FORT MYERS
FDA requests removal of all ranitidine products, including Zantac, from the market
The U.S. Food and Drug Administration Wednesday 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). The agency has determined that […]