U.S. Drug Enforcement Administration Plans to Reclassify Marijuana

Regulations by 2FIRSTS.ai
May.04.2024
U.S. Drug Enforcement Administration Plans to Reclassify Marijuana
The U.S. Drug Enforcement Administration plans to reclassify marijuana as a less dangerous drug, potentially impacting drug policy.

According to a report by Tobaccoreporter on May 2, the Drug Enforcement Administration in the United States is planning to reclassify marijuana as a less dangerous drug, which could have significant implications for drug policy in the United States.

 

This proposed measure has not yet been reviewed by the White House management and Office of Management and Budget. It aims to acknowledge the medical benefits of using marijuana and recognize that the potential for misuse of marijuana is lower compared to some of the most dangerous drugs domestically. It also proposes reclassifying marijuana as a Schedule III controlled substance.

 

However, it is not seeking to legalize marijuana for recreational purposes.

 

Five sources familiar with the matter anonymously discussed this sensitive regulatory review with the Associated Press and confirmed the agency's actions on Tuesday. This move clears the last major regulatory hurdle before the largest policy change in more than 50 years for the agency takes effect.

 

According to the Narcotics Bureau, the following are examples of Schedule I controlled substances:

 

  • Heroin
  • Lysergic acid diethylamide (LSD)
  • Cannabis
  • Methamphetamine
  • Methaqualone (Quaalude)
  • Peyote cactus

 

According to the National Institutes of Health, California became the first state to classify possession of marijuana as illegal. In the 1930s, the Federal Bureau of Narcotics warned of increasing abuse of marijuana, leading 23 states to criminalize its possession by 1937.

 

By 1970, the Controlled Substances Act had been passed, and the federal government classified marijuana as a Schedule I substance.

 

The proposed rule change at the Drug Enforcement Administration (DEA) follows the recommendation of the Department of Health and Human Services (HHS) in August 2023, which suggests reclassifying marijuana from Schedule I to Schedule III. Any changes to the status of marijuana through the DEA rule-making process will not take immediate effect.

 

The American E-Cigarette Association expressed support for the Biden administration's decision to reclassify marijuana.

 

The Executive Director of the Vapor Technology Association (VTA), Tony Abboud, said in an email statement: "This decision clearly emphasizes the current government's commitment to listening to voters and demonstrates a willingness to acknowledge and accept scientific evidence from the real world and across the entire category."

 

In light of today's decision, VTA urges other agencies within the Biden administration, particularly the US FDA, to follow the same overwhelming evidence regarding e-cigarette products as effective harm reduction and smoking cessation tools for adult smokers.

 

In just the past year, the FDA's politically driven, rather than science-based, selective approach has resulted in the approval of over 650 new cigarette products. The VTA reiterates its call for the FDA to stop turning a blind eye to overwhelming scientific evidence that proves flavored nicotine options are beneficial for Americans looking to quit smoking, just as other government agencies do.

 

We welcome news tips, article submissions, interview requests, or comments on this piece.

Please contact us at info@2firsts.com, or reach out to Alan Zhao, CEO of 2Firsts, on LinkedIn


Notice

1.  This article is intended solely for professional research purposes related to industry, technology, and policy. Any references to brands or products are made purely for objective description and do not constitute any form of endorsement, recommendation, or promotion by 2Firsts.

2.  The use of nicotine-containing products — including, but not limited to, cigarettes, e-cigarettes, nicotine pouchand heated tobacco products — carries significant health risks. Users are responsible for complying with all applicable laws and regulations in their respective jurisdictions.

3.  This article is not intended to serve as the basis for any investment decisions or financial advice. 2Firsts assumes no direct or indirect liability for any inaccuracies or errors in the content.

4.  Access to this article is strictly prohibited for individuals below the legal age in their jurisdiction.

 

Copyright

 

This article is either an original work created by 2Firsts or a reproduction from third-party sources with proper attribution. All copyrights and usage rights belong to 2Firsts or the original content provider. Unauthorized reproduction, distribution, or any other form of unauthorized use by any individual or organization is strictly prohibited. Violators will be held legally accountable.

For copyright-related inquiries, please contact: info@2firsts.com

 

AI Assistance Disclaimer

 

This article may have been enhanced using AI tools to improve translation and editorial efficiency. However, due to technical limitations, inaccuracies may occur. Readers are encouraged to refer to the cited sources for the most accurate information.

