Memantine LEK

Country: European Union

Language: German

Source: EMA (European Medicines Agency)

Buy It Now

Active ingredient:

Memantinhydrochlorid

Available from:

Pharmathen S.A.

ATC code:

N06DX01

INN (International Name):

memantine

Therapeutic group:

Psychoanaleptics, Andere anti-Demenz-Medikamenten

Therapeutic area:

Alzheimer

Therapeutic indications:

Behandlung von Patienten mit mittelschwerer bis schwerer Alzheimer-Krankheit.

Product summary:

Revision: 5

Authorization status:

Autorisiert

Authorization date:

2013-04-21

Patient Information leaflet

                                Skip to main content [European Medicines Agency]
Menu	*
EMA WEBSITE TEMPORARILY UNAVAILABLE
This website is currently unavailable due to essential maintenance.
EMERGENCY CONTACT DETAILS
To report a potentially serious problem with a centrally authorised
medicine, call our product emergency hotline on +31 (0)88 781 7600.
To report a product quality defect, including a suspected defect, of a
centrally authorised medicine that could result in a recall or
abnormal restriction on supply, marketing or manufacturing
authorisation holders can call +31 (0)65 008 9457 outside business
hours.
The details of your call may be documented, including personal data if
you provide them (such as your name, contact details and nature of the
issue raised), in accordance with our privacy statement. You can
consult our privacy statement at
https://www.ema.europa.eu/en/about-us/legal/general-privacy-statement
[/en/about-us/legal/general-privacy-statement] once the website is
back online.
RSS feed Twitter YouTube LinkedIn
© 1995-2020 European Medicines Agency
European Union agencies network [European Union agencies network]
An agency of the European Union [European Union flag]
                                
                                Read the complete document
                                
                            

Summary of Product characteristics

                                Skip to main content [European Medicines Agency]
Menu	*
EMA WEBSITE TEMPORARILY UNAVAILABLE
This website is currently unavailable due to essential maintenance.
EMERGENCY CONTACT DETAILS
To report a potentially serious problem with a centrally authorised
medicine, call our product emergency hotline on +31 (0)88 781 7600.
To report a product quality defect, including a suspected defect, of a
centrally authorised medicine that could result in a recall or
abnormal restriction on supply, marketing or manufacturing
authorisation holders can call +31 (0)65 008 9457 outside business
hours.
The details of your call may be documented, including personal data if
you provide them (such as your name, contact details and nature of the
issue raised), in accordance with our privacy statement. You can
consult our privacy statement at
https://www.ema.europa.eu/en/about-us/legal/general-privacy-statement
[/en/about-us/legal/general-privacy-statement] once the website is
back online.
RSS feed Twitter YouTube LinkedIn
© 1995-2020 European Medicines Agency
European Union agencies network [European Union agencies network]
An agency of the European Union [European Union flag]
                                
                                Read the complete document
                                
                            

Documents in other languages

Patient Information leaflet Patient Information leaflet Bulgarian 16-11-2020
Summary of Product characteristics Summary of Product characteristics Bulgarian 16-11-2020
Public Assessment Report Public Assessment Report Bulgarian 29-04-2013
Patient Information leaflet Patient Information leaflet Spanish 16-11-2020
Public Assessment Report Public Assessment Report Spanish 29-04-2013
Patient Information leaflet Patient Information leaflet Czech 16-11-2020
Public Assessment Report Public Assessment Report Czech 29-04-2013
Patient Information leaflet Patient Information leaflet Danish 16-11-2020
Public Assessment Report Public Assessment Report Danish 29-04-2013
Patient Information leaflet Patient Information leaflet Estonian 16-11-2020
Public Assessment Report Public Assessment Report Estonian 29-04-2013
Patient Information leaflet Patient Information leaflet Greek 16-11-2020
Public Assessment Report Public Assessment Report Greek 29-04-2013
Patient Information leaflet Patient Information leaflet English 16-11-2020
Public Assessment Report Public Assessment Report English 29-04-2013
Patient Information leaflet Patient Information leaflet French 16-11-2020
Public Assessment Report Public Assessment Report French 29-04-2013
Patient Information leaflet Patient Information leaflet Italian 16-11-2020
Public Assessment Report Public Assessment Report Italian 29-04-2013
Patient Information leaflet Patient Information leaflet Latvian 16-11-2020
Public Assessment Report Public Assessment Report Latvian 29-04-2013
Patient Information leaflet Patient Information leaflet Lithuanian 16-11-2020
Summary of Product characteristics Summary of Product characteristics Lithuanian 16-11-2020
Public Assessment Report Public Assessment Report Lithuanian 29-04-2013
Patient Information leaflet Patient Information leaflet Hungarian 16-11-2020
Summary of Product characteristics Summary of Product characteristics Hungarian 16-11-2020
Public Assessment Report Public Assessment Report Hungarian 29-04-2013
Patient Information leaflet Patient Information leaflet Maltese 16-11-2020
Public Assessment Report Public Assessment Report Maltese 29-04-2013
Patient Information leaflet Patient Information leaflet Dutch 16-11-2020
Public Assessment Report Public Assessment Report Dutch 29-04-2013
Patient Information leaflet Patient Information leaflet Polish 16-11-2020
Public Assessment Report Public Assessment Report Polish 29-04-2013
Patient Information leaflet Patient Information leaflet Portuguese 16-11-2020
Summary of Product characteristics Summary of Product characteristics Portuguese 16-11-2020
Public Assessment Report Public Assessment Report Portuguese 29-04-2013
Patient Information leaflet Patient Information leaflet Romanian 16-11-2020
Public Assessment Report Public Assessment Report Romanian 29-04-2013
Patient Information leaflet Patient Information leaflet Slovak 16-11-2020
Public Assessment Report Public Assessment Report Slovak 29-04-2013
Patient Information leaflet Patient Information leaflet Slovenian 16-11-2020
Summary of Product characteristics Summary of Product characteristics Slovenian 16-11-2020
Public Assessment Report Public Assessment Report Slovenian 29-04-2013
Patient Information leaflet Patient Information leaflet Finnish 16-11-2020
Public Assessment Report Public Assessment Report Finnish 29-04-2013
Patient Information leaflet Patient Information leaflet Swedish 16-11-2020
Public Assessment Report Public Assessment Report Swedish 29-04-2013
Patient Information leaflet Patient Information leaflet Norwegian 16-11-2020
Summary of Product characteristics Summary of Product characteristics Norwegian 16-11-2020
Patient Information leaflet Patient Information leaflet Icelandic 16-11-2020
Summary of Product characteristics Summary of Product characteristics Icelandic 16-11-2020
Patient Information leaflet Patient Information leaflet Croatian 16-11-2020

Search alerts related to this product

View documents history