Package 63629-2112-1

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 63629-2112-1
Digits Only 6362921121
Product NDC 63629-2112
Description

500 TABLET in 1 BOTTLE (63629-2112-1)

Marketing

Marketing Status
Marketed Since 2003-06-27
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": "369c0baa-babb-4808-a9e9-e7855a80ed2a", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["73a374a6-ea1a-40a1-b6eb-d42654df0895"], "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": "500 TABLET in 1 BOTTLE (63629-2112-1)", "package_ndc": "63629-2112-1", "marketing_start_date": "20030627"}], "brand_name": "Allopurinol", "product_id": "63629-2112_369c0baa-babb-4808-a9e9-e7855a80ed2a", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "63629-2112", "generic_name": "allopurinol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA075798", "marketing_category": "ANDA", "marketing_start_date": "20030627", "listing_expiration_date": "20261231"}