FDA NDC Directory · JSON-LD · Markdown

Flecainide Acetate

NDC 57237-063 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202821
Dosage form / routeTABLET · ORAL
Active ingredientsFLECAINIDE ACETATE (50 mg/1)
Marketing started20150708
Package count1

External sources

Source: openFDA. Public-domain (CC0).