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Zantac was first marketed in 1981, [7] and it was described in 1989 as "one of the most expensive drugs on the market", [8] and "the world's biggest-selling prescription drug". [9] Addiction to taking it ("a habit") was how some of its users described Zantac. [ 10 ]
All Zantac products and generic versions of the heartburn medication should be taken off pharmacy shelves immediately, the Food and Drug Administration announced Wednesday.
It is pulling the drug off shelves after previous recalls by some manufacturers of generic versions of the drug. Sanofi reported Zantac sales of 127 million euros in 2018 69 million euros over the ...
In 2020, the U.S. Food and Drug Administration asked drugmakers to pull Zantac and its generic versions off the market after a cancer-causing substance called NDMA was found in samples of the drug.
Delaware's highest court said on Tuesday it will hear an appeal by GSK and other drugmakers seeking to end more than 70,000 lawsuits claiming discontinued heartburn drug Zantac caused cancer. GSK ...
In October 2019, Sanofi recalled all over-the-counter Zantac in the United States and Canada, [107] [108] [17] Perrigo issued a worldwide recall of ranitidine, [109] [17] Dr. Reddy's issued a recall of all ranitidine products in the United States, [110] [17] and Novitium Pharma recalled all ranitidine hydrochloride capsules in the US. [111] [17]
The U.S. Food and Drug Administration (FDA) in 2020 pulled Zantac and its generic versions off the market, triggering a wave of lawsuits. GSK settles another Zantac lawsuit in California Skip to ...
However, the U.S. Food and Drug Administration asked drugmakers to pull Zantac and its generic versions off the market in 2020, after a cancer-causing substance called NDMA was found in samples of ...