Package 70756-080-51

{"route": ["ORAL"], "spl_id": "f131948c-e75a-4379-b9ec-875fea59a5fe", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0370756080114", "0370756081111"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417", "197418", "197419"], "spl_set_id": ["51a344b6-acf9-4ac4-b743-1e63e3df7958"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70756-080-11)", "package_ndc": "70756-080-11", "marketing_start_date": "20250403"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70756-080-51)", "package_ndc": "70756-080-51", "marketing_start_date": "20250403"}], "brand_name": "Bumetanide", "product_id": "70756-080_f131948c-e75a-4379-b9ec-875fea59a5fe", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "70756-080", "generic_name": "Bumetanide", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "1 mg/1"}], "application_number": "ANDA219291", "marketing_category": "ANDA", "marketing_start_date": "20250403", "listing_expiration_date": "20261231"}