Sun Pharmaceutical Industries Limited (SUNPHARMA)
₹1,758.80 -0.29% last close, 16 Oct
Q2 FY27 results
📅 Next results: 30 Oct 2026 (board meeting)Sun Pharmaceutical Industries Limited's board meets on 30 Oct 2026 to consider its Q2 FY27 results (July-September 2026).
In its latest reported quarter, Q1 FY27, Sun Pharmaceutical's revenue was ₹15,300 Cr (+10.5% year on year, +4.7% on the previous quarter), and net profit ₹2,895 Cr (+27.0% year on year); the operating margin was 28.9%.
| Q1 FY27 (₹ Cr) | Value | YoY vs Q1 FY26 | QoQ |
|---|---|---|---|
| Revenue | ₹15,300 | +10.5% | +4.7% |
| Operating profit | ₹4,418 | +2.7% | +11.7% |
| Net profit | ₹2,895 | +27.0% | +6.8% |
| EPS (₹) | 12.10 | +27.4% | +7.0% |
| Operating margin | 28.9% | — | — |
SUNPHARMA delivery percentage and open interest
NSE end-of-day data for
On Fri, 16 Oct 2026, 62.56% of the SUNPHARMA shares traded on NSE were taken to delivery, against the stock's own 20-session average of 64.85%. That is close to its usual level. In SUNPHARMA futures, open interest rose 0.04% while the futures price fell 0.33%: short buildup (new short positions). NSE's short-selling report for 15 Oct lists 3,500 SUNPHARMA shares sold short, 0.25% of that day's volume.
Delivery in the last 5 sessions: 59.8% · 61.1% · 68.3% · 65.9% · 62.6%
A description of what the exchange published, not a recommendation. Names such as "accumulation" or "long buildup" label a pattern in the numbers. How delivery is analysed
📢 Recent Corporate Announcements
Sun Pharmaceutical Industries Limited has submitted its quarterly compliance certificate under Regulation 74(5) of the SEBI (Depositories and Participants) Regulations, 2018. The certificate was issued by Registrar & Share Transfer Agent MUFG Intime India Private Limited for the quarter ended September 30, 2026. It confirms that all securities received for dematerialisation during the quarter were duly processed, accepted or rejected, and mutilated in accordance with prescribed timelines. This is a standard quarterly administrative filing with no financial or operational impact.
- Compliance certificate submitted under Regulation 74(5) of SEBI Depositories Regulations, 2018
- Applies to the quarter ended September 30, 2026
- Certificate issued by Registrar & Share Transfer Agent MUFG Intime India Private Limited on October 03, 2026
- Filing made to BSE (524715) and NSE (SUNPHARMA) on October 14, 2026
CRISIL and ICRA have assigned 'CRISIL AAA/Stable' and '[ICRA]AAA (Stable)' ratings to Sun Pharma's proposed Rs 15,000 crore Non-Convertible Debenture (NCD) program, while reaffirming existing AAA/A1+ ratings. The credit rating factors in Sun Pharma's proposed $11.75 billion acquisition of US-based Organon & Co. announced in April 2026. Sun Pharma plans to fund the deal via $2.0-2.5 billion in internal cash and $9.5-10.0 billion in additional debt, driving Net Debt to EBITDA to 1.5-2.0x in FY28 before rapid deleveraging.
- Crisil AAA/Stable assigned to proposed Rs 15,000 crore Non-Convertible Debentures (NCDs)
- Ratings factor in the mega $11.75 billion acquisition of Organon & Co., expanding pro-forma sales to ~$12.4 billion
- Acquisition to be funded by $2.0-2.5 billion internal cash surplus and $9.5-10.0 billion incremental debt
- Q1 FY27 operating income rose ~10% YoY to Rs 15,300 crore with operating profit of Rs 4,418 crore
- Net Debt to EBITDA expected to peak at 1.5-2.0x in FY28 followed by strong organic deleveraging
Sun Pharmaceutical Industries' Board approved the issuance of listed, rated, unsecured, redeemable Non-Convertible Debentures (NCDs) via private placement up to ₹10,000 Crore. This planned borrowing represents approximately 16.7% of TTM revenue (₹59,911 Cr) and about 73.5% of current debt (₹13,605 Cr). The Board has delegated tranche-specific terms to its Finance Committee. Additionally, Non-Executive Independent Director Gautam Doshi resigned effective 12 October 2026 citing personal reasons.
