Package 83301-0081-2

{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "4c241a3e-649b-4414-e063-6294a90a3a32", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["282486", "1727569"], "spl_set_id": ["b7cd724b-817b-4b45-8133-1ebf505867e7"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Mullan Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (83301-0081-2)  / 10 mL in 1 VIAL, MULTI-DOSE (83301-0081-1)", "package_ndc": "83301-0081-2", "marketing_start_date": "20260109"}], "brand_name": "Bumetanide", "product_id": "83301-0081_4c241a3e-649b-4414-e063-6294a90a3a32", "dosage_form": "INJECTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "83301-0081", "generic_name": "Bumetanide", "labeler_name": "Mullan Pharmaceutical Inc.", "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": "20260109", "listing_expiration_date": "20271231"}