FDAFDA · Food and drugs·Recall number D-1570-2014
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
Published September 24, 2014 · Recall initiated: August 21, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Impurity/Degradation Specification; high out of specification for CAD II degradant
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Apotex Corp.
- Distributor
- Nationwide
- Lot
- Lot # KK6086, exp 03/2015, UPC 360505375998.
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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