Zydus Lifesciences has received final approval from the United States Food and Drug Administration (USFDA) to manufacture and market Dasatinib Tablets in multiple strengths: 20 mg, 50 mg, 70 mg, 80 mg, 100 mg, and 140 mg. This is a generic version of Sprycel Tablets, which is used for treating Philadelphia chromosome-positive (Ph+) chronic myeloid leukemia (CML) and acute lymphoblastic leukemia (ALL).
According to IQVIA MAT January 2025 data, Dasatinib tablets had annual sales of $1.81 billion in the United States. The approval allows Zydus to enter this segment with its generic version, adding to its portfolio of 415 USFDA approvals. Since FY 2003-04, the company has filed 483 Abbreviated New Drug Applications (ANDAs).
The Dasatinib tablets will be manufactured at Zydus Lifesciences’ facility in Ahmedabad. The plant has been producing various pharmaceutical products for global markets and is part of the company’s USFDA-approved manufacturing network.
In the third quarter of FY25, Zydus reported a 29.62% increase in net profit, reaching ₹1,023.5 crore, compared to ₹789.6 crore in the same quarter of the previous year. Revenue from operations grew by 16.96% YoY, standing at ₹5,269.1 crore. The company attributed this growth to strong sales in India and the US.
As of March 6, 11:23 AM, Zydus Lifesciences Ltd is trading at ₹905.80, up ₹18.35 (2.07%) for the day. However, the stock has declined 10.16% over the past month and 5.83% over the past year.
Zydus has also introduced ANVIMO (Letermovir) in India, a drug aimed at preventing Cytomegalovirus (CMV) infections in transplant patients. The company claims it has reduced the cost of CMV treatment by 91%, making it more accessible.
Bringing it all together, the approval of generic Dasatinib adds another product to Zydus’ US portfolio, increasing its presence in the oncology segment.
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Published on: Mar 6, 2025, 2:46 PM IST
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