H.R. 1843
Referred to CommitteeTo amend the Federal Food, Drug, and Cosmetic Act to increase transparency in generic drug applications.
Introduced 3/5/2025•119th Congress•House
Latest Action
Referred to the House Committee on Energy and Commerce.
3/5/2025 • House
Summary
This bill requires the Food and Drug Administration (FDA) to inform generic drug applicants, upon request or during review, whether the drug is qualitatively and quantitatively the same as the listed brand-name drug (and if not, the reasons why). The FDA must also update or publish guidance on how it makes such determinations.
Introduced in House • 3/5/2025
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Topics & Subjects
Policy Area: Health
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Related Federal Spending
Sponsor & Cosponsors (2)
Party Breakdown
1
Democrats
1
Republicans
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Independents
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Cosponsors (1)
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Bill Journey
Originated in the House
Introduced
March 5, 2025
Referred to the House Committee on Energy and Commerce.
Committee Review
Floor Debate
Passed Chamber
Other Chamber
President
Enacted into Law
Text Versions (1)
Introduced in House3/5/2025