Furextil 500 mg filmom obložene tablete

Name	Furextil 500 mg filmom obložene tablete
Marketing Authorisation Number	HR-H-816131041
Active Substance	cefuroksimaksetil
Composition	jedna tableta sadrži 500 mg cefuroksima u obliku cefuroksimaksetila
Pharmaceutical Form	Filmom obložena tableta
Manufacturer	Alkaloid - INT d.o.o., Ljubljana - Črnuče, Slovenija
Marketing Authorisation Holder	Alkaloid - INT d.o.o., Šlandrova ulica 4, Ljubljana - Črnuče, Slovenija
Marketing Authorisation Date	27.02.2023
MA Period of Validity	unlimited
Classification Number	UP/I-530-09/22-02/207
Registration Number	381-12-01/70-23-03
Prescription	Medicinal product subject to medical prescription
Type of prescription	Medicinal product on medical prescription for non-renewable delivery
Distribution	Supply through pharmacies (community)
Advertising to general public	not allowed
ATC Code	J01DC02
Marketing status	Marketed
Shortage status	Actual
SmPC	download
PL	download
Public Assessment Report	download
Summary of risk management plan	download

Packaging description	MA Number for Packaging	Marketing status	Shortage status
6 tableta u blisteru, u kutiji	HR-H-816131041-01	-	-
7 tableta u blisteru, u kutiji	HR-H-816131041-02	-	-
8 tableta u blisteru, u kutiji	HR-H-816131041-03	-	-
10 tableta u blisteru, u kutiji	HR-H-816131041-04	Marketed	Actual
12 tableta u blisteru, u kutiji	HR-H-816131041-05	Never marketed	-
14 tableta u blisteru, u kutiji	HR-H-816131041-06	Never marketed	-
20 tableta u blisteru, u kutiji	HR-H-816131041-07	-	-
21 tableta u blisteru, u kutiji	HR-H-816131041-08	-	-
100 tableta u blisteru, u kutiji	HR-H-816131041-09	-	-

Medicinal Products