Senate bill · S. 1302 (119th Congress)
Increasing Transparency in Generic Drug Applications Act
U.S. Senate
Sponsor: Margaret Wood Hassan (U.S. Senator for New Hampshire, Democratic)
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From Congress.gov and official rosters. This record was last updated Jul 30, 2026. About our data
Summary
Would amend federal drug law to let a person submitting a generic drug application request information from the FDA about whether laboratory (in vitro) testing may be used to demonstrate that a generic drug works the same as its brand-name counterpart when the two share the same inactive ingredients.
AI summary. Not an official summary. How we handle summaries
Where it stands
Assigned to a committee for review.
- Introduced
- In committee
- Up for a vote
- Passed one chamber
- Passed
- Enacted
Committee
Senate Committee on Health, Education, Labor, and Pensions · U.S. Senate
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Cosponsors
6
Cosponsors listed on Congress.gov, shown A to Z.
- Republican4
- Democratic2
This bill has cosponsors from more than one party.
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Related bills
- H.R. 1768Lower Costs for Everyday Americans ActRelated bill
- H.R. 1843To amend the Federal Food, Drug, and Cosmetic Act to increase transparency in generic drug applications.Related bill
- H.R. 7148Consolidated Appropriations Act, 2026Related bill
- S. 891Bipartisan Health Care ActRelated bill
As identified by Congress.gov.
Full history
- Apr 3, 2025
Introduced
Introduced in U.S. Senate
U.S. Senate
- Apr 3, 2025
Referred to committee
Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
- Apr 3, 2025
Referred to committee
Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
- Apr 3, 2025
Referred to committee
Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
Read the record
- Read on Congress.gov (opens in a new tab) The official record on Congress.gov.