United States · FDA National Drug Code directory
PIRFENIDONE
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 72603-258_5d0eee8c-dc7d-4444-8684-e9c9335291c8
- Product NDC
- 72603-258
- Form
- TABLET, FILM COATED
- Composition / generic term
- PIRFENIDONE
- Labeler
- Northstar Rx LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220524
- Source listing expiry
- 20261231
Source-listed ingredients
- PIRFENIDONE — 267 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 BOTTLE in 1 CARTON (72603-258-03) / 90 TABLET, FILM COATED in 1 BOTTLE (72603-258-01) · 72603-258-03
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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