| Package | eu.epi.february2025 |
| Resource Type | CodeSystem |
| Id | 300000000003 |
| FHIR Version | R5 |
| Source | https://simplifier.net/resolve?scope=eu.epi.february2025@1.0.0&canonical=http://ema.europa.eu/fhir/CodeSystem/300000000003 |
| URL | http://ema.europa.eu/fhir/CodeSystem/300000000003 |
| Version | 5.0.0 |
| Status | active |
| Name | EUepilabellingcodesystem |
| Title | EU EPI Labelling QRD code values |
| Description | EU EPI Labelling QRD code values |
| Content | complete |
No resources found
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No narrative content found in resource
{
"resourceType": "CodeSystem",
"status": "active",
"content": "complete",
"name": "EUepilabellingcodesystem",
"id": "300000000003",
"title": "EU EPI Labelling QRD code values",
"description": "EU EPI Labelling QRD code values",
"version": "5.0.0",
"url": "http://ema.europa.eu/fhir/CodeSystem/300000000003",
"concept": [
{
"code": "000000000000",
"display": "Code for custom sub-sections (reserved)"
},
{
"code": "200000029861",
"display": "LABELLING"
},
{
"code": "200000029862",
"display": "PARTICULARS TO APPEAR ON <THE OUTER PACKAGING> <AND> <THE IMMEDIATE PACKAGING> {NATURE/TYPE}"
},
{
"code": "200000029863",
"display": "1. NAME OF THE MEDICINAL PRODUCT"
},
{
"code": "200000029864",
"display": "2. STATEMENT OF ACTIVE SUBSTANCE(S)"
},
{
"code": "200000029865",
"display": "3. LIST OF EXCIPIENTS"
},
{
"code": "200000029866",
"display": "4. PHARMACEUTICAL FORM AND CONTENTS"
},
{
"code": "200000029867",
"display": "5. METHOD AND ROUTE(S) OF ADMINISTRATION"
},
{
"code": "200000029868",
"display": "6. SPECIAL WARNING THAT THE MEDICINAL PRODUCT MUST BE STORED OUT OF THE SIGHT AND REACH OF CHILDREN"
},
{
"code": "200000029869",
"display": "7. OTHER SPECIAL WARNING(S), IF NECESSARY"
},
{
"code": "200000029870",
"display": "8. EXPIRY DATE"
},
{
"code": "200000029871",
"display": "9. SPECIAL STORAGE CONDITIONS"
},
{
"code": "200000029872",
"display": "10. SPECIAL PRECAUTIONS FOR DISPOSAL OF UNUSED MEDICINAL PRODUCTS OR WASTE MATERIALS DERIVED FROM SUCH MEDICINAL PRODUCTS, IF APPROPRIATE"
},
{
"code": "200000029873",
"display": "11. NAME AND ADDRESS OF THE MARKETING AUTHORISATION HOLDER"
},
{
"code": "200000029874",
"display": "12. MARKETING AUTHORISATION NUMBER(S)"
},
{
"code": "200000029875",
"display": "13. BATCH NUMBER<, DONATION AND PRODUCT CODES>"
},
{
"code": "200000029876",
"display": "14. GENERAL CLASSIFICATION FOR SUPPLY"
},
{
"code": "200000029877",
"display": "15. INSTRUCTIONS ON USE"
},
{
"code": "200000029878",
"display": "16. INFORMATION IN BRAILLE"
},
{
"code": "200000029879",
"display": "17. UNIQUE IDENTIFIER - 2D BARCODE"
},
{
"code": "200000029880",
"display": "18. UNIQUE IDENTIFIER - HUMAN READABLE DATA"
},
{
"code": "200000029881",
"display": "MINIMUM PARTICULARS TO APPEAR ON BLISTERS OR STRIPS {NATURE/TYPE}"
},
{
"code": "200000029882",
"display": "1. NAME OF THE MEDICINAL PRODUCT"
},
{
"code": "200000029883",
"display": "2. NAME OF THE MARKETING AUTHORISATION HOLDER"
},
{
"code": "200000029884",
"display": "3. EXPIRY DATE"
},
{
"code": "200000029885",
"display": "4. BATCH NUMBER<, DONATION AND PRODUCT CODES>"
},
{
"code": "200000029886",
"display": "5. OTHER"
},
{
"code": "200000029887",
"display": "MINIMUM PARTICULARS TO APPEAR ON SMALL IMMEDIATE PACKAGING UNITS {NATURE/TYPE}"
},
{
"code": "200000029888",
"display": "1. NAME OF THE MEDICINAL PRODUCT AND ROUTE(S) OF ADMINISTRATION"
},
{
"code": "200000029889",
"display": "2. METHOD OF ADMINISTRATION"
},
{
"code": "200000029890",
"display": "3. EXPIRY DATE"
},
{
"code": "200000029891",
"display": "4. BATCH NUMBER<, DONATION AND PRODUCT CODES>"
},
{
"code": "200000029892",
"display": "5. CONTENTS BY WEIGHT, BY VOLUME OR BY UNIT"
},
{
"code": "200000029893",
"display": "6. OTHER"
}
],
"experimental": false,
"publisher": "European Medicines Agency",
"jurisdiction": [
{
"text": "European Union"
}
],
"caseSensitive": true,
"count": 34
}