
Zydus Lifesciences has received the final nod from the US Food and Drug Administration (USFDA) for its verapamil hydrochloride extended-release tablets. As per the exchange filings, the approved strengths are 120 mg, 180 mg, and 240 mg. These tablets are prescribed to manage high blood pressure and are commonly used to lower the risk of heart-related incidents such as strokes and heart attacks.
The tablets are the generic equivalent of Calan SR, a reference drug sold in the same strengths in the United States. Zydus plans to manufacture the approved product at its plant in Baddi, Himachal Pradesh. According to IQVIA MAT (September 2025), the US market for verapamil extended-release tablets was valued at $24.5 million over a 12-month period.
This latest approval pushes Zydus’ tally to 428 final USFDA approvals, while the company has filed 487 abbreviated new drug applications (ANDAs) since it started filing in FY2003-04.
In Q2FY26, Zydus Lifesciences posted a consolidated net profit of ₹1,259 crore, a 39% increase from ₹911 crore reported in the same quarter last year. A large part of the increase was due to foreign exchange gains of ₹414 crore, compared with ₹45 crore a year ago.
The company reported revenue of ₹6,123 crore, up 17% year-on-year, supported mainly by growth in the US and Indian formulations businesses. Operating profit also improved, with EBITDA rising to ₹2,014 crore, a jump of 38%, and margins increasing from 27.9% to 32.9%.
Research and development expenses for the quarter stood at ₹482 crore, which is 7.9% of total revenue. The company continues to allocate funds to research areas involving complex generic medicines.
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As of November 26, 2025, 10:15 AM, Zydus Lifesciences share price was trading at ₹937.40, a 0.96% increase from the previous closing price.
With the latest USFDA approval adding to its product portfolio and steady financial results, Zydus continues to increase the number of generic medicines supplied to the US market.
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Published on: Nov 26, 2025, 11:16 AM IST

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