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PRODUCT DETAIL

AKANTIOR 0,8 mg/ml očné roztokové kvapky v jednodávkovom obale

Code 7412E
MA number EU/1/24/1840/003
Product Form: int osd 120 (4x30)x0,3 ml (obal LDPE - jednodávk.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU Orphan
MAH, country: SIFI S.p.A, Italy
Therapeutic Class: 64 - OPHTHALMOLOGICA
ATC:
S SENSORY ORGANS
S01 OPHTHALMOLOGICALS
S01A ANTIINFECTIVES
S01AX Other antiinfectives
S01AX24 Polihexanide
Shelf life: 24
Container: LDPE single-dose container
Route of admin.: Ocular use
Prescription Status: Medicinal product subject to restricted medical prescription.
MA issued: 22.08.2024
Validity: 22.08.2029
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 06.09.2024
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