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United States · Bill · HR

H.R. 5850 (118th)

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.

referredUnited States· United States Congress· EN

Introduced

29 September 2023

Last action

Status

Referred to the Subcommittee on Health.

Sponsors

Subjects

Discovery layer

Source updated

24 July 2024

Records

Official bill H.R. 5850 (118th) from United States at United States Congress. Dated 29 September 2023. Status: Referred to the Subcommittee on Health..

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Documents

2 official files

Introduced in House (text)

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