**Medical cannabis under state licenses and FDA-approved products moved to Schedule III effective April 28, 2026, following an April 23 order by Acting Attorney General Todd Blanche.** This action implemented a December 2025 executive order directing expedited review of marijuana’s placement under the Controlled Substances Act. A separate administrative hearing on broader rescheduling of all botanical marijuana (including adult-use) from Schedule I to Schedule III ran from June 29 to July 15, 2026, with the DEA presenting evidence of currently accepted medical use. Post-hearing briefs are now due, after which an administrative law judge recommendation is expected in late 2026 or early 2027, followed by potential final rulemaking. Ongoing litigation by anti-rescheduling parties challenges the medical reclassification in federal court, while procedural deadlines and agency timelines remain the main near-term catalysts. Traders monitor these steps because full rescheduling hinges on completion of the administrative record and any subsequent agency or judicial action.
基于Polymarket数据的AI实验性摘要。这不是交易建议,也不影响该市场的结算方式。 · 更新于$796,389 交易量
9月30日
14%
12月31日
23%
$796,389 交易量
9月30日
14%
12月31日
23%
The primary resolution source for this market will be official information from the US government, however a consensus of credible reporting will also be used.
市场开放时间: Feb 7, 2026, 5:04 PM ET
Resolver
0x65070BE91...The primary resolution source for this market will be official information from the US government, however a consensus of credible reporting will also be used.
Resolver
0x65070BE91...**Medical cannabis under state licenses and FDA-approved products moved to Schedule III effective April 28, 2026, following an April 23 order by Acting Attorney General Todd Blanche.** This action implemented a December 2025 executive order directing expedited review of marijuana’s placement under the Controlled Substances Act. A separate administrative hearing on broader rescheduling of all botanical marijuana (including adult-use) from Schedule I to Schedule III ran from June 29 to July 15, 2026, with the DEA presenting evidence of currently accepted medical use. Post-hearing briefs are now due, after which an administrative law judge recommendation is expected in late 2026 or early 2027, followed by potential final rulemaking. Ongoing litigation by anti-rescheduling parties challenges the medical reclassification in federal court, while procedural deadlines and agency timelines remain the main near-term catalysts. Traders monitor these steps because full rescheduling hinges on completion of the administrative record and any subsequent agency or judicial action.
基于Polymarket数据的AI实验性摘要。这不是交易建议,也不影响该市场的结算方式。 · 更新于



警惕外部链接哦。
警惕外部链接哦。
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