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Apr 1, 2020 Audience: Patient, Health Professional, Goodrx stendra ISSUE: he FDA announced it is requesting manufacturers to withdraw all prescription and over-the-counter OTC ranitidine drugs from the market immediately. This is the latest step in an ongoing investigation of a contaminant known as N-Nitrosodimethylamine NDMA in ranitidine medications commonly known by the brand name Zantac NDMA is a probable human carcinogen a substance that could cause cancer FDA has determined that the impurity in some ranitidine products increases over time and when stored at goodrx stendra than room temperatures may result in consumer exposure to unacceptable levels of this impurity.elected from data included with permission and copyrighted by First Databank, Inc.

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A voluntary recall is a precautionary action, in this case due to detection of a potential cancer causing chemical, N-nitrosodimethylamine NDMA NDMA is often found in low levels in water and some foods, being a byproduct of manufacturing or of heating/cooking/curing foods.

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