[Federal Register: July 9, 1998 (Volume 63, Number 131)] [Notices] [Page 37138] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr09jy98-112] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Registration By Notice dated February 24, 1998, and published in the Federal Register on March 6, 1998, (63 FR 11310), Johnson Matthey, Inc., Custom Pharmaceuticals Department, 2003 Nolte Drive, West Deptford, New Jersey 08066, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled substances listed below. ------------------------------------------------------------------------ Drug Schedule ------------------------------------------------------------------------ Difenoxin (9168)........................... I Propiram (9649)............................ I Amphetamine (1100)......................... II Methylphenidate (1724)..................... II Phenylacetone (8501)....................... II Dihydrocodeine (9120)...................... II Oxycodone (9143)........................... II Hydromorphone (9150)....................... II Hydrocodone (9193)......................... II Meperidine (9230).......................... II Thebaine (9333)............................ II Alfentanil (9737).......................... II Sufentanil (9740).......................... II Carfentanil (9743)......................... II Fentanyl (9801)............................ II ------------------------------------------------------------------------ The plans to manufacture the listed controlled substances in bulk to supply final dosage form manufacturers. DEA has considered the factors in Title 21, United States Code, Section 823(a) and determined that the registration of Johnson Matthey, Inc. to manufacture the listed controlled substances is consistent with the public interest at this time. Therefore, pursuant to 21 U.S.C 823 and 28 CFR 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 classes of controlled substances listed above is granted. Dated: June 10, 1998. John H. King, Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration. [FR Doc. 98-18214 Filed 7-8-98; 8:45 am] BILLING CODE 4410-09-M