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United States · Bill · S

S. 3633 (110th)

Transparency in Drug Labeling Act

referredUnited States· United States Congress· EN

Introduced

26 September 2008

Last action

Status

Read twice and referred to the Committee on Health, Education, Labor, and Pensions.

Sponsors

Subjects

Discovery layer

Source updated

14 August 2025

Summary

Transparency in Drug Labeling Act - Amends the Federal Food, Drug, and Cosmetic Act to deem a drug to be misbranded unless the labeling of such drug lists the identity of the country of manufacture of each active ingredient and each inactive ingredient of the drug, listed in descending order based on the percentage of the number of such ingredients in the final dosage form manufactured in such countries.

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Documents

3 official files

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Sources

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