Sun Pharma Recalls 41,000 Bottles of Antidepressant in U.S.

Jul 11, 2014


According to a Reuters article, India's Sun Pharmaceutical Industries Ltd. is recalling 41,127 bottles of antidepressant venlafaxine hydrochloride in the United States after the drug failed to dissolve properly, the U.S. Food and Drug Administration said.

"Stability results found the product did not meet the drug release dissolution specifications," the FDA commented in a post on its website. Read the full story