Briviact 50 mg film-coated tablets

Company
UCB (Pharma) Ireland Limited
Active Ingredient
Dosage Form
Film-coated tablet
Legal Category
A - prescription, may not be renewed

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

Licence number Strength ATC Code Dosage Form
EU/1/15/1073/009 50 milligram(s) N03AX, N03AX23 Film-coated tablet
EU/1/15/1073/010 50 milligram(s) N03AX, N03AX23 Film-coated tablet
EU/1/15/1073/011 50 milligram(s) N03AX, N03AX23 Film-coated tablet
EU/1/15/1073/012 50 milligram(s) N03AX, N03AX23 Film-coated tablet
Licence number
EU/1/15/1073/009
Strength
50 milligram(s)
ATC Code
N03AX, N03AX23
Dosage Form
Film-coated tablet
Licence number
EU/1/15/1073/010
Strength
50 milligram(s)
ATC Code
N03AX, N03AX23
Dosage Form
Film-coated tablet
Licence number
EU/1/15/1073/011
Strength
50 milligram(s)
ATC Code
N03AX, N03AX23
Dosage Form
Film-coated tablet
Licence number
EU/1/15/1073/012
Strength
50 milligram(s)
ATC Code
N03AX, N03AX23
Dosage Form
Film-coated tablet

UCB (Pharma) Ireland Limited

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

Telephone
+3531800930075
Email
UCBCares.IE@ucb.com