Package 70771-1523-7

{"route": ["ORAL"], "spl_id": "9d253beb-cd1f-45df-9b23-c521269d419f", "openfda": {"unii": ["DA87705X9K"], "rxcui": ["603203", "603206", "603208"], "spl_set_id": ["daaa1329-3a3f-439c-b13d-b301daa234d4"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70771-1523-3)", "package_ndc": "70771-1523-3", "marketing_start_date": "20200430"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (70771-1523-7)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1523-2)", "package_ndc": "70771-1523-7", "marketing_start_date": "20200430"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (70771-1523-9)", "package_ndc": "70771-1523-9", "marketing_start_date": "20200430"}], "brand_name": "Erlotinib", "product_id": "70771-1523_9d253beb-cd1f-45df-9b23-c521269d419f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Kinase Inhibitor [EPC]", "Protein Kinase Inhibitors [MoA]"], "product_ndc": "70771-1523", "generic_name": "Erlotinib", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Erlotinib", "active_ingredients": [{"name": "ERLOTINIB HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA213065", "marketing_category": "ANDA", "marketing_start_date": "20200430", "listing_expiration_date": "20261231"}