{"@context":{"@vocab":"https://schema.org/"},"@type":"Drug","@id":"https://api.ai-analytics.org/drug-product/68071-3432#drug","name":"Venlafaxine","identifier":[{"@type":"PropertyValue","propertyID":"FDA National Drug Code (NDC)","value":"68071-3432"},{"@type":"PropertyValue","propertyID":"FDA application number","value":"ANDA077653"},{"@type":"PropertyValue","propertyID":"UNII","value":"7D7RX5A8MO"},{"@type":"PropertyValue","propertyID":"SPL Set ID","value":"fe7de51e-8a81-fe68-e053-6294a90a7339"}],"activeIngredient":"VENLAFAXINE HYDROCHLORIDE","administrationRoute":["ORAL"],"dosageForm":"TABLET","manufacturer":{"@type":"Organization","name":"NuCare Pharmaceuticals,Inc."},"drugClass":[],"isAvailableGenerically":true,"legalStatus":"HUMAN PRESCRIPTION DRUG","sameAs":["https://api.ai-analytics.org/drug-approval/ANDA077653","https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fe7de51e-8a81-fe68-e053-6294a90a7339","https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-3432"],"isAccessibleForFree":true,"license":"https://creativecommons.org/publicdomain/zero/1.0/","_source":{"data_provider":"AI Analytics","data_provider_url":"https://api.ai-analytics.org","license":"https://creativecommons.org/publicdomain/zero/1.0/","primary_source":"https://open.fda.gov/apis/drug/ndc/","generated_at":"2026-09-28T17:27:50.609Z"}}