Apotex Corp. recalls Candesartan Cilexetil and Hydrochlorothiazide Tablets 32 mg/12.5 mg, 90 count bottles, Rx only, Manufactured by: Apotex
Recalled September 24, 2014 · FDA recall D-1570-2014 · Apotex
Hazard
Failed Impurity/Degradation Specification; high out of specification for CAD II degradant · FDA Class III
Units
1,494 bottles
Sold at
Nationwide
Description
Failed Impurity/Degradation Specification; high out of specification for CAD II degradant
Product
Candesartan Cilexetil and Hydrochlorothiazide Tablets 32 mg/12.5 mg, 90 count bottles, Rx only, Manufactured by: Apotex Research Pvt. Ltd. Bangalore - 560 099, India NDC 60505-3759-9
Manufacturer(s)
Apotex Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →