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PRODUCT DETAIL

Ximluci 10 mg/ml injekčný roztok

Code 2483E
MA number EU/1/22/1691/001
Product Form: sol inj 1x0,23 ml/2,3 mg (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 64 - OPHTHALMOLOGICA
ATC:
S SENSORY ORGANS
S01 OPHTHALMOLOGICALS
S01L Ocular vascular disorder agents
S01LA Antineovascularisation agents
S01LA04 Ranibizumab
Shelf life: 36
Container: glass vial
Route of admin.: Intravitreal use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 10(4) similar biological application
MA issued: 09.11.2022
Validity: 09.11.2027
SmPC + PL: European Medicines Agency's database
Dokument: Ranibizumab_Prirucka pre pacientov.pdf  
Safety feature Yes
Data update: 06.12.2022
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