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FDA recalls more than 7,000 bottles of antidepressant

FDA recalls duloxetine, antidepressant known as Cymbalta, over possible cancerous chemical

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 because it had the "presence" of N-nitroso-duloxetine, a nitrosamine, which is a chemical that could increase the risk of cancer.

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FDA Has Recalled Thousands of Bottles of Antidepressant Duloxetine, Sold Under Brand Name Cymbalta: Here’s Why

The Duloxetine Delayed-Release Capsules' voluntary recall began on Oct. 10 after the FDA deemed the medication the second-highest risk classification. 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.

Verywell Health on MSN · 20h

Over 7,000 Bottles of Antidepressant Recalled Over Cancer Risk

The recall covers more than 7,000 bottles of duloxtine, sold as Cymbalta, due to the presence of nitrosamines.

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Thousands of Antidepressant Bottles Were Recalled Over 'Impurity' Risk: Here's More Context

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

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FDA recalls more than 7,000 bottles of antidepressant over a possible cancerous chemical

The FDA is recalling more than 7,000 bottles of the antidepressant duloxetine due to a possible cancer-causing chemical.

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