The U.S. Food and Drug Administration has announced that all prescription and over-the-counter ranitidine (Zantac) drugs should be removed from the market immediately. The push to fully remove this drug from the market is part of an on-going investigation by the FDA of a contaminant known as NDMA, a probable human carcinogen.
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On September 13th, the Food and Drug Administration announced that some ranitidine medications contained low-levels of a possible carcinogen called nitrosodimethylamine (NDMA). Those drugs that …
