Zydus Cadila gets USFDA nod to market Vardenafil tablets

Press Trust of India  |  New Delhi 

Drug firm today said it has received tentative approval from the US health regulator to market Hydrochloride tablets used for treatment of in the American market.

The company said in a statement that it has received nod from the Food and Drug Administration (USFDA) to market the tablets in the strengths of 2.5 mg, 5 mg, 10 mg and 20 mg.

The product will be manufactured at the group's formulations manufacturing facility at SEZ, Ahmedabad, it added.

"The drug is an agent that works by blocking a certain enzyme (phosphodiesterase-PDE5) used to treat erectile dysfunction," said.

The group currently has 212 approvals and has so far filed over 330 abbreviated new drug applications (ANDAs) since the commencement of the filing process by the company, it added.

Shares of Cadila Healthcare, the listed entity of the group, were trading over 2 per cent up at Rs 380.55 on BSE in the afternoon.

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First Published: Mon, July 30 2018. 14:20 IST