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FDA takes Zantac off the shelves

The Food and Drug Adminstration has requested all prescription and over-the-counter ranitidine be removed from the market due to the potential for N-Nitrosodimethylamine (NDMA) contamination. Extended exposure to NDMA at high levels can increase the risk of cancer.

https://www.fda.gov/news-events/press-announcements/fda-requests-removal-all -ranitidine-products-zantac-market

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