Bulk Manufacturer of Controlled Substances Application: Johnson Matthey Inc.

Federal Register, Volume 81 Issue 249 (Wednesday, December 28, 2016)

Federal Register Volume 81, Number 249 (Wednesday, December 28, 2016)

Notices

Pages 95647-95648

From the Federal Register Online via the Government Publishing Office www.gpo.gov

FR Doc No: 2016-31283

-----------------------------------------------------------------------

DEPARTMENT OF JUSTICE

Drug Enforcement Administration

Docket No. DEA-392

Bulk Manufacturer of Controlled Substances Application: Johnson Matthey Inc.

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 February 27, 2017.

ADDRESSES: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DRW, 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

Page 95648

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 Assistant Administrator of the DEA Diversion Control Division (``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 September 5, 2016, Johnson Matthey Inc., Pharmaceuticals Materials, 900 River Road, Conshohocken, Pennsylvania 19428, 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

Methylphenidate.................... 1724 II

Codeine............................ 9050 II

Oxycodone.......................... 9143 II

Diphenoxylate...................... 9170 II

Hydrocodone........................ 9193 II

Meperidine......................... 9230 II

Methadone.......................... 9250 II

Methadone intermediate............. 9254 II

Morphine........................... 9300 II

Thebaine........................... 9333 II

Opium tincture..................... 9630 II

------------------------------------------------------------------------

The company plans to manufacture the listed controlled substances in bulk for distribution and sale to its customers. Thebaine (9333) will be used to manufacture other controlled substances for sale in bulk to its customers.

Dated: December 20, 2016.

Louis J. Milione,

Assistant Administrator.

FR Doc. 2016-31283 Filed 12-27-16; 8:45 am

BILLING CODE 4410-09-P

VLEX uses login cookies to provide you with a better browsing experience. If you click on 'Accept' or continue browsing this site we consider that you accept our cookie policy. ACCEPT