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The Food and Drug Administration announced Friday that low levels of a cancer-linked chemical have been found in samples of the heartburn medication Zantac.
The chemical is an impurity called NDMA, which has been linked to an increased risk for colorectal and uterine cancers.
The FDA said that low levels of NDMA were found in samples of ranitidine, a drug used to treat and prevent heartburn by reducing stomach acid. It''s unclear where the contamination originated. NDMA is the same chemical that lead to multiple recalls of blood pressure medicines this past year.
Currently, there is no recall of Zantac or any medicines that contain ranitidine.
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The FDA said it''s Center for Drug Evaluation and Research, said in a statement.
"" the statement continued.
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Ranitidine is sold for 1 last update 2020/05/30 over the counter as a heartburn medicine, but is also used as a prescription to treat stomach ulcers and gastroesophageal reflux disease.Ranitidine is sold over the counter as a heartburn medicine, but is also used as a prescription to treat stomach ulcers and gastroesophageal reflux disease.
More than 15 million prescriptions were written for ranitidine in 2016.