HR 9321 United States House · 118th Congress

American Made Pharmaceuticals Act of 2024

This bill establishes a 7-year demonstration program testing preferential treatment for U.S.-manufactured drugs in Medicare, Medicaid, and CHIP programs. It directs the Secretary to implement the program in at least 8 states, using tools like formulary preference or lower patient cost-sharing for drugs made by qualifying U.S. pharmaceutical companies. To qualify, drugs must be manufactured in the U.S. by companies meeting specific transparency, supply chain diversity, and inventory standards, including critical drugs identified in executive orders or deemed high-risk for shortages. The program aims to assess how U.S. manufacturing preferences affect drug access and costs within federal health programs. The Secretary must submit annual reports to Congress on program results and recommendations.
Bill status in committee 1 of 4 stages cleared
Introduction
Aug 2024
Committee Review
Floor Vote
President
Introduced Aug 6, 2024 Last action Dec 17, 2024
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Total actions
3
Key actions
0
Committee
2
Dec 17, 2024
Committee
Referred to the Subcommittee on Health.
lower
Aug 6, 2024
Committee
Referred to the Committee on Energy and Commerce, and in addition to the Committee on Ways and Means, for a period to be subsequently determined by the Speaker, in each case for consideration of such provisions as fall within the jurisdiction of the committee concerned.
lower
Aug 6, 2024
Introduced
Introduced in House
lower
1 primary · 1 co-sponsor

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