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: Amlodipin Krka 10 mg Tablett
- Invented name part: Amlodipin Krka
- Strength part: 10 mg
- Pharmaceutical dose form part: Tablett
Name usage: Swedish (Kingdom of Sweden)
Authorised dose form: Tablet
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: 23829
Region: Kingdom of Sweden
Marketing authorisation holder: KRKA Sverige AB
Identifier:
Status: Valid (2006-12-15)
Package 1 of 2
PCID:
Description: Blister, 100 tabletter
Marketing status:
Pack size:
Package: 1 Box (Cardboard)
Containing:
Package: 10 Blister (Orientated PolyAmide) (Aluminium) (PolyVinyl Chloride)
Containing: 10 Tablet
Manufactured Item
Dose form: Tablet
Unit of presentation: Tablet
Ingredient
Role: Active
Substance: Amlodipine besilate
Presentation strength: 13.88 milligram(s) / 1 unit(s)
Reference strength: Amlodipine 10 milligram(s) / 1 unit(s)
Package 2 of 2
PCID:
Description: Blister, 30 tabletter
Marketing status:
Pack size:
Package: 1 Box (Cardboard)
Containing:
Package: 3 Blister (Orientated PolyAmide) (Aluminium) (PolyVinyl Chloride)
Containing: 10 Tablet
Manufactured Item
Dose form: Tablet
Unit of presentation: Tablet
Ingredient
Role: Active
Substance: Amlodipine besilate
Presentation strength: 13.88 milligram(s) / 1 unit(s)
Reference strength: Amlodipine 10 milligram(s) / 1 unit(s)
Administrable Product (1 of 1)
Dose form: Tablet
Unit of presentation: Tablet
Route of administration:
Ingredient
Role: Active
Substance: Amlodipine besilate
Presentation strength: 13.88 milligram(s) / 1 unit(s)
Reference strength: Amlodipine 10 milligram(s) / 1 unit(s)