Package 81565-201-02

{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "e70f323d-2e94-4824-bb92-d43013caa497", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0381565201010"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719290"], "spl_set_id": ["08a44bdd-028d-41af-9d4e-70971b0bcc4e"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Phlow Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 TRAY (81565-201-02)  / 2 mL in 1 VIAL (81565-201-01)", "package_ndc": "81565-201-02", "marketing_start_date": "20220201"}], "brand_name": "Furosemide", "product_id": "81565-201_e70f323d-2e94-4824-bb92-d43013caa497", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "81565-201", "generic_name": "FUROSEMIDE", "labeler_name": "Phlow Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "10 mg/mL"}], "application_number": "NDA018902", "marketing_category": "NDA", "marketing_start_date": "20220201", "listing_expiration_date": "20271231"}