Release 4

This page is part of the FHIR Specification (v4.0.1: R4 - Mixed Normative and STU) in it's permanent home (it will always be available at this URL). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions

Medicinalproduct-example.json

Biomedical Research and Regulation Work GroupMaturity Level: N/AStandards Status: InformativeCompartments: Not linked to any defined compartments

Raw JSON (canonical form + also see JSON Format Specification)

Example of medicinalproduct

{
  "resourceType": "MedicinalProduct",
  "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>OperationType</b></td><td><b>AuthorisationReferenceNumber</b></td><td><b>EffectiveDate</b></td><td><b>Manufacturer</b></td><td><b>Regulator</b></td></tr><tr><td>*</td><td>Batchrelease <span>(Details : {http://ema.europa.eu/example/manufacturingOperationType code 'Batchrelease' = 'Batchrelease)</span></td><td>1324TZ</td><td>15/03/2013</td><td><a>Organization/example</a></td><td><a>Organization/example</a></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": [
    {
      "operationType": {
        "coding": [
          {
            "system": "http://ema.europa.eu/example/manufacturingOperationType",
            "code": "Batchrelease"
          }
        ]
      },
      "authorisationReferenceNumber": {
        "system": "http://ema.europa.eu/example/manufacturingAuthorisationReferenceNumber",
        "value": "1324TZ"
      },
      "effectiveDate": "2013-03-15",
      "manufacturer": [
        {
          "reference": "Organization/example"
        }
      ],
      "regulator": {
        "reference": "Organization/example"
      }
    }
  ]
}

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.