Package 70518-4404-1

{"route": ["ORAL"], "spl_id": "4a142f8c-ee72-cae7-e063-6294a90ad762", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["20015399-43f8-4917-8ffe-dd8055c75712"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4404-0)", "package_ndc": "70518-4404-0", "marketing_start_date": "20250726"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (70518-4404-1)", "package_ndc": "70518-4404-1", "marketing_start_date": "20260205"}], "brand_name": "ALLOPURINOL", "product_id": "70518-4404_4a142f8c-ee72-cae7-e063-6294a90ad762", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "70518-4404", "generic_name": "ALLOPURINOL", "labeler_name": "REMEDYREPACK INC.", "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": "20250726", "listing_expiration_date": "20271231"}