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: Stesolid® 10 mg Rektallösning
- Invented name part: Stesolid®
- Strength part: 10 mg
- Pharmaceutical dose form part: Rektallösning
Name usage: Swedish (Kingdom of Sweden)
Authorised dose form: Rectal solution
Legal status of supply: Medicinal product subject to special medical prescription
Domain: Human use
Resource status: Current
Product classification:
Marketing Authorisation 1 of 1
Authorisation number: 9292
Region: Kingdom of Sweden
Marketing authorisation holder: Actavis Group PTC ehf.
Identifier:
Status: Valid (1977-11-18)
Package 1 of 1
PCID:
Description: Endosbehållare, 5 x 2,5 ml
Marketing status:
Pack size:
Package: 1 Box (Cardboard)
Containing:
Package: 5 Bag (Aluminium)
Containing:
Package: 1 Pre-filled gastroenteral tube (Plastic)
Containing: 1 Tube
Manufactured Item
Dose form: Rectal solution
Unit of presentation: Tube
Ingredient
Role: Active
Substance: Diazepam
Concentration strength: 10 milligram(s) / 1 unit(s)
Reference strength: Diazepam 10 milligram(s) / 1 unit(s)
Administrable Product (1 of 1)
Dose form: Rectal solution
Unit of presentation:
Route of administration:
Ingredient
Role: Active
Substance: Diazepam
Concentration strength: 10 milligram(s) / 1 unit(s)
Reference strength: Diazepam 10 milligram(s) / 1 unit(s)