The group also received the final approval from the USFDA to market Ursodiol Tablets, 250 mg (US RLD URSO 250 tablets) and 500 mg (US RLD URSO Forte tablets). It will be manufactured at the group's formulations manufacturing facility at Baddi. It is indicated for the treatment ofpatients with primary biliary cirrhosis, a chronic disease in which the bile ducts in liver are slowly destroyed.
The group now has 226 approvals and has so far filed over 330 ANDAS since the commencement of the filing process in FY 2003-04.
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