{"@context":{"@vocab":"https://schema.org/"},"@type":"Drug","@id":"https://api.ai-analytics.org/drug-product/68001-632#drug","name":"Nadolol","identifier":[{"@type":"PropertyValue","propertyID":"FDA National Drug Code (NDC)","value":"68001-632"},{"@type":"PropertyValue","propertyID":"FDA application number","value":"ANDA210955"},{"@type":"PropertyValue","propertyID":"UNII","value":"FEN504330V"},{"@type":"PropertyValue","propertyID":"SPL Set ID","value":"15822faf-6924-4a63-a4e1-6058b308708c"}],"activeIngredient":"NADOLOL","administrationRoute":["ORAL"],"dosageForm":"TABLET","manufacturer":{"@type":"Organization","name":"BluePoint Laboratories"},"drugClass":[],"isAvailableGenerically":true,"legalStatus":"HUMAN PRESCRIPTION DRUG","sameAs":["https://api.ai-analytics.org/drug-approval/ANDA210955","https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=15822faf-6924-4a63-a4e1-6058b308708c","https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-632"],"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":"2026-09-27T09:26:24.916Z"}}