# Capecitabine

NDC: 0093-7474
Generic name: Capecitabine
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20140307

FDA application: ANDA091649

## Active ingredients

- CAPECITABINE: 500 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0093-7474"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-7474
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5753679a-506c-4ac4-b8b2-b27c664d1d40