The U.S. Food and Drug Administration has recalled thousands of bottles of the antidepressant Duloxetine for potentially ...
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 over 7,000 bottles of the antidepressant duloxetine, which is commonly ...
Thousands of bottles of a commonly prescribed antidepressant drug were recalled because they contained a suspected cancer-causing chemical.
according to a notice from the U.S. Food and Drug Administration. The recall involves the medication duloxetine, which is ...
The recall covers more than 7,000 bottles of duloxtine, sold as Cymbalta, due to the presence of nitrosamines.
The Food and Drug Administration (FDA) issued a Class II recall of more than 7,100 bottles of the antidepressant duloxetine ...
The U.S. Food and Drug Administration has recalled thousands of bottles of the antidepressant duloxetine over the presence of ...
The FDA recalled delayed-release capsules of duloxetine because they potentially contain nitrosamine impurities, which can be ...
A pharmaceutical company issued a recall this month for thousands of bottles of duloxetine, a medicine often prescribed to ...
Over 7,000 bottles of the antidepressant medication duloxetine, sold under the brand name Cymbalta, have been recalled, the ...
The drug is sold under the brand name Cymbalta. The Duloxetine Delayed-Release Capsules' voluntary recall began on Oct. 10 after the FDA deemed the medication the second-highest risk classification.