Recalls / Active ingredient / Desloratadine
Desloratadine
1 FDA drug recall involving the active ingredient “Desloratadine”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2023-12-20 | Class II | Desloratadine Tablets USP 5mg a) 100 count (NDC 68180-153-01) and b) 500 count (NDC 68180-153-02) bottles, Rx | Lupin Pharmaceuticals Inc. |