[Federal Register Volume 81, Number 98 (Friday, May 20, 2016)] [Notices] [Pages 31960-31961] From the Federal Register Online via the Government Publishing Office [www.gpo.gov] [FR Doc No: 2016-11938] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA-392] Bulk Manufacturer of Controlled Substances Application: American Radiolabeled Chemicals ACTION: Notice of application. ----------------------------------------------------------------------- DATES: Registered bulk manufacturers of the affected basic classes, and applicants therefore, may file written comments on or objections to the issuance of the proposed registration in accordance with 21 CFR 1301.33(a) on or before July 19, 2016. ADDRESSES: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/ODW, 8701 Morrissette Drive, Springfield, Virginia 22152. SUPPLEMENTARY INFORMATION: The Attorney General has delegated her authority under the Controlled Substances Act to the Administrator of the Drug Enforcement Administration (DEA), 28 CFR 0.100(b). Authority to exercise all necessary functions with respect to the promulgation and implementation of 21 CFR part 1301, incident to the registration of manufacturers, distributors, dispensers, importers, and exporters of controlled substances (other than final orders in connection with suspension, denial, or revocation of registration) has been redelegated to the Deputy Assistant Administrator of the DEA Office of Diversion Control (``Deputy Assistant Administrator'') pursuant to section 7 of 28 CFR part 0, appendix to subpart R. In accordance with 21 CFR 1301.33(a), this is notice that on March 3, 2016, American Radiolabeled Chemicals, 101 Arc Drive, Saint Louis, Missouri 63146 applied to be registered as a bulk manufacturer of the following basic classes of controlled substances: ------------------------------------------------------------------------ Controlled substance Schedule ------------------------------------------------------------------------ Gamma Hydroxybutyric Acid (2010)............ I Ibogaine (7260)............................. I Lysergic Acid Diethylamide (7315)........... I Tetrahydrocannabinols (7370)................ I Dimethyltryptamine (7435)................... I 1-[1-(2-Thienyl)cyclohexyl]piperidine (7470) I Dihydromorphine (9145)...................... I Heroin (9200)............................... I Normorphine (9313).......................... I Amphetamine (1100).......................... II Methamphetamine (1105)...................... II [[Page 31961]] Amobarbital (2125).......................... II Phencyclidine (7471)........................ II Phenylacetone (8501)........................ II Cocaine (9041).............................. II Codeine (9050).............................. II Dihydrocodeine (9120)....................... II Oxycodone (9143)............................ II Hydromorphone (9150)........................ II Ecgonine (9180)............................. II Hydrocodone (9193).......................... II Meperidine (9230)........................... II Metazocine (9240)........................... II Methadone (9250)............................ II Dextropropoxyphene, bulk (non-dosage forms) II (9273). Morphine (9300)............................. II Oripavine (9330)............................ II Thebaine (9333)............................. II Oxymorphone (9652).......................... II Phenazocine (9715).......................... II Carfentanil (9743).......................... II Fentanyl (9801)............................. II ------------------------------------------------------------------------ The company plans to manufacture small quantities of the listed controlled substances as radiolabeled compounds for biochemical research. Dated: May 16, 2016. Louis J. Milione, Deputy Assistant Administrator. [FR Doc. 2016-11938 Filed 5-19-16; 8:45 am] BILLING CODE 4410-09-P