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Drug Enforcement Administration – Federal Register Recent Federal Regulation Documents
Results 1 - 50 of over 1,100
| Document | Doc Number | Type | Agency | |
|---|---|---|---|---|
| November 17, 2009 | ||||
| Schedules of Controlled Substances: Placement of Carisoprodol into Schedule IV | 59108–59112 [E9–27583] | Proposed Rule | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 21 CFR Part 1308 [Docket No. DEA-333P] Schedules of Controlled Substances: Placement of Carisoprodol Into Schedule IV
AGENCY: Drug Enforcement Administration, Department of Justice. ACTION: Notice of proposed rulemaking. SUMMARY: This proposed rule is issued by the Deputy Administrator of the
Drug Enforcement Administration (DEA) to place the substance carisoprodol, including its salts, isomers, and salts of isomers whenever the existence of... [read document] |
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| November 16, 2009 | ||||
| Agency Information Collection Activities; Proposals, Submissions, and Approvals | 58982 [E9–27346] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration [OMB Number 1117-0034] Agency Information Collection Activities: Proposed Collection; Comments Requested; Collection of
Laboratory Analysis Data on Drug Samples Tested by Non-Federal (State and Local) Crime Laboratories ACTION: 30-day notice of information collection under review. The Department
of Justice (DOJ), Drug Enforcement Administration (DEA) will be submitting the following information collection request to the Office of Management... [read document] |
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| Agency Information Collection Activities; Proposals, Submissions, and Approvals | 58982–58983 [E9–27345] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration [OMB Number 1117-0029] Agency Information Collection Activities: Proposed Collection; Comments Requested: Annual Reporting
Requirement for Manufacturers of Listed Chemicals ACTION: 30-day notice of information collection under review. 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... [read document] |
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| Agency Information Collection Activities; Proposals, Submissions, and Approvals | 58983–58984 [E9–27344] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration [OMB Number 1117-0033] Agency Information Collection Activities: Proposed Collection; Comments Requested: Report of Mail
Order Transaction ACTION: 30-day notice of information collection under review. 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... [read document] |
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| November 12, 2009 | ||||
| Manufacturers of Controlled Substances; Registration | 58313 [E9–27194] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 substances listed in schedule II: Drug... [read document] |
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| Manufacturers of Controlled Substances; Registration | 58313–58314 [E9–27193] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 substances listed in schedule II: Drug... [read document] |
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| Manufacturers of Controlled Substances; Registration | 58313 [E9–27180] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 Ortho-McNeil, 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 controlled substance listed in schedule... [read document] |
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| November 6, 2009 | ||||
| Applications: Manufacturer of Controlled Substances | 57522 [E9–26744] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 22, 2009, ISP Freetown Fine Chemicals, 238 South Main Street, Assonet, Massachusetts 02702, made application by renewal to
the Drug Enforcement Administration (DEA) as a bulk manufacturer of the basic classes of controlled substances listed in schedules I and II: Drug... [read document] |
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| Importer of Controlled Substances; Registrations | 57523–57524 [E9–26756] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 controlled substance listed in schedule II. The... [read document] |
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| Importer of Controlled Substances; Registrations | 57524 [E9–26755] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 controlled substance listed in schedule II. The... [read document] |
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| October 29, 2009 | ||||
| Importer of Controlled Substances; Applications | 55858 [E9–25999] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 08066-1742, 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... [read document] |
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| October 28, 2009 | ||||
| Registration Requirements for Individual Practitioners Operating in a “Locum Tenens” Capacity | 55499–55502 [E9–25937] | Proposed Rule | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 21 CFR Part 1301 [Docket No. DEA-324a] RIN 1117-AB21 Registration Requirements for Individual Practitioners Operating in a
``Locum Tenens'' Capacity AGENCY: Drug Enforcement Administration (DEA), Department of Justice. ACTION: Advance notice of proposed rulemaking. Summary: On December 1, 2006, the
Drug Enforcement Administration (DEA) published in the Federal Register a Final Rule ``Clarification of Registration Requirements for Individual... [read document] |
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| Schedules of Controlled Substances: Placement of 5–Methoxy–N,N–Dimethyltryptamine into Schedule I of the Controlled Substances Act | 55502–55504 [E9–25939] | Proposed Rule | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 21 CFR Part 1308 [Docket No. DEA-331] Schedules of Controlled Substances: Placement of 5-Methoxy-N,N- Dimethyltryptamine
Into Schedule I of the Controlled Substances Act AGENCY: Drug Enforcement Administration (DEA), Department of Justice. ACTION: Notice of proposed rulemaking; reopening of
comment period. SUMMARY: On August 21, 2009, the Drug Enforcement Administration (DEA) published a notice of proposed rulemaking in the Federal Register,... [read document] |
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| Importer of Controlled Substances; Applications | 55583 [E9–25862] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 manufacture of the substance an opportunity... [read document] |
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| Importer of Controlled Substances; Applications | 55583–55584 [E9–25905] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Importer of Controlled Substances; Notice of Application This is notice that on July 9, 2009, Cody Laboratories Inc., 601
Yellowstone Avenue, Cody, Wyoming 82414-9321, 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 Schedule Raw Opium (9600) II Concentrate of Poppy Straw (9670) II The company plans to import... [read document] |
