Bill Sponsor
House Bill 7669
117th Congress(2021-2022)
Drug Shortages Shelf Life Extension Act
Introduced
Introduced
Introduced in House on May 6, 2022
Overview
Text
Introduced
May 6, 2022
Latest Action
May 6, 2022
Origin Chamber
House
Type
Bill
Bill
The primary form of legislative measure used to propose law. Depending on the chamber of origin, bills begin with a designation of either H.R. or S. Joint resolution is another form of legislative measure used to propose law.
Bill Number
7669
Congress
117
Policy Area
Health
Health
Primary focus of measure is science or practice of the diagnosis, treatment, and prevention of disease; health services administration and funding, including such programs as Medicare and Medicaid; health personnel and medical education; drug use and safety; health care coverage and insurance; health facilities. Measures concerning controlled substances and drug trafficking may fall under Crime and Law Enforcement policy area.
Sponsorship by Party
Democrat
California
Democrat
California
Democrat
California
Republican
Nebraska
House Votes (0)
Senate Votes (0)
No House votes have been held for this bill.
Summary

Drug Shortages Shelf Life Extension Act

This bill requires the Food and Drug Administration (FDA) to issue or revise guidance to address issues relating to extending drug expiration dates.

Specifically, the guidance must address recommendations to drug companies relating to (1) submitting stability testing data in applications for market approval for drugs or biological products; (2) establishing on drug labels the longest feasible expiration date scientifically supported by such data, taking into consideration how extended expiration dates may help prevent or mitigate drug shortages and affect product quality; and (3) using innovative approaches to stability modeling to support initial product expiration dates and expiration date extensions.

The FDA must also periodically report to Congress certain information about requests to change the expiration date on a drug label, including the number of such requests from the FDA to the manufacturer and the rationale for each request.

Text (1)
Actions (2)
05/06/2022
Referred to the House Committee on Energy and Commerce.
05/06/2022
Introduced in House
Public Record
Record Updated
Dec 29, 2022 11:48:32 PM