Package 59762-0057-1

Brand: alprazolam xr

Generic: alprazolam
NDC Package

Package Facts

Identity

Package NDC 59762-0057-1
Digits Only 5976200571
Product NDC 59762-0057
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (59762-0057-1)

Marketing

Marketing Status
Marketed Since 2003-01-17
Brand alprazolam xr
Generic alprazolam
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "70f0098e-50b5-4e61-b4e0-141a55d92267", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["433798", "433799", "433800", "433801"], "spl_set_id": ["1338d1c9-7c75-42ed-95f3-9eb1b6fc51d3"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (59762-0057-1)", "package_ndc": "59762-0057-1", "marketing_start_date": "20030117"}], "brand_name": "Alprazolam XR", "product_id": "59762-0057_70f0098e-50b5-4e61-b4e0-141a55d92267", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "59762-0057", "dea_schedule": "CIV", "generic_name": "alprazolam", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "brand_name_suffix": "XR", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".5 mg/1"}], "application_number": "NDA021434", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20030117", "listing_expiration_date": "20261231"}