On April 1, 2020, the FDA announced its request for manufacturers of ranitidine products (Zantac) to immediately withdraw all prescription and over-the-counter (OTC) ranitidine drugs from the market. This is the most recent step in the ongoing investigation into N-Nitrosodimethylamine (NDMA) in ranitidine medication. Ranitidine is the common name of popular prescription and over the counter (OTC) drug, Zantac. The…Read More
