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HR 5316 - 119

Drug Shortage Compounding Patient Access Act of 2025

Referred to the House Committee on Energy and Commerce.

Bill highlights

Votes, text signals, source context, and latest movement from this record.

Bill Text Stats

10
Analyzed sections
N/A
Detected dollar total
0
Tax signals
1
Deadlines

Signal counts

Tax density 0.0%
Spending density 0.0%
Statutory Reference 5
Amendments 3
Deadline 1

Top agencies

N/A

Statutory references

21 U.S.C. 353a 2
21 U.S.C. 353a 1
21 U.S.C. 353b 1
21 U.S.C. 356c 1

House Votes

No House roll call votes have been linked to this bill yet.

Timeline

Sep 11, 2025

Introduced in House

Sep 11, 2025

Introduced in House

Sep 11, 2025

Referred to the House Committee on Energy and Commerce.

Affected Sectors

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Healthcare
15 evidence matches
Impact 100% Confidence 90%

Health

Health

compounded for distribution in limited quantities to a licensed prescriber for urgent administration to a patient in a hospital or other clinical setting, provided that all of the following are met: (A) The drug product appeared on the dru

Energy
2 evidence matches
Impact 94% Confidence 85%

Energy and Commerce Committee Standing House

Drug Shortage Compounding Patient Access Act of 2025 Referred to the House Committee on Energy and Commerce. Health

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Summary

00 Introduced in House Jul 6, 2026

Drug Shortage Compounding Patient Access Act of 2025 This bill relaxes certain requirements for the compounding of drugs facing shortages. Currently, subject to certain requirements, compounded drugs (i.e., drugs altered to meet patient needs) do not require Food and Drug Administration (FDA) approval. There are two general categories of compounding: (1) pharmacy compounding, wherein a licensed pharmacist or physician not registered with the FDA compounds in limited quantities for identified patients; and (2) bulk compounding, wherein an FDA-registered outsourcing facility compounds in bulk for use in medical facilities. The bill permits pharmacy compounding in limited quantities for an urgent medical need not involving a specific patient if, among other requirements, the drug appeared on the FDA’s drug shortage list within a specified period. The bill also formally waives limits on pharmacy compounding of drugs that are essentially copies of commercially available drugs if the drug appeared on the shortage list within a specified period. Separately, the bill extends the period during which an outsourcing facility may compound a drug that appeared on the shortage list to 180 days after the drug’s removal from the list. The bill also requires the FDA to publish annual updates on its evaluation of substances for inclusion on the list of bulk drug substances (i.e., active pharmaceutical ingredients) that may be used in bulk compounding of drugs not on the shortage list. Finally, manufacturers of certain drugs, including life-supporting and life-sustaining drugs, must report to the FDA certain surges in demand for such drugs.

Sponsors

Harris, Andy
Cosponsor

Harris, Andy

Republican · MD-1 · H001052

Joined Oct 24, 2025
Website
N/A
Office
1536 Longworth House Office Building

Amendments

No amendment records are currently available for this bill.
Compiled bill record. Bill pages combine Congress.gov source payloads, normalized relationships, cached text analysis, vote links, and deterministic sector/signal extraction. This is not an official government record or legal advice; use the official source link when accuracy matters.