{"@context":{"@vocab":"https://schema.org/"},"@type":"Drug","@id":"https://api.ai-analytics.org/drug-product/0406-1236#drug","name":"Diphenoxylate Hydrochloride and Atropine Sulfate","alternateName":"diphenoxylate hydrochloride and atropine sulfate","identifier":[{"@type":"PropertyValue","propertyID":"FDA National Drug Code (NDC)","value":"0406-1236"},{"@type":"PropertyValue","propertyID":"FDA application number","value":"ANDA213335"},{"@type":"PropertyValue","propertyID":"UNII","value":"03J5ZE7KA5|W24OD7YW48"},{"@type":"PropertyValue","propertyID":"SPL Set ID","value":"24915aa0-1600-44bb-99fc-46529a794124"}],"activeIngredient":"ATROPINE SULFATE, DIPHENOXYLATE HYDROCHLORIDE","administrationRoute":["ORAL"],"dosageForm":"TABLET","manufacturer":{"@type":"Organization","name":"SpecGx LLC"},"drugClass":[],"isAvailableGenerically":true,"legalStatus":"HUMAN PRESCRIPTION DRUG","sameAs":["https://api.ai-analytics.org/drug-approval/ANDA213335","https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=24915aa0-1600-44bb-99fc-46529a794124","https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0406-1236"],"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":"2026-09-27T04:25:26.088Z"}}