en

PRODUCT DETAIL

Adtralza 150 mg injekčný roztok v naplnenej injekčnej striekačke

Code 8011D
MA number EU/1/21/1554/002
Product Form: sol inj 4 (2x2)x1 ml/150 mg (striek.inj.napl.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 46 - DERMATOLOGICA
ATC:
D DERMATOLOGICALS
D11 OTHER DERMATOLOGICAL PREPARATIONS
D11A OTHER DERMATOLOGICAL PREPARATIONS
D11AH Agents for dermatitis, excluding corticosteroids
D11AH07 Tralokinumab
Shelf life: 36
Route of admin.: Subcutaneous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 17.06.2021
Validity: 17.06.2026
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 30.06.2021
eu-flag.png sk-flag.png