Package 50090-7832-0

{"route": ["ORAL"], "spl_id": "2def7003-b35b-4e0c-9bca-6a0dbd83579b", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["5efa81be-e2c9-4fb7-bd0d-aeca3920a393"], "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": "100 TABLET in 1 BOTTLE (50090-7832-0)", "package_ndc": "50090-7832-0", "marketing_start_date": "20251218"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (50090-7832-1)", "package_ndc": "50090-7832-1", "marketing_start_date": "20251218"}], "brand_name": "Allopurinol", "product_id": "50090-7832_2def7003-b35b-4e0c-9bca-6a0dbd83579b", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "50090-7832", "generic_name": "Allopurinol", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA211820", "marketing_category": "ANDA", "marketing_start_date": "20190312", "listing_expiration_date": "20261231"}