FDA NDC Directory · JSON-LD · Markdown

Rivaroxaban

NDC 59651-849 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA208544
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsRIVAROXABAN (2.5 mg/1)
Marketing started20250410
Package count2

External sources

Source: openFDA. Public-domain (CC0).