Agency for International Development July 2015 – Federal Register Recent Federal Regulation Documents

Manufacturer of Controlled Substances Registration: Apertus Pharmaceuticals
Document Number: 2015-18695
Type: Notice
Date: 2015-07-30
Agency: Agency for Healthcare Research and Quality, Agency for International Development
Apertus Pharmaceuticals applied to be registered as a manufacturer of certain basic classes of controlled substances. The Drug Enforcement Administration (DEA) grants Apertus Pharmaceuticals registration as a manufacturer of those controlled substances.
Manufacturer of Controlled Substances Registration: Cambridge Isotope Lab
Document Number: 2015-18693
Type: Notice
Date: 2015-07-30
Agency: Agency for Healthcare Research and Quality, Agency for International Development
Cambridge Isotope Lab applied to be registered as a manufacturer of a certain basic class of controlled substance. The Drug Enforcement Administration (DEA) grants Cambridge Isotope Lab registration as a manufacturer of this controlled substance.
Manufacturer of Controlled Substances Registration: American Radiolabeled Chemicals, Inc.
Document Number: 2015-18692
Type: Notice
Date: 2015-07-30
Agency: Agency for Healthcare Research and Quality, Agency for International Development
American Radiolabeled Chemicals, Inc. applied to be registered as a manufacturer of certain basic classes of controlled substances. The Drug Enforcement Administration (DEA) grants American Radiolabeled Chemicals, Inc. registration as a manufacturer of those controlled substances.
Importer of Controlled Substances Registration: Stepan Company
Document Number: 2015-18691
Type: Notice
Date: 2015-07-30
Agency: Agency for Healthcare Research and Quality, Agency for International Development
Stepan Company applied to be registered as an importer of certain basic class of controlled substances. The Drug Enforcement Administration (DEA) grants Stepan Company registration as an importer of this controlled substance.
Importer of Controlled Substances Registration: Pharmacore
Document Number: 2015-18690
Type: Notice
Date: 2015-07-30
Agency: Agency for Healthcare Research and Quality, Agency for International Development
Pharmacore applied to be registered as an importer of a certain basic class of controlled substance. The Drug Enforcement Administration (DEA) grants Pharmacore registration as an importer of this controlled substance.
Syed Jawed Akhtar-Zaidi, M.D.; Decision and Order
Document Number: 2015-17719
Type: Notice
Date: 2015-07-20
Agency: Agency for Healthcare Research and Quality, Agency for International Development
Schedules of Controlled Substances: Temporary Placement of Acetyl Fentanyl Into Schedule I
Document Number: 2015-17563
Type: Rule
Date: 2015-07-17
Agency: Agency for Healthcare Research and Quality, Agency for International Development
The Administrator of the Drug Enforcement Administration is issuing this final order to temporarily schedule the synthetic opioid, N-(1-phenethylpiperidin-4-yl)-N-phenylacetamide (acetyl fentanyl), and its optical, positional, and geometric isomers, salts and salts of isomers, into schedule I pursuant to the temporary scheduling provisions of the Controlled Substances Act. This action is based on a finding by the Administrator that the placement of this opioid substance into schedule I of the Controlled Substances Act is necessary to avoid an imminent hazard to the public safety. As a result of this order, the regulatory controls and administrative, civil, and criminal sanctions applicable to schedule I controlled substances will be imposed on persons who handle (manufacture, distribute, import, export, engage in research, or possess), or propose to handle, acetyl fentanyl.
Proposed Aggregate Production Quotas for Schedule I and II Controlled Substances and Assessment of Annual Needs for the List I Chemicals Ephedrine, Pseudoephedrine, and Phenylpropanolamine for 2016
Document Number: 2015-17561
Type: Notice
Date: 2015-07-17
Agency: Agency for Healthcare Research and Quality, Agency for International Development
The Drug Enforcement Administration proposes to establish the 2016 aggregate production quotas for controlled substances in schedules I and II of the Controlled Substances Act and assessment of annual needs for the list I chemicals ephedrine, pseudoephedrine, and phenylpropanolamine.
Manufacturer of Controlled Substances Registration: Navinta LLC
Document Number: 2015-17525
Type: Notice
Date: 2015-07-17
Agency: Agency for Healthcare Research and Quality, Agency for International Development
Navinta LLC applied to be registered as a manufacturer of certain basic classes of controlled substances. The Drug Enforcement Administration (DEA) grants Navinta LLC registration as a manufacturer of those controlled substances.
Manufacturer of Controlled Substances Registration: Mallinckrodt, LLC
Document Number: 2015-17523
Type: Notice
Date: 2015-07-17
Agency: Agency for Healthcare Research and Quality, Agency for International Development
Mallinckrodt, LLC applied to be registered as a manufacturer of certain basic classes of controlled substances. The Drug Enforcement Administration (DEA) grants Mallinckrodt, LLC registration as a manufacturer of those controlled substances.
Manufacturer of Controlled Substances Registration: Siegfried USA, LLC
Document Number: 2015-17520
Type: Notice
Date: 2015-07-17
Agency: Agency for Healthcare Research and Quality, Agency for International Development
Siegfried USA, LLC applied to be registered as a manufacturer of certain basic classes of controlled substances. The Drug Enforcement Administration (DEA) grants Siegfried USA, LLC registration as a manufacturer of those controlled substances.
Importer of Controlled Substances Registration: Siegfried USA, LLC
Document Number: 2015-17518
Type: Notice
Date: 2015-07-17
Agency: Agency for Healthcare Research and Quality, Agency for International Development
Siegfried USA, LLC applied to be registered as an importer of certain basic classes of controlled substances. The Drug Enforcement Administration (DEA) grants Siegfried USA, LLC registration as an importer of those controlled substances.
Importer of Controlled Substances Registration: Meda Pharmaceuticals, Inc.
Document Number: 2015-17514
Type: Notice
Date: 2015-07-17
Agency: Agency for Healthcare Research and Quality, Agency for International Development
Meda Pharmaceuticals, Inc. applied to be registered as an importer of a certain basic class of controlled substance. The Drug Enforcement Administration (DEA) grants Meda Pharmaceuticals, Inc. registration as an importer of this controlled substance.
Notice of July 9 Advisory Committee on Voluntary Foreign Aid Meeting
Document Number: 2015-17027
Type: Notice
Date: 2015-07-13
Agency: Agency for International Development, Agencies and Commissions
Pursuant to the Federal Advisory Committee Act, notice is hereby given of a meeting of the Advisory Committee on Voluntary Foreign Aid (ACVFA). Date: Thursday, July 9, 2015 Time: 2:00-4:00 p.m. Location: Horizon Ballroom, The Ronald Reagan Building, 1300 Pennsylvania Ave, NW., Washington, DC 20004.
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