Package 0009-0090-04

{"route": ["ORAL"], "spl_id": "f5323eac-81d0-4096-ac15-2f25220c5c28", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0300090094010", "0300090090012", "0300090029012", "0300090055011"], "unii": ["YU55MQ3IZY"], "rxcui": ["141927", "141928", "197321", "197322", "214003", "214004", "308047", "308048"], "spl_set_id": ["388e249d-b9b6-44c3-9f8f-880eced0239f"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["PHARMACIA & UPJOHN COMPANY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0009-0090-01)", "package_ndc": "0009-0090-01", "marketing_end_date": "20260831", "marketing_start_date": "19811016"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0009-0090-04)", "package_ndc": "0009-0090-04", "marketing_end_date": "20261231", "marketing_start_date": "19811016"}], "brand_name": "Xanax", "product_id": "0009-0090_f5323eac-81d0-4096-ac15-2f25220c5c28", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "0009-0090", "dea_schedule": "CIV", "generic_name": "alprazolam", "labeler_name": "PHARMACIA & UPJOHN COMPANY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Xanax", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": "1 mg/1"}], "application_number": "NDA018276", "marketing_category": "NDA", "marketing_end_date": "20261231", "marketing_start_date": "19811016"}