Xarelto 20 mg film-coated tablets

Company
Bayer Limited
Active Ingredient
Dosage Form
Film-coated tablet
Legal Category
B - prescription, may be renewed
Date of revision
06/2024

*Additional information is available within the SPC or upon request to the company

Licence number Strength ATC Code Dosage Form
EU/1/08/472/017 20 milligram(s) B01AF, B01AF01 Film-coated tablet
EU/1/08/472/018 20 milligram(s) B01AF, B01AF01 Film-coated tablet
EU/1/08/472/019 20 milligram(s) B01AF, B01AF01 Film-coated tablet
EU/1/08/472/020 20 milligram(s) B01AF, B01AF01 Film-coated tablet
EU/1/08/472/021 20 milligram(s) B01AF, B01AF01 Film-coated tablet
Licence number
EU/1/08/472/017
Strength
20 milligram(s)
ATC Code
B01AF, B01AF01
Dosage Form
Film-coated tablet
Licence number
EU/1/08/472/018
Strength
20 milligram(s)
ATC Code
B01AF, B01AF01
Dosage Form
Film-coated tablet
Licence number
EU/1/08/472/019
Strength
20 milligram(s)
ATC Code
B01AF, B01AF01
Dosage Form
Film-coated tablet
Licence number
EU/1/08/472/020
Strength
20 milligram(s)
ATC Code
B01AF, B01AF01
Dosage Form
Film-coated tablet
Licence number
EU/1/08/472/021
Strength
20 milligram(s)
ATC Code
B01AF, B01AF01
Dosage Form
Film-coated tablet

Bayer Limited

1st Floor The Grange Offices, The Grange, Brewery Road, Stillorgan, Co. Dublin, A94 H2K7, Ireland

Telephone
+35312163300
Email
Medinfo.ireland@bayer.com