7,100 bottles of Duloxetine, brand name Cymbalta, have been recalled for potential toxic chemical contamination. Find your lot number here.
more than 7,000 bottles of duloxetine—an antidepressant sold under the brand name Cymbalta that’s often prescribed to treat chronic pain. Thewas initiated due to the medication containing levels of N-nitroso-duloxetine, a chemical that can be toxic if consumed at certain levels.that are commonly found in food and water products.
Class II recalls are the second most serious of the FDA recall classification system . It indicates that recalled products have the potential to trigger"temporary or medically reversible adverse health consequences," according to the FDA.No. This recall pertains specifically to the 20mg Duloxetine Delayed-Release Capsules, packaged in 500-count bottles. The lot number for the affected products is 220128, and they have an expiration date of 12/2024.
Duloxetine, or Cymbalta, belongs to a class of medications known as selective serotonin and norepinephrine reuptake inhibitors . They work by increasing the activity of serotonin and norepinephrine, both of which are known to play a role in regulating mood and pain. These medications are used to treat depression, anxiety and sometimes nerve pain. Although SSNRIs are typically taken daily, it can take several weeks before their therapeutic effects are noticeable.
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