HR 4438 · 95th Congress · Drugs
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.
Bill Progress
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Introduced2
Committee3
House Vote4
Senate5
EnactedLatest: Referred to House Committee on Interstate and Foreign Commerce.(1977-03-03)
Plain Language Summary
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Amends the Federal Food, Drug, and Cosmetic Act to require that 180 days after enactment of this Act prescription drugs manufactured in final dosage form and distributed or packed by a different person, company, or corporation show on the label both the identity of the distributor or packer and the identity or registration number of the manufacturer.…
Summarized by Claude AI · Non-partisan · For informational purposes only