Package 80425-0383-2
Brand: allopurinol
Generic: allopurinolPackage Facts
Identity
Package NDC
80425-0383-2
Digits Only
8042503832
Product NDC
80425-0383
Description
60 TABLET in 1 BOTTLE (80425-0383-2)
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": "15d70b80-3ae2-bc32-e063-6394a90a163e", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["15d758f9-2ec5-ecf5-e063-6394a90a7a2c"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0383-1)", "package_ndc": "80425-0383-1", "marketing_start_date": "20240411"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0383-2)", "package_ndc": "80425-0383-2", "marketing_start_date": "20240411"}], "brand_name": "Allopurinol", "product_id": "80425-0383_15d70b80-3ae2-bc32-e063-6394a90a163e", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "80425-0383", "generic_name": "allopurinol", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA018659", "marketing_category": "ANDA", "marketing_start_date": "20240411", "listing_expiration_date": "20261231"}