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PRODUCT DETAIL

Lytenava 25 mg/ml injekčný roztok

Code 6598E
MA number EU/1/24/1798/001
Product Form: sol inj 1x0,3 ml/7,5 mg (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Outlook Therapeutics Limited, Ireland
Therapeutic Class: 64 - OPHTHALMOLOGICA
ATC:
S SENSORY ORGANS
S01 OPHTHALMOLOGICALS
S01L Ocular vascular disorder agents
S01LA Antineovascularisation agents
S01LA08 Bevacizumab
Shelf life: 24
Container: glass vial
Route of admin.: Intravitreal use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 10a well-established use application
MA issued: 27.05.2024
Validity: 27.05.2029
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 13.06.2024
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