{"@context":{"@vocab":"https://schema.org/"},"@type":"Drug","@id":"https://api.morvs.ai/drug-product/0363-0270#drug","name":"Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride","identifier":[{"@type":"PropertyValue","propertyID":"FDA National Drug Code (NDC)","value":"0363-0270"},{"@type":"PropertyValue","propertyID":"FDA application number","value":"ANDA215232"},{"@type":"PropertyValue","propertyID":"UNII","value":"2S068B75ZU|6V9V2RYJ8N"},{"@type":"PropertyValue","propertyID":"SPL Set ID","value":"4daddd32-615f-aedf-e063-6394a90a5b09"}],"activeIngredient":"FEXOFENADINE HYDROCHLORIDE, PSEUDOEPHEDRINE HYDROCHLORIDE","administrationRoute":["ORAL"],"dosageForm":"TABLET, FILM COATED, EXTENDED RELEASE","manufacturer":{"@type":"Organization","name":"WALGREEN CO."},"drugClass":[],"isAvailableGenerically":true,"legalStatus":"HUMAN OTC DRUG","sameAs":["https://api.morvs.ai/drug-approval/ANDA215232","https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4daddd32-615f-aedf-e063-6394a90a5b09","https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-0270"],"isAccessibleForFree":true,"license":"https://creativecommons.org/publicdomain/zero/1.0/","_source":{"data_provider":"AI Analytics","brand_name":"MORVS","brand_url":"https://morvs.ai/","data_provider_url":"https://api.morvs.ai","license":"https://creativecommons.org/publicdomain/zero/1.0/","primary_source":"https://open.fda.gov/apis/drug/ndc/","generated_at":"2026-11-03T04:22:19.800Z"}}