Memantine Sandoz 20 mg film-coat. tabl.

Country: Belgium

Language: English

Source: AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

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Active ingredient:

Memantine Hydrochloride 20 mg - Eq. Memantine 16,62 mg

Available from:

Sandoz SA-NV

ATC code:

N06DX01

Pharmaceutical form:

Film-coated tablet

Administration route:

Oral use

Therapeutic area:

Memantine

Product summary:

CTI Extended: 439196-06; 439196-03; 439196-02; 439196-01; 439196-05; 439196-04; 439196-09; 439196-08; 439196-07; 439196-12; 439196-11; 439196-10; 439196-15; 439196-14; 439196-25; 439196-23; 439196-21; 439196-20; 439196-26; 439196-13; 439196-19; 439196-18; 439196-17; 439196-16; 439196-24; 439196-22; 439196-29; 439196-27; 439196-28

Authorization status:

Commercialised: No

Authorization date:

2013-06-13

Documents in other languages

Patient Information leaflet Patient Information leaflet German 01-07-2022
Patient Information leaflet Patient Information leaflet French 01-07-2022
RMP RMP French 10-11-2022
Patient Information leaflet Patient Information leaflet Dutch 01-07-2022
RMP RMP Dutch 10-11-2022