Divalproex Sodium Delayed Release Tablets, USP, 500 mg, a) 100 count (NDC 68382-033-01) and b) 500 count (NDC 68382-033-05) bottles, Rx only, manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ
Recall Number: D-0617-2017
Firm: Zydus Pharmaceuticals USA Inc
Classification: Class II
Status: Terminated
Report Date: 20170405
Initiation Date: 20170315
Termination Date: 20200910
Reason for Recall
Failed Dissolution Specifications; 9 month long term stability
Product Description
Divalproex Sodium Delayed Release Tablets, USP, 500 mg, a) 100 count (NDC 68382-033-01) and b) 500 count (NDC 68382-033-05) bottles, Rx only, manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