This page is part of the FHIR Specification (v4.4.0: R5 Preview #2). 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 |
This is the narrative for the resource. See also the XML, JSON or Turtle format. This example conforms to the profile MedicinalProductDefinition.
Generated Narrative with Details
id: example
identifier: {mpid}
productClassification: WHOAnatomicalTherapeuticChemicalATCClassificationSystem|B01AF02 (Details : {http://ema.europa.eu/example/WHOAnatomicalTherapeuticChemicalATCClassificationSystem code 'WHOAnatomicalTherapeuticChemicalATCClassificationSystem|B01AF02' = 'WHOAnatomicalTherapeuticChemicalATCClassificationSystem|B01AF02)
attachedDocument: DocumentReference/example
masterFile: DocumentReference/example
name
productName: Equilidem 2.5 mg film-coated tablets
namePart
part: Equilidem
type: INV (Details : {[not stated] code 'INV' = 'INV)
namePart
part: 2.5 mg
type: STR (Details : {[not stated] code 'STR' = 'STR)
namePart
part: film-coated tablets
type: FRM (Details : {[not stated] code 'FRM' = 'FRM)
CountryLanguages
- Country Jurisdiction Language * EU (Details : {http://ema.europa.eu/example/countryCode code 'EU' = 'EU) EU (Details : {http://ema.europa.eu/example/jurisdictionCode code 'EU' = 'EU) EN (Details : {http://ema.europa.eu/example/languageCode code 'EN' = 'EN)
- | Type | EffectiveDate | Authorization |
* | 2013-03-15 --> (ongoing) |
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.