Olanzapine Viatris 15 mg film-coated tablets

Company
Viatris 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/1/08/475/25 15 milligram(s) C09DB02, N05AH, N05AH03 Film-coated tablet
EU/1/08/475/26 15 milligram(s) C09DB02, N05AH, N05AH03 Film-coated tablet
EU/1/08/475/27 15 milligram(s) C09DB02, N05AH, N05AH03 Film-coated tablet
EU/1/08/475/28 15 milligram(s) C09DB02, N05AH, N05AH03 Film-coated tablet
EU/1/08/475/29 15 milligram(s) C09DB02, N05AH, N05AH03 Film-coated tablet
Licence number
EU/1/08/475/25
Strength
15 milligram(s)
ATC Code
C09DB02, N05AH, N05AH03
Dosage Form
Film-coated tablet
Licence number
EU/1/08/475/26
Strength
15 milligram(s)
ATC Code
C09DB02, N05AH, N05AH03
Dosage Form
Film-coated tablet
Licence number
EU/1/08/475/27
Strength
15 milligram(s)
ATC Code
C09DB02, N05AH, N05AH03
Dosage Form
Film-coated tablet
Licence number
EU/1/08/475/28
Strength
15 milligram(s)
ATC Code
C09DB02, N05AH, N05AH03
Dosage Form
Film-coated tablet
Licence number
EU/1/08/475/29
Strength
15 milligram(s)
ATC Code
C09DB02, N05AH, N05AH03
Dosage Form
Film-coated tablet

Viatris Limited

Damastown Industrial Park, Mulhuddart, Dublin 15, Dublin, Ireland

Telephone
+353 (0)1 8711600
Email
info.ie@viatris.com