Recalls / Active ingredient / Voriconazole
Voriconazole
4 FDA drug recalls involving the active ingredient “Voriconazole”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2025-03-24 | Class II | Voriconazole Tablets, 50 mg, packaged in cartons of 3 blister cards with 10 individual blistered doses (30 Uni | Amerisource Health Services LLC |
| 2025-03-13 | Class II | Voriconazole Tablets 50mg, 30-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pitham | Glenmark Pharmaceuticals Inc., USA |
| 2025-03-13 | Class II | Voriconazole Tablets 200 mg, 30-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pith | Glenmark Pharmaceuticals Inc., USA |
| 2024-02-05 | Class II | Voriconazole for Oral Suspension, 40mg/mL, Orange-Flavored, 49g/75mL when reconstituted. Mixing Directions: Ta | Lupin Pharmaceuticals Inc. |