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[FR Doc E9-9806] 101. 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 February 25, 2009, Rhodes Technologies, 498 Washington Street, Coventry, Rhode Island 02816, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled

Published: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-9807] 102. 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 February 20, 2009, Stepan Company, Natural Products Dept., 100 W. Hunter Avenue, Maywood, New Jersey 07607, made application by renewal to the Drug Enforcement Administration (DEA) as a bulk manufacturer of the basic classes of controlled

Published: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-9797] 103. Bob's Pharmacy and Diabetic Supplies; Revocation of Registration

On August 15, 2008, I, the Deputy Administrator of the Drug Enforcement Administration, issued an Order to Show Cause and Immediate Suspension of Registration to Bob's Pharmacy and Diabetic Supplies (Respondent), of Winter Haven, Florida. The Show Cause Order proposed the revocation of Respondent's DEA Certificate of Registration, FB0181216,

Published: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-9778] 104. Importer of Controlled Substances; Notice of Application

This is notice that on March 10, 2009, Penick Corporation, 33 Industrial Park Road, Pennsville, New Jersey 08070, 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: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-9782] 105. 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: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-9780] 106. 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: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-9784] 107. Importer of Controlled Substances; Notice of Registration

By Notice dated February 5, 2009, and published in the Federal Register on February 11, 2009 (74 FR 6920), Roche Diagnostics Operations Inc., Attn: Regulatory Compliance, 9115 Hague Road, Indianapolis, Indiana 46250, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as an importer of the basic classes of

Published: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-9785] 108. Importer of Controlled Substances; Notice of Registration

By Notice dated January 14, 2009, and published in the Federal Register on January 22, 2009 (74 FR 4054), ISP Freetown Fine Chemicals, 238 South Main Street, Assonet, Massachusetts 02702, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as an importer of Phenylacetone (8501), a basic class of controlled

Published: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-9788] 109. Importer of Controlled Substances; Notice of Registration

By Notice dated January 9, 2009, and published in the Federal Register on January 21, 2009 (74 FR 3642), Noramco Inc., 1440 Olympic Drive, Athens, Georgia 30601, made application by letter to the Drug Enforcement Administration (DEA) to be registered as an importer of Thebaine (9333), a basic class of controlled substance listed in schedule

Published: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-9789] 110. Importer of Controlled Substances; Notice of Registration

By Notice dated January 30, 2009, and published in the Federal Register on February 6, 2009 (74 FR 6309), Mallinckrodt Inc., 3600 North Second Street, St. Louis, Missouri 63147, 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

Published: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-9791] 111. Importer of Controlled Substances; Notice of Registration

By Notice dated December 22, 2008, and published in the Federal Register on December 31, 2008 (73 FR 80431), Johnson Matthey Inc., Pharmaceutical Materials, 2003 Nolte Drive, West Deptford, New Jersey 080661742, has made application by letter to the Drug Enforcement Administration (DEA) to be registered as an importer of the basic classes of

Published: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-9794] 112. Importer of Controlled Substances; Notice of Registration

By Notice dated December 22, 2008, and published in the Federal Register on December 31, 2008 (73 FR 80432), Johnson Matthey Inc., Pharmaceutical Materials, 2003 Nolte Drive, West Deptford, New Jersey 080661742, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as an importer of the basic classes of

Published: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-9795] 113. Manufacturer of Controlled Substances; Notice of Registration

By Notice dated December 22, 2008, and published in the Federal Register on December 31, 2008 (73 FR 80431), Norac Inc., 405 S. Motor Avenue, P.O. Box 577, Azusa, California 917023232, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of Tetrahydrocannabinols (7370), a basic class

Published: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-9799] 114. 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 11, 2009, AMRI Rensselaer, Inc., 33 Riverside
[[Page 19599]]
Avenue, Rensselaer, New York 12144, made application by renewal to the Drug Enforcement Administration (DEA) as a bulk manufacturer of the basic classes of controlled

Published: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-9800] 115. 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 February 2, 2009, Cambrex Charles City, Inc., 1205 11th Street, Charles City, Iowa 50616, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled

Published: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-9801] 116. 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 January 6, 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 Lisdexamfetamine (1205), a basic

Published: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-9802] 117. 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 February 11, 2009, Siemens Healthcare Diagnostics Inc., Attn: RA, 100 GBC Drive, Mail Stop 514, Newark, Delaware 19702, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the

Published: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-9803] 118. 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 10, 2009, Penick Corporation, 33 Industrial 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

Published: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-9804] 119. 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 May 22, 2008, 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 Methamphetamine (1105), a basic

Published: 2009-04-29 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-8612] 120. Joseph Baumstarck, M.D.; Revocation of Registration

On May 19, 2008, I, the Deputy Administrator of the Drug Enforcement Administration, issued an Order to Show Cause and Immediate Suspension of Registration to Joseph Baumstarck, M.D. (Respondent), of Lovell, Wyoming. The Order proposed the revocation of Respondent's DEA Certificate of Registration, BB2806480, which authorizes him to dispense

Published: 2009-04-15 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-8613] 121. Scott Sandarg, D.M.D.; Revocation of Registration

On July 25, 2007, the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, issued an Order to Show Cause to Scott Sandarg, D.M.D. (Respondent), of Irvine, California. The Show Cause Order proposed the revocation of Respondent's DEA Certificate of Registration, BS6026525, which authorizes him to dispense

Published: 2009-04-15 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-8624] 122. George C. Aycock, M.D.; Revocation of Registration

On June 25, 2008, the Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration, issued an Order to Show Cause to George C. Aycock, M.D. (Respondent), of Sumter, South Carolina. The Show Cause Order proposed the revocation of Respondent's DEA Certificate of Registration, AA1071947, which authorizes him to

Published: 2009-04-15 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-6054] 123. Agency Information Collection Activities: Proposed Collection; Comments

Prescription Drug Monitoring Program Questionnaire

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

Published: 2009-03-20 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-4945] 124. Importer of Controlled Substances; Notice of Registration

By Notice dated November 26, 2008, and published in the Federal Register on December 5, 2008, (73 FR 74194), Cerilliant Corporation, 811 Paloma Drive, Suite A, Round Rock, Texas 786652402, made application by renewal to the Drug Enforcement Administration (DEA) to be registered as an importer of the basic classes of controlled substances

Published: 2009-03-09 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

[FR Doc E9-4271] 125. 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 registration under 21 U.S.C. 952(a)(2), authorizing the importation of such a substance, provide manufacturers holding registrations for the

Published: 2009-03-02 DEPARTMENT OF JUSTICE : Drug Enforcement Administration

 

Years: 2000200120022003200420052006200720082009

Pages: «23456