Buronil 25 mg - Filmtabletten, Buronil 50 mg - Filmtabletten New
Recall
|
Medicines
|
15/05/2025
The marketing authorisation holder informed its customers on May 13, 2025, that the powder used to manufacture the tablets may contain metal particles.
| Name of the medicinal product | 1) Buronil 25 mg - Filmtabletten 2) Buronil 50 mg - Filmtabletten |
|---|---|
| Marketing authorisation number(s) | 1) 14476 2) 17209 |
| CIP code | 1) 0065548 und 0008728 2) 0705775 und 0705781 |
| Marketing authorisation holder | Medilink A/S |
| Manufacturer | Orkla Care A/S |
| Batch number(s) | 1) 747283, 747284 2) 747293, 747294, 747299, 74729A, 74729B, 74729C |
| Expiry date | 04/30/2028 |
| Classification of the recall | 2 |
| Depth of recall | Pharmacies |
| BASG reference number | INS-640.001-5163 |
Further inquiry note
Page last modified:
15/05/2025