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 |