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May 11, 2020
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On Sept. 13, 2019, the U.S. Food and Drug Administration announced that tests found some samples of ranitidine, a popular heartburn medication known by the brand name Zantac, contained a contaminant, N-Nitrosodimethylamine (NDMA). At that time, the FDA encouraged healthcare professionals and patients to report any adverse events or side effects. On April 1, 2020,...

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