Release 4B 5

This page is part of the FHIR Specification (v4.3.0: R4B (v5.0.0: R5 - STU ). The This is the current published version which supercedes in it's permanent home (it will always be available at this version is 5.0.0 . URL). For a full list of available versions, see the Directory of published versions . Page versions: R5 R4B R5 R4B

Medicinalproductdefinition-example.xml

Example MedicinalProductDefinition/example (XML)

Biomedical Research and Regulation Work Group Maturity Level : N/A Standards Status : Informative Compartments : Not linked to any No defined compartments

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

Jump past Narrative

General example (id = "example") 

<?xml version="1.0" encoding="UTF-8"?>


  
  
    
    
      
      
      

<MedicinalProductDefinition xmlns="http://hl7.org/fhir">
  <id value="example"/> 
  <text> 
    <status value="generated"/> 
    <div xmlns="http://www.w3.org/1999/xhtml">
      <p> <b> Generated Narrative</b> </p> 
      <p> <b> Id</b> : example</p> 
      <p> <b> Identifier</b> : {mpid}</p> 
      <p> <b> Classification</b> : <span title="Codes: {http://ema.europa.eu/example/WHOAnatomicalTherapeuticChemicalATCClassificationSystem
         B01AF02}
      
      
      
      
        
        
      
      
        
        
      
      
        
        
        
        
        
          
            
            
            
            
          
          
            
            
            
            
          
        
      
      
      
        
          
          
          
          
        
        
          
          
          
          
        
      
    
  
  
    
    
  
  
    
      
      
    
  
  
    
  
  
    
  
  
    
    
      
      
        
          
        
      
    
    
      
      
        
          
        
      
    
    
      
      
        
          
        
      
    
    
      
        
          
          
        
      
      
        
          
          
        
      
      
        
          
          
        
      
    
  
  
    
      
        
          
          
        
      
    
    
      
    
  

         B01AF02}">ATC: B01AF02</span> </p> 
      <p> <b> Attached Document</b> : (SmPC)</p>       <p> <b> Master File</b> : (Pharmacovigilence Master File)</p>       <p> <b> Product Name</b> : Equilidem 2.5 mg film-coated tablets</p>       <blockquote>         <p> <b> Name Part</b> </p> <p> <b> part</b> :Equilidem</p>         <p> <b> type</b> : <span title="Codes: ">Invented</span> </p>       </blockquote>       <blockquote>         <p> <b> Name Part</b> </p> <p> <b> part</b> :2.5 mg</p>         <p> <b> type</b> : <span title="Codes: ">Strength</span> </p>       </blockquote>       <blockquote>         <p> <b> Name Part</b> </p>         <p> <b> part</b> :film-coated tablets</p>         <p> <b> type</b> : <span title="Codes: ">Form</span> </p>         <p> <b> Country &amp; Languages</b> </p>         <table class="grid">          <tr>             <td> -</td>             <td> <b> Country</b> </td>             <td> <b> Jurisdiction</b> </td>             <td> <b> Language</b> </td>           </tr>           <tr>             <td> *</td>             <td> <span title="Codes: {http://ema.europa.eu/example/countryCode EU}">EU</span> </td>             <td> <span title="Codes: {http://ema.europa.eu/example/jurisdictionCode EU}">EU</span> </td>             <td> <span title="Codes: {urn:ietf:bcp:47}">EN</span> </td>           </tr>         </table>       </blockquote>       <p> <b> Manufacturing &amp; Business Operations</b> </p>       <table class="grid">        <tr>           <td> -</td>           <td> <b> Type</b> </td>           <td> <b> EffectiveDate</b> </td>           <td> <b> Authorization</b> </td>         </tr>         <tr>           <td> *</td>           <td> Batch Release</td>           <td> 2013-03-15 --&gt; (ongoing)</td>           <td> <span> 1324TZ</span> </td>         </tr>       </table>     </div>   </text>   <identifier>     <system value="http://ema.europa.eu/example/MPID"/>     <value value="{mpid}"/>   </identifier>   <classification>     <coding>       <system value="http://ema.europa.eu/example/WHOAnatomicalTherapeuticChemicalATCClassificationSystem"/>       <code value="B01AF02"/>     </coding>   </classification>   <attachedDocument>     <reference value="DocumentReference/example"/>   </attachedDocument>   <masterFile>     <reference value="DocumentReference/example"/>   </masterFile>   <name>     <productName value="Equilidem 2.5 mg film-coated tablets"/>     <part>       <part value="Equilidem"/>       <type>         <coding>           <code value="INV"/>         </coding>       </type>     </part>     <part>       <part value="2.5 mg"/>       <type>         <coding>           <code value="STR"/>         </coding>       </type>     </part>     <part>       <part value="film-coated tablets"/>       <type>         <coding>           <code value="FRM"/>         </coding>       </type>     </part>     <usage>       <country>         <coding>           <system value="http://ema.europa.eu/example/countryCode"/>           <code value="EU"/>         </coding>       </country>       <jurisdiction>         <coding>           <system value="http://ema.europa.eu/example/jurisdictionCode"/>           <code value="EU"/>         </coding>       </jurisdiction>       <language>         <coding>           <system value="urn:ietf:bcp:47"/>           <code value="en"/>         </coding>       </language>     </usage>   </name>   <operation>     <type>       <concept>         <coding>           <system value="http://ema.europa.eu/example/manufacturingOperationType"/>           <code value="Batchrelease"/>         </coding>       </concept>     </type>     <effectiveDate>       <start value="2013-03-15"/>     </effectiveDate>   </operation> 


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MedicinalProductDefinition

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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.