Package 0781-5560-31

{"route": ["ORAL"], "spl_id": "e593fadb-cac5-44ca-8fd6-93c626cd40a7", "openfda": {"upc": ["0307815560317"], "unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["6d69e73a-76cb-4ece-9cf9-e9adb4f523b4"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (0781-5560-13)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5560-06)", "package_ndc": "0781-5560-13", "marketing_start_date": "20250613"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0781-5560-31)", "package_ndc": "0781-5560-31", "marketing_start_date": "20250613"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (0781-5560-92)", "package_ndc": "0781-5560-92", "marketing_start_date": "20250613"}], "brand_name": "Montelukast", "product_id": "0781-5560_e593fadb-cac5-44ca-8fd6-93c626cd40a7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "0781-5560", "generic_name": "Montelukast", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Montelukast", "active_ingredients": [{"name": "MONTELUKAST SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA200889", "marketing_category": "ANDA", "marketing_start_date": "20120803", "listing_expiration_date": "20261231"}