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capecitabine

NDC 55111-497 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDr. Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA204345
Dosage form / routeTABLET · ORAL
Active ingredientsCAPECITABINE (500 mg/1)
Marketing started20201210
Package count2

External sources

Source: openFDA. Public-domain (CC0).