Increasing Transparency in Generic Drug Applications Act of 2022
Official title: To amend section 505(j) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 355(j)) with respect to a process to inform persons submitting an abbreviated ap… Show full official titleShow less
Official title: To amend section 505(j) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 355(j)) with respect to a process to inform persons submitting an abbreviated application for a new drug whether the new drug is qualitatively or quantitatively the same as a listed drug, and for other purposes.
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Referred to the Subcommittee on Health.
Increasing Transparency in Generic Drug Applications Act of 2022
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).
- Introduced in House Formatted Text PDF Formatted XML
Cite this page
U.S. Congress. (2026). H.R. 7032: Increasing Transparency in Generic Drug Applications Act of 2022. 117th Congress. Open America. https://openamerica.io/bill/117-HR-7032/
"H.R. 7032: Increasing Transparency in Generic Drug Applications Act of 2022." 117th Congress, 2026, Open America, https://openamerica.io/bill/117-HR-7032/.
H.R. 7032, 117th Cong. (2026), https://openamerica.io/bill/117-HR-7032/.
[H.R. 7032: Increasing Transparency in Generic Drug Applications Act of 2022](https://openamerica.io/bill/117-HR-7032/)