Diamilla 75 microgram film-coated tablets
Recall
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Medicines
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24/10/2016
The marketing authorization holder informed its supplied customers in a letter dated October 12, 2016, that an impurity, "lmpurity D", was detected in the course of stability tests, which in the measured concentration does not indicate any health risk for patients. A recall of the above mentioned batches will be carried out on wholesale level.
| Name of the medicinal product | Diamilla 75 Mikrogramm Filmtabletten |
|---|---|
| Marketing authorisation number(s) | 1-30055 |
| Marketing authorisation holder | Actavis Group |
| Batch number(s) | 3DX167B, 4DX103C, 5DX123AC 3DX167C, 3DX168A, 5DX073AA |
| Classification of the recall | 2 |
| BASG reference number | INS-640.001-1864 |
Further inquiry note
Page last modified:
12/07/2022