Agency: Drug Enforcement Administration

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[FR Doc E9-27344] 1. Agency Information Collection Activities: Proposed Collection; Comments

The Department of Justice (DOJ), Drug Enforcement Administration (DEA), will be submitting the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995. The proposed information collection is published to obtain comments from the public

Published: 2009-11-16 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-27345] 2. Agency Information Collection Activities: Proposed Collection; Comments

The Department of Justice (DOJ), Drug Enforcement Administration (DEA), will be submitting the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995. The proposed information collection is published to obtain comments from the public

Published: 2009-11-16 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

[FR Doc E9-27346] 3. Agency Information Collection Activities: Proposed Collection; Comments

The Department of Justice (DOJ), Drug Enforcement Administration (DEA) will be submitting the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995. The proposed information collection is published to obtain comments from the public

Published: 2009-11-16 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-27180] 4. Manufacturer of Controlled Substances; Notice of Registration

By Notice dated June 15, 2009, and published in the Federal Register on June 23, 2009, (74 FR 29719), Noramco Inc., Division of OrthoMcNeil, Inc., 1440 Olympic Drive, Athens, Georgia 30601, made application by letter to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of Tapentadol (9780), a basic class of

Published: 2009-11-12 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-27193] 5. Manufacturer of Controlled Substances; Notice of Registration

By Notice dated April 17, 2009, and published in the Federal Register on April 29, 2009, (74 FR 19599), Stepan Company, Natural Products Dept., 100 W. Hunter Avenue, Maywood, New Jersey 07607, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled

Published: 2009-11-12 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-27194] 6. Manufacturer of Controlled Substances; Notice of Registration

By Notice dated June 15, 2009, and published in the Federal Register on June 23, 2009, (74 FR 29719), Boehringer Ingelheim Chemicals, Inc., 2820 N. Normandy Drive, Petersburg, Virginia 23805, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled

Published: 2009-11-12 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-26755] 7. Importer of Controlled Substances; Notice of Registration

By Notice dated June 3, 2009, and published in the Federal Register on June 9, 2009, (74 FR 27347), Stepan Company, Natural Products Department, 100 W. Hunter Avenue, Maywood, New Jersey 07607, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as an importer of Coca Leaves (9040), a basic class of

Published: 2009-11-06 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-26756] 8. Importer of Controlled Substances; Notice of Registration

By Notice dated June 15, 2009, and published in the Federal Register on June 23, 2009, (74 FR 29718), Boehringer Ingelheim Chemicals, Inc., 2820 N. Normandy Drive, Petersburg, Virginia 23805, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as an importer of Phenylacetone (8501), a basic class of

Published: 2009-11-06 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

[FR Doc E9-25999] 9. Importer of Controlled Substances; Notice of Application

Pursuant to Title 21 Code of Federal Regulations 1301.34(a), this is notice that on September 11, 2009, Johnson Matthey, Inc., Pharmaceutical Materials, 2003 Nolte Drive, West Deptford, New Jersey 080661742, made application by renewal to the Drug Enforcement Administration (DEA) for registration as an importer of the basic classes of

Published: 2009-10-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-25895] 10. Manufacturer of Controlled Substances; Notice of Application

Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on March 27, 2009, Varian, Inc., Lake Forest, 25200 Commercentre Drive, Lake Forest, California 92630 8810, made application by renewal to the Drug Enforcement
Administration (DEA) as a bulk manufacturer of the basic classes of controlled

Published: 2009-10-28 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-25899] 11. Manufacturer of Controlled Substances; Notice of Application

Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on August 26, 2009, Cayman Chemical Company, 1180 East Ellsworth Road, Ann Arbor, Michigan 48108, made application by renewal to the Drug Enforcement Administration (DEA) as a bulk manufacturer of the basic classes of controlled substances

Published: 2009-10-28 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-26002] 12. Manufacturer of Controlled Substances; Notice of Application

Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on September 10, 2009, Johnson Matthey Inc., Custom Pharmaceuticals Department, 2003 Nolte Drive, West Deptford, New Jersey 080661742, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk

Published: 2009-10-28 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-26003] 13. Manufacturer of Controlled Substances; Notice of Application

Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on June 18, 2009, Archimica, Inc., 2460 W. Bennett Street, Springfield, Missouri 658071229, made application by letter to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of Tapentadol (9780), a basic class of

Published: 2009-10-28 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-25882] 14. Manufacturer of Controlled Substances; Notice of Registration

