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Warfarin Sodium

NDC 51672-4034 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040301
Dosage form / routeTABLET · ORAL
Active ingredientsWARFARIN SODIUM (7.5 mg/1)
Marketing started19990715
Package count2

External sources

Source: openFDA. Public-domain (CC0).