Patient Safety and Generic Labeling Improvement Act
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Patient Safety and Generic Labeling Improvement Act - Amends the Federal Food, Drug, and Cosmetic Act to allow the holder of an approved abbreviated new drug application (generic drug approval) to change the labeling of a drug so approved in the same manner authorized by regulation for the holder of an approved new drug application.
Allows conforming changes to be ordered to the labeling of the equivalent listed drug and each drug approved under the abbreviated new drug application process that corresponds to such listed drug.
Read twice and referred to the Committee on Health, Education, Labor, and Pensions. (text of measure as introduced: CR S2498)
- Introduced in Senate Formatted Text PDF Formatted XML
Cite this page
U.S. Congress. (2026). S. 2295: Patient Safety and Generic Labeling Improvement Act. 112th Congress. Open America. https://openamerica.io/bill/112-S-2295/
"S. 2295: Patient Safety and Generic Labeling Improvement Act." 112th Congress, 2026, Open America, https://openamerica.io/bill/112-S-2295/.
S. 2295, 112th Cong. (2026), https://openamerica.io/bill/112-S-2295/.
[S. 2295: Patient Safety and Generic Labeling Improvement Act](https://openamerica.io/bill/112-S-2295/)