Package 0781-1061-05

Brand: alprazolam

Generic: alprazolam
NDC Package

Package Facts

Identity

Package NDC 0781-1061-05
Digits Only 0781106105
Product NDC 0781-1061
Description

500 TABLET in 1 BOTTLE (0781-1061-05)

Marketing

Marketing Status
Discontinued 2027-03-19
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": "4c8c7366-aa3b-4124-9d64-67fb0ead6e15", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["197321", "197322", "308047", "308048"], "spl_set_id": ["d9b0e228-17cf-40d7-b62e-5050311c571c"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0781-1061-01)", "package_ndc": "0781-1061-01", "marketing_end_date": "20270319", "marketing_start_date": "19951229"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (0781-1061-05)", "package_ndc": "0781-1061-05", "marketing_end_date": "20270319", "marketing_start_date": "19951229"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (0781-1061-10)", "package_ndc": "0781-1061-10", "marketing_end_date": "20270319", "marketing_start_date": "19951229"}], "brand_name": "Alprazolam", "product_id": "0781-1061_4c8c7366-aa3b-4124-9d64-67fb0ead6e15", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "0781-1061", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".25 mg/1"}], "application_number": "ANDA074112", "marketing_category": "ANDA", "marketing_end_date": "20270319", "marketing_start_date": "19951229"}