Prescription Drug Freshness Act
Bill journey · stage 2 of 5
Under committee review
What it doesSummary introduced in house (May 18, 1983)
Prescription Drug Freshness Act - Requires the prominent labeling, as to the date beyond which the product shall not be used, of prescription and over-the-counter drugs and pharmaceuticals whose effectiveness or potency becomes diminished after storage.
Authorizes the Food and Drug Administration to establish the "beyond use" dates for all applicable products and the manner in which they shall be labeled.
What just happenedMay 24, 1983
Referred to Subcommittee on Health and the Environment.
Who’s behind it
- May 24, 1983CommitteeH11000
Referred to Subcommittee on Health and the Environment.
Health and Environment Subcommittee - May 18, 1983IntroReferralH11100
Referred to House Committee on Energy and Commerce.
Energy and Commerce Committee - May 18, 1983IntroReferralIntro-H
Introduced in House
- May 18, 1983IntroReferral1000
Introduced in House