Drovelis 3 mg/14.2 mg film-coated tablets

Active Ingredient
Dosage Form
Film-coated tablet
Legal Category
B - prescription, may 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/1/21/1547/001 3 mg / 14.2 mg G03AA18 Film-coated tablet
EU/1/21/1547/002 3 mg / 14.2 mg G03AA18 Film-coated tablet
EU/1/21/1547/003 3 mg / 14.2 mg G03AA18 Film-coated tablet
EU/1/21/1547/004 3 mg / 14.2 mg G03AA18 Film-coated tablet
Licence number
EU/1/21/1547/001
Strength
3 mg / 14.2 mg
ATC Code
G03AA18
Dosage Form
Film-coated tablet
Licence number
EU/1/21/1547/002
Strength
3 mg / 14.2 mg
ATC Code
G03AA18
Dosage Form
Film-coated tablet
Licence number
EU/1/21/1547/003
Strength
3 mg / 14.2 mg
ATC Code
G03AA18
Dosage Form
Film-coated tablet
Licence number
EU/1/21/1547/004
Strength
3 mg / 14.2 mg
ATC Code
G03AA18
Dosage Form
Film-coated tablet

Gedeon Richter Ireland

4045 Kingswood Road, Citywest Business Campus, Dublin 24, Ireland

Telephone
+442076048806