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Ranolazine

NDC 13668-759 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerTorrent Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214035
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsRANOLAZINE (500 mg/1)
Marketing started20260511
Package count1

External sources

Source: openFDA. Public-domain (CC0).