Drug Enforcement Administration February 2024 – Federal Register Recent Federal Regulation Documents

Bulk Manufacturer of Controlled Substances Application: S&B Pharma LLC
Document Number: 2024-03719
Type: Notice
Date: 2024-02-23
Agency: Drug Enforcement Administration, Department of Justice
S&B Pharma LLC has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to SUPPLEMENTARY INFORMATION listed below for further drug information.
Importer of Controlled Substances Application: S&B Pharma LLC DBA Norac Pharma
Document Number: 2024-03718
Type: Notice
Date: 2024-02-23
Agency: Drug Enforcement Administration, Department of Justice
S&B Pharma LLC DBA Norac Pharma has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to SUPPLEMENTARY INFORMATION listed below for further drug information.
Importer of Controlled Substances Application: Meridian Medical Technologies, LLC
Document Number: 2024-03714
Type: Notice
Date: 2024-02-23
Agency: Drug Enforcement Administration, Department of Justice
Meridian Medical Technologies, LLC has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to SUPPLEMENTARY INFORMATION listed below for further drug information.
Bulk Manufacturer of Controlled Substances Application: Siemens Healthcare Diagnostics Inc.
Document Number: 2024-03712
Type: Notice
Date: 2024-02-23
Agency: Drug Enforcement Administration, Department of Justice
Siemens Healthcare Diagnostics Inc. has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to Supplementary Information listed below for further drug information.
Importer of Controlled Substances Application: Patheon API Services, Inc.
Document Number: 2024-03688
Type: Notice
Date: 2024-02-23
Agency: Drug Enforcement Administration, Department of Justice
Patheon API Services, Inc. has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to Supplementary Information listed below for further drug information.
Bulk Manufacturer of Controlled Substances Application: Patheon API Services Inc.
Document Number: 2024-03686
Type: Notice
Date: 2024-02-23
Agency: Drug Enforcement Administration, Department of Justice
Patheon API Services Inc. has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to SUPPLEMENTARY INFORMATION listed below for further drug information.
Importer of Controlled Substances Application: Pall Life Sciences PR, LLC
Document Number: 2024-03683
Type: Notice
Date: 2024-02-23
Agency: Drug Enforcement Administration, Department of Justice
Pall Life Sciences PR, LLC has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to SUPPLEMENTARY INFORMATION listed below for further drug information.
Importer of Controlled Substances Application: Pfizer, Inc.
Document Number: 2024-03709
Type: Notice
Date: 2024-02-23
Agency: Drug Enforcement Administration, Department of Justice
Pfizer, Inc. has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to Supplementary Information listed below for further drug information.
Importer of Controlled Substances Application: Janssen Pharmaceuticals Inc.
Document Number: 2024-03689
Type: Notice
Date: 2024-02-23
Agency: Drug Enforcement Administration, Department of Justice
Janssen Pharmaceuticals Inc. has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to Supplementary Information listed below for further drug information.
Henry Manning Pickett, M.D.; Default Decision and Order
Document Number: 2024-03548
Type: Notice
Date: 2024-02-22
Agency: Drug Enforcement Administration, Department of Justice
Conforming Amendment Regarding the Veterinary Medicine Mobility Act of 2014
Document Number: 2024-02322
Type: Rule
Date: 2024-02-08
Agency: Drug Enforcement Administration, Department of Justice
The Veterinary Medicine Mobility Act of 2014 (VMMA), which became law on August 1, 2014, amended the Controlled Substances Act to address separate registration requirements for veterinarians. The VMMA allows a veterinarian to transport and dispense controlled substances in the usual course of veterinary practice at a site other than the veterinarian's registered principal place of business or professional practice without obtaining a separate registration, subject to certain limitations. The Drug Enforcement Administration is amending its regulations to codify the VMMA. This rule merely conforms DEA regulations to statutory amendments of the Controlled Substances Act that have already taken effect and makes no substantive change to existing legal requirements.
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