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/ and changes regularly. See the Directory of published versions
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:
Marketing Authorisation 1 of 1
Authorisation number: 12391
Region: Kingdom of Sweden
Marketing authorisation holder: Perrigo Sverige AB
Identifier:
Status: Valid (1994-10-28)
Package 1 of 1
PCID:
Description: Dospåsar, 12 st
Marketing status:
Pack size:
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:
Ingredient
Role: Active
Substance: Paracetamol
Presentation strength: 500 milligram(s) / 1 Sachet
Reference strength: Paracetamol 500 milligram(s) / 1 Sachet