Over 7,100 bottles of Duloxetine were recalled, including 500 delayed-release 20mg capsules. The lot number is 220128, and ...

The recall involves 7,101 bottles of duloxetine delayed-release capsules distributed nationwide within the United States, according to the FDA. The recalled capsules are 20mg in strength ...

The recall, announced on October 10, affects only 20 mg Duloxetine Delayed-Release Capsules made by Towa Pharmaceutical Europe, targeting over 7,100 bottles with lot number 220128 and an ...

N-nitroso-duloxetine is toxic if swallowed and suspected of causing cancer, according to the National Library of Medicine. The recalled capsules are 20mg in strength and sold in 500-count bottles.

The recall involves 7,101 bottles of duloxetine delayed-release capsules distributed nationwide within the United States, according to the FDA. The recalled capsules are 20mg in strength, and sold in ...

The U.S. Food and Drug Administration (FDA) has been forced to recall thousands of bottles of the antidepressant medication ...

of Connecticut, according to a recall notice. They were prescribed in 20mg delayed-release capsules, in 500-count bottles. Duloxetine may also be recognized by other brand names, including ...