Package 80425-0206-1
Brand: allopurinol
Generic: allopurinolPackage Facts
Identity
Package NDC
80425-0206-1
Digits Only
8042502061
Product NDC
80425-0206
Description
30 TABLET in 1 BOTTLE (80425-0206-1)
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": "2a99b834-0c9d-6f97-e063-6394a90a8407", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["ec09fbcf-6e20-8438-e053-2a95a90a6376"], "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 (80425-0206-1)", "package_ndc": "80425-0206-1", "marketing_start_date": "20231027"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0206-2)", "package_ndc": "80425-0206-2", "marketing_start_date": "20231027"}], "brand_name": "Allopurinol", "product_id": "80425-0206_2a99b834-0c9d-6f97-e063-6394a90a8407", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "80425-0206", "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": "ANDA203154", "marketing_category": "ANDA", "marketing_start_date": "20221027", "listing_expiration_date": "20261231"}