News
31 Aug 2011
Dr Reddy's Launches OTC Drug in US Market?
Dr. Reddy's Laboratories has launched its OTC Fexofenadine HCl and Pseudoephedrine HCl extended release tablets 180 /240 mg in the U.S. market.
Dr. Reddy's Laboratories announced yesterday that it has launched its OTC Fexofenadine HCl and Pseudoephedrine HCl extended release tablets 180 /240 mg in the U.S. market.
The FDA approved Dr. Reddy's Abbreviated New Drug Application (ANDA) for Fexofenadine HCl and Pseudoephedrine HCl extended release tablets on June 22nd, 2011.
Dr. Reddy's will market the product under store brand labels in the U.S. market.
The product is a bioequivalent version of sanofi-aventis' Allegra? D24 Hour extended release tablets which received Rx-to-OTC switch approval from the FDA on January 24th, 2011.
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