Zantac and its generic varieties are coming off store shelves after the Food and Drug Administration revealed it found a chemical that could be linked to cancer.
The FDA issued a warning that the popular heartburn drug Zantac had been found to contain N-nitrosodimethylamine, or NDMA, a known human carcinogen (cancer-causing substance).
This warning came after a pharmacy in Connecticut discovered elevated levels of NDMA while testing Zantac. It has been reported that the levels of cancer-causing NDMA are anywhere from 3,000 to 26,000 times higher than the legally allowable limit set by the FDA.
Pharmacy chains CVS and Walgreens have already announced they would suspend sales of Zantac brand pills and generic versions that contain ranitidine, the active ingredient of the drug commonly used to treat heartburn.
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