Teva Pharmaceuticals USA, Inc. issued a voluntary Nationwide recall of Losartan Potassium 25 mg and 100 mg tablets that were sold exclusively to Golden State Medical Supply, according to the U.S. Food and Drug Administration.
This recall is due to an impurity found in six lots of active pharmaceutical ingredient manufactured by Hetero Labs Limited.
Losartan Potassium is used for the treatment of hypertension, hypertensive patients and nephropathy in Type 2 diabetics.
To date, Teva has not received any reports of adverse events related to the lots being recalled.
For more information, visit the FDA's Website.
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