Vantobra
Recall
|
Medicines
|
21/02/2019
The marketing authorisation holder informed its customers on February 19, 2019 that the marketing authorisation of „Vantobra 170 mg Lösung für einen Vernebler“ will be withdrawn. Therefore all batches within shelf-life are recalled as a precautionary measure. The withdrawal of the marketing authorisation is not based on safety-related issues and a new marketing authorisation will be granted.
| Name of the medicinal product | Vantobra 170 mg Lösung für einen Vernebler |
|---|---|
| Marketing authorisation number(s) | EU/1/14/932/001 |
| Marketing authorisation holder | Pari Pharma GmbH |
| Batch number(s) | Alle Chargen |
| Classification of the recall | 3 |
| BASG reference number | INS - 640.001 - 2744 |
Further inquiry note
Page last modified:
07/11/2019