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PRODUCT DETAIL

Afqlir 40 mg/ml, injekčný roztok v injekčnej liekovke

Code 8745E
MA number EU/1/24/1867/002
Product Form: sol inj 1x0,240 ml/9,6 mg (liek.inj.skl. + 1 ihla s filtrom)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Sandoz GmbH, Austria
Therapeutic Class: 64 - OPHTHALMOLOGICA
ATC:
S SENSORY ORGANS
S01 OPHTHALMOLOGICALS
S01L Ocular vascular disorder agents
S01LA Antineovascularisation agents
S01LA05 Aflibercept
Shelf life: 36
Route of admin.: Intravitreal use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 10(4) similar biological application
MA issued: 13.11.2024
Validity: 13.11.2029
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 16.01.2025
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