Breakdown | TTM | Dec 2025 | Dec 2024 | Dec 2022 | Dec 2022 | Dec 2021 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 314.88B | 317.24B | 290.02B | 233.67B | 246.17B | 247.75B |
Gross Profit | 184.62B | 186.97B | 160.16B | 69.38B | 129.75B | 80.49B |
EBITDA | 70.40B | 66.05B | 61.79B | 45.36B | 40.09B | 85.29B |
Net Income | 34.86B | 34.86B | 31.73B | 26.48B | 19.27B | 53.35B |
Balance Sheet | ||||||
Total Assets | 497.85B | 497.85B | 450.72B | 339.22B | 398.90B | 338.54B |
Cash, Cash Equivalents and Short-Term Investments | 82.36B | 82.36B | 63.25B | 45.58B | 62.24B | 56.21B |
Total Debt | 82.63B | 82.63B | 66.48B | 32.79B | 52.86B | 53.39B |
Total Liabilities | 171.38B | 171.38B | 152.21B | 93.48B | 130.38B | 119.25B |
Stockholders Equity | 326.53B | 326.53B | 298.43B | 245.76B | 268.40B | 219.30B |
Cash Flow | ||||||
Free Cash Flow | 0.00 | 19.57B | -11.27B | 23.12B | -3.34B | 14.55B |
Operating Cash Flow | 0.00 | 39.25B | 24.35B | 50.16B | 23.87B | 33.29B |
Investing Cash Flow | 0.00 | -18.76B | -45.37B | -32.12B | -39.78B | 5.99B |
Financing Cash Flow | 0.00 | 1.20B | 8.00B | -29.69B | 18.14B | -13.65B |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
72 Outperform | ₹647.71B | 28.35 | 0.84% | 4.49% | 11.22% | ||
72 Outperform | ₹878.69B | 23.73 | 0.63% | 12.40% | 63.16% | ||
72 Outperform | ₹993.71B | 21.73 | 1.13% | 14.52% | 9.46% | ||
71 Outperform | ₹607.11B | 17.90 | 0.39% | 7.76% | -2.84% | ||
62 Neutral | ₹550.97B | 73.11 | 0.13% | 10.99% | ― | ||
54 Neutral | ₹468.76B | 92.06 | 0.14% | 17.31% | 242.99% | ||
51 Neutral | $7.81B | -0.22 | -40.01% | 2.29% | 21.48% | -2.11% |
CuraTeQ Biologics, a subsidiary of Aurobindo Pharma, has received a positive opinion from the European Medicines Agency’s Committee for Medicinal Products for Human Use for its trastuzumab biosimilar, Dazublys®, intended for treating HER2-positive breast cancers. This endorsement marks an important step for Aurobindo Pharma in strengthening its biosimilars portfolio, with expectations for European Commission approval by July, furthering its commitment to launching at least ten biosimilars by 2030 to enhance cancer care and address unmet patient needs.