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
0480-3610_72544fc9-cc24-4975-8111-9cfeb0497b8f
Product NDC
0480-3610
Form
TABLET, FILM COATED
Composition / generic term
Pirfenidone
Labeler
Teva Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20220511
Source listing expiry
20271231

Source-listed ingredients

  • PIRFENIDONE — 267 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 270 TABLET, FILM COATED in 1 BOTTLE (0480-3610-87) · 0480-3610-87

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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