Keppra 500 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/1/00/146/006 500 Milligram N03AX14 Film-coated tablet
EU/1/00/146/007 500 Milligram N03AX14 Film-coated tablet
EU/1/00/146/008 500 Milligram N03AX14 Film-coated tablet
EU/1/00/146/009 500 Milligram N03AX14 Film-coated tablet
EU/1/00/146/010 500 Milligram N03AX14 Film-coated tablet
EU/1/00/146/011 500 Milligram N03AX14 Film-coated tablet
EU/1/00/146/012 500 Milligram N03AX14 Film-coated tablet
EU/1/00/146/013 500 Milligram N03AX14 Film-coated tablet
Licence number
EU/1/00/146/006
Strength
500 Milligram
ATC Code
N03AX14
Dosage Form
Film-coated tablet
Licence number
EU/1/00/146/007
Strength
500 Milligram
ATC Code
N03AX14
Dosage Form
Film-coated tablet
Licence number
EU/1/00/146/008
Strength
500 Milligram
ATC Code
N03AX14
Dosage Form
Film-coated tablet
Licence number
EU/1/00/146/009
Strength
500 Milligram
ATC Code
N03AX14
Dosage Form
Film-coated tablet
Licence number
EU/1/00/146/010
Strength
500 Milligram
ATC Code
N03AX14
Dosage Form
Film-coated tablet
Licence number
EU/1/00/146/011
Strength
500 Milligram
ATC Code
N03AX14
Dosage Form
Film-coated tablet
Licence number
EU/1/00/146/012
Strength
500 Milligram
ATC Code
N03AX14
Dosage Form
Film-coated tablet
Licence number
EU/1/00/146/013
Strength
500 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