This page is part of the FHIR Specification (v4.3.0: R4B - STU). 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)
General example
{ "resourceType": "MedicinalProductDefinition", "id": "example", "text": { "status": "generated", "div": "<div xmlns=\"http://www.w3.org/1999/xhtml\">\n\t\t\t<p><b>Generated Narrative</b></p>\n\t\t\t<p><b>Id</b>: example</p>\n\t\t\t<p><b>Identifier</b>: {mpid}</p>\n\t\t\t<p><b>Classification</b>: <span title=\"Codes: {http://ema.europa.eu/example/WHOAnatomicalTherapeuticChemicalATCClassificationSystem B01AF02}\">ATC: B01AF02</span></p>\n\t\t\t<p><b>Attached Document</b>: (SmPC)</p>\n\t\t\t<p><b>Master File</b>: (Pharmacovigilence Master File)</p>\n\t\t\t<p><b>Product Name</b>: Equilidem 2.5 mg film-coated tablets</p>\n\t\t\t<blockquote>\n\t\t\t\t<p><b>Name Part</b></p><p><b>part</b>:Equilidem</p>\n\t\t\t\t<p><b>type</b>: <span title=\"Codes: \">Invented</span></p>\n\t\t\t</blockquote>\n\t\t\t<blockquote>\n\t\t\t\t<p><b>Name Part</b></p><p><b>part</b>:2.5 mg</p>\n\t\t\t\t<p><b>type</b>: <span title=\"Codes: \">Strength</span></p>\n\t\t\t</blockquote>\n\t\t\t<blockquote>\n\t\t\t\t<p><b>Name Part</b></p>\n\t\t\t\t<p><b>part</b>:film-coated tablets</p>\n\t\t\t\t<p><b>type</b>: <span title=\"Codes: \">Form</span></p>\n\t\t\t\t<p><b>Country & Languages</b></p>\n\t\t\t\t<table class=\"grid\">\n\t\t\t\t\t<tr>\n\t\t\t\t\t\t<td>-</td>\n\t\t\t\t\t\t<td><b>Country</b></td>\n\t\t\t\t\t\t<td><b>Jurisdiction</b></td>\n\t\t\t\t\t\t<td><b>Language</b></td>\n\t\t\t\t\t</tr>\n\t\t\t\t\t<tr>\n\t\t\t\t\t\t<td>*</td>\n\t\t\t\t\t\t<td><span title=\"Codes: {http://ema.europa.eu/example/countryCode EU}\">EU</span></td>\n\t\t\t\t\t\t<td><span title=\"Codes: {http://ema.europa.eu/example/jurisdictionCode EU}\">EU</span></td>\n\t\t\t\t\t\t<td><span title=\"Codes: {http://ema.europa.eu/example/languageCode EN}\">EN</span></td>\n\t\t\t\t\t</tr>\n\t\t\t\t</table>\n\t\t\t</blockquote>\n\t\t\t<p><b>Manufacturing & Business Operations</b></p>\n\t\t\t<table class=\"grid\">\n\t\t\t\t<tr>\n\t\t\t\t\t<td>-</td>\n\t\t\t\t\t<td><b>Type</b></td>\n\t\t\t\t\t<td><b>EffectiveDate</b></td>\n\t\t\t\t\t<td><b>Authorization</b></td>\n\t\t\t\t</tr>\n\t\t\t\t<tr>\n\t\t\t\t\t<td>*</td>\n\t\t\t\t\t<td>Batch Release</td>\n\t\t\t\t\t<td>2013-03-15 --> (ongoing)</td>\n\t\t\t\t\t<td><span>1324TZ</span></td>\n\t\t\t\t</tr>\n\t\t\t</table>\n\t\t</div>" }, "identifier": [ { "system": "http://ema.europa.eu/example/MPID", "value": "{mpid}" } ], "classification": [ { "coding": [ { "system": "http://ema.europa.eu/example/WHOAnatomicalTherapeuticChemicalATCClassificationSystem", "code": "B01AF02" } ] } ], "attachedDocument": [ { "reference": "DocumentReference/example" } ], "masterFile": [ { "reference": "DocumentReference/example" } ], "name": [ { "productName": "Equilidem 2.5 mg film-coated tablets", "namePart": [ { "part": "Equilidem", "type": { "coding": [ { "code": "INV" } ] } }, { "part": "2.5 mg", "type": { "coding": [ { "code": "STR" } ] } }, { "part": "film-coated tablets", "type": { "coding": [ { "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" } ] } } ] } ], "operation": [ { "type": { "concept": { "coding": [ { "system": "http://ema.europa.eu/example/manufacturingOperationType", "code": "Batchrelease" } ] } }, "effectiveDate": { "start": "2013-03-15" } } ] }
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.