FDA NDC Directory · JSON-LD · Markdown

Warfarin Sodium

NDC 51672-4030 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040301
Dosage form / routeTABLET · ORAL
Active ingredientsWARFARIN SODIUM (3 mg/1)
Marketing started19990715
Package count3

External sources

Source: openFDA. Public-domain (CC0).