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HR 1843 119th Congress House Health

To amend the Federal Food, Drug, and Cosmetic Act to increase transparency in generic drug applications.

Introduced: March 5, 2025 Introduced by: Dunn, Neal P. Republican · Florida See on congress.gov
 Everywhere this bill has been 2 steps
Introduced
In committee
Reported out
Passed House
Passed Senate
To President
Became law
Mar 5, 2025
Referred to the House Committee on Energy and Commerce.
Mar 5, 2025
Introduced in House
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 Plain-English summary Congressional Research Service

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.

What's happening now March 5, 2025

Referred to the House Committee on Energy and Commerce.

 Hearings & markups 1
 Related & companion bills 4
 Bill text 1 version

Source documents hosted by congress.gov.

 Committees of jurisdiction 1
 Lobbying activity 59

Registered lobbyists who named this bill in their disclosure filings. Source: federal Lobbying Disclosure Act filings.

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APA
U.S. Congress. (2026). H.R. 1843: To amend the Federal Food, Drug, and Cosmetic Act to increase transparency in generic drug applications.. 119th Congress. Open America. https://openamerica.io/bill/119-HR-1843/
MLA
"H.R. 1843: To amend the Federal Food, Drug, and Cosmetic Act to increase transparency in generic drug applications.." 119th Congress, 2026, Open America, https://openamerica.io/bill/119-HR-1843/.
Bluebook (legal)
H.R. 1843, 119th Cong. (2026), https://openamerica.io/bill/119-HR-1843/.
Markdown link
[H.R. 1843: To amend the Federal Food, Drug, and Cosmetic Act to increase transparency in generic drug applications.](https://openamerica.io/bill/119-HR-1843/)
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