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United States · Bill · S

S. 1898 (117th)

Affordable Medications Act

referredUnited States· United States Congress· EN

Introduced

27 May 2021

Last action

27 May 2021 · Introduced

Status

Read twice and referred to the Committee on Finance.

Sponsors

Sen. Smith, Tina [D-MN], Sen. Warren, Elizabeth [D-MA], Sen. Blumenthal, Richard [D-CT], Sen. Klobuchar, Amy [D-MN], Sen. Merkley, Jeff [D-OR], Sen. Reed, Jack [D-RI], Sen. Baldwin, Tammy [D-WI], Sen. Hassan, Margaret Wood [D-NH], Sen. Booker, Cory A. [D-NJ], Sen. Sanders, Bernard [I-VT], Sen. Brown, Sherrod [D-OH], Sen. Gillibrand, Kirsten E. [D-NY], Sen. Whitehouse, Sheldon [D-RI], Sen. Durbin, Richard J. [D-IL]

Subjects

Healthcare, Taxation

Source updated

3 January 2025

Healthcare · Taxation

Summary

Affordable Medications Act This bill revises and expands various requirements relating to prescription drug pricing and affordability.  Specifically, the bill expands financial reporting requirements for drug manufacturers and establishes corresponding civil penalties for noncompliance; it also adds reporting requirements for certain nonprofit patient-assistance programs. Further, the bill requires the Centers for Medicare & Medicaid Services (CMS) to negotiate prices for certain prescription drugs under Medicare and requires the Centers for Medicare and Medicaid Innovation within the CMS to test specified models for negotiating drug prices. It also establishes reporting requirements, and corresponding civil penalties for noncompliance, for pharmaceutical companies with respect to spikes in prescription drug prices. The bill establishes an excise tax on prescription drugs subject to price spikes, lessens prescription drug cost-sharing requirements under qualified health plans and group health plans, and modifies requirements for the importation of prescription drugs. It also requires drug manufacturers to provide rebates for drugs dispensed to certain low-income individuals under the Medicare program and limits the time frame that trade agreements are required to provide market exclusivity for biological products. Additionally, the bill (1) requires the Food and Drug Administration to establish a database of generic drugs; (2) modifies other provisions related to generic drugs, prescription drug advertising, disclosure of wholesale acquisition prices, and patent-infringement proceedings; and (3) revises certain time frames and conditions related to drug exclusivity. Finally, it establishes an innovation incentive fund for new or more effective treatments of bacterial infections and establishes the Center for Clinical Research within the National Institutes of Health.

This text is taken from the official record. PoliticalRepo does not editorialize.

Timeline

  1. 27 May 2021

    Introduced

    Read twice and referred to the Committee on Finance.

    Source: IntroReferral

  2. 27 May 2021

    Introduced

    Introduced in Senate

    Source: IntroReferral

Votes

No vote records are attached yet.

Versions

Documents

3 official files

Introduced in Senate (text)

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  • Introduced in Senate (text)

    Introduced in Senate · EN · 27 May 2021

    ViewDownloadOpen at official source

  • Introduced in Senate (PDF)

    Introduced in Senate · EN · 27 May 2021

    ViewDownloadOpen at official source

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  • Introduced in Senate

    summary · EN · 27 May 2021

    Open at official source

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Sponsors

Related records

Sources

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