Zynrelef (60 mg + 1,8 mg) / 2,3 ml roztok na rany s predĺženým uvoľňovaním

Code 5741D
MA number EU/1/20/1478/001
Product Form: sol vup 1x60 mg/1,8 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
eu-flag.png sk-flag.png