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[FR Doc E9-25893] 26. 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 April 9, 2009, Aldrich Chemical Company Inc., DBA Isotec, 3858 Benner Road, Miamisburg, Ohio 453424304, 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 E9-25895] 27. 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] 28. 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] 29. 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] 30. 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] 31. 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] 32. 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] 33. 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] 34. 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 E9-25128] 35. 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: 2009-10-20 DEPARTMENT OF JUSTICE : Drug Enforcement Administration
[FR Doc E9-24714] 36. Importer of Controlled Substances; Notice of Registration
By Notice dated June 22, 2009, and published in the Federal Register on June 26, 2009, (74 FR 30620), 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 an importer of the basic classes of controlled substances
Published: 2009-10-14 DEPARTMENT OF JUSTICE : Drug Enforcement Administration
[FR Doc E9-22502] 37. 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: 2009-09-18 DEPARTMENT OF JUSTICE : Drug Enforcement Administration
[FR Doc E9-22451] 38. 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), Aptuit, 10245 Hickman Mills Drive, Kansas City, Missouri 64137, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as an importer of Marihuana (7360), a basic class of controlled substance listed in
Published: 2009-09-18 DEPARTMENT OF JUSTICE : Drug Enforcement Administration
[FR Doc E9-22452] 39. Importer of Controlled Substances Notice of Registration
By Notice dated June 15, 2009, and published in the Federal Register on June 24, 2009, (74 FR 30111), AllTech Associates Inc., 2051 Waukegan Road, Deerfield, Illinois 60015, made application to the Drug Enforcement Administration (DEA) to be registered as an importer of the basic classes of controlled substances listed in schedules I and II:
Published: 2009-09-18 DEPARTMENT OF JUSTICE : Drug Enforcement Administration
[FR Doc E9-22505] 40. 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 29719), Aptuit (Allendale) Inc., 75 Commerce Drive, Allendale, New Jersey 07401, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as an importer of the basic classes of controlled substances listed in schedule
Published: 2009-09-18 DEPARTMENT OF JUSTICE : Drug Enforcement Administration
[FR Doc E9-22506] 41. Importer 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), Noramco, Inc., Division of
OrthoMcNeil, Inc., 500 Swedes Landing Road, Wilmington, Delaware 19801, made application by letter to the Drug Enforcement
Administration (DEA) to be registered as an importer of Tapentadol
(9780), a basic class of
Published: 2009-09-18 DEPARTMENT OF JUSTICE : Drug Enforcement Administration
[FR Doc E9-22503] 42. 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 July 2, 2009, GE Healthcare, 3350 North Ridge Avenue, Arlington Heights, Illinois 600041412, made application by renewal to the Drug Enforcement Administration (DEA) as a bulk manufacturer of Cocaine (9041), a basic class of controlled
Published: 2009-09-18 DEPARTMENT OF JUSTICE : Drug Enforcement Administration
[FR Doc E9-22453] 43. Manufacturer of Controlled Substances Notice of Registration
By Notice dated June 3, 2009, and published in the Federal Register on June 9, 2009, (74 FR 27350), Norac Inc., 405 S. Motor Avenue, P.O. Box 577, Azusa, California 917023232, made application by letter to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of Nabilone (7379), a basic class of controlled substance
Published: 2009-09-18 DEPARTMENT OF JUSTICE : Drug Enforcement Administration
[FR Doc E9-22123] 44. 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: 2009-09-15 DEPARTMENT OF JUSTICE : Drug Enforcement Administration
[FR Doc E9-21778] 45. 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
[[Page 46618]]
the Paperwork Reduction Act of 1995. The proposed information
collection is published to obtain comments
Published: 2009-09-10 DEPARTMENT OF JUSTICE : Drug Enforcement Administration
[FR Doc E9-21781] 46. 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: 2009-09-10 DEPARTMENT OF JUSTICE : Drug Enforcement Administration
[FR Doc E9-21698] 47. Identification of Institution-based Individual Practitioners
The Drug Enforcement Administration (DEA) is soliciting public comments on how best to standardize the specific internal code number associated with each individual practitioner permitted by the hospital or other institutional practitioner to administer, dispense, or prescribe controlled substances using that institution's DEA registration. DEA is
Published: 2009-09-09 DEPARTMENT OF JUSTICE : Drug Enforcement Administration
[FR Doc E9-21525] 48. Manufacturer of Controlled Substances; Notice of Application
Pursuant to Sec. 1301.33(a), Title 21 of the Code of Federal Regulations (CFR), this is notice that on July 1, 2009, Alltech Associates Inc., 2051 Waukegan Road, Deerfield, Illinois 60015, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled
Published: 2009-09-08 DEPARTMENT OF JUSTICE : Drug Enforcement Administration
[FR Doc E9-21526] 49. 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 18, 2009, Research Triangle Institute, Kenneth H. Davis Jr., Hermann Building, East Institute Drive, P.O. Box 12194, Research Triangle, North Carolina 27709, made application by renewal to the Drug Enforcement Administration (DEA) as
Published: 2009-09-08 DEPARTMENT OF JUSTICE : Drug Enforcement Administration
[FR Doc E9-21527] 50. 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 19598), AMRI Rensselaer, Inc., 33 Riverside Avenue, Rensselaer, New York 12144, 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 in
Published: 2009-09-08 DEPARTMENT OF JUSTICE : Drug Enforcement Administration
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