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Ivabradine

NDC 46708-680 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA215238
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsIVABRADINE HYDROCHLORIDE (7.5 mg/1)
Marketing started20241220
Package count2

External sources

Source: openFDA. Public-domain (CC0).