FDA NDC Directory · JSON-LD · Markdown

Capecitabine

NDC 68001-643 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA210203
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCAPECITABINE (150 mg/1)
Marketing started20250418
Package count1

External sources

Source: openFDA. Public-domain (CC0).