Recalls / Active ingredient / Pregabalin
Pregabalin
5 FDA drug recalls involving the active ingredient “Pregabalin”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2024-05-16 | Class III | Pregabalin Capsules 50mg, 1000-count bottle, Rx Only, Manufactured for: Rising Pharma Holdings, Inc., East Bru | Rising Pharma Holding, Inc. |
| 2021-10-22 | Class II | Pregabalin Capsules, 50 mg, 100 count bottle, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cr | SUN PHARMACEUTICAL INDUSTRIES INC |
| 2021-03-15 | Class II | PREGABALIN CAPSULES 300MG 90 ; NDC 43598-298-90; RX; CAPSULES | Cardinal Health Inc. |
| 2016-01-11 | Class II | Lyrica (pregabalin) capsules, 75 mg, 90-count bottle, Rx only, Distributed by: Parke-Davis, Division of Pfizer | Pfizer Inc. |
| 2016-01-11 | Class II | Lyrica (pregabalin) capsules, 50 mg, 90-count bottle, Rx only, Distributed by: Parke-Davis, Division of Pfizer | Pfizer Inc. |