f). As noted in a previous notice at 40 FR 43745-46 (September 23, 1975), all applicants for registration to import a basic class of any controlled substance in Schedule I or II are and will continue to be required to demonstrate to the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration that the requirements for such registration pursuant to 21 U.S.C. 958(a), 21 U.S.C. 823(a), and 21 CFR 1311.42(a), (b), (c), (d), (e), and (f) are satisfied. Dated: December 15, 1995. Gene R. Haislip, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 95-31389 Filed 12-27-95; 8:45 am] BILLING CODE 4410-09-M