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
69097-988_398a92b7-8db3-4604-9004-892c41721294
Product NDC
69097-988
Form
TABLET, COATED
Composition / generic term
Pirfenidone
Labeler
Cipla USA Inc.
Marketing category
ANDA
Marketing start / end (source format)
20220802
Source listing expiry
20261231

Source-listed ingredients

  • PIRFENIDONE — 801 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET, COATED in 1 BOTTLE (69097-988-05) · 69097-988-05
  • 270 TABLET, COATED in 1 BOTTLE (69097-988-93) · 69097-988-93

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.

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