Memantine LEK
Maa: Euroopan unioni
Kieli: tanska
Lähde: EMA (European Medicines Agency)
Pakkausseloste
(PIL)
16-11-2020
Valmisteyhteenveto
(SPC)
16-11-2020
Julkisesta arviointikertomuksesta
(PAR)
29-04-2013
Aktiivinen ainesosa:
memantinhydrochlorid
Saatavilla:
Pharmathen S.A.
ATC-koodi:
N06DX01
INN (Kansainvälinen yleisnimi):
memantine
Terapeuttinen ryhmä:
Psychoanaleptics, , Andre demensmedicin
Terapeuttinen alue:
Alzheimers sygdom
Käyttöaiheet:
Behandling af patienter med moderat til svær Alzheimers sygdom.
Tuoteyhteenveto:
Revision: 5
Valtuutuksen tilan:
autoriseret
Valtuutus päivämäärä:
2013-04-21
Pakkausseloste
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Valmisteyhteenveto
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.
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© 1995-2020 European Medicines Agency
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An agency of the European Union [European Union flag]
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