Package 67046-1514-3
Brand: allopurinol
Generic: allopurinolPackage Facts
Identity
Package NDC
67046-1514-3
Digits Only
6704615143
Product NDC
67046-1514
Description
30 TABLET in 1 BLISTER PACK (67046-1514-3)
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": "2d6cdaf0-8651-d103-e063-6394a90a9352", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["2d6ce57f-a9df-319e-e063-6394a90ac93f"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1514-3)", "package_ndc": "67046-1514-3", "marketing_start_date": "20250205"}], "brand_name": "Allopurinol", "product_id": "67046-1514_2d6cdaf0-8651-d103-e063-6394a90a9352", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "67046-1514", "generic_name": "allopurinol", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "NDA016084", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20250205", "listing_expiration_date": "20261231"}