 "Zydus Cadila gets USFDA nod to market treatment for gout, excess uric acid")
The company has received final approval from the United States Food and Drug Administration (USFDA) to market Allopurinol tablets USP in the strengths of 100mg and 300 mg, Zydus Cadila said in a filing to the BSE.
The product will be manufactured at the group's formulations manufacturing facility at Baddi, it added.
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The group has more than 160 approvals and so far filed over 300 abbreviated new drug applications (ANDAs) since the commencement of its filing process, it added.
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