{"effective_time":"20221105","id":"34685b34-d41c-4a8b-b6db-9cd17e4ced70","openfda":{"application_number":["ANDA214048"],"brand_name":["betamethasone dipropionate"],"generic_name":["BETAMETHASONE DIPROPIONATE"],"is_original_packager":[true],"manufacturer_name":["Zydus Lifesciences Limited"],"package_ndc":["70771-1550-1","70771-1550-4"],"product_ndc":["70771-1550"],"product_type":["HUMAN PRESCRIPTION DRUG"],"route":["TOPICAL"],"rxcui":["197405"],"spl_id":["34685b34-d41c-4a8b-b6db-9cd17e4ced70"],"spl_set_id":["f531da27-2435-49a3-8992-c65240c6a7fe"],"substance_name":["BETAMETHASONE DIPROPIONATE"],"unii":["826Y60901U"]},"package_label_principal_display_panel":["PACKAGE LABEL.PRINCIPAL DISPLAY PANEL Betamethasone Dipropionate Ointment USP, 0.05% NDC 70771-1550-1 in tube of 15 gm Rx Only tube label carton label"],"set_id":"f531da27-2435-49a3-8992-c65240c6a7fe","spl_product_data_elements":["betamethasone dipropionate betamethasone dipropionate BETAMETHASONE DIPROPIONATE BETAMETHASONE MINERAL OIL PETROLATUM"],"spl_unclassified_section":[""],"version":"3"}