233,000 bottles of duloxetine, the generic name for a popular antidepressant, were recently recalled. Here's what to know about the medication. Hotspots ranked Start the day smarter ☀️ ...

This commonly prescribed medication was also hit with a recall earlier this year...for the same possible cancer-causing ...

More than 233,000 bottles of an antidepressant have been recalled by the FDA due to the presence of duloxetine posing the risk of cancer. Hotspots ranked Start the day smarter ☀️ Funniest cap ...

Towa issued the recall for 7,107 bottles, which covers 500-count bottles of 20mg Duloxetine Delayed-Release Capsules, Lot number: 220128, Exp. Date 12/2024, according to the Oct. 11 Class II recall. 3 ...

More than 233,000 bottles of duloxetine capsules sold by Rising Pharmaceuticals were voluntarily recalled on Nov. 19, and the U.S. Food and Drug Administration assigned the recall as a class II ...

Over 7,100 bottles of Duloxetine were recalled, including 500 delayed-release 20mg capsules. The lot number is 220128, and the expiration date is 12/2024, per the FDA report.

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 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 ...

Some bottles of the antidepressant duloxetine, sold under the brand name Cymbalta, ... The bottles include 500 delayed-release 20mg capsules. The lot number is 220128, ...

The Food and Drug Administration (FDA) issued a Class II recall of more than 7,100 bottles of the antidepressant duloxetine due to the possible presence of a carcinogen. Duloxetine belongs to a ...