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    You are here: Home > Pharmacy News | Health Articles/Tips > Aurobindo > December 08, 2010

      Aurobindo Pharma Gets USFDA Approval For Duloxetine Hydrochloride Capsules


      (RTTNews) - The Hyderabad-based Aurobindo Pharma Ltd. announced that the company had received tentative approval from the US FDA to manufacture and market Duloxetine Hydrochloride Delayed-Release capsules 20mg (base), 30mg (base) and 60mg (base).

      Duloxetine Hydrochloride Delay-Release capsules are the generic equivalent of Eli Lilly and Company's Cymbalta Delayed-Release capsules 20mg (base), 30mg (base) and 60mg (base).

      Duloxetine Hydrochloride Delayed-Release capsules are indicated for the treatment of major depressive disorder and fall under the Neurological therapeutic category.

      As per IMS data, the product has a market size of around $2.9 billion for the twelve months ended June 2010.

      At the BSE, Aurobindo Pharma shares are being traded at Rs.1,301, up by 0.143% from the previous close.

      December 08, 2010


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