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Pirfenidone

NDC 59651-239 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA212596
Dosage form / routeTABLET · ORAL
Active ingredientsPIRFENIDONE (801 mg/1)
Marketing started20250811
Package count1

External sources

Source: openFDA. Public-domain (CC0).