Renvela 800 mg film-coated tablets

Company
SANOFI
Active Ingredient
Dosage Form
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/1/09/521/1 800 milligram(s) A06AX, A06AX05 Tablet
EU/1/09/521/2 800 milligram(s) A06AX, A06AX05 Tablet
EU/1/09/521/3 800 milligram(s) A06AX, A06AX05 Tablet
Licence number
EU/1/09/521/1
Strength
800 milligram(s)
ATC Code
A06AX, A06AX05
Dosage Form
Tablet
Licence number
EU/1/09/521/2
Strength
800 milligram(s)
ATC Code
A06AX, A06AX05
Dosage Form
Tablet
Licence number
EU/1/09/521/3
Strength
800 milligram(s)
ATC Code
A06AX, A06AX05
Dosage Form
Tablet

SANOFI

Citywest Business Campus, Dublin 24, Ireland, 24 Dublin