VANFLYTA 17.7 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/1/23/1768/001 17.7 mg L01EX11 Film-coated tablet
EU/1/23/1768/002 17.7 mg L01EX11 Film-coated tablet
Licence number
EU/1/23/1768/001
Strength
17.7 mg
ATC Code
L01EX11
Dosage Form
Film-coated tablet
Licence number
EU/1/23/1768/002
Strength
17.7 mg
ATC Code
L01EX11
Dosage Form
Film-coated tablet

Daiichi Sankyo Ireland Ltd

Unit 29, Block 3, Northwood Court, Northwood Avenue, Santry, Dublin 9, Ireland