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Propafenone Hydrochloride

NDC 68382-522 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerZydus Pharmaceuticals (USA) Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214184
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsPROPAFENONE HYDROCHLORIDE (225 mg/1)
Marketing started20220202
Package count2

External sources

Source: openFDA. Public-domain (CC0).