Ebixa 20 mg film-coated tablets

Active Ingredient
Strength
  • Memantine hydrochloride: 20 mg
Dosage Form
Film-coated tablet
Legal Category
A - prescription, may not be renewed
Last Updated
25/09/2026
Licence Info section shown.
Licence numbers with strength, ATC code and dosage form
Licence number Strength ATC Code Dosage Form
EU/1/02/219/023 20 mg N06DX01 Film-coated tablet
EU/1/02/219/024 20 mg N06DX01 Film-coated tablet
EU/1/02/219/025 20 mg N06DX01 Film-coated tablet
EU/1/02/219/026 20 mg N06DX01 Film-coated tablet
EU/1/02/219/027 20 mg N06DX01 Film-coated tablet
EU/1/02/219/028 20 mg N06DX01 Film-coated tablet
EU/1/02/219/029 20 mg N06DX01 Film-coated tablet
EU/1/02/219/030 20 mg N06DX01 Film-coated tablet
EU/1/02/219/031 20 mg N06DX01 Film-coated tablet
EU/1/02/219/032 20 mg N06DX01 Film-coated tablet
EU/1/02/219/033 20 mg N06DX01 Film-coated tablet
EU/1/02/219/034 20 mg N06DX01 Film-coated tablet
EU/1/02/219/035 20 mg N06DX01 Film-coated tablet
Licence number
EU/1/02/219/023
Strength
20 mg
ATC Code
N06DX01
Dosage Form
Film-coated tablet
Licence number
EU/1/02/219/024
Strength
20 mg
ATC Code
N06DX01
Dosage Form
Film-coated tablet
Licence number
EU/1/02/219/025
Strength
20 mg
ATC Code
N06DX01
Dosage Form
Film-coated tablet
Licence number
EU/1/02/219/026
Strength
20 mg
ATC Code
N06DX01
Dosage Form
Film-coated tablet
Licence number
EU/1/02/219/027
Strength
20 mg
ATC Code
N06DX01
Dosage Form
Film-coated tablet
Licence number
EU/1/02/219/028
Strength
20 mg
ATC Code
N06DX01
Dosage Form
Film-coated tablet
Licence number
EU/1/02/219/029
Strength
20 mg
ATC Code
N06DX01
Dosage Form
Film-coated tablet
Licence number
EU/1/02/219/030
Strength
20 mg
ATC Code
N06DX01
Dosage Form
Film-coated tablet
Licence number
EU/1/02/219/031
Strength
20 mg
ATC Code
N06DX01
Dosage Form
Film-coated tablet
Licence number
EU/1/02/219/032
Strength
20 mg
ATC Code
N06DX01
Dosage Form
Film-coated tablet
Licence number
EU/1/02/219/033
Strength
20 mg
ATC Code
N06DX01
Dosage Form
Film-coated tablet
Licence number
EU/1/02/219/034
Strength
20 mg
ATC Code
N06DX01
Dosage Form
Film-coated tablet
Licence number
EU/1/02/219/035
Strength
20 mg
ATC Code
N06DX01
Dosage Form
Film-coated tablet

Lundbeck (Ireland) Limited

4045 Kingswood Road, Citywest Business Park, Co Dublin, Ireland

Telephone
+441908638972