FDA Clears New, Safer Formulation of Ranitidine After Full Safety Evaluation
Written By : Dr. Kamal Kant Kohli
Published On 2025-12-01 05:00 GMT | Update On 2025-12-01 10:17 GMT
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The U.S. Food and Drug Administration has approved reformulated ranitidine tablets, marking the return of this important acid-reducing medication to the U.S. market after a five-year absence. The approval follows extensive safety testing and manufacturing improvements that address previous concerns about N-nitrosodimethylamine (NDMA) impurity formation during the product’s shelf-life.
Ranitidine, an H2 receptor antagonist, is widely used to treat conditions including gastroesophageal reflux disease (GERD), peptic ulcers, and Zollinger-Ellison syndrome.
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