Package 50090-7353-0
Brand: allopurinol
Generic: allopurinolPackage Facts
Identity
Package NDC
50090-7353-0
Digits Only
5009073530
Product NDC
50090-7353
Description
90 TABLET in 1 BOTTLE (50090-7353-0)
Marketing
Marketing Status
Brand
allopurinol
Generic
allopurinol
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "484827e8-5874-4a62-a760-6956cdb13601", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["d9a20bf5-15b9-4643-b829-40eacd4e849d"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7353-0)", "package_ndc": "50090-7353-0", "marketing_start_date": "20241016"}], "brand_name": "Allopurinol", "product_id": "50090-7353_484827e8-5874-4a62-a760-6956cdb13601", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "50090-7353", "generic_name": "Allopurinol", "labeler_name": "A-S Medication Solutions", "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": "20230803", "listing_expiration_date": "20261231"}