| Breakdown | TTM | Dec 2025 | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 157.71B | 152.62B | 147.56B | 111.74B | 81.84B | 71.43B |
| Gross Profit | 95.31B | 92.44B | 91.73B | 69.62B | 50.11B | 48.99B |
| EBITDA | 31.75B | 31.24B | 32.71B | 26.57B | 19.56B | 16.52B |
| Net Income | 3.85B | 10.13B | 10.22B | 4.63B | 6.48B | 7.41B |
Balance Sheet | ||||||
| Total Assets | 613.95B | 587.97B | 560.71B | 520.43B | 203.94B | 185.22B |
| Cash, Cash Equivalents and Short-Term Investments | 60.89B | 49.24B | 25.74B | 37.26B | 29.65B | 32.24B |
| Total Debt | 164.33B | 183.62B | 162.77B | 180.19B | 51.47B | 44.81B |
| Total Liabilities | 293.97B | 310.85B | 307.96B | 295.54B | 109.24B | 100.15B |
| Stockholders Equity | 258.69B | 216.44B | 197.84B | 178.67B | 84.33B | 76.27B |
Cash Flow | ||||||
| Free Cash Flow | 0.00 | 17.18B | 10.22B | 1.26B | -7.48B | -5.87B |
| Operating Cash Flow | 0.00 | 40.61B | 29.54B | 18.52B | 11.77B | 11.60B |
| Investing Cash Flow | 0.00 | -2.34B | -10.04B | -142.82B | -16.99B | -36.25B |
| Financing Cash Flow | 0.00 | -18.54B | -23.33B | 130.49B | 2.42B | 25.64B |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
71 Outperform | ₹252.74B | 53.77 | ― | 0.19% | 8.57% | -2.93% | |
63 Neutral | ₹506.62B | 95.62 | ― | 0.12% | 10.62% | -66.88% | |
63 Neutral | ₹109.29B | 37.58 | ― | 0.74% | 3.80% | 64.94% | |
61 Neutral | ₹86.88B | 24.65 | ― | 0.22% | 63.34% | 109.89% | |
61 Neutral | ₹138.18B | 42.65 | ― | 0.80% | 3.63% | -1.21% | |
55 Neutral | ₹224.11B | -925.86 | ― | 0.08% | 2.66% | -153.15% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
Biocon Biologics has been recognized as an Asia IP Elite for 2025 by Intellectual Asset Management (IAM), marking the ninth consecutive year of this accolade. This recognition highlights the company’s strong intellectual property strategy and its role in expanding access to affordable therapies, reinforcing its position as a leader in the global biosimilars market.
Biocon Limited has announced that CRISIL Ratings Limited has reaffirmed its credit ratings for the company’s bank facilities, maintaining a long-term rating of Crisil AA+/Stable and a short-term rating of Crisil A1+. This reaffirmation reflects Biocon’s strong financial position and stability, which is crucial for its continued operations and growth in the competitive biopharmaceutical industry.
Biocon Limited announced that India Ratings and Research has assigned and affirmed credit ratings for the company’s various debt instruments. The ratings reflect a stable outlook for the bank loan facilities and high creditworthiness for proposed commercial papers, indicating a positive financial position and potential for growth.
Biocon Limited has announced the scheduling of an Extraordinary General Meeting (EGM) on December 31, 2025, to be conducted via video conferencing in compliance with regulatory guidelines. This meeting is significant for stakeholders as it reflects Biocon’s commitment to transparency and adherence to corporate governance standards, potentially impacting its operational strategies and investor relations.
Biocon Biologics has announced a settlement agreement with Amgen Inc., paving the way for the commercialization of its Denosumab biosimilars, Vevzuo® and Evfraxy®, in Europe and other international markets starting December 2, 2025. This strategic move follows a similar settlement in the U.S. and is expected to enhance Biocon’s global reach in the oncology and bone health sectors, providing patients with more affordable treatment options. The European Commission had already approved these biosimilars in July 2025, marking a significant step in Biocon’s mission to expand its footprint in the global biosimilars market.
Biocon Limited announced that the U.S. FDA has classified its Biocon Biologics’ Drug Substance Facility in Bengaluru as Voluntary Action Indicated (VAI) following an inspection. This classification pertains to the production of Human Recombinant Insulin and Biosimilar Pegfilgrastim Drug Substance for the U.S. market, reinforcing Biocon’s commitment to maintaining high standards of quality and compliance.
Biocon Limited’s subsidiary, Biocon Pharma Limited, has received approval from the U.S. FDA for its ANDA for Tofacitinib Extended-Release Tablets, with final approval for the 11mg strength and tentative approval for the 22mg strength. This approval enhances Biocon’s portfolio in complex drug products, potentially strengthening its market position and offering new treatment options for conditions such as Rheumatoid Arthritis and Ulcerative Colitis.
Biocon Limited has announced its Q2 FY26 earnings call, scheduled for November 12, 2025. This presentation is part of the company’s regulatory compliance with the Securities and Exchange Board of India. The earnings call is expected to provide insights into Biocon’s financial performance and strategic direction, potentially impacting its market positioning and stakeholder interests.
Biocon Limited announced the successful completion of a GMP inspection by the U.S. FDA at its newly inaugurated manufacturing site in Cranbury, New Jersey. The facility, which represents a strategic expansion of Biocon’s operations in the United States, received one observation that will be addressed promptly and is not expected to affect business operations. This site is key to enhancing Biocon’s supply chain efficiency and expanding access to its high-quality, affordable therapies in the region, with several products already commissioned and more launches planned.
Biocon Limited announced that its subsidiary, Biocon Pharma Limited, in collaboration with Carnegie Pharmaceuticals LLC, has received tentative approval from the U.S. FDA for the ANDA for Rifaximin Tablets, 550 mg. This development marks a significant step for Biocon in expanding its portfolio in the U.S. market, potentially enhancing its competitive positioning and offering new treatment options for conditions like hepatic encephalopathy and irritable bowel syndrome with diarrhea.
Biocon Biologics, a subsidiary of Biocon Limited, has announced a settlement and license agreement with Amgen Inc., allowing the company to commercialize its denosumab biosimilars, Bosaya and Aukelso, in the U.S. market starting October 1, 2025. This development follows the U.S. FDA’s approval and provisional interchangeability designation for these products, which are biosimilars to Amgen’s Prolia and Xgeva. The agreement resolves pending patent litigation and marks Biocon Biologics’ entry into the bone health space, enhancing its oncology portfolio and reaffirming its position as a global leader in biosimilars.