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PRODUCT DETAIL

MYNZEPLI 40 mg/ml, injekčný roztok v naplnenej injekčnej striekačke

Code 1026F
MA number EU/1/25/1964/002
Product Form: sol inj 1x0,09 ml/3,6 mg (striek.inj.napl.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: ADVANZ PHARMA LIMITED, Ireland
Therapeutic Class: 64 - OPHTHALMOLOGICA
ATC:
S SENSORY ORGANS
S01 OPHTHALMOLOGICALS
S01L Ocular vascular disorder agents
S01LA Antineovascularisation agents
S01LA05 Aflibercept
Shelf life: 24
Route of admin.: Intravitreal use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 10(4) similar biological application
MA issued: 18.08.2025
Validity: 18.08.2030
SmPC + PL: European Medicines Agency's database
Dokument: Aflibercept_Príručka pre pacienta.pdf  
Dokument: Aflibercept_Príručka pre predpisujúceho lekára.pdf  
Safety feature Yes
Data update: 08.09.2025
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