Package 70518-0476-1
Brand: Allopurinol
Generic: allopurinolPackage Facts
Identity
Package NDC
70518-0476-1
Digits Only
7051804761
Product NDC
70518-0476
Description
30 TABLET in 1 BLISTER PACK (70518-0476-1)
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": "47f7337b-b613-9bb5-e063-6294a90a09b2", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["9138122e-844c-4613-b70e-e60d5ffcbd13"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-0476-1)", "package_ndc": "70518-0476-1", "marketing_start_date": "20250210"}], "brand_name": "Allopurinol", "product_id": "70518-0476_47f7337b-b613-9bb5-e063-6294a90a09b2", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "70518-0476", "generic_name": "allopurinol", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA075798", "marketing_category": "ANDA", "marketing_start_date": "20170512", "listing_expiration_date": "20271231"}