Brintellix 5 mg film-coated tablets

Company
Lundbeck (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/1/13/891/001 5 milligram(s) N06AX26 Film-coated tablet
EU/1/13/891/002 5 milligram(s) N06AX26 Film-coated tablet
EU/1/13/891/003 5 milligram(s) N06AX26 Film-coated tablet
EU/1/13/891/004 5 milligram(s) N06AX26 Film-coated tablet
EU/1/13/891/005 5 milligram(s) N06AX26 Film-coated tablet
EU/1/13/891/006 5 milligram(s) N06AX26 Film-coated tablet
EU/1/13/891/007 5 milligram(s) N06AX26 Film-coated tablet
Licence number
EU/1/13/891/001
Strength
5 milligram(s)
ATC Code
N06AX26
Dosage Form
Film-coated tablet
Licence number
EU/1/13/891/002
Strength
5 milligram(s)
ATC Code
N06AX26
Dosage Form
Film-coated tablet
Licence number
EU/1/13/891/003
Strength
5 milligram(s)
ATC Code
N06AX26
Dosage Form
Film-coated tablet
Licence number
EU/1/13/891/004
Strength
5 milligram(s)
ATC Code
N06AX26
Dosage Form
Film-coated tablet
Licence number
EU/1/13/891/005
Strength
5 milligram(s)
ATC Code
N06AX26
Dosage Form
Film-coated tablet
Licence number
EU/1/13/891/006
Strength
5 milligram(s)
ATC Code
N06AX26
Dosage Form
Film-coated tablet
Licence number
EU/1/13/891/007
Strength
5 milligram(s)
ATC Code
N06AX26
Dosage Form
Film-coated tablet

Lundbeck (Ireland) Limited

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

Telephone
+441908638972
Email
ukinfo@lundbeck.com