Package 47335-721-83

{"route": ["ORAL"], "spl_id": "53dfe063-e9bf-4069-b4cc-5a83a27d18ec", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["101V0R1N2E"], "rxcui": ["834235", "834241"], "spl_set_id": ["1f7541bd-bf32-422b-b99a-89193cf193ca"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (47335-721-13)", "package_ndc": "47335-721-13", "marketing_start_date": "20190705"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (47335-721-81)", "package_ndc": "47335-721-81", "marketing_start_date": "20190705"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (47335-721-83)", "package_ndc": "47335-721-83", "marketing_start_date": "20190705"}], "brand_name": "Febuxostat", "product_id": "47335-721_53dfe063-e9bf-4069-b4cc-5a83a27d18ec", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "47335-721", "generic_name": "Febuxostat", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Febuxostat", "active_ingredients": [{"name": "FEBUXOSTAT", "strength": "40 mg/1"}], "application_number": "ANDA205467", "marketing_category": "ANDA", "marketing_start_date": "20190705", "listing_expiration_date": "20261231"}