UnicomIG
0.1.0 - ci-build

UnicomIG, published by UNICOM. This guide is not an authorized publication; it is the continuous build for version 0.1.0 built by the FHIR (HL7® FHIR® Standard) CI Build. This version is based on the current content of https://github.com/hl7-eu/unicom-ig/tree/master and changes regularly. See the Directory of published versions

Example Bundle: 012-Panodil-500mg-SolutionInSachet-SE-FullProduct

Panodil 500 mg pulver till oral lösning i dospåse

EURDID: 2283

Full name: Panodil 500 mg pulver till oral lösning i dospåse

- Invented name part: Panodil

- Strength part: 500 mg

- Pharmaceutical dose form part: pulver till oral lösning i dospåse

Name usage: Swedish (Kingdom of Sweden)

Authorised dose form: Powder for oral solution in sachet

Legal status of supply: Medicinal product not subject to medical prescription

Domain: Human use

Resource status: Current

Product classification:

  • 100000097305 Paracetamol
  • N02BE01 Paracetamol

Marketing Authorisation 1 of 1

Authorisation number: 12391

Region: Kingdom of Sweden

Marketing authorisation holder: Perrigo Sverige AB

Identifier:

  • LOC-100005555

Status: Valid (1994-10-28)

Package 1 of 1

PCID:

Description:
Dospåsar, 12 st

Marketing status:

  • Kingdom of Sweden: Marketed

Pack size:

  • 12 Sachet

Package: 1 Box (Cardboard)

Containing: 12 Sachet

Manufactured Item

Dose form: Powder for oral solution

Unit of presentation: Sachet

Ingredient

Role: Active

Substance: Paracetamol

Presentation strength: 500 milligram(s) / 1 Sachet

Reference strength:
Paracetamol 500 milligram(s) / 1 Sachet

Administrable Product (1 of 1)

Dose form: Oral solution

Unit of presentation:

Route of administration:

  • Oral use

Ingredients:

Ingredient

Role: Active

Substance: Paracetamol

Presentation strength: 500 milligram(s) / 1 Sachet

Reference strength:
Paracetamol 500 milligram(s) / 1 Sachet