By Notice dated June 15, 2009, and published in the Federal Register on June 23, 2009, (74 FR 29718), Austin Pharma LLC., 811 Paloma Drive, Suite A, Round Rock, Texas 786652402, 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

Published: 2009-10-28 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-25885] 15. Manufacturer of Controlled Substances; Notice of Registration

By Notice dated February 5, 2009 and published in the Federal Register on February 11, 2009, (74 FR 6921), Siegfried (USA), Inc., 33 Industrial Park Road, Pennsville, New Jersey 08070, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled substances

Published: 2009-10-28 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-25886] 16. Manufacturer of Controlled Substances Notice of Registration

By Notice dated June 22, 2009, and published in the Federal Register on June 26, 2009, (74 FR 30621), Wildlife Laboratories Inc., 1401 Duff Drive, Suite 400, Fort Collins, Colorado 80524, made application to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of Carfentanil (9743), a basic class of controlled

Published: 2009-10-28 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-25887] 17. Manufacturer of Controlled Substances; Notice of Registration

By Notice dated June 15, 2009, and published in the Federal Register on June 23, 2009, (74 FR 29720), Noramco Inc., Division of OrthoMcNeil, Inc., 1440 Olympic Drive, Athens, Georgia 30601, made application by letter to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of Noroxymorphone (9668), a basic class of

Published: 2009-10-28 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-25937] 18. Registration Requirements for Individual Practitioners Operating in a ``Locum

Summary: On December 1, 2006, the Drug Enforcement Administration (DEA) published in the Federal Register a Final Rule ``Clarification of Registration Requirements for Individual Practitioners'' (71 FR 69478). The Final Rule makes it clear that when an individual practitioner practices in more than one State, he or she must obtain a separate

Published: 2009-10-28 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-25892] 19. Manufacturer of Controlled Substances; Notice of Registration

By Notice dated July 1, 2009, and published in the Federal Register on July 13, 2009, (74 FR 33476), Organix Inc., 240 Salem Street, Woburn, Massachusetts 01801, made application by letter to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of Marihuana (7360), a basic class of controlled substance listed in

Published: 2009-10-28 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-25905] 20. Importer of Controlled Substances; Notice of Application

This is notice that on July 9, 2009, Cody Laboratories Inc., 601 Yellowstone Avenue, Cody, Wyoming 824149321, made application by renewal to the Drug Enforcement Administration (DEA) for registration as an importer of the basic classes of controlled substances listed in schedule II:
Drug

Published: 2009-10-28 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-25894] 21. Manufacturer of Controlled Substances; Notice of Registration

By Notice dated June 22, 2009, and published in the Federal Register on June 30, 2009, (74 FR 31314), Chattem Chemicals Inc., 3801 St. Elmo Avenue, Building 18, Chattanooga, Tennessee 37409, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled

Published: 2009-10-28 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-26000] 22. Importer of Controlled Substances; Notice of Application

Pursuant to 21 U.S.C. 958(i), the Attorney General shall, prior to issuing a registration under this section to a bulk manufacturer of a controlled substance in schedule I or II, and prior to issuing a regulation under 21 U.S.C. 952(a)(2) authorizing the importation of such a substance, provide manufacturers holding registrations for the bulk

Published: 2009-10-28 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-25901] 23. Manufacturer of Controlled Substances; Notice of Registration

By Notice dated June 15, 2009, and published in the Federal Register on June 23, 2009, (74 FR 29717), Chattem Chemicals Inc., 3801 St. Elmo Avenue, Building 18, Chattanooga, Tennessee 37409, made application by letter to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled

Published: 2009-10-28 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-26001] 24. Importer of Controlled Substances; Notice of Application

Pursuant to 21 U.S.C. 958(i), the Attorney General shall, prior to issuing a registration under this Section to a bulk manufacturer of a controlled substance in schedule I or II, and prior to issuing a regulation under 21 U.S.C. 952(a)(2) authorizing the importation of such a substance, provide manufacturers holding registrations for the bulk

Published: 2009-10-28 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-25862] 25. Importer of Controlled Substances Notice of Application

Pursuant to 21 U.S.C. 958(i), the Attorney General shall, prior to issuing a registration under this Section to a bulk manufacturer of a controlled substance in schedule I or II, and prior to issuing a regulation under 21 U.S.C. 952(a)(2) authorizing the importation of such a substance, provide manufacturers holding registrations for the bulk

Published: 2009-10-28 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

Years: 2000200120022003200420052006200720082009

Pages: 12345»