Package 70518-0476-1

Brand: Allopurinol

Generic: allopurinol
NDC Package

Package 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
Marketed Since 2025-02-10
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"}