[Federal Register Volume 84, Number 218 (Tuesday, November 12, 2019)] [Notices] [Page 61074] From the Federal Register Online via the Government Publishing Office [www.gpo.gov] [FR Doc No: 2019-24543] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA-539] Bulk Manufacturer of Controlled Substances Application: Cambrex Charles City 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 on or before January 13, 2020. ADDRESSES: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152. SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.33(a), this is notice that on May 15, 2019, Cambrex Charles City, 1205 11th Street, Charles City, Iowa 50616-3466 applied to be registered as a bulk manufacturer of the following basic classes of controlled substances: ------------------------------------------------------------------------ Controlled substance Drug code Schedule ------------------------------------------------------------------------ Gamma Hydroxybutyric Acid............ 2010 I Amphetamine.......................... 1100 II Lisdexamfetamine..................... 1205 II Methylphenidate...................... 1724 II ANPP (4-Anilino-N-phenethyl-4- 8333 II piperidine). Phenylacetone........................ 8501 II Cocaine.............................. 9041 II Codeine.............................. 9050 II Oxycodone............................ 9143 II Hydromorphone........................ 9150 II Hydrocodone.......................... 9193 II Morphine............................. 9300 II Oripavine............................ 9330 II Thebaine............................. 9333 II Opium extracts....................... 9610 II Opium fluid extract.................. 9620 II Opium tincture....................... 9630 II Opium, powdered...................... 9639 II Oxymorphone.......................... 9652 II Noroxymorphone....................... 9668 II Fentanyl............................. 9801 II ------------------------------------------------------------------------ The company plans to manufacture the listed controlled substances in bulk for conversion to other controlled substances and sale to its customers, for dosage form development, for clinical trials, and for use in stability qualification studies. Dated: October 30, 2019. William T. McDermott, Assistant Administrator. [FR Doc. 2019-24543 Filed 11-8-19; 8:45 am] BILLING CODE 4410-09-P