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FDA inspection OAI
US FDA inspected Eugia Pharma Specialities Ltd Unit‑III (Jan 27–Feb 06, 2026), found 11 observations and has classified the inspection as 'Official Action Indicated' (OAI); company states no financial/operational impact.
Share transfer notice
Aurobindo Pharma published on June 11, 2026 (Business Standard and Nava Telangana) a newspaper notice announcing a special window for re‑lodgement of transfer requests of physical shares and submitted copies to exchanges.
Aurobindo Pharma Ltd (AUROPHARMA) is currently trading at 1,469.30 per share. Stock prices fluctuate during market hours on NSE and BSE based on demand, company updates, and overall market conditions. Refer to the live price chart above for the most recent price movement.
Aurobindo Pharma Limited is a global pharmaceutical company that develops, manufactures and markets active pharmaceutical ingredients (APIs), generic formulations, injectables and a growing biosimilars portfolio across regulated and growth markets, operating multiple manufacturing sites and R&D centres to serve over 150 countries with a broad ANDA/DMF filing base and expanding biologics capabilities. Q3FY26 consolidated revenue reached Rs. 8,646 crore, up 8.4% YoY, with EBITDA of Rs. 1,773 crore (20.5% margin) and net profit of Rs. 910 crore; management highlighted stable US base business, strong European growth (+27% YoY) and R&D spend of Rs. 409 crore (4.7% of sales) focused on biosimilars and specialty products development. Biosimilars (CuraTeQ) are a strategic growth pillar: multiple 2025 approvals in EEA/UK/Canada, filings planned in EMA and Health Canada, two Phase‑3 programs ongoing and planned US/EU BLA/MAA engagement for denosumab and omalizumab in 2026, positioning Aurobindo for a biotech revenue inflection toward 2028–2029. Operationally, Aurobindo reported meaningful capex and cash generation: net capex of US$79mn in the quarter, free cash flow generation of US$118mn and a strong net cash position (~US$251mn after appropriations), enabling both organic capacity build and selective M&A such as the Lannett transaction under regulatory review. Key near‑term drivers include: commercialization momentum in Europe, ramp of Pen‑G/6‑APA capacity with Govt MIP support, continued ANDA approvals and product launches in the US, and biosimilars commercialization and filings that together create multi‑year earnings visibility across segments.
Over the past 52 weeks, Aurobindo Pharma Ltd has traded between a low of ₹1,017.00 and a high of ₹1,550.00. The 52-week high and low indicate the stock’s price range over the last year and help investors understand its volatility and recent trading levels.
Aurobindo Pharma Ltd has a market capitalization of approximately 85,035.17. Market capitalization represents the total value of a company’s outstanding shares and helps investors understand its size, stability, and relative risk compared to other listed companies.
Aurobindo Pharma Ltd’s investment profile depends on its business fundamentals, valuation, and long-term outlook. The stock currently trades at a PE ratio of 24.26 and operates in the its sector sector. Investors typically assess financial performance, growth prospects, and individual risk tolerance before making investment decisions.
Based on its market capitalization of 85,035.17 Cr, Aurobindo Pharma Ltd is classified as a Mid Cap stock. Large-cap stocks are generally more stable, while mid-cap and small-cap stocks tend to offer higher growth potential along with higher price volatility.
Aurobindo Pharma Ltd operates in the its sector sector. Sector classification matters because companies in the same sector are often affected by similar economic conditions, regulatory changes, and competitive dynamics, which can influence overall stock performance.
The Price-to-Earnings (PE) ratio of Aurobindo Pharma Ltd is 24.26. The PE ratio compares a company’s share price to its earnings and is commonly used to assess valuation. Comparing the PE ratio with sector peers and historical levels provides better context.
Final USFDA approval to manufacture and market Tofacitinib Tablets in 5 mg and 10 mg strengths.
Aurobindo Pharma said it received final USFDA approval to manufacture and market Tofacitinib Tablets, 5 mg and 10 mg, which are bioequivalent to Xeljanz tablets.
Aurobindo said it received final USFDA approval to manufacture and market Rivaroxaban Tablets USP, 2.5 mg, and plans to launch it in Q1FY26.
The stock rose after its subsidiary received USFDA final approval to manufacture and market Dasatinib tablets, with the company indicating a Q1 FY26 launch.
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Bearish
3
Neutral
8
Bullish
3
Bearish
6
Neutral
8
Bullish
32
Bearish
3
Neutral
0
Bullish
29
Discovery themes featuring this stock
Aurobindo Pharma Limited is a global pharmaceutical company that develops, manufactures and markets active pharmaceutical ingredients (APIs), generic formulations, injectables and a growing biosimilars portfolio across regulated and growth markets, operating multiple manufacturing sites and R&D centres to serve over 150 countries with a broad ANDA/DMF filing base and expanding biologics capabilities.
Q3FY26 consolidated revenue reached Rs. 8,646 crore, up 8.4% YoY, with EBITDA of Rs. 1,773 crore (20.5% margin) and net profit of Rs. 910 crore; management highlighted stable US base business, strong European growth (+27% YoY) and R&D spend of Rs. 409 crore (4.7% of sales) focused on biosimilars and specialty products development.
Biosimilars (CuraTeQ) are a strategic growth pillar: multiple 2025 approvals in EEA/UK/Canada, filings planned in EMA and Health Canada, two Phase‑3 programs ongoing and planned US/EU BLA/MAA engagement for denosumab and omalizumab in 2026, positioning Aurobindo for a biotech revenue inflection toward 2028–2029.
Operationally, Aurobindo reported meaningful capex and cash generation: net capex of US$79mn in the quarter, free cash flow generation of US$118mn and a strong net cash position (~US$251mn after appropriations), enabling both organic capacity build and selective M&A such as the Lannett transaction under regulatory review.
Key near‑term drivers include: commercialization momentum in Europe, ramp of Pen‑G/6‑APA capacity with Govt MIP support, continued ANDA approvals and product launches in the US, and biosimilars commercialization and filings that together create multi‑year earnings visibility across segments.
Pharmaceuticals & Biotechnology
Pharmaceuticals
85,035 Cr
Low Risk
24.3
34.1
1.2
2.2
1,550.00
1,017.00
Sales CAGR
Profit CAGR
ROE
ROCE
Discovery themes featuring this stock
| Symbol | Watchlist | Price | Market Cap | P/E | P/B | Div Yield (%) | ROE (%) | ROCE (%) | ROA (%) |
1275.05 | 1,06,424 Cr | 25.36 | 2.81 | 0.63 | 11.07 | 12.54 | 7.15 | ||
2275.00 | 1,03,975 Cr | 19.50 | 4.63 | 0.79 | 23.76 | 24.88 | 13.96 | ||
2382.00 | 97,948 Cr | 51.20 | 6.01 | 0.04 | 11.74 | 13.13 | 6.90 | ||
1462.65 | 85,035 Cr | 24.26 | 2.24 | 0.00 | 9.25 | 11.76 | 5.99 | ||
1393.00 | 75,122 Cr | 84.52 | 14.17 | 0.14 | 16.77 | 16.14 | 8.47 | ||
416.40 | 67,559 Cr | 175.21 | 1.99 | 0.12 | 1.14 | 3.64 | 0.58 | ||
5301.00 | 63,388 Cr | 27.54 | 4.59 | 1.00 | 16.66 | 18.61 | 11.27 | ||
| Median: 7 Co. | — | 1462.65 | 85,035 Cr | 27.54 | 4.59 | 0.14 | 11.74 | 13.13 | 7.15 |
