Rule 8 Aug 2025 business impact, administrative practice and procedure, controlled substances, drug traffic control, drug enforcement, reporting and recordkeeping requirements, regulatory compliance, legal obligations

⚖️Business Implications of Dipentylone as a Controlled Substance

The Drug Enforcement Administration (DEA) is establishing a specific listing and DEA Controlled Substances Code Number (drug code) for 1-(1,3-benzodioxol-5-yl)-2-(dimethylamino)pentan-1-one (dipentylone; N,N-dimethylpentylone) in schedule I of the Controlled Substances Act (CSA). Although dipentylone is not specifically listed in schedule I of the CSA with its own unique drug code, it is a schedule I controlled substances in the United States because it is a positional isomer of N-ethylpenthylone (controlled August 31, 2018), which is a schedule I hallucinogen. Therefore, DEA is simply amending the schedule I hallucinogenic substances list in its regulations to separately include dipentylone.

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Rule 25 Jul 2025 compliance, regulations, pharmaceuticals, controlled substances, drug enforcement administration, law, benzodiazepines

⚖️Extension of Temporary Scheduling for Designer Benzodiazepines

The Acting Administrator of the Drug Enforcement Administration (DEA) is issuing this temporary scheduling order to extend the temporary schedule I status of five designer benzodiazepines--clonazolam, diclazepam, etizolam, flualprazolam, and flubromazolam. In an order dated July 26, 2023, DEA temporarily placed these five substances in schedule I of the Controlled Substances Act. This temporary order will extend the temporary scheduling of five designer benzodiazepines for one year, or until the permanent scheduling action for these substances is completed, whichever occurs first. As a result of this order, the regulatory controls and administrative, civil, and criminal sanctions applicable to schedule I controlled substances will continue to be imposed on persons who handle (manufacture, distribute, reverse distribute, import, export, engage in research, conduct instructional activities or chemical analysis with, or possess) or propose to handle these five specified controlled substances.

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Proposed Rule 25 Jul 2025 compliance, regulatory, administrative practice and procedure, reporting and recordkeeping requirements, business impact, controlled substances, drug traffic control, drug enforcement, benzodiazepines

⚖️Proposed Rule for Scheduling Designer Benzodiazepines as Controlled Substances

The Drug Enforcement Administration proposes placing clonazolam, diclazepam, etizolam, flualprazolam, and flubromazolam and their salts, isomers, and salts of isomers, whenever the existence of such salts, isomers, and salts of isomers is possible within the specific chemical designation, as identified in this proposed rule, in schedule I of the Controlled Substances Act. These five substances were temporarily scheduled in an order dated July 26, 2023, and subsequently extended until July 26, 2026, pursuant to an extension published elsewhere in this issue of the Federal Register. This action will also enable the United States to meet its obligations under the 1971 Convention on Psychotropic Substances. If finalized, this action would make permanent the existing regulatory controls and administrative, civil, and criminal sanctions applicable to schedule I controlled substances on persons who handle (manufacture, distribute, import, export, engage in research, conduct instructional activities or chemical analysis, or possess), or propose to handle these five specific controlled substances.

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Notice 17 Jul 2025 regulatory compliance, pharmaceuticals, manufacturing, controlled substances, drug enforcement, cerilliant corporation

💊Cerilliant Corporation's Bulk Manufacturer Application Overview

Cerilliant Corporation 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.

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Notice 17 Jul 2025 regulatory compliance, manufacturing, controlled substances, drug enforcement

💊AMPAC Fine Chemicals LLC Controlled Substances Application Notice

AMPAC Fine Chemicals 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.

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Notice 17 Jul 2025 compliance, import regulations, pharmaceutical, controlled substances, justice department, drug enforcement, cerilliant corporation

⚖️Cerilliant Corporation's Application for Import of Controlled Substances

Cerilliant Corporation 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.

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Notice 17 Jul 2025 compliance, business regulation, manufacturing, controlled substances, drug enforcement, curia missouri inc.

💊Curia Missouri Inc.'s Application for Controlled Substance Manufacturing

Curia Missouri 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.

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Notice 17 Jul 2025 regulatory compliance, pharmaceutical industry, dea, controlled substances, import application

💊DEA Notice

AndersonBrecon, Inc. DBA PCI Pharma Services 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.

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Notice 17 Jul 2025 regulatory compliance, pharmaceutical, controlled substances, drug enforcement, curia new york

💊Curia New York Applies for Controlled Substances Manufacturing Registration

Curia New York, 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.

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Notice 16 Jul 2025 compliance, healthcare, regulatory, north carolina, dea, controlled substances, drug enforcement administration

⚖️DEA Revocation

The Drug Enforcement Administration revokes the registration of Sasha Melissa Ikramelahai due to allegations of material falsification and lack of state authority to handle controlled substances in North Carolina. The case underscores the significance of regulatory compliance in the healthcare sector, emphasizing the severe consequences businesses face when failing to uphold licensure integrity.

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