{"@context":{"@vocab":"https://schema.org/"},"@type":"Drug","@id":"https://api.ai-analytics.org/drug-product/49884-789#drug","name":"olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide","identifier":[{"@type":"PropertyValue","propertyID":"FDA National Drug Code (NDC)","value":"49884-789"},{"@type":"PropertyValue","propertyID":"FDA application number","value":"ANDA206137"},{"@type":"PropertyValue","propertyID":"UNII","value":"864V2Q084H|6M97XTV3HD|0J48LPH2TH"},{"@type":"PropertyValue","propertyID":"SPL Set ID","value":"268d12e8-1cfc-4086-b613-8fd94f2d7c4e"}],"activeIngredient":"AMLODIPINE BESYLATE, HYDROCHLOROTHIAZIDE, OLMESARTAN MEDOXOMIL","administrationRoute":["ORAL"],"dosageForm":"TABLET, FILM COATED","manufacturer":{"@type":"Organization","name":"Par Health USA, LLC"},"drugClass":[],"isAvailableGenerically":true,"legalStatus":"HUMAN PRESCRIPTION DRUG","sameAs":["https://api.ai-analytics.org/drug-approval/ANDA206137","https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=268d12e8-1cfc-4086-b613-8fd94f2d7c4e","https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49884-789"],"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":"2026-09-28T07:55:32.001Z"}}