Package 65219-570-04

{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "aaff61c4-203b-4905-9138-0f98959ad013", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["282486", "1727569"], "spl_set_id": ["a007f3aa-3977-4be3-a9a2-db3d458bca58"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (65219-570-04)  / 4 mL in 1 VIAL, SINGLE-DOSE (65219-570-01)", "package_ndc": "65219-570-04", "marketing_start_date": "20220926"}], "brand_name": "Bumetanide", "product_id": "65219-570_aaff61c4-203b-4905-9138-0f98959ad013", "dosage_form": "INJECTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "65219-570", "generic_name": "Bumetanide", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": ".25 mg/mL"}], "application_number": "ANDA216434", "marketing_category": "ANDA", "marketing_start_date": "20220926", "listing_expiration_date": "20261231"}