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Propafenone Hydrochloride

NDC 59651-278 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA213096
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsPROPAFENONE HYDROCHLORIDE (425 mg/1)
Marketing started20230221
Package count3

External sources

Source: openFDA. Public-domain (CC0).