drugs Class II Updated 2014-11-12

Sun Pharma Global Inc. recalls Venlafaxine Hydrochloride Extended-Release Tablets, 37.5 mg,

Recalled Product

Venlafaxine Hydrochloride Extended-Release Tablets, 37.5 mg, 30-count bottles and 90-count bottles, RX only, Manufactured for Sun Pharma Global Inc. Dubai, United Arab Emirates by Sun Pharmaceutical Industries Limited, Halol, India

Hazard / Issue

Failed Dissolution Specifications; 12 month stability time point

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Batch Number: JKM3855A Mfg. Date: 06/25/2013 Exp. Date: 05/31/2015 Batch Number: JKM3855B Mfg. Date: 06/25/2013 Exp. Date: 05/31/2015 Batch Number: JKM7265A Mfg. Date: 12/25/2013 Exp. Date: 11/30/2015 Batch Number: JKM7265B Mfg. Date: 12/25/2013 Exp. Date: 11/30/2015
View official government recall

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