Package 70518-3660-2

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 70518-3660-2
Digits Only 7051836602
Product NDC 70518-3660
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-3660-2)

Marketing

Marketing Status
Marketed Since 2024-05-23
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": "3b01dd3d-2d9e-d5bd-e063-6294a90aed3f", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["36526c80-5a70-47c4-a0a6-785ccc346703"], "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 (70518-3660-0)", "package_ndc": "70518-3660-0", "marketing_start_date": "20230224"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-3660-2)", "package_ndc": "70518-3660-2", "marketing_start_date": "20240523"}], "brand_name": "Allopurinol", "product_id": "70518-3660_3b01dd3d-2d9e-d5bd-e063-6294a90aed3f", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "70518-3660", "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": "ANDA211820", "marketing_category": "ANDA", "marketing_start_date": "20230224", "listing_expiration_date": "20261231"}