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

Recall date

July 21, 2015

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D1834-2015

FDA classification

Class III

Brand / firm

Apotex Inc.

Sold / distributed

Nationwide and Puerto Rico

Why it was recalled

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

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

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.