CVS Health Corp. has suspended sales of the popular heartburn drug Zantac, as well as its own generic, called ranitidine, following a Food and Drug Administration alert earlier this month that the medicine contained a possible carcinogen.
Ranitidine is a common stomach acid drug that’s available over the counter and by prescription to people of all ages.
(MORE: The Zantac problem: What’s NDMA?
“Zantac brand products and CVS brand ranitidine products have not been recalled, and the FDA is not recommending that patients stop taking ranitidine at this time,” the company said in a statement. Customers who previously purchased the heartburn medicine at CVS can return it to the stores for a refund.
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Packages of Zantac, a popular medication which decreases stomach acid production and prevents heartburn, sit on a shelf at a drugstore, Sept. 19, 2019 in New York City.
(MORE: Possible chemical carcinogen found in some Zantac products: FDA)
Results from FDA lab tests showed some heartburn pills contained an impurity called N-nitrosodimethylamine (NDMA) in small amounts. As a probable carcinogen, NDMA may be capable of increasing cancer risk when taken in high doses over a long period of time.
On Sept. 18, a division of the Swiss pharmaceutical company Novartis said it was halting worldwide distribution of ranitidine.
Canada’s federal government has also asked companies to stop distributing ranitidine products while it completes an assessment of the drug to see if it is safe.