Package 80425-0444-2

{"route": ["ORAL"], "spl_id": "26f8b6d9-81c1-a02c-e063-6394a90aefdf", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321"], "spl_set_id": ["26f8b63c-6dad-8fac-e063-6394a90a5435"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0444-1)", "package_ndc": "80425-0444-1", "marketing_start_date": "20241106"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0444-2)", "package_ndc": "80425-0444-2", "marketing_start_date": "20241106"}], "brand_name": "Alprazolam", "product_id": "80425-0444_26f8b6d9-81c1-a02c-e063-6394a90aefdf", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "80425-0444", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": "1 mg/1"}], "application_number": "ANDA203346", "marketing_category": "ANDA", "marketing_start_date": "20241106", "listing_expiration_date": "20261231"}