Federal Register Notices > Manufacturers 2009 > Noramco Inc.

FR Doc E9-14704[Federal Register: June 23, 2009 (Volume 74, Number 119)] [Notices] [Page 29720] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr23jn09-84]

DEPARTMENT OF JUSTICE

DRUG ENFORCEMENT ADMINISTRATION

Manufacturer of Controlled Substances; Notice of Application

Pursuant to Section 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on May 1, 2009, Noramco Inc., Division of Ortho-McNeil, Inc., 1440 Olympic Drive, Athens, Georgia 30601, made application by letter to the Drug Enforcement Administration (DEA) for registration as a bulk manufacturer of Noroxymorphone (9668), a basic class of controlled substance listed in schedule II.

The company plans to bulk manufacture the above listed controlled substance for distribution to its customers. Any other such applicant and any person who is presently registered with DEA to manufacture such a substance may file comments or objections to the issuance of the proposed registration pursuant to 21 CFR 1301.33(a).

Any such written comments or objections should be addressed, in quintuplicate, to the Drug Enforcement Administration, Office of Diversion Control, Federal Register Representative (ODL), 8701 Morrissette Drive, Springfield, VA 22152; and must be filed no later than August 24, 2009.

Dated: June 15, 2009.

Joseph T. Rannazzisi, 
Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.

[FR Doc. E9-14704 Filed 6-22-09; 8:45 am]

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