Package 50090-6968-0

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 50090-6968-0
Digits Only 5009069680
Product NDC 50090-6968
Description

90 TABLET in 1 BOTTLE (50090-6968-0)

Marketing

Marketing Status
Marketed Since 2023-12-21
Brand allopurinol
Generic allopurinol
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "aaf62490-cdc7-4b5c-b665-2b901a8799f2", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["420d338d-4d0d-4e38-bfe2-a83256821b45"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6968-0)", "package_ndc": "50090-6968-0", "marketing_start_date": "20231221"}], "brand_name": "Allopurinol", "product_id": "50090-6968_aaf62490-cdc7-4b5c-b665-2b901a8799f2", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "50090-6968", "generic_name": "Allopurinol", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA204467", "marketing_category": "ANDA", "marketing_start_date": "20220701", "listing_expiration_date": "20261231"}