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PRODUCT DETAIL

Sugammadex Mylan 100 mg/ml injekčný roztok

Code 9161D
MA number EU/1/21/1583/002
Product Form: sol inj 10x2 ml/200 mg (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 19 - ANTIDOTA, DETOXICANTIA
ATC:
V VARIOUS
V03 ALL OTHER THERAPEUTIC PRODUCTS
V03A ALL OTHER THERAPEUTIC PRODUCTS
V03AB Antidotes
V03AB35 Sugammadex
Shelf life: 24
Container: glass vial
Route of admin.: Intravenous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 10(1) generic application
MA issued: 15.11.2021
Validity: 15.11.2026
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 10.10.2023
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