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.
Reported: October 7, 2015 Initiated: July 21, 2015 #D1834-2015
Product Description
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.
Reason for Recall
Failed Dissolution Specification: One lot of product did not meet the first stage dissolution specification limits.
Details
- Recalling Firm
- Apotex Inc.
- Units Affected
- 2,075 bottles
- Distribution
- Nationwide and Puerto Rico
- Location
- Toronto, Ontario
Frequently Asked Questions
What product 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.. Recalled by Apotex Inc.. Units affected: 2,075 bottles.
Why was this product recalled? ▼
Failed Dissolution Specification: One lot of product did not meet the first stage dissolution specification limits.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 7, 2015. Severity: Low. Recall number: D1834-2015.
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