Drug Enforcement Administration October 31, 2023 – Federal Register Recent Federal Regulation Documents

Proposed Adjustments to the 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 2023
Document Number: 2023-23931
Type: Notice
Date: 2023-10-31
Agency: Drug Enforcement Administration, Department of Justice
The Drug Enforcement Administration (DEA) proposes to adjust the 2023 aggregate production quotas for several controlled substances in schedules I and II of the Controlled Substances Act (CSA) and the assessment of annual needs for the list I chemical phenylpropanolamine.
Designation of Halides of 4-Anilinopiperidine as List I Chemicals
Document Number: 2023-23927
Type: Rule
Date: 2023-10-31
Agency: Drug Enforcement Administration, Department of Justice
The Drug Enforcement Administration (DEA) is finalizing the modification of the listing of the list I chemical, N-phenylpiperidin- 4-amine (also known as 4-anilinopiperidine; N-phenyl-4-piperidinamine; 4-AP) (hereinafter referred to as 4-anilinopiperidine), to include halides of 4-anilinopiperidine. This rule finalizes the modification of the listing of 4-anilinopiperidine as a list I chemical.
Controlled Substance Destruction Alternatives to Incineration
Document Number: 2023-23984
Type: Proposed Rule
Date: 2023-10-31
Agency: Drug Enforcement Administration, Department of Justice
The Drug Enforcement Administration (DEA) is seeking information about destruction processes which may be used to render controlled substances to a non-retrievable state. DEA invites comment from stakeholders in the controlled substance disposal industry, as well as registrants engaged in the destruction and disposal of controlled substances in their possession or inventory, to the questions provided below.
Schedules of Controlled Substances: Placement of Zuranolone in Schedule IV
Document Number: 2023-23982
Type: Rule
Date: 2023-10-31
Agency: Drug Enforcement Administration, Department of Justice
On August 4, 2023, the United States Food and Drug Administration approved a new drug application for ZURZUVAE (zuranolone) capsules for the treatment of post-partum depression. The Department of Health and Human Services provided the Drug Enforcement Administration (DEA) with a scheduling recommendation to place zuranolone and its salts in schedule IV of the Controlled Substances Act (CSA). In accordance with the CSA, as amended by the Improving Regulatory Transparency for New Medical Therapies Act, DEA is hereby issuing an interim final rule placing zuranolone, including its salts, in schedule IV of the CSA. This action facilitates the public availability of zuranolone as a schedule IV controlled substance.
Siamak Arassi, M.D.; Decision and Order
Document Number: 2023-23958
Type: Notice
Date: 2023-10-31
Agency: Drug Enforcement Administration, Department of Justice
Fares F. Yasin, M.D.; Decision and Order
Document Number: 2023-23957
Type: Notice
Date: 2023-10-31
Agency: Drug Enforcement Administration, Department of Justice
Stephen E. Van Noy, P.A.; Decision and Order
Document Number: 2023-23955
Type: Notice
Date: 2023-10-31
Agency: Drug Enforcement Administration, Department of Justice
Demille W. Madoux, M.D.; Decision and Order
Document Number: 2023-23953
Type: Notice
Date: 2023-10-31
Agency: Drug Enforcement Administration, Department of Justice
Dmitry Anatolevich Shelchkov, M.D.; Decision and Order
Document Number: 2023-23950
Type: Notice
Date: 2023-10-31
Agency: Drug Enforcement Administration, Department of Justice
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