{"resourceType":"MedicinalProduct","id":"example","meta":{"versionId":"1","lastUpdated":"2023-12-05T15:41:44.136+00:00","security":[{"system":"http://terminology.hl7.org/CodeSystem/v3-ActReason","code":"HTEST","display":"test health data"}]},"text":{"status":"generated","div":"
\n Generated Narrative with Details\n
\n\n id: example
\n\n identifier: {mpid}
\n\n productClassification: WHOAnatomicalTherapeuticChemicalATCClassificationSystem|B01AF02 (Details : {http://ema.europa.eu/example/WHOAnatomicalTherapeuticChemicalATCClassificationSystem code 'WHOAnatomicalTherapeuticChemicalATCClassificationSystem|B01AF02' = 'WHOAnatomicalTherapeuticChemicalATCClassificationSystem|B01AF02)
\n\n attachedDocument: DocumentReference/example
\n\n masterFile: DocumentReference/example
\n\n\n\n name\n
\n\n productName: Equilidem 2.5 mg film-coated tablets
\n\n\n\n namePart\n
\n\n part: Equilidem
\n\n type: INV (Details: [not stated] code INV = 'INV', stated as 'null')
\n\n\n\n namePart\n
\n\n part: 2.5 mg
\n\n type: STR (Details: [not stated] code STR = 'STR', stated as 'null')
\n\n\n\n namePart\n
\n\n part: film-coated tablets
\n\n type: FRM (Details: [not stated] code FRM = 'FRM', stated as 'null')
\nCountryLanguages
\n\n
\n\n \n- \n\n Country\n \n\n Jurisdiction\n \n\n Language\n \n\n \n* \nEU (Details : {http://ema.europa.eu/example/countryCode code 'EU' = 'EU) \nEU (Details : {http://ema.europa.eu/example/jurisdictionCode code 'EU' = 'EU) \nEN (Details : {http://ema.europa.eu/example/languageCode code 'EN' = 'EN) \n
- | \n\n OperationType\n | \n\n AuthorisationReferenceNumber\n | \n\n EffectiveDate\n | \n\n Manufacturer\n | \n\n Regulator\n | \n
* | \nBatchrelease (Details : {http://ema.europa.eu/example/manufacturingOperationType code 'Batchrelease' = 'Batchrelease) | \n1324TZ | \n15/03/2013 | \n\n Organization/example\n | \n\n Organization/example\n | \n