Package 42571-438-85

{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "4829e889-87d2-9d87-e063-6294a90a11cb", "openfda": {"nui": ["N0000175366", "N0000175590"], "upc": ["0342571437862", "0342571438562", "0342571436759"], "unii": ["7LXU5N7ZO5"], "rxcui": ["1719286", "1719290", "1719291"], "spl_set_id": ["2f547f7c-0322-465c-9764-43f955d98ab2"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (42571-438-85)  / 10 mL in 1 VIAL (42571-438-56)", "package_ndc": "42571-438-85", "marketing_start_date": "20231116"}], "brand_name": "Furosemide", "product_id": "42571-438_4829e889-87d2-9d87-e063-6294a90a11cb", "dosage_form": "INJECTION", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "42571-438", "generic_name": "Furosemide", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "100 mg/10mL"}], "application_number": "ANDA218188", "marketing_category": "ANDA", "marketing_start_date": "20231116", "listing_expiration_date": "20271231"}