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Food and Drug Administration. As of Sept. Both companies cited the potential cancer-causing impurity NDMA as the reason. People who were diagnosed with cancer after taking the medication have begun filing Zantac lawsuits. Manufacturer Sandoz Inc. In a statement, the company said officials had confirmed that batches of Sandoz Ranitidine Hydrochloride Capsules mg and mg contained unacceptable levels of NDMA.
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Select Legend. It works by decreasing the amount of fluid made in your stomach.
This action is being taken out of an abundance of caution due to a recent Product Alert from the U.
Bromide and Length Administration FDA predestined it is requesting that makes withdraw all over-the-counter and prescription drugs containing ranitidine, the only ingredient in Canadian and U.
The FDA has requested that US manufacturers test their own drugs and it has begun testing other heartburn drugs, including those in the same category as Zantac as well those in the proton-pump inhibitor category, like Nexium.
The heartburn drug Zantac has been on the market for decades, and was considered safe enough to be sold over the counter and regularly given to infants.
That ascendent feeling in your chest after you eat a pleasant meal could be heartburn. Approximate than 60 million Americans experience side at least once a month.
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