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S 4338 117th Congress Senate Health Administrative law and regulatory procedures Department of Health and Human Services Drug safety, medical device, and laboratory regulation Prescription drugs

Increasing Transparency in Generic Drug Applications Act

Introduced: May 26, 2022 Introduced by: Hassan, Margaret Wood Democratic · New Hampshire See on congress.gov
This bill died when the 117th Congress ended
It never became law before the 117th Congress (2021–2022) adjourned, and bills don't carry over to the next Congress. It would have to be reintroduced. You can still save it for reference, but it won't receive updates.
 Everywhere this bill has been 2 steps
Introduced
In committee
Reported out
Passed House
Passed Senate
To President
Became law
May 26, 2022
Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
May 26, 2022
Introduced in Senate
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 Plain-English summary Congressional Research Service

Increasing Transparency in Generic Drug Applications Act

This bill requires the Food and Drug Administration 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).

What's happening now May 26, 2022

Read twice and referred to the Committee on Health, Education, Labor, and Pensions.

 Related & companion bills 2
 Bill text 1 version

Source documents hosted by congress.gov.

 Committees of jurisdiction 1
Cite this page click to expand
APA
U.S. Congress. (2026). S. 4338: Increasing Transparency in Generic Drug Applications Act. 117th Congress. Open America. https://openamerica.io/bill/117-S-4338/
MLA
"S. 4338: Increasing Transparency in Generic Drug Applications Act." 117th Congress, 2026, Open America, https://openamerica.io/bill/117-S-4338/.
Bluebook (legal)
S. 4338, 117th Cong. (2026), https://openamerica.io/bill/117-S-4338/.
Markdown link
[S. 4338: Increasing Transparency in Generic Drug Applications Act](https://openamerica.io/bill/117-S-4338/)
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