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
59651-238_50958060-c904-4374-997d-59df54007fa4
Product NDC
59651-238
Form
TABLET
Composition / generic term
Pirfenidone
Labeler
Aurobindo Pharma Limited
Marketing category
ANDA
Marketing start / end (source format)
20250811
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 (59651-238-27) / 90 TABLET in 1 BOTTLE (59651-238-90) · 59651-238-27

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →