Package 72162-1149-0

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 72162-1149-0
Digits Only 7216211490
Product NDC 72162-1149
Product ID 72162-1149_90912dd4-5abf-4fd3-8fc1-3afd057b743f
Description

1000 TABLET in 1 BOTTLE (72162-1149-0)

Marketing

Marketing Status
Marketed Since 2003-06-27
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": "90912dd4-5abf-4fd3-8fc1-3afd057b743f", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["90912dd4-5abf-4fd3-8fc1-3afd057b743f"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-1149-0)", "package_ndc": "72162-1149-0", "marketing_start_date": "20030627"}], "brand_name": "Allopurinol", "product_id": "72162-1149_90912dd4-5abf-4fd3-8fc1-3afd057b743f", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "72162-1149", "generic_name": "allopurinol", "labeler_name": "Bryant Ranch Prepack", "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": "20030627", "listing_expiration_date": "20261231"}