{"@context":{"@vocab":"https://schema.org/"},"@type":"Drug","@id":"https://api.morvs.ai/drug-product/76282-302#drug","name":"Alfuzosin hydrochloride","identifier":[{"@type":"PropertyValue","propertyID":"FDA National Drug Code (NDC)","value":"76282-302"},{"@type":"PropertyValue","propertyID":"FDA application number","value":"ANDA090284"},{"@type":"PropertyValue","propertyID":"UNII","value":"75046A1XTN"},{"@type":"PropertyValue","propertyID":"SPL Set ID","value":"f075a897-7bef-4799-b7e2-7e051c461443"}],"activeIngredient":"ALFUZOSIN HYDROCHLORIDE","administrationRoute":["ORAL"],"dosageForm":"TABLET, EXTENDED RELEASE","manufacturer":{"@type":"Organization","name":"Exelan Pharmaceuticals Inc."},"drugClass":[],"isAvailableGenerically":true,"legalStatus":"HUMAN PRESCRIPTION DRUG","sameAs":["https://api.morvs.ai/drug-approval/ANDA090284","https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f075a897-7bef-4799-b7e2-7e051c461443","https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76282-302"],"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":"2026-10-31T16:51:17.946Z"}}