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propafenone hydrochloride

NDC 68462-409 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA205268
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsPROPAFENONE HYDROCHLORIDE (325 mg/1)
Marketing started20170908
Package count1

External sources

Source: openFDA. Public-domain (CC0).