Package 59726-125-70

{"route": ["TOPICAL"], "spl_id": "daa285c7-be37-4292-9966-13bd7ee54bc2", "openfda": {"nui": ["N0000175379", "N0000175564"], "unii": ["5965120SH1"], "rxcui": ["645146"], "spl_set_id": ["869ce741-3094-4123-9059-0669f3591b2f"], "pharm_class_pe": ["Arteriolar Vasodilation [PE]"], "pharm_class_epc": ["Arteriolar Vasodilator [EPC]"], "manufacturer_name": ["P & L Development, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 CAN in 1 PACKAGE (59726-125-60)  / 60 mL in 1 CAN", "package_ndc": "59726-125-60", "marketing_start_date": "20231001"}, {"sample": false, "description": "3 CAN in 1 PACKAGE (59726-125-70)  / 60 mL in 1 CAN", "package_ndc": "59726-125-70", "marketing_start_date": "20231001"}], "brand_name": "Minoxidil", "product_id": "59726-125_daa285c7-be37-4292-9966-13bd7ee54bc2", "dosage_form": "AEROSOL, FOAM", "pharm_class": ["Arteriolar Vasodilation [PE]", "Arteriolar Vasodilator [EPC]"], "product_ndc": "59726-125", "generic_name": "Minoxidil", "labeler_name": "P & L Development, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Minoxidil", "active_ingredients": [{"name": "MINOXIDIL", "strength": "50 mg/mL"}], "application_number": "ANDA208092", "marketing_category": "ANDA", "marketing_start_date": "20231001", "listing_expiration_date": "20271231"}