The U.S. Food and Drug Administration Wednesday announced it is requesting manufacturers withdraw all prescription and over-the-counter ranitidine drugs — commonly known by the brand name Zantac — from the market immediately. This is the latest step in an ongoing investigation of a contaminant known as N-Nitrosodimethylamine, or NDMA, in ranitidine medications.
Fda Orders Zantac Pulled From Store Shelves
The Gazette, The Gazette (Cedar Rapids)
Wed, 04/01/2020 - 11:36am
Sections: u.s.
Topics: Iowa Linn County Cedar Rapids
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