UFIS-SWE-IG
0.1.0 - ci-build

UFIS-SWE-IG, 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/joofio/ufis-swe-ig/ and changes regularly. See the Directory of published versions

Example Bundle: Sandimmun50mgmlkoncentrat-SE-PLC-MPD-BBDL

Sandimmun 50 mg/ml koncentrat till infusionsvätska, lösning

MPID: SE-100003469-00010263
EURDID: 745

Full name: Sandimmun 50 mg/ml koncentrat till infusionsvätska, lösning

- Invented name part: Sandimmun

- Strength part: 50 mg/ml

- Pharmaceutical dose form part: koncentrat till infusionsvätska, lösning

Name usage: Swedish (Kingdom of Sweden)

Authorised dose form: Concentrate for solution for infusion

Legal status of supply: Medicinal product subject to medical prescription

Domain: Human use

Resource status: Current

Product classification:

  • 100000096879 ciclosporin

Marketing Authorisation 1 of 1

Authorisation number: 10263

Region: Kingdom of Sweden

Marketing authorisation holder: Novartis Sverige AB

Identifier:

  • LOC-123456789

Status: Valid (1985-09-06)

Package 1 of 1

PCID:

Description:
Ampull, 10 x 1 ml

Marketing status:

  • Kingdom of Sweden: Marketed

Pack size:

  • 10 Ampoule

Package: 1 Box (Cardboard)

Containing:

Package: 10 Ampoule (Glass type I)

Containing: 1 millilitre(s)

Manufactured Item

Dose form: Concentrate for solution for infusion

Unit of presentation: Ampoule

Ingredient

Role: Active

Substance: Ciclosporin

Concentration strength: 50 milligram(s) / 1 millilitre(s)

Reference strength:
Ciclosporin 50 milligram(s) / 1 millilitre(s)

Administrable Product (1 of 1)

Dose form: Solution for infusion

Unit of presentation:

Route of administration:

  • Intravenous use

Ingredients:

Ingredient

Role: Active

Substance: Ciclosporin

Concentration strength: 50 milligram(s) / 1 millilitre(s)

Reference strength:
Ciclosporin 50 milligram(s) / 1 millilitre(s)