Package 70518-4556-0

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 70518-4556-0
Digits Only 7051845560
Product NDC 70518-4556
Description

100 TABLET in 1 BOTTLE, PLASTIC (70518-4556-0)

Marketing

Marketing Status
Marketed Since 2026-01-26
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": "495f354a-81fd-fe7c-e063-6294a90a860c", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["52ce5aab-76cf-465d-8f14-c745d382cd15"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (70518-4556-0)", "package_ndc": "70518-4556-0", "marketing_start_date": "20260126"}], "brand_name": "Allopurinol", "product_id": "70518-4556_495f354a-81fd-fe7c-e063-6294a90a860c", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "70518-4556", "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": "ANDA204467", "marketing_category": "ANDA", "marketing_start_date": "20260126", "listing_expiration_date": "20271231"}