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.
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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Timeline
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Votes
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Versions
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Documents
1 official file
Introduced in Senate
summary · EN · 5 November 1975
Sponsors
No sponsors or actors listed by the source.
Related records
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Sources
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- Official source: https://www.congress.gov/bill/94th-congress/senate-bill/2621
- Open data entity: https://api.congress.gov/v3/bill/94/s/2621