# dasatinib

NDC: 70710-1741
Generic name: dasatinib
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250303

FDA application: ANDA218719

## Active ingredients

- DASATINIB: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70710-1741"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1741
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=11703145-29ea-480a-9810-bc70663b783f