| Breakdown | TTM | Dec 2025 | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 13.15B | 12.86B | 11.53B | 10.43B | 11.40B | 9.00B |
| Gross Profit | 9.18B | 8.76B | 7.10B | 1.34B | 7.56B | 6.29B |
| EBITDA | 3.28B | 3.11B | 2.46B | 1.13B | 2.23B | 2.73B |
| Net Income | 1.11B | 782.93M | 318.74M | -325.33M | 606.62M | 1.48B |
Balance Sheet | ||||||
| Total Assets | 0.00 | 33.11B | 30.93B | 29.04B | 28.75B | 26.32B |
| Cash, Cash Equivalents and Short-Term Investments | 285.24M | 585.61M | 302.26M | 221.92M | 338.29M | 1.23B |
| Total Debt | 0.00 | 5.88B | 9.37B | 7.98B | 6.83B | 8.46B |
| Total Liabilities | -23.64B | 9.47B | 12.93B | 11.30B | 10.64B | 11.65B |
| Stockholders Equity | 23.64B | 23.72B | 18.09B | 17.83B | 18.22B | 14.79B |
Cash Flow | ||||||
| Free Cash Flow | 0.00 | -1.11B | -492.22M | -467.44M | -2.27B | -3.07B |
| Operating Cash Flow | 0.00 | 1.32B | 1.35B | 1.80B | 1.05B | 469.28M |
| Investing Cash Flow | 0.00 | -1.99B | -1.67B | -2.33B | -2.85B | -4.04B |
| Financing Cash Flow | 0.00 | 626.54M | 467.75M | 457.98M | 828.58M | 4.36B |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
74 Outperform | ₹1.01T | 16.94 | ― | 0.63% | 14.10% | 9.72% | |
72 Outperform | ₹701.66B | 29.68 | ― | 0.80% | 9.32% | 11.25% | |
67 Neutral | ₹94.31B | 26.36 | ― | 4.73% | -19.94% | -22.49% | |
63 Neutral | ₹406.35B | 42.03 | ― | 2.16% | 4.17% | 41.51% | |
54 Neutral | ₹58.19B | 42.06 | ― | 0.16% | 10.46% | 111.15% | |
53 Neutral | ₹569.55B | 56.14 | ― | 0.24% | 30.27% | ― | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
Shilpa Medicare Limited has disclosed that the Delhi High Court has issued an ex-parte ad-interim injunction restraining the company, its material subsidiary Shilpa Pharma Lifesciences and wholly owned subsidiary FTF Pharma from manufacturing, stockpiling, importing, exporting or supplying pharmaceutical products containing the compound Ruxolitinib and/or its salts in any form that may infringe a specified Indian patent. A court-appointed Local Commissioner inspected the company’s premises and collected records, with Shilpa Medicare stating it fully cooperated and that the Ruxolitinib-related product was used solely for research purposes, resulting in no financial impact or disruption to its ongoing business operations. The company has acknowledged the order, is complying with its directions and is evaluating legal options, including filing responses or appeals, as it manages the potential intellectual property dispute while maintaining normal operations.
Shilpa Medicare Limited has received initial authorization from Europe for its Rotigotine transdermal patch, a generic version of Neupro®, used to treat Restless Legs Syndrome and Parkinson’s disease. This milestone marks Shilpa’s first transdermal patch to gain marketing authorization in Europe, with a targeted launch in FY27, and represents a significant step in expanding its market presence in the European pharmaceutical sector.
Shilpa Medicare Limited announced the completion of a USFDA inspection at its Unit IV facility in Jadcherla, Telangana, which resulted in eight observations but no repeat issues. The facility’s contribution to the company’s US sales is minimal, accounting for less than 1% of the total business for the first half of FY25-26. The company plans to address the observations comprehensively within the stipulated timeframe, maintaining its compliance with international regulatory standards.
Shilpa Medicare Limited has announced that it will release its second-quarter earnings results for the fiscal year 2026 on November 13, 2025, with an earnings call scheduled for November 17, 2025. This announcement is significant as it provides stakeholders with insights into the company’s financial performance and strategic direction, potentially impacting its market positioning and investor relations.