The FDA recalled more than 7,000 bottles of duloxetine, which is sold under the brand name Cymbalta, over the presence of a toxic chemical.
from the agency, the recall involves 7,107 bottles of duloxetine, which is sold under the brand name Cymbalta. Duloxetine is part of a class of drugs called selective serotonin/norepinephrine reuptake inhibitors , which are used to treat depression, anxiety and other mood disorders,The FDA issued the recall due to the presence of N-nitroso-duloxetine above the proposed interim limit.
The recalled capsules are 20mg in strength and sold in 500-count bottles. The lot number for the recalled products is 220128 with an expiration date of December 2024 and manufactured by Towa Pharmaceutical Europe, according to the FDA.
The FDA did not issue specific guidance on what to do with the recalled duloxetine. Patients who take this medication should contact their health care provider.36-year-old's Etsy side hustle brings in up to $54,000 a month, takes 10 hours a week — it paid off her student loan debt
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