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PRODUCT DETAIL

Xbryk 120 mg injekčný roztok

Code 9118E
MA number EU/1/24/1889/001
Product Form: sol inj 1x1,7 ml/120 mg (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Samsung Bioepis NL B.V., Netherland
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: 12.02.2025
Validity: 12.02.2030
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 03.03.2025
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