- Approved issuance of listed, rated, unsecured NCDs up to ₹10,000 Crore on a private placement basis
- Finance Committee authorised to finalise tranche-specific terms, conditions, and allotment
- Resignation of Non-Executive Independent Director Mr. Gautam Doshi effective 12 October 2026
- The ₹10,000 Cr borrowing limit compares against existing debt of ₹13,605 Cr and net worth of ₹22,371 Cr
Sun Pharmaceutical Industries' Board approved the issuance of listed, rated, unsecured, redeemable Non-Convertible Debentures (NCDs) via private placement up to ₹10,000 Crore. This planned borrowing represents approximately 16.7% of TTM revenue (₹59,911 Cr) and about 73.5% of current debt (₹13,605 Cr). The Board has delegated tranche-specific terms to its Finance Committee. Additionally, Non-Executive Independent Director Gautam Doshi resigned effective 12 October 2026 citing personal reasons.
- Approved issuance of listed, rated, unsecured NCDs up to ₹10,000 Crore on a private placement basis
- Finance Committee authorised to finalise tranche-specific terms, conditions, and allotment
- Resignation of Non-Executive Independent Director Mr. Gautam Doshi effective 12 October 2026
- The ₹10,000 Cr borrowing limit compares against existing debt of ₹13,605 Cr and net worth of ₹22,371 Cr
Sun Pharmaceutical Industries has established the Sun Professorship in Dermatology at the Icahn School of Medicine at Mount Sinai through a $2.5 million endowment. Mark G. Lebwohl, M.D., has been installed as the inaugural professor to lead dermatology research and education in perpetuity. With Sun Pharma operating as the second-largest U.S. dermatology player by prescription volume and innovative medicines accounting for ~22% of sales, the move deepens academic ties in a core therapy area. However, given the company's TTM revenue of ₹59,911 Cr, the $2.5 million (~₹21 Cr) financial outlay is immaterial.
- $2.5 million endowment funded by Sun Pharma to support academic leadership in perpetuity
- Mark G. Lebwohl, M.D., installed as inaugural professor at Mount Sinai
- Company identified as the second-largest U.S. dermatology company by prescription volume
- Global Innovative Medicines portfolio accounts for approximately 22% of company sales
Sun Pharmaceutical Industries has issued a Postal Ballot notice seeking shareholder approvals for financing arrangements related to the proposed acquisition of Organon & Co. The company is seeking approvals to enhance investment/loan limits under Section 186, borrowing limits under Section 180(1)(c), and creation of security/encumbrances over assets and shares. Additionally, Sun Pharma is seeking approval for ESOP 2026, which will be implemented via secondary market share purchases without equity dilution. E-voting runs from 02 October 2026 to 31 October 2026, with results expected on or before 03 November 2026.
- Seeking shareholder approval for enhanced borrowing limits and security creation to finance the acquisition of Organon & Co.
- Proposed ESOP 2026 will use secondary market acquisitions of equity shares, involving no fresh issue or equity dilution
- E-voting starts on Friday, 02 October 2026 at 09:00 AM IST and ends on Saturday, 31 October 2026 at 05:00 PM IST
- Cut-off date for eligibility to vote is Friday, 25 September 2026, with results declared on or before 03 November 2026
Sun Pharmaceutical announced positive two-year efficacy and safety data for LEQSELVI (deuruxolitinib 8 mg) in severe alopecia areata at the EADV Congress 2026. In an open-label extension study, 93.9% of baseline responders maintained their hair regrowth response (SALT score ≤20) at Week 108. Additionally, 76.6% of baseline nonresponders achieved response by Week 52, with 96.8% of those maintaining it through Week 108. The long-term safety profile showed no reports of deaths, thrombosis, or major adverse cardiovascular events at the FDA-approved dose.
