Glenmark receives ANDA approval for hydrochlorothiazide tablets
Drug Approval

Glenmark receives ANDA approval for hydrochlorothiazide tablets

According to IQVIA sales data for the 12-month period ending November 2021, the Ziac tablets, 2.5 mg/6.25 mg, 5 mg/6.25 mg, and 10 mg/6.25 mg market achieved annual sales of approximately US $ 30.3 million

  • By IPP Bureau | January 27, 2022

Glenmark Pharmaceuticals has received final approval by the United States Food & Drug Administration (U.S. FDA) for bisoprolol fumarate and hydrochlorothiazide tablets.

According to IQVIA sales data for the 12-month period ending November 2021, the Ziactablets of different mg achieved annual sales of approximately US $ 30.3 million. 

Glenmark’s current portfolio consists of 172 products authorized for distribution in the U.S. marketplace and 46 ANDA’s pending approval with the U.S. FDA.

In addition to these internal filings, Glenmark continues to identify and explore external development partnerships to supplement and accelerate the growth of its existing pipeline and portfolio. 

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