Zejula 100 mg film-coated tablets
Licence Info section shown.
| Licence number | Strength | ATC Code | Dosage Form |
|---|---|---|---|
| EU/1/17/1235/004 | 100 mg | L01XK02 | Film-coated tablet |
| EU/1/17/1235/005 | 100 mg | L01XK02 | Film-coated tablet |
| EU/1/17/1235/006 | 100 mg | L01XK02 | Film-coated tablet |
| EU/1/17/1235/007 | 100 mg | L01XK02 | Film-coated tablet |
- Licence number
- EU/1/17/1235/004
- Strength
- 100 mg
- ATC Code
- L01XK02
- Dosage Form
- Film-coated tablet
- Licence number
- EU/1/17/1235/005
- Strength
- 100 mg
- ATC Code
- L01XK02
- Dosage Form
- Film-coated tablet
- Licence number
- EU/1/17/1235/006
- Strength
- 100 mg
- ATC Code
- L01XK02
- Dosage Form
- Film-coated tablet
- Licence number
- EU/1/17/1235/007
- Strength
- 100 mg
- ATC Code
- L01XK02
- Dosage Form
- Film-coated tablet
GlaxoSmithKline (Ireland) Ltd
12 Riverwalk, Citywest Business Campus, Dublin 24, Ireland, D24 Dublin
- Telephone
- +3531800244255