One of the company's wholly-owned subsidiaries has received final approval from the USFDA for its abbreviated new drug application (ANDA) for generic version of Zetia, ezetimibe tablets, Sun Pharma said in a BSE filing.
The approval is for the tablets in the strength of 10 mg. The tablets are generic versions of Merck's Zetia, Sun Pharma said.
"As per IMS, ezetimibe tablets had annual sales of approximately USD 2.7 billion in the US for the 12 months ended April 2017," it added.