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| Importer of Controlled Substances; Applications | 55584 [E9–25903] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Importer of Controlled Substances; Notice of Application This is notice that on September 18, 2009, Clinical Supplies
Management, 342 42nd Street South, Fargo, North Dakota 58103, made application to the Drug Enforcement Administration (DEA) for registration as an importer of Poppy Straw
Concentrate (9670), a basic class of controlled substance listed in schedule II. The company plans to import an ointment for the treatment of wounds which... [read document] |
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| Importer of Controlled Substances; Applications | 55584–55585 [E9–26001] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 manufacture of the substance an opportunity... [read document] |
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| Importer of Controlled Substances; Applications | 55584 [E9–26000] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 manufacture of the substance an opportunity... [read document] |
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| Importer of Controlled Substances; Registrations | 55585–55586 [E9–25908] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 27349), Mylan Technologies Inc., 110 Lake Street, Saint Albans, Vermont 05478, made application to the Drug Enforcement Administration (DEA) to
be registered as an importer of the basic classes of controlled substances listed in schedule II: Drug Schedule Methylphenidate (1724) II Fentanyl... [read document] |
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| Importer of Controlled Substances; Registrations | 55585 [E9–25891] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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), Archimica, Inc., 2460 W. Bennett Street, Springfield, Missouri 65807-1229, made application by letter to the Drug Enforcement
Administration (DEA) to be registered as a bulk manufacturer of Lisdexamfetamine (1205), a basic class of controlled substance listed in schedule II. The... [read document] |
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| Importer of Controlled Substances; Registrations | 55585 [E9–25888] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 27349), Mylan Pharmaceuticals Inc., 781 Chestnut Ridge Road, Morgantown, West Virginia 26505, made application by letter to the Drug Enforcement
Administration (DEA) to be registered as an importer of the basic classes of controlled substances listed in schedule II: Drug Schedule Methylphenidate... [read document] |
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| Manufacturer of Controlled Substances; Applications | 55586 [E9–26003] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 65807-1229, made application by letter to the Drug
Enforcement Administration (DEA) to be registered as a bulk manufacturer of Tapentadol (9780), a basic class of controlled substance listed in... [read document] |
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| Manufacturer of Controlled Substances; Applications | 55586 [E9–25890] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 26, 2009, Lonza Riverside, 900 River Road, Conshohocken, Pennsylvania 19428, 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 schedules I and II: Drug... [read document] |
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| Manufacturer of Controlled Substances; Applications | 55586–55587 [E9–25889] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 31, 2009, Lin Zhi International Inc., 687 North Pastoria Avenue, Sunnyvale, California 94085, 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 schedules... [read document] |
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| Importer of Controlled Substances; Registrations | 55586 [E9–25906] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Importer of Controlled Substances; Notice of Registration By Notice dated June 22, 2009, and published in the Federal
Register on June 29, 2009, (74 FR 31049), Noramco, Inc., Division of Ortho-McNeil, Inc., 1440 Olympic Drive, Athens, Georgia 30601, made application by letter to the Drug
Enforcement Administration (DEA) to be registered as an importer of Tapentadol (9780), a basic class of controlled substance listed in schedule II. The... [read document] |
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| Manufacturer of Controlled Substances; Applications | 55587 [E9–25899] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 listed in schedule I: Drug Schedule... [read document] |
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| Manufacturer of Controlled Substances; Applications | 55587–55588 [E9–25895] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 substances listed in schedule II: Drug... [read document] |
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| Manufacturer of Controlled Substances; Applications | 55587 [E9–25884] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 16, 2009, American Radiolabeled Chemical, Inc., 101 Arc Drive, St. Louis, Missouri 63146, made application by renewal to the Drug
Enforcement Administration (DEA) as a bulk manufacturer of the basic classes of controlled substances listed in schedules I and II: Drug... [read document] |
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| Manufacturer of Controlled Substances; Registrations | 55588–55589 [E9–25887] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 Ortho-McNeil, 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 controlled substance listed in... [read document] |
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| Manufacturer of Controlled Substances; Applications | 55588 [E9–26002] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 08066-1742,
made application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of... [read document] |
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| Manufacturer of Controlled Substances; Applications | 55588 [E9–25893] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 45342-4304, made application by renewal to
the Drug Enforcement Administration (DEA) as a bulk manufacturer of the basic classes of controlled substances listed in schedules I and II:... [read document] |
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| Manufacturer of Controlled Substances; Registrations | 55589 [E9–25892] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 schedule I. The company plans to... [read document] |
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| Manufacturer of Controlled Substances; Registrations | 55589 [E9–25886] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 substance listed in schedule II. The... [read document] |
