This page is part of the FHIR Specification (v4.2.0: R5 Preview #1). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions
. Page versions: R5 R4B
| Biomedical Research and Regulation Work Group | Maturity Level: N/A | Standards Status: Informative | Compartments: Not linked to any defined compartments |
Raw JSON (canonical form + also see JSON Format Specification)
Example of medicinalproductdefinition
{
"resourceType": "MedicinalProductDefinition",
"id": "example",
"text": {
"status": "generated",
"div": "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p><b>Generated Narrative with Details</b></p><p><b>id</b>: example</p><p><b>identifier</b>: {mpid}</p><p><b>productClassification</b>: WHOAnatomicalTherapeuticChemicalATCClassificationSystem|B01AF02 <span>(Details : {http://ema.europa.eu/example/WHOAnatomicalTherapeuticChemicalATCClassificationSystem code 'WHOAnatomicalTherapeuticChemicalATCClassificationSystem|B01AF02' = 'WHOAnatomicalTherapeuticChemicalATCClassificationSystem|B01AF02)</span></p><p><b>attachedDocument</b>: <a>DocumentReference/example</a></p><p><b>masterFile</b>: <a>DocumentReference/example</a></p><blockquote><p><b>name</b></p><p><b>productName</b>: Equilidem 2.5 mg film-coated tablets</p><blockquote><p><b>namePart</b></p><p><b>part</b>: Equilidem</p><p><b>type</b>: INV (Details: [not stated] code INV = 'INV', stated as 'null')</p></blockquote><blockquote><p><b>namePart</b></p><p><b>part</b>: 2.5 mg</p><p><b>type</b>: STR (Details: [not stated] code STR = 'STR', stated as 'null')</p></blockquote><blockquote><p><b>namePart</b></p><p><b>part</b>: film-coated tablets</p><p><b>type</b>: FRM (Details: [not stated] code FRM = 'FRM', stated as 'null')</p></blockquote><h3>CountryLanguages</h3><table><tr><td>-</td><td><b>Country</b></td><td><b>Jurisdiction</b></td><td><b>Language</b></td></tr><tr><td>*</td><td>EU <span>(Details : {http://ema.europa.eu/example/countryCode code 'EU' = 'EU)</span></td><td>EU <span>(Details : {http://ema.europa.eu/example/jurisdictionCode code 'EU' = 'EU)</span></td><td>EN <span>(Details : {http://ema.europa.eu/example/languageCode code 'EN' = 'EN)</span></td></tr></table></blockquote><h3>ManufacturingBusinessOperations</h3><table><tr><td>-</td><td><b>Type[x]</b></td><td><b>EffectiveDate</b></td><td><b>Authorization</b></td></tr><tr><td>*</td><td>Batchrelease (Details: http://ema.europa.eu/example/manufacturingOperationType code Batchrelease = 'Batchrelease', stated as 'null')</td><td>2013-03-15 --> (ongoing)</td><td/></tr></table></div>"
},
"identifier": [
{
"system": "http://ema.europa.eu/example/MPID",
"value": "{mpid}"
}
],
"productClassification": [
{
"coding": [
{
"system": "http://ema.europa.eu/example/WHOAnatomicalTherapeuticChemicalATCClassificationSystem",
"code": "WHOAnatomicalTherapeuticChemicalATCClassificationSystem|B01AF02"
}
]
}
],
"attachedDocument": [
{
"reference": "DocumentReference/example"
}
],
"masterFile": [
{
"reference": "DocumentReference/example"
}
],
"name": [
{
"productName": "Equilidem 2.5 mg film-coated tablets",
"namePart": [
{
"part": "Equilidem",
"type": {
"code": "INV"
}
},
{
"part": "2.5 mg",
"type": {
"code": "STR"
}
},
{
"part": "film-coated tablets",
"type": {
"code": "FRM"
}
}
],
"countryLanguage": [
{
"country": {
"coding": [
{
"system": "http://ema.europa.eu/example/countryCode",
"code": "EU"
}
]
},
"jurisdiction": {
"coding": [
{
"system": "http://ema.europa.eu/example/jurisdictionCode",
"code": "EU"
}
]
},
"language": {
"coding": [
{
"system": "http://ema.europa.eu/example/languageCode",
"code": "EN"
}
]
}
}
]
}
],
"manufacturingBusinessOperation": [
{
"typeCoding": {
"system": "http://ema.europa.eu/example/manufacturingOperationType",
"code": "Batchrelease"
},
"effectiveDate": {
"start": "2013-03-15"
},
"authorization": {
"identifier": {
"system": "http://ema.europa.eu/example/manufacturingAuthorisationReferenceNumber",
"value": "1324TZ"
}
}
}
]
}
Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.