Renagel 800 mg film-coated tablets

Company
SANOFI
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/1/99/123/008 800 milligram(s) V03AE, V03AE02 Film-coated tablet
EU/1/99/123/009 800 milligram(s) V03AE, V03AE02 Film-coated tablet
EU/1/99/123/010 800 milligram(s) V03AE, V03AE02 Film-coated tablet
EU/1/99/123/011 800 milligram(s) V03AE, V03AE02 Film-coated tablet
EU/1/99/123/012 800 milligram(s) V03AE, V03AE02 Film-coated tablet
EU/1/99/123/013 800 milligram(s) V03AE, V03AE02 Film-coated tablet
Licence number
EU/1/99/123/008
Strength
800 milligram(s)
ATC Code
V03AE, V03AE02
Dosage Form
Film-coated tablet
Licence number
EU/1/99/123/009
Strength
800 milligram(s)
ATC Code
V03AE, V03AE02
Dosage Form
Film-coated tablet
Licence number
EU/1/99/123/010
Strength
800 milligram(s)
ATC Code
V03AE, V03AE02
Dosage Form
Film-coated tablet
Licence number
EU/1/99/123/011
Strength
800 milligram(s)
ATC Code
V03AE, V03AE02
Dosage Form
Film-coated tablet
Licence number
EU/1/99/123/012
Strength
800 milligram(s)
ATC Code
V03AE, V03AE02
Dosage Form
Film-coated tablet
Licence number
EU/1/99/123/013
Strength
800 milligram(s)
ATC Code
V03AE, V03AE02
Dosage Form
Film-coated tablet

SANOFI

Citywest Business Campus, Dublin 24, Ireland, 24 Dublin

Email
iemedinfo@sanofi.com