Recalls / Active ingredient / Nebivolol Hydrochloride
Nebivolol Hydrochloride
3 FDA drug recalls involving the active ingredient “Nebivolol Hydrochloride”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2025-11-18 | Class III | Nebivolol Tablets, 20 mg, 90 Tablets, Rx Only, Manufactured by: Glenmark Pharmaceuticals Limited, Pithampur, M | Glenmark Pharmaceuticals Inc., USA |
| 2024-12-06 | Class II | Nebivolol Tablets, 2.5. mg, 30-count bottles, Rx only, Distributed by: Aurobindo Pharma USA, Inc., 279 Princet | Aurobindo Pharma USA Inc |
| 2014-05-12 | Class II | Bystolic (nebivolol), 20 mg/tablet, 30 tablets per bottle, Rx only, Licensed from Mylan Laboratories Inc., Und | Forest Pharmaceuticals Inc |