The U.S. Food and Drug Administration has recalled over 7,000 bottles of the antidepressant duloxetine, which is commonly sold under the name Cymbalta. According to the FDA, the drug was recalled ...

The U.S. Food and Drug Administration announced a Class II recall for more than 7,100 bottles of Duloxetine — a generic antidepressant for Cymbalta — due to a cancerous chemical. A voluntary ...

But Cymbalta is approved to treat other conditions as well. They also belong to different drug classes, have slightly ...

Opens in a new tab or window Over 7,000 bottles of the antidepressant duloxetine (Cymbalta) were recalled ... of the investigational schizophrenia drug ANAVEX3-71 showed dose-dependent ...

The U.S. Food and Drug Administration announced a Class II recall for more than 7,100 bottles of Duloxetine — a generic antidepressant for Cymbalta — due to a cancerous chemical. A voluntary ...

The voluntary recall for 7,107 bottles of the generic form of Cymbalta, known as Duloxetine, was initiated on Oct. 10 by Breckenridge Pharmaceutical Inc. The recall lot was #220128, expiring in ...

More than 7,000 bottles of the duoxetine antidepressant drug Cymbalta, have been removed from shelves after the U.S. Food and Drug Administration (FDA) detected elevated levels of N-nitroso ...

a generic form of the popular antidepressant Cymbalta. The recall was initiated due to the discovery of N-nitroso-duloxetine, a chemical impurity classified as a nitrosamine. Nitrosamines are ...

Thousands of bottles of the antidepressant medication duloxetine have been recalled, according to the Food and Drug Administration. The medication, sold under the brand name Cymbalta, contains a ...