Package 80425-0518-2
Brand: allopurinol
Generic: allopurinolPackage Facts
Identity
Package NDC
80425-0518-2
Digits Only
8042505182
Product NDC
80425-0518
Description
60 TABLET in 1 BOTTLE (80425-0518-2)
Marketing
Marketing Status
Brand
allopurinol
Generic
allopurinol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "36c1d44f-f581-f2ef-e063-6294a90a9f43", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["36c1c908-1eed-ed2a-e063-6294a90a16f9"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0518-1)", "package_ndc": "80425-0518-1", "marketing_start_date": "20250529"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0518-2)", "package_ndc": "80425-0518-2", "marketing_start_date": "20250529"}], "brand_name": "ALLOPURINOL", "product_id": "80425-0518_36c1d44f-f581-f2ef-e063-6294a90a9f43", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "80425-0518", "generic_name": "ALLOPURINOL", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALLOPURINOL", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA217748", "marketing_category": "ANDA", "marketing_start_date": "20250529", "listing_expiration_date": "20261231"}