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Aurobindo Pharma’s Eugia Pharma Gains USFDA Approval for Dasatinib Tablets

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Aurobindo Pharma’s Eugia Pharma Gains USFDA Approval for Dasatinib Tablets

Aurobindo Pharma Ltd ( (IN:AUROPHARMA) ) has shared an announcement.

Aurobindo Pharma Limited announced that its subsidiary, Eugia Pharma Specialities Limited, has received final approval from the USFDA to manufacture and market Dasatinib Tablets, which are bioequivalent to Sprycel Tablets by Bristol-Myers Squibb. The product, expected to launch in Q1FY26, targets a market estimated at $1.8 billion. This approval marks the 181st ANDA approval for Eugia Pharma, enhancing its position in the oncology sector and potentially impacting stakeholders positively by expanding its product offerings in the US market.

More about Aurobindo Pharma Ltd

Aurobindo Pharma Limited is an integrated global pharmaceutical company headquartered in Hyderabad, India. It develops, manufactures, and commercializes a wide range of generic pharmaceuticals, branded specialty pharmaceuticals, and active pharmaceutical ingredients globally in over 150 countries. The company has more than 30 manufacturing and packaging facilities approved by leading regulatory agencies and offers a robust product portfolio across seven major therapeutic areas.

YTD Price Performance: -11.16%

Average Trading Volume: 32,467

Current Market Cap: 697.3B INR

For a thorough assessment of AUROPHARMA stock, go to TipRanks’ Stock Analysis page.

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