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FDAFDA · Food and drugs·Recall number D-0243-2015

Candesartan Cilexetil Tablets, 16 mg, a) 30-count bottle (NDC 60505-3620-3) b) 90-count bottles (NDC 60505-3620-9) Rx Only, Manufactured by Apotex Research Pvt. Ltd., Bangalore- 560 099, India, Manufactured for Apotex Corp., Weston, FL 33326

Published November 12, 2014 · Recall initiated: October 16, 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 Impurities/Degradation Specifications: Out of specification (OOS) results were observed for CAD-II, CAD-V and Total Impurities.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Apotex Inc.
Distributor
Nationwide.
Lot
Lot #: a) KR3943; Exp. 11/15 Lot #: b) KT6058, KT6060; Exp. Date 11/15
Risk classification
Class III
Area (FDA)
drug
Country
Canada

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