Package 58151-506-91

Brand: xanax xr

Generic: alprazolam
NDC Package

Package Facts

Identity

Package NDC 58151-506-91
Digits Only 5815150691
Product NDC 58151-506
Product ID 58151-506_d8ad22b9-9ba3-4193-a678-23d5563d9511
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (58151-506-91)

Marketing

Marketing Status
Discontinued 2027-02-28
Brand xanax xr
Generic alprazolam
Sample Package No

Linked Drug Pages (1)

Xanax XR ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d8ad22b9-9ba3-4193-a678-23d5563d9511", "openfda": {"nui": ["N0000175694", "M0002356"], "upc": ["0358151506910", "0358151504916", "0358151503919", "0358151505913"], "unii": ["YU55MQ3IZY"], "rxcui": ["433798", "433799", "433800", "433801", "687022", "687023", "687024", "687025"], "spl_set_id": ["c8990714-c2f5-4b0c-9f1c-91d77156d962"], "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": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (58151-506-91)", "package_ndc": "58151-506-91", "marketing_end_date": "20270228", "marketing_start_date": "20240726"}], "brand_name": "Xanax XR", "product_id": "58151-506_d8ad22b9-9ba3-4193-a678-23d5563d9511", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "58151-506", "dea_schedule": "CIV", "generic_name": "alprazolam", "labeler_name": "Viatris Specialty LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Xanax", "brand_name_suffix": "XR", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": "3 mg/1"}], "application_number": "NDA021434", "marketing_category": "NDA", "marketing_end_date": "20270228", "marketing_start_date": "20240726"}