- 93.9% of baseline responders maintained treatment response (SALT score ≤20) at Week 108
- 76.6% of baseline nonresponders reached response by Week 52, with 96.8% maintaining it through Week 108
- No reports of deaths, thrombosis, or major adverse cardiovascular events at the approved 8 mg twice-daily dose
- LEQSELVI is featured in 7 of Sun Pharma's 22 presentations across its dermatology and immunology portfolio at EADV 2026
Sun Pharmaceutical Industries has published its ESG Overview for FY 2025-26, prepared under GRI Standards 2021 and externally assured by DNV Business Assurance India. Key highlights include a 15.86% reduction in absolute Scope 1 and 2 carbon emissions and a 16.05% drop in absolute water consumption compared to the 2020 baseline. The company sourced 43% of its energy from renewables and invested INR 206.8 crore (INR 2,068 million) in CSR initiatives. The reporting boundary covers 44 manufacturing and R&D facilities accounting for ~97% of revenues.
- 15.86% absolute reduction and 48.64% intensity drop in Scope 1 and 2 carbon emissions vs 2020 baseline
- 16.05% reduction in absolute water consumption with 48.72% decrease in specific water intensity vs 2020
- 43% of total energy sourced from renewable power
- INR 2,068 million spent on CSR initiatives, impacting ~2.23 million lives in India
- Board composition maintains 50% independent directors and 95.24% average meeting attendance
Sun Pharmaceutical Industries Limited has concluded its Postal Ballot process initiated via notice dated 25 August 2026. Remote e-voting was conducted between 28 August 2026 and 26 September 2026. The company announced that the resolution set out in the notice was approved by shareholders with the requisite majority. Voting results and the Scrutinizer's Report have been submitted to exchanges and published on the company website.
- Postal Ballot notice was dated 25 August 2026
- Remote e-voting period commenced on 28 August 2026
- Voting concluded on 26 September 2026
- Resolution approved by shareholders by requisite majority
Sun Pharma has entered into an exclusive licensing, commercialization, and manufacturing agreement with LIB Therapeutics for Lerodalcibep (brand name Lyrokaul), a once-monthly PCSK9 inhibitor. The agreement covers worldwide rights excluding the US and China, targeting an ex-US/China PCSK9 market valued at US$ 3.7 billion that is growing at a 38% CAGR. Lyrokaul received EU regulatory approval on September 21, 2026. Deal financials include an upfront payment, future milestone payments, and net sales royalties, though specific deal amounts were not disclosed.
- Exclusive rights to manufacture and commercialize Lerodalcibep globally, excluding the US and China
- Targets an ex-US and China addressable PCSK9 market of US$ 3.7 billion (growing at 38% CAGR), with Europe representing US$ 2.9 billion
- Product received European Union marketing authorization on September 21, 2026 under the brand Lyrokaul
- Upfront, milestone payments, and sales royalties payable to LIB Therapeutics; exact figures not disclosed
Sun Pharmaceutical Industries Limited released its September 2026 corporate investor presentation detailing historical performance and therapeutic segment splits. The company reported FY26 gross sales of Rs 58,220.1 crore (Rs 582 Bn) with an EBITDA margin of 30.3% and Innovative Medicines contributing 22% of total sales. Geographically, India formulations formed 33% of FY26 revenues with an 8.4% domestic market share, while US formulations accounted for 29%. The presentation reinforces the company's financial profile without announcing any new business events, capex plans, or material transactions.
