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Flecainide Acetate

NDC 65162-643 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075442
Dosage form / routeTABLET · ORAL
Active ingredientsFLECAINIDE ACETATE (150 mg/1)
Marketing started20091201
Package count2

External sources

Source: openFDA. Public-domain (CC0).