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PROPAFENONE HYDROCHLORIDE

NDC 16571-737 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA205956
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsPROPAFENONE HYDROCHLORIDE (325 mg/1)
Marketing started20201216
Package count2

External sources

Source: openFDA. Public-domain (CC0).