Package 72205-101-07

{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "387edfd4-be85-41cd-8a6d-14e6a022b5a9", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0372205102019", "0372205101012"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["282486", "1727569"], "spl_set_id": ["387edfd4-be85-41cd-8a6d-14e6a022b5a9"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (72205-101-07)  / 4 mL in 1 VIAL (72205-101-01)", "package_ndc": "72205-101-07", "marketing_start_date": "20220806"}], "brand_name": "Bumetanide", "product_id": "72205-101_387edfd4-be85-41cd-8a6d-14e6a022b5a9", "dosage_form": "INJECTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "72205-101", "generic_name": "Bumetanide", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": ".25 mg/mL"}], "application_number": "ANDA215364", "marketing_category": "ANDA", "marketing_start_date": "20220806", "listing_expiration_date": "20261231"}