Package 59651-285-01

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 59651-285-01
Digits Only 5965128501
Product NDC 59651-285
Product ID 59651-285_311ca755-c022-4251-97eb-dd9be86a993f
Description

100 TABLET in 1 BOTTLE (59651-285-01)

Marketing

Marketing Status
Marketed Since 2025-04-14
Brand allopurinol
Generic allopurinol
Sample Package No

Linked Drug Pages (1)

Allopurinol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "311ca755-c022-4251-97eb-dd9be86a993f", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320"], "spl_set_id": ["311ca755-c022-4251-97eb-dd9be86a993f"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59651-285-01)", "package_ndc": "59651-285-01", "marketing_start_date": "20250414"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (59651-285-99)", "package_ndc": "59651-285-99", "marketing_start_date": "20250414"}], "brand_name": "Allopurinol", "product_id": "59651-285_311ca755-c022-4251-97eb-dd9be86a993f", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "59651-285", "generic_name": "Allopurinol", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA215091", "marketing_category": "ANDA", "marketing_start_date": "20250414", "listing_expiration_date": "20261231"}