Candesartan Cilexetil Tablets, 16 mg, 30 Tablets (5 x 6) blister pack, Rx, Distributed by: American Health Packaging Columbus, Ohio 43217, NDC 68084-877-25(carton), NDC 68084-877-95(individual dose)
FDA recall notice · announced February 17, 2016 · Amerisource Health Services
Class III FDA/FSIS Class III: use is not likely to cause adverse health consequences.
The product
Candesartan Cilexetil Tablets, 16 mg, 30 Tablets (5 x 6) blister pack, Rx, Distributed by: American Health Packaging Columbus, Ohio 43217, NDC 68084-877-25(carton), NDC 68084-877-95(individual dose)
Reason for recall
Failed Impurities/Degradation Specifications; 9 month stability (manufacturer)
Notes
Distribution: Nationwide
Lot/code information: Lot # 153855, exp 01/2017
Quantity: 716 cartons
Status: Terminated
Products in this recall event:
- Candesartan Cilexetil Tablets, 16 mg, 30 Tablets (5 x 6) blister pack, Rx, Distributed by: American Health Packaging Columbus, Ohio 43217, NDC 68084-877-25(carton), NDC 68084-877-95(individual dose) (D-0660-2016)
Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.