Package 70710-1926-1

{"route": ["INTRAVENOUS"], "spl_id": "fd646c47-7fcd-4d60-8f6c-29e13f611c6d", "openfda": {"upc": ["0370710192617"], "unii": ["OJ245FE5EU", "48N6U1781G"], "rxcui": ["2560228"], "spl_set_id": ["0f17c50f-3761-4470-bf3b-63837a287b8a"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (70710-1926-1)  / 20 mL in 1 VIAL", "package_ndc": "70710-1926-1", "marketing_start_date": "20230919"}], "brand_name": "Sodium phenylacetate and Sodium benzoate", "product_id": "70710-1926_fd646c47-7fcd-4d60-8f6c-29e13f611c6d", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Ammonium Ion Binding Activity [MoA]", "Ammonium Ion Binding Activity [MoA]", "Nitrogen Binding Agent [EPC]", "Nitrogen Binding Agent [EPC]"], "product_ndc": "70710-1926", "generic_name": "Sodium phenylacetate and Sodium benzoate", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium phenylacetate and Sodium benzoate", "active_ingredients": [{"name": "SODIUM BENZOATE", "strength": "100 mg/mL"}, {"name": "SODIUM PHENYLACETATE", "strength": "100 mg/mL"}], "application_number": "ANDA217526", "marketing_category": "ANDA", "marketing_start_date": "20230919", "listing_expiration_date": "20261231"}