# Dasatinib

NDC: 68001-660
Generic name: dasatinib
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20251124

FDA application: ANDA217217

## Active ingredients

- DASATINIB: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-660"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-660
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=02b04c6f-4ea5-4fcb-bf6d-2631d5ab31e4