Briviact 10 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/1/15/1073/001 10 milligram(s) N03AX, N03AX23 Film-coated tablet
EU/1/15/1073/002 10 milligram(s) N03AX, N03AX23 Film-coated tablet
EU/1/15/1073/003 10 milligram(s) N03AX, N03AX23 Film-coated tablet
EU/1/15/1073/004 10 milligram(s) N03AX, N03AX23 Film-coated tablet
Licence number
EU/1/15/1073/001
Strength
10 milligram(s)
ATC Code
N03AX, N03AX23
Dosage Form
Film-coated tablet
Licence number
EU/1/15/1073/002
Strength
10 milligram(s)
ATC Code
N03AX, N03AX23
Dosage Form
Film-coated tablet
Licence number
EU/1/15/1073/003
Strength
10 milligram(s)
ATC Code
N03AX, N03AX23
Dosage Form
Film-coated tablet
Licence number
EU/1/15/1073/004
Strength
10 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