- Innovative Medicines reached 22% of sales in FY26 compared to 7.3% in FY18, with 29 marketed products globally
- Reported FY26 gross sales of Rs 582,201 mn with an EBITDA of Rs 177,314 mn (30.3% margin)
- India formulations contributed Rs 192,904 mn (33% of sales), maintaining rank No. 1 with an 8.4% market share
- US formulations generated Rs 168,242 mn (29% of sales), ranking 13th in the US generics market
- R&D investment stood at 6.1% of sales across 40 manufacturing facilities globally
Sun Pharmaceutical Industries announced that its subsidiaries (SPII, Taro Ltd., and Taro USA) have executed a settlement agreement with a plaintiff in the ongoing US Generic Pharmaceuticals Pricing Antitrust Litigation. The settlement resolves the action in the Eastern District of Pennsylvania for a confidential payment amount without any admission of wrongdoing. In exchange, the subsidiaries secure a full release of all asserted claims across affiliates, officers, and employees. Against Sun Pharma's TTM net profit of Rs 12,104 Cr, the resolution helps eliminate a lingering legacy legal overhang, though financial specifics remain undisclosed.
- Subsidiaries SPII, Taro Pharmaceutical Industries Ltd., and Taro Pharmaceuticals U.S.A. signed the settlement agreement on September 11, 2026
- Settlement involves a confidential payment amount for a full release of all claims asserted in the litigation
- Pertains to In re Generic Pharmaceuticals Pricing Antitrust Litigation in the Eastern District of Pennsylvania, U.S.
- Entered into without admission of any wrongdoing by the company or its subsidiaries
Sun Pharmaceutical Industries has incorporated a wholly owned indirect subsidiary, 'Sun Pharma Global Treasury Centre IFSC Limited', in GIFT City, Gandhinagar. The entity was incorporated on September 8, 2026, through Sun Pharma Laboratories Limited with an initial equity subscription of approximately ₹9.50 crore. The new unit will handle global treasury, funding, liquidity, and cash management operations for the Sun Pharma Group. Given Sun Pharma's TTM revenue of ₹59,911 crore and net worth of ₹22,371 crore, the financial outlay represents less than 0.05% of net worth and is immaterial to consolidated financials.
- Incorporated Sun Pharma Global Treasury Centre IFSC Limited on 08 September 2026
- Initial equity subscription of approximately INR 9.50 Crore in cash
- 100% shareholding held indirectly via wholly owned subsidiary Sun Pharma Laboratories Limited
- Pending approval/registration from the International Financial Services Centres Authority (IFSCA)
Sun Pharma has been assigned investment-grade issuer credit ratings of 'Baa1' (Stable) by Moody's and 'BBB+' (Stable) by S&P Global, both two notches above India's sovereign rating. The rating action incorporates Sun Pharma's proposed acquisition of Organon & Co. for an enterprise value of $11.75 billion, backed by $12 billion in committed bank financing. Moody's expects gross debt/EBITDA leverage to peak at ~3.0x by closing (targeted March 2027) before de-leveraging to ~2.0x within 18 months. Sun Pharma anticipates generating approximately $350 million in cost synergies over two to four years post-acquisition.
- Assigned Baa1 by Moody's and BBB+ by S&P Global, both with a Stable outlook.
- Ratings incorporate the proposed acquisition of Organon & Co. for an enterprise value of $11.75 billion.
- Secured $12 billion in committed acquisition bridge financing from international banks.
- Expected cost synergies of around $350 million over 2 to 4 years post-deal completion.
- Pro-forma gross debt/EBITDA leverage projected to rise to ~3.0x at closing (March 2027) from historical levels below 1.0x.
Sun Pharmaceutical Industries Limited has submitted an intimation under Regulation 30 regarding its schedule of upcoming institutional investor and analyst meetings. The company is slated to attend five physical conferences between September 10 and September 22, 2026, including summits hosted by UBS, Jefferies, Kotak, J.P. Morgan, and Anand Rathi. The interactions will include both group and one-on-one formats across Mumbai and Delhi. The company confirmed that no Unpublished Price Sensitive Information (UPSI) will be shared during these meetings.
