| Breakdown | TTM | Mar 2025 | Mar 2024 | Mar 2023 | Mar 2022 | Mar 2021 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 247.51B | 227.08B | 200.11B | 166.42B | 164.05B | 151.63B |
| Gross Profit | 157.85B | 153.27B | 128.99B | 94.10B | 95.05B | 94.18B |
| EBITDA | 64.56B | 50.51B | 36.27B | 15.73B | 19.66B | 25.24B |
| Net Income | 43.25B | 32.82B | 19.14B | 4.30B | -15.28B | 12.17B |
Balance Sheet | ||||||
| Total Assets | 335.00B | 292.05B | 239.97B | 229.56B | 218.21B | 236.10B |
| Cash, Cash Equivalents and Short-Term Investments | 62.82B | 42.01B | 21.79B | 19.52B | 21.04B | 41.11B |
| Total Debt | 62.17B | 54.48B | 29.22B | 45.42B | 41.58B | 51.29B |
| Total Liabilities | 137.72B | 119.11B | 96.24B | 104.13B | 95.99B | 97.52B |
| Stockholders Equity | 196.33B | 172.03B | 142.90B | 124.64B | 121.53B | 138.03B |
Cash Flow | ||||||
| Free Cash Flow | 23.29B | 13.18B | 27.19B | 3.98B | -5.38B | 11.44B |
| Operating Cash Flow | 29.03B | 30.00B | 36.48B | 18.97B | 3.67B | 18.22B |
| Investing Cash Flow | -28.42B | -41.72B | -17.12B | -12.87B | 12.92B | -12.40B |
| Financing Cash Flow | -2.77B | 17.32B | -21.84B | -3.37B | -15.72B | -18.85B |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
72 Outperform | ₹1.05T | 20.49 | ― | 0.57% | 15.49% | 64.37% | |
72 Outperform | ₹891.83B | 22.07 | ― | 1.19% | 14.01% | 14.62% | |
70 Outperform | ₹1.06T | 21.88 | ― | 0.63% | 14.10% | 9.72% | |
68 Neutral | ₹1.05T | 45.14 | ― | 0.87% | 6.93% | 21.55% | |
66 Neutral | ₹1.44T | 51.30 | ― | 0.84% | 9.11% | 18.76% | |
59 Neutral | ₹863.55B | 55.46 | ― | 0.04% | 23.22% | -19.19% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
Lupin Limited said the U.S. Food and Drug Administration has completed an inspection of its Ankleshwar manufacturing facility in India, conducted from March 2 to March 7, 2026. The review closed with a Form 483 containing two observations, indicating issues the regulator expects the company to remediate.
Lupin plans to address the U.S. FDA’s observations and submit a response within the required timeframe, reaffirming its commitment to CGMP compliance across all sites. While the presence of observations signals some gaps in quality or processes, the limited number may help reassure investors and partners that the facility remains broadly aligned with regulatory expectations.
Lupin Limited reported that the Maharashtra Goods & Service Tax Department has concluded its inspection and search proceedings at the company’s registered office, which began in late February and ended on March 2, 2026. The company stated it fully cooperated by providing all requested information and documents, and confirmed that no official communication indicating adverse findings has been received from the tax authorities, with no impact on its financials arising from the inspection.
The update signals that, at this stage, the GST inquiry does not pose an immediate financial or operational risk to Lupin, offering reassurance to investors and other stakeholders. While the absence of adverse remarks reduces near-term regulatory overhang, the market is likely to watch for any future communication from the authorities that could clarify whether the matter is definitively closed or subject to further review.
Global drugmaker Lupin Limited has received an Establishment Inspection Report from the U.S. Food and Drug Administration for its Goa, India manufacturing facility, with a Voluntary Action Indicated classification. The report follows an FDA inspection conducted in November 2025 and signals that any observed issues are minor and can be addressed without regulatory sanctions.
Management said the outcome underscores Lupin’s emphasis on quality and compliance and supports its ability to reliably supply medicines to international markets, particularly the U.S. The favorable regulatory status at Goa strengthens Lupin’s manufacturing footprint and reinforces stakeholder confidence in its global operations and ongoing access to key regulated markets.
Lupin Limited announced that its CEO, Vinita Gupta, has been named to the 2026 CNBC Changemakers list of Women Transforming Business, recognizing her role in making medicines more accessible and affordable for Americans. The honor underscores Lupin’s rapid ascent under her leadership to become the third-largest generic medicine supplier to the U.S. by volume and highlights its growing portfolio in complex generics, inhalation therapies, and biosimilars.
Gupta’s strategic emphasis on the U.S. market includes the FDA approval in late 2025 of Lupin’s first biosimilar Pegfilgrastim, reinforcing its push into high-value, specialty medicines. Her drive to expand domestic manufacturing through a planned state-of-the-art inhalation facility in Coral Springs, Florida, is positioned to bolster U.S. medicine security, increase production of key respiratory drugs such as Albuterol, and improve access for patients, further strengthening Lupin’s competitive standing and stakeholder confidence.
Lupin Limited has been ranked the number one pharmaceutical company globally and the top company across all sectors in India in the S&P Global Corporate Sustainability Assessment 2025, with an overall score of 91 out of 100. This places Lupin among the top 1% of companies worldwide in the assessment and secures its inclusion in the S&P Global Sustainability Yearbook 2026 for the third consecutive year.
The recognition underscores Lupin’s position as a global sustainability leader and reflects its strong performance on economic, environmental, and social criteria relative to more than 9,200 companies assessed across 59 industries. Management indicated that this achievement reinforces Lupin’s long-term strategy of integrating ESG principles across its value chain and supports its efforts to drive positive outcomes for patients, communities, and stakeholders, potentially strengthening its reputation with investors and regulators.
Lupin Limited has entered into a strategic collaboration with nonprofit drug developer TB Alliance to advance the clinical development and commercialization of the investigational drug Telacebec for multiple mycobacterial diseases, including tuberculosis, leprosy and Buruli ulcer. Under the agreement, TB Alliance will lead development while Lupin contributes its global manufacturing, regulatory and supply chain capabilities to ensure worldwide access, reinforcing Lupin’s focus on addressing unmet medical needs and potentially strengthening its role in the global fight against neglected infectious diseases.
Lupin Limited has entered into a licensing and supply agreement, via its subsidiary Lupin Atlantis Holdings, with Spain-based Galenicum Health for finished injectable formulations of Semaglutide, a GLP-1 receptor agonist used in Type 2 diabetes and obesity management. Under the deal, Galenicum will develop, manufacture and supply the product, while Lupin will manage regulatory approvals and commercialization across 23 countries, including Canada, Europe, Southeast Asia and Latin America, sharpening Lupin’s push into the fast-growing GLP-1 market. The partnership is positioned as a strategic milestone that expands Lupin’s Semaglutide portfolio and leverages its existing commercial footprint to scale access to cost-effective diabetes and obesity treatments, while supporting Galenicum’s ambition to become a leading B2B GLP-1 supplier amid surging global demand for these therapies.