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PRODUCT DETAIL

Dupixent 300 mg injekčný roztok naplnený v injekčnom pere

Code 3092E
MA number EU/1/17/1229/028
Product Form: sol inj 6(2x3)x2 ml/300 mg (pero inj.napl.skl. - multibal.)
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
D11AH05 Dupilumab
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: 26.09.2017
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 20.02.2023
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