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      Dr Reddy`s gets USFDA approval for Primidone

      Posted AtMyiris.com

      Drug maker, DR Reddy`s (Q, N,C,F)* Laboratories has received final approval from the US Food and Drug Administration (USFDA) to market (on prescription basis) its anti-convulsant drug Primidone, in the strengths of 15 mg/ml and 30 mg/ml.

      The drug will be available in both tablet and oral form.


      Shares of the company declined Rs 25.45, or 5.66%, to trade at Rs 424. The total volume of shares traded was 440,443 at the BSE (12.24 p.m., Wednesday).

      * Q - Quote , N - News , C - Chart , F - Financials


      October 16, 2008


       

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