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.
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Over 7,100 bottles of prescription antidepressants recalled over potentially cancer-causing substanceNEW YORK (WPIX) – A pharmaceutical company issued a recall this month for thousands of bottles of duloxetine, a medicine ...
N-nitroso-duloxetine belongs to the nitrosamine class of compounds, some of which are classified as probable or possible human carcinogens.
The U.S. Food and Drug Administration is urging patients not to stop taking their prescribed medication if it falls under the ...
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