The Food and Drug Administration on Wednesday said the heartburn drug Zantac should immediately be pulled from shelves and consumers should dispose of any pills or liquid they have at home.
During safety tests last summer, extremely high levels of the contaminant NDMA, believed to be a carcinogen, were discovered in samples of the drug. The active ingredient in Zantac is ranitidine, and the FDA said that over time, NDMA appears as an impurity in ranitidine in levels exceeding federal standards, NPR reports.
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