XELJANZ 10 mg film-coated tablets

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 Info section shown.
Licence numbers with strength, ATC code and dosage form
Licence number Strength ATC Code Dosage Form
EU/1/17/1178/005 10 milligram(s) L04AF01 Film-coated tablet
EU/1/17/1178/006 10 milligram(s) L04AF01 Film-coated tablet
EU/1/17/1178/007 10 milligram(s) L04AF01 Film-coated tablet
EU/1/17/1178/008 10 milligram(s) L04AF01 Film-coated tablet
EU/1/17/1178/009 10 milligram(s) L04AF01 Film-coated tablet
Licence number
EU/1/17/1178/005
Strength
10 milligram(s)
ATC Code
L04AF01
Dosage Form
Film-coated tablet
Licence number
EU/1/17/1178/006
Strength
10 milligram(s)
ATC Code
L04AF01
Dosage Form
Film-coated tablet
Licence number
EU/1/17/1178/007
Strength
10 milligram(s)
ATC Code
L04AF01
Dosage Form
Film-coated tablet
Licence number
EU/1/17/1178/008
Strength
10 milligram(s)
ATC Code
L04AF01
Dosage Form
Film-coated tablet
Licence number
EU/1/17/1178/009
Strength
10 milligram(s)
ATC Code
L04AF01
Dosage Form
Film-coated tablet

Pfizer Healthcare Ireland Unlimited Company

The Watermarque Building, Ringsend Road, Dublin 4, D04 K7N3, Ireland, D04 K7N3 Dublin

Telephone
+3531800633363