{"@context":{"@vocab":"https://schema.org/"},"@type":"Drug","@id":"https://api.morvs.ai/drug-product/82804-024#drug","name":"Duloxetine Delayed-Release","alternateName":"DULOXETINE HYDROCHLORIDE","identifier":[{"@type":"PropertyValue","propertyID":"FDA National Drug Code (NDC)","value":"82804-024"},{"@type":"PropertyValue","propertyID":"FDA application number","value":"ANDA203088"},{"@type":"PropertyValue","propertyID":"UNII","value":"9044SC542W"},{"@type":"PropertyValue","propertyID":"SPL Set ID","value":"f5e7503a-b28f-4cd0-a4ee-47bdca88d54b"}],"activeIngredient":"DULOXETINE HYDROCHLORIDE","administrationRoute":["ORAL"],"dosageForm":"CAPSULE, DELAYED RELEASE PELLETS","manufacturer":{"@type":"Organization","name":"Proficient Rx LP"},"drugClass":[],"isAvailableGenerically":true,"legalStatus":"HUMAN PRESCRIPTION DRUG","sameAs":["https://api.morvs.ai/drug-approval/ANDA203088","https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f5e7503a-b28f-4cd0-a4ee-47bdca88d54b","https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82804-024"],"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":"2026-10-28T16:45:12.799Z"}}