Zynrelef (400 mg + 12 mg) / 14 ml roztok na rany s predĺženým uvoľňovaním

Code 5743D
MA number EU/1/20/1478/003
Product Form: sol vup 1x400 mg/12 mg (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 01 - ANAESTHETICA (LOKÁLNE)
Shelf life: 24
Container: glass vial
Route of admin.: Intralesional use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 10b fixed combination application
MA issued: 24.09.2020
Validity: 24.09.2025
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 16.10.2020
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