Package 51655-523-52
Brand: allopurinol
Generic: allopurinolPackage Facts
Identity
Package NDC
51655-523-52
Digits Only
5165552352
Product NDC
51655-523
Description
30 TABLET in 1 BOTTLE, PLASTIC (51655-523-52)
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": "494dda25-b095-7fc2-e063-6394a90a8a36", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["f3198e1b-6344-ad96-e053-2995a90a4aaf"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-523-52)", "package_ndc": "51655-523-52", "marketing_start_date": "20220906"}], "brand_name": "Allopurinol", "product_id": "51655-523_494dda25-b095-7fc2-e063-6394a90a8a36", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "51655-523", "generic_name": "allopurinol", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA203154", "marketing_category": "ANDA", "marketing_start_date": "20220906", "listing_expiration_date": "20271231"}