FDA NDC Directory · JSON-LD · Markdown

Capecitabine

NDC 0093-7474 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091649
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCAPECITABINE (500 mg/1)
Marketing started20140307
Package count1

External sources

Source: openFDA. Public-domain (CC0).