en

PRODUCT DETAIL

Wyost 120 mg injekčný roztok

Code 6451E
MA number EU/1/24/1812/001
Product Form: sol inj 1x1,7 ml/120 mg (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 87 - VARIA I
ATC:
M MUSCULO-SKELETAL SYSTEM
M05 DRUGS FOR TREATMENT OF BONE DISEASES
M05B DRUGS AFFECTING BONE STRUCTURE AND MINERALIZATION
M05BX Other drugs affecting bone structure and mineralization
M05BX04 Denosumab
Shelf life: 36
Container: glass vial
Route of admin.: Subcutaneous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 10(4) similar biological application
MA issued: 17.05.2024
Validity: 17.05.2029
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 30.05.2024
eu-flag.png sk-flag.png