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Pirfenidone

NDC 42385-925 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLaurus Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA212722
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPIRFENIDONE (534 mg/1)
Marketing started20220719
Package count1

External sources

Source: openFDA. Public-domain (CC0).