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PRODUCT DETAIL

LUMIGAN 0,3 mg/ml očná roztoková instilácia v jednodávkovom obale

Code 3851A
MA number EU/1/02/205/005
Product Form: int opo 5x0,4 ml/0,12 mg (fľ.LDPE)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: AbbVie Deutschland GmbH & Co. KG, Germany
Therapeutic Class: 64 - OPHTHALMOLOGICA
ATC:
S SENSORY ORGANS
S01 OPHTHALMOLOGICALS
S01E ANTIGLAUCOMA PREPARATIONS AND MIOTICS
S01EE PROSTAGLADIN ANALOGUES
S01EE03 Bimatoprost
Shelf life: 12
Container: bottle LDPE
Route of admin.: Ocular use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 8(3) application
MA issued: 08.03.2022
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 23.05.2022
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