www.fdanews.com/articles/131131-watson-8217-s-generic-version-of-lotrel-receives-fda-approval
Watson’s Generic Version of Lotrel Receives FDA Approval
October 15, 2010
Watson Pharmaceuticals, Inc. announced that its subsidiary, Watson Laboratories, Inc., has received approval from the United States Food and Drug Administration on its Abbreviated New Drug Application for Amlodipine Besylate/Benazepril 5/20mg, 10/20mg, 2.5/10mg, and 5/10mg capsules, the generic equivalent to Novartis’ Lotrel capsules.
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