![]() NDMA levels in Zantac and Ranitidine products, however, have been found to be 3,000 to 26,000 times higher than legally allowed levels which were set by the FDA. However, it’s found in such low amounts in food and water that the FDA considers them safe for consumption. NDMA is known to be an environmental contaminant and is commonly found in: NDMA is a known human carcinogen according to the U.S. NDMA is a semi-volatile organic compound used as a stabilizer in gasoline, rocket fuel and other petroleum-based industrial products and is a byproduct of pesticide manufacturing and other industries. Food and Drug Administration (FDA) are warning that popular heartburn drug Zantac, and other generic or store brand formulations of over-the-counter acid-reducers and prescription forms of Ranitidine, may contain a cancer-causing agent, N-nitrosodimethylamine (NDMA). Finally, in 2020, the FDA concluded its investigation and announced a recall of Zantac and other drugs based on ranitidine. As a precaution, manufacturers of Zantac and other ranitidine-based drugs voluntarily recalled the drugs that same year.Īt the same time, the FDA was investigating ranitidine and had announced a warning, although as of 2019 it hadn’t issued a recall or instructed patients to stop taking the drug, despite the recalls. Investigations into ranitidine began, prompting drugstore chains to begin pulling ranitidine-based drugs, including Zantac, from their shelves in 2019. In 2018, ranitidine was found to be linked to the cancer-causing NDMA (N-nitrosodimethylamine). After the patent on Zantac expired in 1997, numerous competitors began to sell generic versions of Zantac, all based on ranitidine. ![]() ![]() Zantac is based on a substance called ranitidine. Although it wasn’t exactly known how it worked, Zantac was approved for treating stomach ulcers and other conditions linked to too much stomach acid. GM Silverado & Sierra Roof-Rail Airbag Failure. ![]()
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