Ludiomil - Filmtabletten New
Recall
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Medicines
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26/06/2025
The marketing authorisation holder informed its customers on June 26, 2025, that the nitrosamine quantities in the batches mentioned may be above the permitted acceptable daily dose. For this reason, these batches are being recalled as a precautionary measure.
| Name of the medicinal product | 1) Ludiomil 25 mg – Filmtabletten 2) Ludiomil 50 mg - Filmtabletten 3) Ludiomil 75 mg - Filmtabletten |
|---|---|
| Marketing authorisation number(s) | 1) 15240 2) 15241 3) 16036 |
| CIP code | 1) 0533191 2) 0116004 3) 0193513 |
| Marketing authorisation holder | Amdipharm Limited |
| Distributor | Movianto Deutschland GmbH |
| Batch number(s) | Batch, Expiry Date F0016, 05/2026 F0012, 11/2026 F0018, 03/2026 |
| Classification of the recall | 2 |
| Depth of recall | Pharmacies |
| BASG reference number | INS-640.001-5217 |
Further inquiry note
Page last modified:
26/06/2025