Package 72189-647-90

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 72189-647-90
Digits Only 7218964790
Product NDC 72189-647
Product ID 72189-647_426262e6-821a-c825-e063-6294a90a21a9
Description

90 TABLET in 1 BOTTLE (72189-647-90)

Marketing

Marketing Status
Marketed Since 2025-10-30
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": "426262e6-821a-c825-e063-6294a90a21a9", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["426262e6-8219-c825-e063-6294a90a21a9"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-647-90)", "package_ndc": "72189-647-90", "marketing_start_date": "20251030"}], "brand_name": "Allopurinol", "product_id": "72189-647_426262e6-821a-c825-e063-6294a90a21a9", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "72189-647", "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": "ANDA217748", "marketing_category": "ANDA", "marketing_start_date": "20251030", "listing_expiration_date": "20261231"}