Teva Pharmaceutical Industries has announced that the FDA has granted tentative approval for the company's abbreviated new drug application to market its generic version of Novartis's hypertension treatment Diovan tablets, 40mg, 80mg, 160mg and 320mg.
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Final approval of this product is expected upon expiry of patent protection for the brand product in September 2012, as well as any periods of marketing exclusivity that may be awarded.
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