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The Epidiolex Effect: Will Other CBD Drugs Receive FDA and DEA Approval?

Freedom Leaf

On September 28, the DEA designated Epidiolex —a plant-based CBD pharmaceutical manufactured by the UK-based GW Pharmaceuticals—a Schedule V drug in the government’s list of controlled substances. schedules were created by the Controlled Substances Act (CSA) in 1970 and are interpreted and enforced by the DEA. will top $1.9

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Constitutionality of Cannabis: Federal Lawsuit Against DEA, DOJ Proceeds

Marijuana Lawyer Blog

Department of Justice, challenging the constitutionality of the federal law designating marijuana a Schedule I controlled substance proceeded recently to the next level with oral arguments before the U.S. Defendants are acting-Attorney General Matthew Whitaker, the acting director of the DEA and the federal government.

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House Passes Bill to Expand Cannabis and CBD Research

Cannabis Law Report

8454 , the Medical Marijuana and Cannabidiol Research Expansion Act (Research Expansion Act). Drug Enforcement Administration (DEA) to register practitioners to conduct cannabis and CBD research and manufacturers to supply cannabis for research purposes. Food and Drug Administration (FDA). Food and Drug Administration (FDA).

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CBD Lawsuit Reflects Trucker Termination for THC Tainted Drug Products

The Blunt Truth

Medical Marijuana, Inc., We have noted previously that the federal Drug Enforcement Agency (DEA) recently announced that drugs that include CBD (cannabidiol) with less than 0.1% of THC (tetrahydrocannabinols) are now considered Schedule V drugs provided they are approved by the federal Food and Drug Administration (FDA).

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Nevada veterinarians can now treat patients with certain cannabis products

Cannabis Law Report

Nevada voters approved medical marijuana for people by ballot initiative in 2000. or less THC are exempted from the federal Controlled Substances Act, the products do fall under the Federal Food, Drug, and Cosmetic Act if they are used therapeutically or included in animal food. 1, 2017, following a 2016 ballot measure.

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New U.S. Research Efforts Could Catalyze Medical Cannabis’ Adoption in the Pharmaceutical Industry

Veriheal

Groff North America is proud to be producing research-grade marijuana, so we can continue growing the field of cannabis-based medicine,” reads an official statement from the company’s website. Drug Enforcement Agency (DEA). The final goal is to introduce medicinal cannabis products to the pharmaceutical drug market.

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Navigating Medical Cannabis for Veterans: Benefits and Federal Laws

Veriheal

Despite the widespread adoption, the Food and Drug Administration still classifies cannabis as a Schedule One drug. According to the United States Drug Enforcement Administration (DEA), Schedule One drugs are “drugs with no currently accepted medical use and a high potential for abuse.” No, they can’t.

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