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United States · Bill · S

S. 2621 (94th)

A bill to amend the Federal Food, Drug, and Cosmetic Act to require that the identity of the manufacturer of a prescription drug appear on the label of the package from which the drug is to be dispensed.

referredUnited States· United States Congress· EN

Introduced

5 November 1975

Last action

Status

Referred to Senate Committee on Labor and Public Welfare.

Sponsors

Subjects

Discovery layer

Source updated

21 April 2025

Summary

Revises the Federal Food, Drug, and Cosmetic Act to require that the name and place of business of the manufacturer and distributor, if different, of a prescription drug appear on the label of the package from which the drug is to be dispensed.

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Documents

1 official file

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Sources

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