Package 42799-119-01

{"route": ["ORAL"], "spl_id": "462dc93e-f284-3a48-e063-6394a90a7ce1", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0342799120010", "0342799119014", "0342799121017"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417", "197418", "197419"], "spl_set_id": ["32c4372e-54ea-4fc8-b9f8-827fa4c8edd3"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Edenbridge Pharmaceuticals LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42799-119-01)", "package_ndc": "42799-119-01", "marketing_start_date": "20151015"}], "brand_name": "Bumetanide", "product_id": "42799-119_462dc93e-f284-3a48-e063-6394a90a7ce1", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "42799-119", "generic_name": "Bumetanide", "labeler_name": "Edenbridge Pharmaceuticals LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": ".5 mg/1"}], "application_number": "NDA018225", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20151015", "listing_expiration_date": "20261231"}