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PRODUCT DETAIL

Baiama 40 mg/ml, injekčný roztok v injekčnej liekovke

Code 9101E
MA number EU/1/24/1887/001
Product Form: sol inj 1x0,1 ml/4 mg (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Formycon AG, Germany
Therapeutic Class: 64 - OPHTHALMOLOGICA
ATC:
S SENSORY ORGANS
S01 OPHTHALMOLOGICALS
S01L Ocular vascular disorder agents
S01LA Antineovascularisation agents
S01LA05 Aflibercept
Shelf life: 24
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: 13.01.2025
Validity: 13.01.2030
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 27.02.2025
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