Lupin gets USFDA nod for generic version of Tadalafil tablets

Press Trust of India  |  New Delhi 

Drug firm Thursday said it has received approval from the US health regulator to market a generic version of tablets, used to treat pulmonary arterial

The company has received approval from the (USFDA) to market a generic version of Eli Lilly and Company's tablets in 20 mg strength, said in a statement.

It is indicated for the treatment of pulmonary arterial (PAH) to improve exercise ability.

As per IQVIA MAT December 2018 data, said, the tablets, 20 mg had annual sales of around USD 474.3 million in the US.

Lupin shares were trading 2.42 per cent down at Rs 821.85 apiece on the BSE.

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First Published: Thu, February 07 2019. 15:15 IST