Diversion Control Division, US Department of Justice, Drug Enforcement Administration

RESOURCES > Federal Register Notices > Importers Notice of Application - 2000 > Morton Grove Pharmaceuticals, Inc.; Notice of Withdrawal

Importers Notice of Application - 2000

[Federal Register: September 14, 2000 (Volume 65, Number 179)] [Notices] [Page 55644] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr14se00-87]


DEPARTMENT OF JUSTICE

Drug Enforcement Administration

Importer of Controlled Substances; Notice of Withdrawal

As set forth in the Federal Register (FR Doc. 99-21588) Vol. 64, No. 161 at page 45565, dated August 20, 1999, Morton Grove Pharmaceuticals, Inc., 6451 W. Main Street, Morton Grove, Illinois 60053, made application to the Drug Enforcement Administration for registration as an importer of codeine (9050).

Two registered bulk manufacturers of codeine requested a hearing to deny the proposed registration of Morton Grove Pharmaceuticals. Morton Grove Pharmaceuticals requested by letter that its application be withdrawn. Therefore, Morton Grove Pharmaceuticals' application to import codeine is hereby withdrawn.

Dated: August 21, 2000.

John H. King,
Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.

[FR Doc. 00-23621 Filed 9-13-00; 8:45 am]

BILLING CODE 4410-09-M

 

NOTICE: This is an unofficial version. An official version of this publication may be obtained directly from the Government Printing Office (GPO).

Emergency Disaster Relief
National Prescription Drug Take Back Day. Turn in your unused or expired medication for safe disposal here.
RX Abuse Online

U.S. DEPARTMENT OF JUSTICE  •  DRUG ENFORCEMENT ADMINISTRATION
Diversion Control Division  •  8701 Morrissette Drive  •  Springfield, VA 22152  •  1-800-882-9539

DOJ Legal Policies and Disclaimers    |    DOJ Privacy Policy    |    FOIA    |    Section 508 Accessibility