We welcome any corrections or feedback. Please contact us at: info@2firsts.com

UAE Sets Dh1-Per-ml Minimum Excise Price for Vape Liquids From Sept. 1 While Keeping 100% Tax Rate
UAE Sets Dh1-Per-ml Minimum Excise Price for Vape Liquids From Sept. 1 While Keeping 100% Tax Rate
The UAE Ministry of Finance will introduce a minimum excise price for e-liquids used in vaping and electronic smoking devices from September 1, 2026. The minimum excise price will be set at AED 1 per millilitre. The existing 100% excise tax rate will continue to apply to tobacco and electronic smoking products. The measure changes the minimum taxable base rather than the tax rate, with the UAE government saying it aims to establish unified tax standards, improve market compliance and prevent pricing loopholes.
Regulations
Aug.07 by 2Firsts Perspectives
South Korea Vape Strategies Diverge as BAT Reconsiders Exit and PMI Takes VEEV to About 14,000 Stores
South Korea Vape Strategies Diverge as BAT Reconsiders Exit and PMI Takes VEEV to About 14,000 Stores
BAT Rothmans says it previously considered exiting South Korea's vaping market because of competitive pressure from unregulated products, but is now reassessing conditions following changes to the country's nicotine regulatory framework. Vuse and other BAT vaping products remain available through existing distribution channels. The statement followed a South Korean media report that interpreted BAT's broader withdrawal from selected Vapour markets as a full exit from South Korea. Meanwhile, Philip Morris International launched VEEV inPRIME in the country in June and began expanding distribution to around 14,000 convenience stores and other retail channels in July. The contrasting moves highlight differing investment strategies as South Korea's regulated vaping market evolves.
Aug.14
From a 2017 Launch to 48% of South Korea’s Heated Tobacco Market, KT&G Looks Back on a Decade of lil
From a 2017 Launch to 48% of South Korea’s Heated Tobacco Market, KT&G Looks Back on a Decade of lil
KT&G announced on Aug. 13, 2026, that it has opened “lil Archive,” a brand exhibition space in Seoul showcasing the evolution, technology platforms and future direction of its heated tobacco brand lil since its launch in 2017. KT&G said lil now spans three major platforms — lil SOLID, lil HYBRID and lil AIBLE — with more than 30 dedicated consumables, and held a 48% share of South Korea's heated tobacco market in the second quarter of 2026. The opening comes as lil enters its 10th year, with KT&G continuing to position the brand for expansion beyond its domestic market.
Aug.14
2FIRSTS EXCLUSIVE|China Breaks Up $6.8 Million Illegal Hookah Tobacco Operation as Market Expands
2FIRSTS EXCLUSIVE|China Breaks Up $6.8 Million Illegal Hookah Tobacco Operation as Market Expands
Chinese authorities have dismantled an illegal hookah tobacco operation worth more than 46 million yuan ($6.8 million), detaining five foreign suspects and seizing over 500,000 boxes of tobacco paste. The case comes as hookah expands across China’s nightlife sector and attracts overseas operators, including former vaping entrepreneurs. It also raises a central regulatory question: whether waterpipe tobacco will follow China’s private-sector e-cigarette licensing model or be reserved for the state tobacco system, as with nicotine pouches, in the years ahead.
Jul.31
JTI Makes Third Bet on South Korea as Ploom AURA Enters a Market Dominated by lil and IQOS
JTI Makes Third Bet on South Korea as Ploom AURA Enters a Market Dominated by lil and IQOS
Japan Tobacco International is stepping up its heated tobacco push in South Korea with Ploom AURA. Since its official launch in April 2026, the device's limited First Edition and Glacier White version have sold out, while distribution has expanded across Seoul, Incheon, Gyeonggi Province and airport duty-free channels. The rollout marks JTI's third major attempt to build a stronger heated tobacco position in South Korea, following Ploom TECH in 2019 and Ploom X Advanced in 2024. At the group level, JT plans to invest about ¥800 billion, approximately $5 billion, in reduced-risk products from 2026 through 2028, with heated products and Ploom identified as its primary investment priority.
Aug.14
Research | Swedish Study Finds Oral Lesions in 79% of Examined Nicotine Pouch Users, With Distinct Tissue Responses
Research | Swedish Study Finds Oral Lesions in 79% of Examined Nicotine Pouch Users, With Distinct Tissue Responses
A new Swedish study found oral mucosal lesions in 79% of examined nicotine pouch users and 89% of tobacco-derived snus users, with different tissue-response patterns between the two categories. For manufacturers and regulators, the findings shift attention toward product formulation, flavouring, pouch materials and local oral exposure, not only whether a product contains tobacco. The study found no higher prevalence of caries or periodontal disease, but it could not establish causality, long-term outcomes or differences between individual products or designs.
Special Report
Jul.27