FDA NDC Directory · JSON-LD · Markdown

RIVAROXABAN

NDC 68180-709 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208555
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsRIVAROXABAN (2.5 mg/1)
Marketing started20250306
Package count2

External sources

Source: openFDA. Public-domain (CC0).