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	neponovljivi recept
Distribution	Supply through pharmacies (community)
Advertising to general public	not allowed
ATC Code	J01DC02
Marketing status	stavljeno u promet
Shortage status	u tijeku
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	stavljeno u promet	u tijeku
12 tableta u blisteru, u kutiji	HR-H-816131041-05	nije stavljeno u promet	-
14 tableta u blisteru, u kutiji	HR-H-816131041-06	nije stavljeno u promet	-
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