Package 70710-1742-6

Brand: dasatinib

Generic: dasatinib
NDC Package

Package Facts

Identity

Package NDC 70710-1742-6
Digits Only 7071017426
Product NDC 70710-1742
Description

60 TABLET in 1 BOTTLE (70710-1742-6)

Marketing

Marketing Status
Marketed Since 2025-03-03
Brand dasatinib
Generic dasatinib
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46121457-8af5-4016-827f-ead2f0b33b83", "openfda": {"upc": ["0370710174361", "0370710174163", "0370710174262"], "unii": ["RBZ1571X5H"], "rxcui": ["643105", "643107", "643109", "799047", "1045402", "1045406"], "spl_set_id": ["11703145-29ea-480a-9810-bc70663b783f"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (70710-1742-6)", "package_ndc": "70710-1742-6", "marketing_start_date": "20250303"}], "brand_name": "dasatinib", "product_id": "70710-1742_46121457-8af5-4016-827f-ead2f0b33b83", "dosage_form": "TABLET", "pharm_class": ["Cytochrome P450 3A4 Inhibitors [MoA]", "Kinase Inhibitor [EPC]", "Protein Kinase Inhibitors [MoA]"], "product_ndc": "70710-1742", "generic_name": "dasatinib", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "dasatinib", "active_ingredients": [{"name": "DASATINIB", "strength": "50 mg/1"}], "application_number": "ANDA218719", "marketing_category": "ANDA", "marketing_start_date": "20250303", "listing_expiration_date": "20261231"}