Package 72888-021-01

{"route": ["ORAL"], "spl_id": "47c8ef6a-8934-2514-e063-6294a90abae6", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0372888021010", "0372888020013", "0372888019017"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417", "197418", "197419"], "spl_set_id": ["94078edd-b9c0-449e-baaf-a9afceccb407"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Advagen Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72888-021-01)", "package_ndc": "72888-021-01", "marketing_start_date": "20250116"}], "brand_name": "Bumetanide", "product_id": "72888-021_47c8ef6a-8934-2514-e063-6294a90abae6", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "72888-021", "generic_name": "Bumetanide", "labeler_name": "Advagen Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "2 mg/1"}], "application_number": "ANDA213942", "marketing_category": "ANDA", "marketing_start_date": "20250116", "listing_expiration_date": "20271231"}