{"effective_time":"20260702","id":"a25a56d4-e46c-40ec-a20e-a31be11f91a1","openfda":{"application_number":["ANDA214290"],"brand_name":["Sugammadex"],"generic_name":["SUGAMMADEX"],"is_original_packager":[true],"manufacturer_name":["Zydus Lifesciences Limited"],"package_ndc":["70771-1856-1","70771-1856-6","70771-1857-1","70771-1857-6"],"product_ndc":["70771-1856","70771-1857"],"product_type":["HUMAN PRESCRIPTION DRUG"],"route":["INTRAVENOUS"],"rxcui":["1726992","1727000"],"spl_id":["a25a56d4-e46c-40ec-a20e-a31be11f91a1"],"spl_set_id":["b1ec2b5e-a571-4511-ab44-d4193441330a"],"substance_name":["SUGAMMADEX SODIUM"],"unii":["ERJ6X2MXV7"]},"package_label_principal_display_panel":["PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 70771-1856-1 Sugammadex Injection 200 mg/ 2 mL (100 mg/mL) – Vial Label For Intravenous Use Only Storage: 25°C (77°F) Protect from light 2 mL Single-Dose Vial Discard unused portion Rx only NDC 70771-1857-1 Sugammadex Injection 500 mg/5 mL (100 mg/mL) For Intravenous Use Only Storage: 25°C (77°F) Protect from light 5 mL Single-Dose Vial Discard unused portion Rx only vial label vial label"],"set_id":"b1ec2b5e-a571-4511-ab44-d4193441330a","spl_product_data_elements":["Sugammadex Sugammadex SUGAMMADEX SODIUM SUGAMMADEX HYDROCHLORIC ACID SODIUM HYDROXIDE WATER Sugammadex Sugammadex SUGAMMADEX SODIUM SUGAMMADEX HYDROCHLORIC ACID SODIUM HYDROXIDE WATER"],"spl_unclassified_section":[""],"version":"1"}