{"@context":{"@vocab":"https://schema.org/"},"@type":"Drug","@id":"https://api.morvs.ai/drug-product/76420-236#drug","name":"Duloxetine","identifier":[{"@type":"PropertyValue","propertyID":"FDA National Drug Code (NDC)","value":"76420-236"},{"@type":"PropertyValue","propertyID":"FDA application number","value":"ANDA090776"},{"@type":"PropertyValue","propertyID":"UNII","value":"9044SC542W"},{"@type":"PropertyValue","propertyID":"SPL Set ID","value":"7c755ca3-0855-4b54-80a8-01b85f8e644a"}],"activeIngredient":"DULOXETINE HYDROCHLORIDE","administrationRoute":["ORAL"],"dosageForm":"CAPSULE, DELAYED RELEASE PELLETS","manufacturer":{"@type":"Organization","name":"Asclemed USA, Inc."},"drugClass":[],"isAvailableGenerically":true,"legalStatus":"HUMAN PRESCRIPTION DRUG","sameAs":["https://api.morvs.ai/drug-approval/ANDA090776","https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7c755ca3-0855-4b54-80a8-01b85f8e644a","https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76420-236"],"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":"2026-11-02T15:52:29.749Z"}}