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Propafenone Hydrochloride

NDC 0832-0740 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerUpsher-Smith Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212744
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsPROPAFENONE HYDROCHLORIDE (225 mg/1)
Marketing started20200625
Marketing ended20261130
Package count1

External sources

Source: openFDA. Public-domain (CC0).