<?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}">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>
</MedicinalProductDefinition>