RU-486 Suspension and Review Act of 2005
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RU-486 Suspension and Review Act of 2005 - Deems the approved application for the drug mifepristone (marketed as Mifeprex, commonly known as RU-486, and used for the chemically induced termination of intrauterine pregnancy) to have been withdrawn.
Deems the drug misoprostol as misbranded under the Federal Food, Drug, and Cosmetic Act (FFDCA) if it bears labeling providing that the drug may be used for the medical termination of intrauterine pregnancy.
Directs the Comptroller General to review and report on the process by which the Food and Drug Administration (FDA) approved mifepristone. Provides for the reinstatement of the approved application for such drug if the report determines the approval to have been in accordance with FFDCA.
Read twice and referred to the Committee on Health, Education, Labor, and Pensions. (text of measure as introduced: CR S2020-2021)
- Introduced in Senate Formatted Text PDF Formatted XML
Cite this page
U.S. Congress. (2026). S. 511: RU-486 Suspension and Review Act of 2005. 109th Congress. Open America. https://openamerica.io/bill/109-S-511/
"S. 511: RU-486 Suspension and Review Act of 2005." 109th Congress, 2026, Open America, https://openamerica.io/bill/109-S-511/.
S. 511, 109th Cong. (2026), https://openamerica.io/bill/109-S-511/.
[S. 511: RU-486 Suspension and Review Act of 2005](https://openamerica.io/bill/109-S-511/)