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| Manufacturer of Controlled Substances; Registrations | 55589–55590 [E9–25885] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 listed in schedules I and II: Drug... [read document] |
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| Manufacturer of Controlled Substances; Registrations | 55590 [E9–25901] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 substances listed in schedule II: Drug... [read document] |
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| Manufacturer of Controlled Substances; Registrations | 55590–55591 [E9–25894] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 substances listed in schedules I and II:... [read document] |
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| Manufacturer of Controlled Substances; Registrations | 55590 [E9–25882] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 78665-2402, 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 schedules I and II: Drug Schedule... [read document] |
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| October 23, 2009 | ||||
| Dismissal of Proceeding: Samuel H. Albert, M.D. | 54851–54853 [E9–25480] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. 07-6] Samuel H. Albert, M.D.; Dismissal of Proceeding On October 25, 2006, the Deputy Assistant Administrator,
Office of Diversion Control, issued an Order to Show Cause to Samuel H. Albert, M.D. (Respondent), of Fountain Valley, California. ALJ Ex. 1, at 1. The Show Cause Order proposed
the denial of Respondent's ``pending application for a DEA Certificate of Registration'' as a practitioner on the grounds that on this... [read document] |
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| October 21, 2009 | ||||
| Controlled Substances: Final Revised Aggregate Production Quotas (2009) | 54077–54080 [E9–25274] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA-317F] Controlled Substances: Final Revised Aggregate Production Quotas for 2009 AGENCY: Drug Enforcement
Administration (DEA), Justice. ACTION: Notice of final aggregate production quotas for 2009. SUMMARY: This notice establishes final 2009 aggregate production quotas for
controlled substances in schedules I and II of the Controlled Substances Act (CSA). The DEA has taken into consideration comments received in response to a... [read document] |
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| Controlled Substances: Established Initial Aggregate Production Quotas (2010) | 54080–54083 [E9–25275] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration [DEA 318E] Controlled Substances: Established Initial Aggregate Production Quotas for 2010 AGENCY: Drug Enforcement
Administration (DEA), Justice. ACTION: Notice of aggregate production quotas for 2010. SUMMARY: This notice establishes initial 2010 aggregate production quotas for controlled
substances in schedules I and II of the Controlled Substances Act (CSA). DATES: Effective Date: October 21, 2009. FOR FURTHER INFORMATION CONTACT:... [read document] |
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| October 20, 2009 | ||||
| Agency Information Collection Activities; Proposals, Submissions, and Approvals | 53760 [E9–25128] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration [OMB Number 1117-0038] Agency Information Collection Activities: Proposed Collection; Comments Requested: Reporting and
Recordkeeping for Digital Certificates ACTION: 60-Day Notice of Information Collection under review. 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... [read document] |
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| October 14, 2009 | ||||
| Importer of Controlled Substances; Notice of Registration | 52819 [E9–24714] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 listed in schedule II: Drug Schedule... [read document] |
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| October 6, 2009 | ||||
| Schedules of Controlled Substances: Placement of Fospropofol into Schedule IV | 51234–51236 [E9–23971] | Rule | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 21 CFR Part 1308 [Docket No. DEA-327F] Schedules of Controlled Substances; Placement of Fospropofol Into Schedule IV
AGENCY: Drug Enforcement Administration, Department of Justice. ACTION: Final rule. SUMMARY: With the issuance of this final rule, the Deputy Administrator of the Drug
Enforcement Administration (DEA) places the substance fospropofol, including its salts, isomers and salts of isomers whenever the existence of such salts,... [read document] |
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| September 25, 2009 | ||||
| Manufacturer of Controlled Substances; Applications: Cerilliant Corp., Round Rock, TX | 49020–49021 [E9–23067] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 16, 2009, Cerilliant Corporation, 811 Paloma Drive, Suite A, Round Rock, Texas 78665-2402, made application by renewal to the Drug
Enforcement Administration (DEA) as a bulk manufacturer of the basic classes of controlled substances listed in schedules I and II: Drug... [read document] |
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| September 24, 2009 | ||||
| Importer of Controlled Substances; Applications: Fisher Clinical Services, Allentown, PA | 48780 [E9–23066] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 manufacture of the substance an opportunity... [read document] |
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| September 18, 2009 | ||||
| Importer of Controlled Substances; Registration | 47961 [E9–22506] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 Ortho-McNeil, 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 controlled substance listed in schedule... [read document] |
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| Importer of Controlled Substances; Registration | 47961–47962 [E9–22505] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 II: Drug Schedule Lisdexamfetamine (1205)... [read document] |
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| Importer of Controlled Substances; Applications | 47961 [E9–22502] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 manufacture of the substance an opportunity... [read document] |
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| Manufacturer of Controlled Substances; Registration | 47962–47963 [E9–22453] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 91702-3232, 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 listed in schedule II. The company... [read document] |
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| Manufacturer of Controlled Substances; Application | 47962 [E9–22503] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 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 60004-1412, made application by renewal to the Drug
Enforcement Administration (DEA) as a bulk manufacturer of Cocaine (9041), a basic class of controlled substance in schedule II. The company... [read document] |
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