Package 72572-190-25

{"route": ["INTRAVENOUS"], "spl_id": "4e63826f-f7be-4cc6-b21d-03aec09b9c5e", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0372572190015"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719291"], "spl_set_id": ["7ecaa5af-d186-4380-b105-e7e528f75cc7"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 BOX (72572-190-25)  / 4 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "72572-190-25", "marketing_start_date": "20220923"}], "brand_name": "FUROSEMIDE", "product_id": "72572-190_4e63826f-f7be-4cc6-b21d-03aec09b9c5e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "72572-190", "generic_name": "furosemide", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FUROSEMIDE", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "ANDA202747", "marketing_category": "ANDA", "marketing_start_date": "20220923", "listing_expiration_date": "20261231"}