Package 70518-4286-0

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 70518-4286-0
Digits Only 7051842860
Product NDC 70518-4286
Product ID 70518-4286_401b7e29-7b73-7dfa-e063-6394a90a3128
Description

30 TABLET in 1 BLISTER PACK (70518-4286-0)

Marketing

Marketing Status
Marketed Since 2025-02-11
Brand allopurinol
Generic allopurinol
Sample Package No

Linked Drug Pages (1)

Allopurinol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "401b7e29-7b73-7dfa-e063-6394a90a3128", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["4dbced9a-ef6f-455e-8d5d-b635409521db"], "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 (70518-4286-0)", "package_ndc": "70518-4286-0", "marketing_start_date": "20250211"}], "brand_name": "Allopurinol", "product_id": "70518-4286_401b7e29-7b73-7dfa-e063-6394a90a3128", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "70518-4286", "generic_name": "allopurinol", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA075798", "marketing_category": "ANDA", "marketing_start_date": "20250211", "listing_expiration_date": "20261231"}