The FDA recently announced a recall of over 7,000 bottles of duloxetine after detecting elevated levels of ...
The U.S. Food and Drug Administration (FDA) has issued a nationwide recall of thousands of bottles of antidepressants. These ...
The U.S. Food and Drug Administration is urging patients not to stop taking their prescribed medication if it falls under the ...
The recall of the Duloxetine Delayed-Release Capsules, produced by Towa Pharmaceutical Europe, was initiated on October 10 and has been given the second highest risk classification by the FDA.