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Ranbaxy gets nod for Cefprozil

Our Bureau

New Delhi, July 2

Ranbaxy Laboratories has said it has received approval from the US Food and Drug Administration to manufacture and market Cefprozil for oral suspension USP, 125 mg/5ml and 250 mg/5ml. The Office of Generic Drugs, USFDA has determined the Ranbaxy formulations to be bio-equivalent and have the same therapeutic effect as that of the reference listed drug Cefzil for oral suspension by Bristol Myers Squibb Company Pharmaceutical Research Institute, a company release said. The total annual market sales for Cefprozil are estimated at $93 million.

More Stories on : Regulatory Bodies & Rulings | Pharmaceuticals | Ranbaxy Laboratories Ltd

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