Package 67184-0593-2

{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "b392cf53-2b1f-46b5-86dc-c0df49f16730", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0367184059317", "0367184059416"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["282486", "1727569"], "spl_set_id": ["ef5fe12a-f8ee-4ba7-932b-51bbaccf6575"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Qilu Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (67184-0593-2)  / 4 mL in 1 VIAL (67184-0593-1)", "package_ndc": "67184-0593-2", "marketing_start_date": "20240919"}], "brand_name": "Bumetanide", "product_id": "67184-0593_b392cf53-2b1f-46b5-86dc-c0df49f16730", "dosage_form": "INJECTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "67184-0593", "generic_name": "Bumetanide", "labeler_name": "Qilu Pharmaceutical Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": ".25 mg/mL"}], "application_number": "ANDA219116", "marketing_category": "ANDA", "marketing_start_date": "20240919", "listing_expiration_date": "20261231"}