Package 80425-0099-2

Brand: alprazolam

Generic: alprazolam
NDC Package

Package Facts

Identity

Package NDC 80425-0099-2
Digits Only 8042500992
Product NDC 80425-0099
Description

60 TABLET in 1 BOTTLE (80425-0099-2)

Marketing

Marketing Status
Marketed Since 1993-10-01
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": "2a994e77-4ae4-1307-e063-6394a90a5bd3", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["YU55MQ3IZY"], "rxcui": ["308048"], "spl_set_id": ["b39e2bc8-b68f-0f4e-e053-2995a90a00fd"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0099-2)", "package_ndc": "80425-0099-2", "marketing_start_date": "19931001"}], "brand_name": "Alprazolam", "product_id": "80425-0099_2a994e77-4ae4-1307-e063-6394a90a5bd3", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "80425-0099", "dea_schedule": "CIV", "generic_name": "Alprazolam", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Alprazolam", "active_ingredients": [{"name": "ALPRAZOLAM", "strength": ".5 mg/1"}], "application_number": "ANDA074342", "marketing_category": "ANDA", "marketing_start_date": "19931001", "listing_expiration_date": "20261231"}