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Proposed

Bill · 119th Congress · HR 8339

Drug Origin Transparency Act of 2026

Refreshed 2 h ago

Introduced 2026-04-16Topic: health care

Summary

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This bill changes federal drug law to require more detailed reporting on where drugs and their ingredients come from. Companies that report drug manufacturing amounts to the Food and Drug Administration would have to include supplier details for active ingredients and in-process materials, as specified by the Secretary, and the amounts made using each supplier's materials. Reports would be due more often than once a year, but no more than four times a year. Drug labels, including labels on active pharmaceutical ingredients, would have to show the name, place of business, and facility identifier of the original manufacturer, and drug labeling would have to list the original manufacturer of each active ingredient, any other manufacturer, and the packer or distributor.

Full text and official record on Congress.gov

Sponsors

Action history

DateChamberActionStatus effect
2026-04-16HouseReferred to the House Committee on Energy and Commerce.refer
2026-04-16Introduced in Houseintroduce
2026-04-16Introduced in Houseintroduce
Source: GovInfo Bill Status (Library of Congress), fetched 2026-10-31. Provisions and opinion polling arrive in a later release.