Package 59762-3719-1

Brand: alprazolam

Generic: alprazolam
NDC Package

Package Facts

Identity

Package NDC 59762-3719-1
Digits Only 5976237191
Product NDC 59762-3719
Description

100 TABLET in 1 BOTTLE (59762-3719-1)

Marketing

Marketing Status
Marketed Since 1981-10-16
Brand alprazolam
Generic alprazolam
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0deddc26-2764-4879-a0e4-a29fff246244", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321", "197322", "308047", "308048"], "spl_set_id": ["13930c94-d83a-414f-be35-b1fef35f738d"], "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": "100 TABLET in 1 BOTTLE (59762-3719-1)", "package_ndc": "59762-3719-1", "marketing_start_date": "19811016"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (59762-3719-3)", "package_ndc": "59762-3719-3", "marketing_start_date": "19811016"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (59762-3719-4)", "package_ndc": "59762-3719-4", "marketing_start_date": "19811016"}], "brand_name": "Alprazolam", "product_id": "59762-3719_0deddc26-2764-4879-a0e4-a29fff246244", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "59762-3719", "dea_schedule": "CIV", "generic_name": "alprazolam", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".25 mg/1"}], "application_number": "NDA018276", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "19811016", "listing_expiration_date": "20261231"}