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dasatinib

NDC 70710-1745 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218719
Dosage form / routeTABLET · ORAL
Active ingredientsDASATINIB (100 mg/1)
Marketing started20250303
Package count1

External sources

Source: openFDA. Public-domain (CC0).