Zydus Lifesciences bags USFDA nod for BP drug Bisoprolol Fumarate
The drug will be manufactured at the group's formulation manufacturing facility at, SEZ, Ahmedabad, India.;
Ahmedabad: Pharma major, Zydus Lifesciences Limited (formerly known as Cadila Healthcare Limited), has recently received final approval from the United States Food and Drug Administration (USFDA) to market Bisoprolol Fumarate Tablets USP 5 mg and 10 mg.
Bisoprolol Fumarate Tablets are used to treat high blood pressure. They can be used alone or in combination with other high blood pressure medications to lower blood pressure. High blood pressure is also known as hypertension.
The drug will be manufactured at the group's formulation manufacturing facility at, SEZ, Ahmedabad, India and will be distributed by Viona Pharmaceuticals Inc.
Read also: Zydus Lifesciences bags USFDA approval for Empagliflozin, Metformin Hydrochloride Tablets
Bisoprolol Fumarate Tablets had annual sales of USD 30 million in the United States according to IQVIA data (IQVIA MAT May 2022). The group now has 318 approvals and has so far filed over 420* ANDAs since the commencement of the filing process in FY 2003-04.
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