Package 0143-9159-01

{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "febcfbde-87d9-4c2f-819f-dfb4a04082f8", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286", "1719290", "1719291", "2683305", "2683306"], "spl_set_id": ["ddfc41a9-37d4-49c1-bbf3-969a98cd649c"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (0143-9159-01)  / 100 mL in 1 VIAL", "package_ndc": "0143-9159-01", "marketing_start_date": "20240531"}], "brand_name": "Furosemide", "product_id": "0143-9159_febcfbde-87d9-4c2f-819f-dfb4a04082f8", "dosage_form": "INJECTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "0143-9159", "generic_name": "Furosemide", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "NDA018267", "marketing_category": "NDA", "marketing_start_date": "20240531", "listing_expiration_date": "20261231"}