Package 70771-1907-0

{"route": ["ORAL"], "spl_id": "183fab96-5c7b-4fcc-a475-5d1832bbf9c6", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320", "245422"], "spl_set_id": ["9232f484-a5f6-4c63-b7f4-b510d2827159"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (70771-1907-0)", "package_ndc": "70771-1907-0", "marketing_start_date": "20250617"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (70771-1907-9)", "package_ndc": "70771-1907-9", "marketing_start_date": "20250617"}], "brand_name": "Allopurinol", "product_id": "70771-1907_183fab96-5c7b-4fcc-a475-5d1832bbf9c6", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "70771-1907", "generic_name": "Allopurinol", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "200 mg/1"}], "application_number": "ANDA210117", "marketing_category": "ANDA", "marketing_start_date": "20250617", "listing_expiration_date": "20261231"}