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Apotex Inc. recalls Verapamil Hydrochloride Extended-Release tablets, USP, 240 mg, 500-count bottles, Rx Only, Apotex Corp. Manufactured by

Recalled October 7, 2015 · FDA recall D1834-2015 · Apotex

Hazard
Failed Dissolution Specification: One lot of product did not meet the first stage dissolution specification limits. · FDA Class III
Units
2,075 bottles
Sold at
Nationwide and Puerto Rico

Description

Failed Dissolution Specification: One lot of product did not meet the first stage dissolution specification limits.

Product
Verapamil Hydrochloride Extended-Release tablets, USP, 240 mg, 500-count bottles, Rx Only, Apotex Corp. Manufactured by Apotex Research Private Limited, Bangalore, Karnataka 560 099, India; Manufactured for: Apotex Corp., Weston, FL 33326. NDC 60505-2742-5.
Manufacturer(s)
Apotex Inc.
Made in
Canada

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →

Apotex Inc. recalls Verapamil Hydrochloride Extended-Release tablets, USP, 240 mg, 500-count bottles, Rx Only, Apotex Corp. Manufactured by | RecallWatchUSA