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Increasing Transparency in Generic Drug Applications Act
3/14/2024, 12:02 AM
Congressional Summary of S 4338
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).
Read the Full Bill
Current Status of Bill S 4338
Bill S 4338 is currently in the status of Bill Introduced since May 26, 2022. Bill S 4338 was introduced during Congress 117 and was introduced to the Senate on May 26, 2022. Bill S 4338's most recent activity was Read twice and referred to the Committee on Health, Education, Labor, and Pensions. as of May 26, 2022
Bipartisan Support of Bill S 4338
Total Number of Sponsors
1Democrat Sponsors
1Republican Sponsors
0Unaffiliated Sponsors
0Total Number of Cosponsors
1Democrat Cosponsors
0Republican Cosponsors
1Unaffiliated Cosponsors
0Policy Area and Potential Impact of Bill S 4338
Primary Policy Focus
HealthPotential Impact Areas
- Administrative law and regulatory procedures
- Department of Health and Human Services
- Drug safety, medical device, and laboratory regulation
- Prescription drugs
Alternate Title(s) of Bill S 4338
Increasing Transparency in Generic Drug Applications Act
Increasing Transparency in Generic Drug Applications Act
A bill to provide for increased transparency in generic drug applications.
Comments
Sponsors and Cosponsors of S 4338
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