| Breakdown | TTM | Dec 2025 | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 233.76B | 227.08B | 200.11B | 166.42B | 164.05B | 151.63B |
| Gross Profit | 159.68B | 153.27B | 128.99B | 94.10B | 95.05B | 94.18B |
| EBITDA | 53.87B | 50.51B | 36.27B | 15.73B | 19.66B | 25.24B |
| Net Income | 36.99B | 32.82B | 19.14B | 4.30B | -15.28B | 12.17B |
Balance Sheet | ||||||
| Total Assets | 0.00 | 292.05B | 239.97B | 229.56B | 218.21B | 236.10B |
| Cash, Cash Equivalents and Short-Term Investments | 29.90B | 42.01B | 21.79B | 19.52B | 21.04B | 41.11B |
| Total Debt | 0.00 | 54.48B | 29.22B | 45.42B | 41.58B | 51.29B |
| Total Liabilities | -172.94B | 119.11B | 96.24B | 104.13B | 95.99B | 97.52B |
| Stockholders Equity | 172.94B | 172.03B | 142.90B | 124.64B | 121.53B | 138.03B |
Cash Flow | ||||||
| Free Cash Flow | 0.00 | 13.18B | 27.19B | 3.98B | -5.38B | 11.44B |
| Operating Cash Flow | 0.00 | 30.00B | 36.48B | 18.97B | 3.67B | 18.22B |
| Investing Cash Flow | 0.00 | -41.72B | -17.12B | -12.87B | 12.92B | -12.40B |
| Financing Cash Flow | 0.00 | 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 |
|---|---|---|---|---|---|---|---|
74 Outperform | ₹1.07T | 18.21 | ― | 0.62% | 14.10% | 9.72% | |
72 Outperform | ₹965.64B | 22.32 | ― | 0.57% | 15.49% | 64.37% | |
72 Outperform | ₹934.84B | 19.00 | ― | 1.19% | 14.01% | 14.62% | |
68 Neutral | ₹1.23T | 22.52 | ― | 0.86% | 6.93% | 21.55% | |
66 Neutral | ₹1.28T | 59.93 | ― | 0.85% | 9.11% | 18.76% | |
59 Neutral | ₹899.73B | 51.09 | ― | 0.05% | 23.22% | -19.19% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
Lupin Limited announced that it has received approval from the U.S. FDA for its biosimilar product, Armlupeg (pegfilgrastim-unne), marking its first biosimilar approval. This product, intended to decrease infection incidence in certain cancer patients and increase survival in radiation-exposed patients, will be manufactured at Lupin’s Pune facility. The approval signifies a significant step in Lupin’s strategy to provide affordable and accessible medicines in the U.S., enhancing its biosimilar portfolio and strengthening its market position. The biosimilar market is lucrative, with the pegfilgrastim market alone valued at USD 1,295 million annually in the U.S., indicating potential for substantial revenue growth and impact on stakeholders.
Lupin Limited announced that the U.S. FDA conducted an inspection at its manufacturing facility in Goa, India, resulting in a Form-483 with seven observations. The company is committed to addressing these observations and maintaining compliance with CGMP standards, which is crucial for its operational integrity and market reputation.
Lupin Limited has launched Risperidone for extended-release injectable suspension in the U.S., marking the first product from its proprietary PrecisionSphere™ platform. This launch, supported by a 180-day CGT exclusivity, underscores Lupin’s commitment to expanding its portfolio of complex injectables and enhancing global access to advanced long-acting treatments. The product is bioequivalent to Risperdal Consta® and is used for treating schizophrenia and bipolar I disorder, with significant market potential in the U.S.
Lupin Limited announced that it has received the Establishment Inspection Report (EIR) from the U.S. FDA for its Aurangabad facility after a product-specific Pre-Approval Inspection. This achievement highlights Lupin’s dedication to maintaining high standards of quality and compliance, reinforcing its reputation as a trusted provider of healthcare solutions globally. The receipt of the EIR is a significant milestone for Lupin, potentially enhancing its operational capabilities and market positioning, particularly in the U.S., which is a critical market for the company.
Lupin Limited announced that its Bioresearch Center in Pune received zero observations from the U.S. FDA following a successful inspection and assessment. This outcome underscores Lupin’s commitment to quality and compliance, enhancing its reputation in the pharmaceutical industry and potentially strengthening its market position.
Lupin Limited has launched an authorized generic version of Ravicti® (Glycerol Phenylbutyrate) Oral Liquid, 1.1g/mL, in the United States, aimed at managing urea cycle disorders (UCDs) in patients who cannot be managed by dietary protein restriction and/or amino acid supplementation alone. This strategic move is expected to enhance Lupin’s presence in the U.S. pharmaceutical market, potentially increasing its market share and providing a cost-effective treatment option for patients with UCDs.
Lupin Limited announced that the U.S. FDA conducted a Pre-Approval Inspection at its Somerset, New Jersey manufacturing facility, which concluded with one observation. The company is committed to addressing the observation promptly to ensure compliance with CGMP standards, reflecting its dedication to maintaining high-quality manufacturing practices.
Lupin Limited announced that the U.S. FDA has classified its Pithampur Unit-2 manufacturing facility inspection as ‘Official Action Indicated’ (OAI) following an earlier inspection that resulted in a Form-483 with four observations. The company is actively working with the FDA to address the compliance issues and ensure adherence to CGMP standards across all its facilities. This development may have implications for Lupin’s operations and its standing in the pharmaceutical industry, particularly in the U.S. market.
Lupin Limited’s subsidiary, Nanomi B.V., has entered into a definitive agreement to acquire VISUfarma B.V., a specialty pharmaceutical company based in Amsterdam, Netherlands. VISUfarma focuses on ophthalmology and has a significant commercial presence across major European countries, offering products for dry eye, glaucoma, and other eye-related conditions. This acquisition is expected to enhance Lupin’s market positioning in the European ophthalmology sector, potentially expanding its product offerings and market reach.
Lupin Limited has announced the successful passing of resolutions via a postal ballot, including the re-appointment of Mr. Mark D. McDade as an Independent Director and a revision in the remuneration of Managing Director Mr. Nilesh D. Gupta. These resolutions, passed with the requisite majority, reflect the company’s ongoing governance and operational adjustments, potentially impacting its strategic direction and stakeholder relations.
Lupin Limited has announced that it has received approval from the U.S. FDA for its Abbreviated New Drug Application for Lenalidomide Capsules, which are bioequivalent to Revlimid® Capsules by Bristol-Myers Squibb. These capsules, intended for treating multiple myeloma and transfusion-dependent anemia, will be manufactured at Lupin’s Pithampur facility in India. The approval marks a significant milestone for Lupin, potentially enhancing its market presence in the U.S. pharmaceutical sector, given the high annual sales of Lenalidomide Capsules in the U.S. market.