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Propafenone Hydrochloride

NDC 72162-1752 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA076550
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsPROPAFENONE HYDROCHLORIDE (225 mg/1)
Marketing started20150331
Package count1

External sources

Source: openFDA. Public-domain (CC0).