Drug recall D-0469-2021
Product
PREGABALIN CAPSULES 300MG 90 ; NDC 43598-298-90; RX; CAPSULES
Reason for recall
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots and codes
T2000309
Recall details
- Recalling firm
- Cardinal Health Inc., Dublin, OH
- Quantity
- 6 CONTAINERS
- Distribution
- FL, GA, SC
- Type
- Voluntary: Firm initiated
- Recall initiated
- March 15, 2021
- Terminated
- June 17, 2024
Related products
- Pregabalin – drug information
- NDC 43598-295 Pregabalin · Pregabalin 150 mg/1 · Dr.Reddys Laboratories Inc
- NDC 43598-294 Pregabalin · Pregabalin 100 mg/1 · Dr.Reddys Laboratories Inc
- NDC 43598-293 Pregabalin · Pregabalin 75 mg/1 · Dr.Reddys Laboratories Inc
- NDC 43598-292 Pregabalin · Pregabalin 50 mg/1 · Dr.Reddys Laboratories Inc
- NDC 43598-297 Pregabalin · Pregabalin 225 mg/1 · Dr.Reddys Laboratories Inc
- NDC 43598-296 Pregabalin · Pregabalin 200 mg/1 · Dr.Reddys Laboratories Inc
- NDC 43598-291 Pregabalin · Pregabalin 25 mg/1 · Dr.Reddys Laboratories Inc
- NDC 43598-298 Pregabalin · Pregabalin 300 mg/1 · Dr.Reddys Laboratories Inc