| Breakdown | TTM | Dec 2025 | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 30.34B | 30.35B | 28.30B | 26.57B | 32.30B | 27.08B |
| Gross Profit | 18.74B | 18.26B | 15.98B | 14.85B | 18.81B | 14.98B |
| EBITDA | 3.83B | 3.60B | 1.38B | 420.00M | 2.26B | -1.43B |
| Net Income | -1.23B | -470.00M | -4.63B | -5.59B | -2.44B | 6.86B |
Balance Sheet | ||||||
| Total Assets | 0.00 | 81.35B | 76.49B | 76.83B | 82.43B | 77.73B |
| Cash, Cash Equivalents and Short-Term Investments | 5.88B | 6.13B | 5.23B | 1.50B | 3.79B | 2.38B |
| Total Debt | 0.00 | 20.21B | 23.56B | 21.84B | 21.98B | 26.73B |
| Total Liabilities | -46.57B | 34.78B | 39.87B | 40.21B | 40.41B | 40.12B |
| Stockholders Equity | 46.57B | 43.53B | 33.59B | 33.54B | 38.49B | 33.77B |
Cash Flow | ||||||
| Free Cash Flow | 0.00 | -2.64B | 30.00M | -560.00M | 2.01B | -4.53B |
| Operating Cash Flow | 0.00 | -220.00M | 2.19B | 1.53B | 4.13B | -2.87B |
| Investing Cash Flow | 0.00 | -7.83B | -1.37B | -1.25B | -2.01B | 14.70B |
| Financing Cash Flow | 0.00 | 4.09B | 3.34B | -3.15B | -710.00M | -11.71B |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
74 Outperform | ₹662.29B | 19.03 | ― | 0.33% | 7.33% | -3.79% | |
74 Outperform | ₹376.77B | 45.06 | ― | 0.28% | 9.66% | 25.79% | |
72 Outperform | ₹683.80B | 28.65 | ― | 0.80% | 9.32% | 11.25% | |
71 Outperform | ₹973.45B | 17.04 | ― | 0.63% | 14.10% | 9.72% | |
53 Neutral | ₹545.85B | 54.31 | ― | 0.24% | 30.27% | ― | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
47 Neutral | ₹223.81B | -996.96 | ― | ― | 1.19% | 93.08% |
Wockhardt has filed a Marketing Authorisation Application with the European Medicines Agency for its novel antibiotic WCK 5222, branded as Zaynich, a fixed-dose combination of Zidebactam and Cefepime designed to treat resistant Gram-negative infections. The EMA has deemed the drug eligible for Accelerated Assessment, and Wockhardt expects approval across all EMA countries, complementing fast-track review already under way at the U.S. FDA and filings in India; as the first New Chemical Entity discovered and developed in India to seek pan-European authorisation, the move marks a significant milestone for both the company and the country’s innovation credentials in addressing life-threatening multi-drug resistant infections.