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Event Type Medicine - Pharmaceutical Recalls  Date Time 2019-09-25 22:17:00 
Country US  City Weston, FL 
Latitude 26.100  Longitude -80.400 
URL https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/apotex-corp-issues-voluntary-nationwide-recall-ranitidine-tablets-75mg-and-150mg-all-pack-sizes-and     
[fda.gov] FLORIDA - Apotex Corp Issues Voluntary Nationwide Recall of Ranitidine Tablets 75mg And 150mg - All Pack Sizes And Formats Due To The Potential For Detection Of An Amount Of Unexpected Impurity N-Nitrosodimethylamine (NDMA) Impurity In The Product

"Apotex Corp. is voluntarily, on a precautionary basis, recalling Ranitidine Tablets 75mg and 150mg (All pack sizes and Formats) to the Retail level. Apotex has learned from the U.S. Food and Drug Administration and other Global regulators that some ranitidine medicines including brand and generic formulations of ranitidine regardless of the manufacturer, contain a nitrosamine impurity called N-nitrosodimethylamine (NDMA) at low levels."

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