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

27 March 1979

Last action

—

Status

Referred to Senate Committee on Labor and Human Resources.

Summary

Amends the Federal Food, Drug, and Cosmetic Act to require that labels of prescription drugs manufactured in final dosage form show the name and place of business of the manufacturer and, if different, the name and place of business of the packer or distributor.

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Versions

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Documents

1 official file

Introduced in Senate
summary · EN · 27 March 1979
Open at official source

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Sources

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Official source: https://www.congress.gov/bill/96th-congress/senate-bill/786
Open data entity: https://api.congress.gov/v3/bill/96/s/786