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H.R. 685In committee

SAVE Moms and Babies Act of 2025

Introduced: Jan 23, 2025

Latest action date: Jan 23, 2025

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Current stage

In committee

The most advanced recorded stage is committee consideration.

Introduced

Jan 23, 2025

Latest action

Jan 23, 2025

Recorded roll calls

0

Civixly topics

What this legislation is about

Civixly topics make federal and state legislation comparable. They are derived from the official CRS policy area and legislative subjects.

Official CRS policy area

Health

View 7 official legislative subjects
AbortionDrug safety, medical device, and laboratory regulationHealth information and medical recordsHealth personnelHealth technology, devices, suppliesMarketing and advertisingPrescription drugs

Bill Summary

Support And Value Expectant Moms and Babies Act of 2025 or the SAVE Moms and Babies Act of 2025

This bill prohibits the Food and Drug Administration (FDA) from approving any new drug (either as a brand-name drug or a generic) intended to terminate a pregnancy and imposes additional restrictions on such drugs that are already approved.

Under the bill, an already-approved drug intended to terminate a pregnancy may be dispensed to a patient only with a prescription. Furthermore, the FDA may not approve any labeling change that would authorize (1) using the drug after 70 days of gestation, or (2) dispensing the drug by any means other than in-person administration by the prescribing health care practitioner.

The FDA must also impose additional restrictions on such already-approved drugs, including by (1) requiring the prescribing health care practitioner to receive a special certification, (2) prohibiting the practitioner from also acting as the dispensing pharmacist, and (3) requiring the practitioner to have the ability to provide surgical intervention to the patient.

The bill also rescinds any investigational use exemption already granted to such a drug if the bill would have prohibited the FDA from granting the exemption. (Currently, the FDA may grant an exemption to certain market approval requirements if a drug is intended solely for use in safety and effectiveness investigations.)

Committee activity

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Amendments

Proposed changes to this measure, with their latest official outcome or action from Congress.gov.

No amendments are listed for this measure.

Checked against Congress.gov Sep 14, 2026.

Action timeline

Newest action first. Action language comes from the official Congress.gov record.

View full action timeline3 actions
  1. Introduced in House

    IntroReferralLibrary of Congress
  2. Referred to the House Committee on Energy and Commerce.

    IntroReferralHouse floor actions
  3. Introduced in House

    IntroReferralLibrary of Congress

Roll-call votes

Recorded House and Senate votes connected to this bill. Your representatives appear first when available.

No connected roll-call votes are currently available for this bill.

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Federal legislative data comes from Congress.gov and official House and Senate vote records.

Base metadata check pending · Summary check pending · Action timeline checked Sep 14, 2026 · Complete sponsorship check pending · Topics checked Sep 14, 2026 · Committees checked Sep 14, 2026 · Status checked Sep 14, 2026 · Related bills checked Sep 14, 2026.