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IVABRADINE

NDC 50742-362 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerIngenus Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA214051
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIVABRADINE HYDROCHLORIDE (5 mg/1)
Marketing started20240715
Package count1

External sources

Source: openFDA. Public-domain (CC0).