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
Full name: Ventoline 2 mg/ml lösning för nebulisator
- Invented name part: Ventoline
- Strength part: 2 mg/ml
- Pharmaceutical dose form part: lösning för nebulisator
Name usage: Swedish (Kingdom of Sweden)
Authorised dose form: Nebuliser solution
Legal status of supply: Medicinal product subject to medical prescription
Domain: Human use
Resource status: Current
Product classification:
Marketing Authorisation 1 of 1
Authorisation number: 11088
Region: Kingdom of Sweden
Marketing authorisation holder: GlaxoSmithKline AB
Identifier:
Status: Valid (1990-02-02)
Package 1 of 1
PCID:
Description: Endosbehållare 6 x 10 x 2,5 ml
Marketing status:
Pack size:
Package: 1 Box (Cardboard)
Containing:
Package: 6 Pouch (Aluminium)
Containing: 60 Pipette
Manufactured Item
Dose form: Nebuliser solution
Unit of presentation: Pipette
Ingredient
Role: Active
Substance: Salbutamol sulfate
Concentration strength: 2.4 milligram(s) / 1 millilitre(s)
Reference strength: salbutamol 2 milligram(s) / 1 millilitre(s)
Administrable Product (1 of 1)
Dose form: Nebuliser solution
Unit of presentation:
Route of administration:
Ingredient
Role: Active
Substance: Salbutamol sulfate
Concentration strength: 2.4 milligram(s) / 1 millilitre(s)
Reference strength: salbutamol 2 milligram(s) / 1 millilitre(s)