Package 72189-417-90

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 72189-417-90
Digits Only 7218941790
Product NDC 72189-417
Product ID 72189-417_4c4bb472-bcf4-c5df-e063-6394a90a787d
Description

90 TABLET in 1 BOTTLE (72189-417-90)

Marketing

Marketing Status
Discontinued 2029-10-31
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": "4c4bb472-bcf4-c5df-e063-6394a90a787d", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["f3bd5852-8e43-6b5d-e053-2995a90a194f"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-417-30)", "package_ndc": "72189-417-30", "marketing_end_date": "20291031", "marketing_start_date": "20230202"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-417-90)", "package_ndc": "72189-417-90", "marketing_end_date": "20291031", "marketing_start_date": "20230202"}], "brand_name": "ALLOPURINOL", "product_id": "72189-417_4c4bb472-bcf4-c5df-e063-6394a90a787d", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "72189-417", "generic_name": "ALLOPURINOL", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALLOPURINOL", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA204467", "marketing_category": "ANDA", "marketing_end_date": "20291031", "marketing_start_date": "20230202"}