Dr Reddy’s Gets FDA Approval to Market Fexofenadine

by Kathy Jones on  April 14, 2011 at 8:12 PM Corporate News
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The US Food and Drug Administration has given its approval for a Abbreviated New Drug Application (ANDA) by Dr Reddy's Laboratories for the production of its Fexofenadine HCl tablets.
 Dr Reddy’s Gets FDA Approval to Market Fexofenadine
Dr Reddy’s Gets FDA Approval to Market Fexofenadine
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The tablets are generic version of Sanofi-Aventis' Allegra tablets and will be sold over the counter under store brand labels.

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Dr Reddy's revealed that it had got the approval for the drug on April 12, more than three months after the US District Court of New Jersey had given clearance for the company to manufacture the generic version of Allegra-D 24 in US.


Source: Medindia
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