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United States · Bill · HR

H.R. 63 (110th)

RU-486 Suspension and Review Act of 2007

referredUnited States· United States Congress· EN

Introduced

4 January 2007

Last action

2 February 2007 · Referred

Status

Referred to the Subcommittee on Health.

Sponsors

Rep. Bartlett, Roscoe G. [R-MD-6], Rep. Norwood, Charles W. [R-GA-9], Rep. Musgrave, Marilyn N. [R-CO-4], Rep. Herger, Wally [R-CA-2], Rep. Lewis, Ron [R-KY-2], Rep. Alexander, Rodney [R-LA-5], Rep. Fortenberry, Jeff [R-NE-1], Rep. Manzullo, Donald A. [R-IL-16], Rep. Goode, Virgil H., Jr. [R-VA-5], Rep. Franks, Trent [R-AZ-8], Sen. Blackburn, Marsha [R-TN], Rep. Smith, Christopher H. [R-NJ-4], Rep. Davis, Jo Ann [R-VA-1], Rep. Davis, Geoff [R-KY-4], Rep. Gingrey, Phil [R-GA-11], Sen. Wicker, Roger F. [R-MS], Rep. King, Steve [R-IA-4], Rep. Davis, Lincoln [D-TN-4], Rep. Hoekstra, Peter [R-MI-2], Rep. Wilson, Joe [R-SC-2], Rep. Sali, Bill [R-ID-1], Rep. Murphy, Tim [R-PA-18], Rep. Pitts, Joseph R. [R-PA-16], Sen. Boozman, John [R-AR], Rep. Tiberi, Patrick J. [R-OH-12], Rep. Jones, Walter B., Jr. [R-NC-3], Rep. Renzi, Rick [R-AZ-1], Rep. Ehlers, Vernon J. [R-MI-3], Rep. Hall, Ralph M. [R-TX-4], Rep. Hayes, Robin [R-NC-8], Rep. Shimkus, John [R-IL-15], Rep. Hunter, Duncan [R-CA-52], Rep. Tiahrt, Todd [R-KS-4], Rep. Sullivan, John [R-OK-1], Rep. Hensarling, Jeb [R-TX-5], Rep. Terry, Lee [R-NE-2], Rep. Westmoreland, Lynn A. [R-GA-3], Rep. McCotter, Thaddeus G. [R-MI-11], Rep. Everett, Terry [R-AL-2], Rep. LaHood, Ray [R-IL-18], Rep. Schmidt, Jean [R-OH-2], Rep. Bachus, Spencer [R-AL-6], Rep. Whitfield, Ed [R-KY-1], Rep. Chabot, Steve [R-OH-1], Rep. Inglis, Bob [R-SC-4], Rep. Rogers, Harold [R-KY-5], Rep. Souder, Mark E. [R-IN-3], Rep. Lamborn, Doug [R-CO-5]

Subjects

Healthcare

Source updated

14 August 2025

Healthcare

Official sourceDownload fileView documentsShare

Summary

RU-486 Suspension and Review Act of 2007 - 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commonly known as RU-486, and used for the chemically induced termination of intrauterine pregnancy) to have been withdrawn.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 to be 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.

This text is taken from the official record. PoliticalRepo does not editorialize.

Timeline

  1. 4 January 2007

    Introduced

    Referred to the House Committee on Energy and Commerce.

    Source: IntroReferral

  2. 4 January 2007

    Introduced

    Introduced in House

    Source: IntroReferral

  3. 4 January 2007

    Introduced

    Introduced in House

    Source: IntroReferral

  4. 2 February 2007

    Referred

    Referred to the Subcommittee on Health.

    Source: Committee

Votes

No vote records are attached yet.

Versions

Documents

3 official files

Introduced in House (text)

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  • Introduced in House (text)

    Introduced in House · EN · 4 January 2007

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  • Introduced in House (PDF)

    Introduced in House · EN · 4 January 2007

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  • Introduced in House

    summary · EN · 4 January 2007

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Sponsors

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Related records

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Sources

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