Keppra 750 mg film-coated tablets

Active Ingredient
Dosage Form
Film-coated tablet
Legal Category
B - prescription, may be renewed

*further information is available on request to the holder of the authorisation or in the SPC

Licence Info section shown.
Licence numbers with strength, ATC code and dosage form
Licence number Strength ATC Code Dosage Form
EU/1/00/146/014 750 Milligram N03AX14 Film-coated tablet
EU/1/00/146/015 750 Milligram N03AX14 Film-coated tablet
EU/1/00/146/016 750 Milligram N03AX14 Film-coated tablet
EU/1/00/146/017 750 Milligram N03AX14 Film-coated tablet
EU/1/00/146/018 750 Milligram N03AX14 Film-coated tablet
EU/1/00/146/019 750 Milligram N03AX14 Film-coated tablet
Licence number
EU/1/00/146/014
Strength
750 Milligram
ATC Code
N03AX14
Dosage Form
Film-coated tablet
Licence number
EU/1/00/146/015
Strength
750 Milligram
ATC Code
N03AX14
Dosage Form
Film-coated tablet
Licence number
EU/1/00/146/016
Strength
750 Milligram
ATC Code
N03AX14
Dosage Form
Film-coated tablet
Licence number
EU/1/00/146/017
Strength
750 Milligram
ATC Code
N03AX14
Dosage Form
Film-coated tablet
Licence number
EU/1/00/146/018
Strength
750 Milligram
ATC Code
N03AX14
Dosage Form
Film-coated tablet
Licence number
EU/1/00/146/019
Strength
750 Milligram
ATC Code
N03AX14
Dosage Form
Film-coated tablet

UCB (Pharma) Ireland Limited

United Drug House, Magna Drive, Magna Business Park, Citywest Road, Dublin 24, Ireland

Telephone
+3531800930075