Blog: Zantac - Page 2

On April 1st, 2020, the US Food and Drug Administration (FDA) recalled all Zantac and ranitidine products from the market due to substantial evidence linking the drug to hazardous levels of the carcinogenic chemical N-nitrosodimethylamine, or NDMA. As a result, tens of thousands of former Zantac users have come forward to proceed with legal action …

The US Food and Drug Administration (FDA) is responsible for protecting public health by enacting measures that ensure the efficacy, safety, and security of human and veterinary drugs, biological products, and medical devices. The FDA also ensures the safety of our nation’s food supply, cosmetics, and products that emit radiation. They conduct years of testing …

N-nitrosodimethylamine, or NDMA, is a naturally-occurring chemical that can become carcinogenic if repeatedly ingested in large amounts. In recent years, the chemical has been discovered in various prescription medications, most notably in the antacid drug Zantac.  NDMA is actually all around us– the FDA has established a safe intake limit of 96 nanograms per day. …