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Camber Pharmaceuticals – Recall of losartan

February 28, 2019 - The FDA announced the voluntary, consumer-level recall of several lots of Camber Pharmaceuticals’ losartan tablets due to the detection of trace amounts of N-Nitroso N-Methyl 4-amino butyric acid (NMBA), a possible process impurity or contaminant in an active pharmaceutical ingredient, manufactured by Hetero Labs.

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