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Zydus Cadila receives USFDA nod to market blood pressure lowering drug

It will be manufactured at the group's formulations manufacturing facility at SEZ, Ahmedabad

Press Trust of India  |  New Delhi 

Zydus
Zydu

Drug firm Tuesday said it has received final approval from the US health regulator to market and tablets USP, used to treat high blood pressure, in the US.

The company has received approval from the US Food and Drug Administration (USFDA) to market the medication in two different strengths, said in a statement.

It will be manufactured at the group's formulations manufacturing facility at SEZ, Ahmedabad.

belongs to a class of drugs known as beta blockers. It works by blocking the action of certain natural chemicals in the body, such as epinephrine on the heart and blood vessels.

is a water pill' (diuretic) and causes the body to get rid of extra salt and water.

The Zydus group now has 253 product approvals since the commencement of the filing process in 2003-04.

Shares of Cadila Healthcare, the listed entity of the group, was trading at Rs 336.90 per scrip, up 1.26 per cent on BSE.

First Published: Tue, March 12 2019. 15:10 IST
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