FDA pulls Zantac, other heartburn meds off the market
April 2, 2020
The U.S. Food and Drug Administration has ordered all manufacturers and retailers to pull all prescription and over-the-counter ranitidine drugs, known by the brand name Zantac, from the market immediately after discovering a contaminant in the heartburn medication. The contaminant, N-nitrosodimethylamine or NDMA, is a probable carcinogen in humans.
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