House bill HR5850-118
Energy and Commerce Committee
To nullify modifications made by the Food and Drug Administration on January 3, 2023, to the risk evaluation and mitigation strategy under section 505-1 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 355-1) for mifepristone, and for other purposes.
• Last activity on Oct 06, 2023
• Introduced Sep 29, 2023
• By Rep. Mann, Tracey [R-KS-1]