Sun Pharma Global Inc. recalls Venlafaxine Hydrochloride Extended-Release Tablets, 37.5 mg, 30-count bottles and 90-count bottles, RX only, Manufacture
Recalled November 12, 2014 · FDA recall D-0236-2015 · Sun Pharma Global
Hazard
Failed Dissolution Specifications; 12 month stability time point · FDA Class II
Units
68194
Sold at
Nationwide and Puerto Rico
Description
Failed Dissolution Specifications; 12 month stability time point
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
Manufacturer(s)
Sun Pharma Global Inc.
Made in
United Arab Emirates
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →