Package 70518-4412-0

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 70518-4412-0
Digits Only 7051844120
Product NDC 70518-4412
Product ID 70518-4412_3b8a5bce-a7fd-e2db-e063-6394a90a8021
Description

30 TABLET in 1 BLISTER PACK (70518-4412-0)

Marketing

Marketing Status
Marketed Since 2025-07-31
Brand allopurinol
Generic allopurinol
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3b8a5bce-a7fd-e2db-e063-6394a90a8021", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["8f50e91e-66a7-4fd4-888a-9f1986aa661c"], "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 (70518-4412-0)", "package_ndc": "70518-4412-0", "marketing_start_date": "20250731"}], "brand_name": "Allopurinol", "product_id": "70518-4412_3b8a5bce-a7fd-e2db-e063-6394a90a8021", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "70518-4412", "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": "ANDA018659", "marketing_category": "ANDA", "marketing_start_date": "20250731", "listing_expiration_date": "20261231"}