A Duloxetine recall by the FDA has flagged more than 7,100 bottles of the Cymbalta generic drug due to a cancerous chemical.

The U.S. Food and Drug Administration has recalled over 7,000 bottles of the antidepressant duloxetine, which is commonly ...

Some bottles of the antidepressant duloxetine, sold under the brand name Cymbalta, were recalled due to the presence of a ...

The U.S. Food and Drug Administration has recalled thousands of bottles of the antidepressant Duloxetine for potentially ...

Over 7,000 bottles of the antidepressant medication duloxetine, sold under the brand name Cymbalta, have been recalled, the ...

The U.S. Food and Drug Administration has recalled thousands of bottles of the antidepressant duloxetine over the presence of ...

Thousands of bottles of a popular antidepressant medication are being recalled due to the presence of what the National ...

The FDA recalled delayed-release capsules of duloxetine because they contain nitrosamines, which are everywhere but can be ...

The U.S. Food and Drug Administration (FDA) has announced a substantial recall of duloxetine, the generic form of the widely ...

The Food and Drug Administration (FDA) issued a Class II recall of more than 7,100 bottles of the antidepressant duloxetine ...

The recall was initiated due to the discovery of N-nitroso-duloxetine, a chemical impurity classified as a nitrosamine.

Thousands of bottles of a commonly prescribed antidepressant drug were recalled because they contained a suspected cancer-causing chemical.