Package 70518-3133-2

{"route": ["ORAL"], "spl_id": "3d57c911-aacb-9d85-e063-6394a90a3c5a", "openfda": {"unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["ecaa9b4b-5941-4af5-930c-35e9f3b2b4ba"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3133-0)", "package_ndc": "70518-3133-0", "marketing_start_date": "20210618"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3133-1)", "package_ndc": "70518-3133-1", "marketing_start_date": "20210701"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3133-2)", "package_ndc": "70518-3133-2", "marketing_start_date": "20250827"}], "brand_name": "Montelukast", "product_id": "70518-3133_3d57c911-aacb-9d85-e063-6394a90a3c5a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "70518-3133", "generic_name": "Montelukast", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Montelukast", "active_ingredients": [{"name": "MONTELUKAST SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA202843", "marketing_category": "ANDA", "marketing_start_date": "20210618", "listing_expiration_date": "20261231"}