Drug recall D-0593-2021
Product
HALOPERIDOL TABLETS 20mg, USP, 100-count bottle, Rx Only Distributed by: Usher-Smith Laboratories, LLC, Maple Grove, MN 55369, NDC: 0832-1560-11
Reason for recall
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots and codes
2007346C
Recall details
- Recalling firm
- Cardinal Health Inc., Dublin, OH
- Quantity
- 35 BOTTLE
- Distribution
- FL, GA, SC
- Type
- Voluntary: Firm initiated
- Recall initiated
- March 15, 2021
- Terminated
- June 17, 2024
Related products
- Haloperidol – drug information
- NDC 0832-1520 Haloperidol · Haloperidol 1 mg/1 · Upsher-Smith Laboratories, LLC
- NDC 0832-1550 Haloperidol · Haloperidol 10 mg/1 · Upsher-Smith Laboratories, LLC
- NDC 0832-1560 Haloperidol · Haloperidol 20 mg/1 · Upsher-Smith Laboratories, LLC
- NDC 0832-1510 Haloperidol · Haloperidol .5 mg/1 · Upsher-Smith Laboratories, LLC
- NDC 0832-1530 Haloperidol · Haloperidol 2 mg/1 · Upsher-Smith Laboratories, LLC
- NDC 0832-1540 Haloperidol · Haloperidol 5 mg/1 · Upsher-Smith Laboratories, LLC