FDA Requests Removal of All Ranitidine Products (Zantac) from …
The U.S. Food and Drug Administration today announced it is requesting manufacturers withdraw all prescription and over-the-counter (OTC) ranitidine drugs from the market immediately.
Popular heartburn drug ranitidine recalled: What you need to …
Oct 1, 2019 · If you or a family member take ranitidine (Zantac) to relieve heartburn, you may have heard that the FDA has found a probable human carcinogen (a substance that could cause cancer) in it. The story is unfolding quickly and many details remain murky.
FDA Updates and Press Announcements on NDMA in Zantac (ranitidine)
FDA has advised companies to recall their ranitidine if testing shows levels of NDMA above the acceptable daily intake (96 nanograms per day or 0.32 parts per million for ranitidine).
All Ranitidine Products (Zantac): Press Release - FDA Requests …
ISSUE: The FDA 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...
Zantac Recall | FDA Removal of Zantac (Ranitidine) Products
May 28, 2024 · American Health Packaging Issues Voluntary Nationwide Recall of Ranitidine Syrup (Ranitidine Oral Solution USP) 150 mg/10 mL Liquid Unit Dose Cups Due to the Detection of N-nitrosodimethylamine (NDMA) Impurity.
The FDA Announces Two More Antacid Recalls Due to Cancer Risk
Jan 10, 2020 · On Wednesday, the Food and Drug Administration announced voluntary recalls of prescription forms of ranitidine by two generic drug companies, Appco Pharma and Northwind Pharmaceuticals, bringing...
FDA Recalls Popular Heartburn Drug Ranitidine: What You …
Nov 30, 2020 · The recall included all prescription and over-the-counter (OTC) medications containing ranitidine. The National Foundation for Cancer Research (NFCR) understands that individuals who have taken or are currently taking ranitidine …
Zantac and other heartburn drugs recalled over possible cancer …
Apr 1, 2020 · Washington — U.S. health regulators are telling drugmakers to immediately pull their popular heartburn drugs off the market after determining that a contamination issue with the medications poses a...
Zantac (Ranitidine) Recall | Is Your Heartburn Drug Affected?
Jul 28, 2020 · Valisure closed the petition by asking the FDA to recall all Zantac and ranitidine products. According to Valisure, any ranitidine product poses a risk of generating "very high levels of NDMA in the human body."
FDA announces voluntary recall of Sandoz ranitidine capsules …
The U.S. Food and Drug Administration is alerting health care professionals and patients of a voluntary recall of 14 lots of prescription ranitidine capsules distributed by Sandoz Inc., used to...