Medicinal Products

Memantin Grindeks 10 mg filmom obložene tablete

Name Memantin Grindeks 10 mg filmom obložene tablete
Marketing Authorisation Number HR-H-073848955
Active Substance memantinklorid
Composition jedna filmom obložena tableta sadrži 10 mg memantinklorida što odgovara 8,3 mg memantina
Pharmaceutical Form filmom obložena tableta
Packaging [MA Number for Packaging] 10 tableta u blisteru, u kutiji  [HR-H-073848955-01]
14 tableta u blisteru, u kutiji  [HR-H-073848955-02]
20 tableta u blisteru, u kutiji  [HR-H-073848955-03]
28 tableta u blisteru, u kutiji  [HR-H-073848955-04]
30 tableta u blisteru, u kutiji  [HR-H-073848955-05]
40 tableta u blisteru, u kutiji  [HR-H-073848955-06]
50 tableta u blisteru, u kutiji  [HR-H-073848955-07]
56 tableta u blisteru, u kutiji  [HR-H-073848955-08]
60 tableta u blisteru, u kutiji  [HR-H-073848955-09]
90 tableta u blisteru, u kutiji  [HR-H-073848955-10]
98 tableta u blisteru, u kutiji  [HR-H-073848955-11]
100 tableta u blisteru, u kutiji  [HR-H-073848955-12]
112 tableta u blisteru, u kutiji  [HR-H-073848955-13]
Manufacturer AS Grindeks, Riga, Latvija
Marketing Authorisation Holder AS Grindeks, Krustpils iela 53, Riga, Latvija
Marketing Authorisation Date 15.01.2021
MA Period of Validity 15.01.2026
Classification Number UP/I-530-09/20-01/88
Registration Number 381-12-01/70-21-04
Prescription na recept
Type of prescription ograničeni recept
Distribution u ljekarni
Advertising to general public zabranjeno
ATC Code N06DX01
SmPC download
PL download
Public Assessment Report download
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