Package 58151-452-01
Brand: xanax
Generic: alprazolamPackage Facts
Identity
Package NDC
58151-452-01
Digits Only
5815145201
Product NDC
58151-452
Description
100 TABLET in 1 BOTTLE (58151-452-01)
Marketing
Marketing Status
Brand
xanax
Generic
alprazolam
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "27062ff4-9ce3-4d8a-aeae-f4468efb623a", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0358151455010", "0358151454013", "0358151452019", "0358151453016"], "unii": ["YU55MQ3IZY"], "rxcui": ["141927", "141928", "197321", "197322", "214003", "214004", "308047", "308048"], "spl_set_id": ["bb5cf72e-3a41-41a8-9a38-80f974eca33f"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Viatris Specialty LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (58151-452-01)", "package_ndc": "58151-452-01", "marketing_start_date": "20251029"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (58151-452-05)", "package_ndc": "58151-452-05", "marketing_start_date": "20251029"}], "brand_name": "Xanax", "product_id": "58151-452_27062ff4-9ce3-4d8a-aeae-f4468efb623a", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "58151-452", "dea_schedule": "CIV", "generic_name": "alprazolam", "labeler_name": "Viatris Specialty LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Xanax", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".25 mg/1"}], "application_number": "NDA018276", "marketing_category": "NDA", "marketing_start_date": "20251029", "listing_expiration_date": "20261231"}