- UBS India Summit 2026 scheduled for 10-Sept-26 in Mumbai (Physical Group & One-on-one)
- Jefferies India Forum 2026 scheduled for 16-Sept-26 in Delhi (Physical Group & One-on-one)
- Kotak Institutional Equities Healthcare Forum 2026 on 17-Sept-26 in Mumbai
- J.P. Morgan India Conference 2026 and Anand Rathi G-200 Summit on 21-Sept-26 and 22-Sept-26 in Mumbai
- No Unpublished Price Sensitive Information (UPSI) will be disclosed at these meetings
Financial Performance
Revenue Growth by Segment
Consolidated revenue grew 10% YoY in FY24 to INR 48,560 Cr and 8.6% YoY in Q2 FY26 to INR 14,405.2 Cr. Domestic formulations, the largest segment, contributed 33% of revenue in H1 FY25. The global specialty business grew to represent 18% of FY24 revenue and approximately 20% of total sales by Q2 FY26. Emerging Markets revenue grew 9.2% YoY to INR 9,416 Cr in FY25, while the US business saw a 4.1% decline to $496 million in Q2 FY26 due to generic pricing pressures.
Geographic Revenue Split
India formulations account for 33% of total revenue as of H1 FY25. The US market is a significant contributor, though it faced a 4.1% quarterly decline to $496 million in Q2 FY26. Emerging Markets (including Bangladesh, South Africa, and Russia) contributed INR 9,416 Cr in FY25, representing a 9.2% YoY growth. The 'Rest of World' markets (excluding India and US) are also expanding, though Japan faced moderate growth due to pricing pressures.
Profitability Margins
Adjusted Profit After Tax (APAT) margin was 19.5% in FY24 (INR 9,457 Cr) compared to 18.3% in FY23. Gross margin stood at 79.3% in Q2 FY26. Net profit for Q2 FY26 was INR 3,118 Cr, up 2.6% YoY. Margins are supported by the increasing mix of high-margin specialty products but are partially offset by R&D investments of 7-8% of revenue and high marketing expenses for new launches.
EBITDA Margin
EBITDA margin improved to 31.3% in Q2 FY26 compared to 29.6% in Q2 FY25, driven by a higher contribution from specialty medicines and operational efficiencies. Absolute EBITDA for Q2 FY26 was INR 4,527.1 Cr, registering a 14.9% YoY increase.
Capital Expenditure
The company has approved a major greenfield investment of INR 3,000 Cr for a formulations manufacturing facility in Madhya Pradesh. Annual organic maintenance capex is expected to remain moderate at $200-250 million (approx. INR 1,600-2,100 Cr), funded entirely through internal cash accruals.
Credit Rating & Borrowing
The company maintains a 'Stable' outlook from CRISIL Ratings. Debt reduced to INR 2,081 Cr as of September 30, 2024, from INR 2,846 Cr in March 2024. Interest coverage is exceptionally strong at 60.99 times, and the company holds a net cash surplus exceeding INR 25,000 Cr ($2.9 billion) as of Q2 FY26.
Operational Drivers
Raw Materials
Bulk drugs (APIs) and formulations are the primary raw material components, with bulk drugs accounting for approximately 5% of total revenue. Specific chemical names are not disclosed.
Import Sources
Not specifically disclosed, though the company operates manufacturing facilities in India, Bangladesh, South Africa, Malaysia, Romania, Egypt, Morocco, Nigeria, and Russia to support local supply chains.
Capacity Expansion
Current expansion includes a new INR 3,000 Cr greenfield formulations facility in Madhya Pradesh. The company also recently acquired all outstanding shares of Taro Pharmaceutical Industries Ltd for INR 2,902 Cr to consolidate its global generics footprint.
Raw Material Costs
Raw material costs are managed through vertical integration, particularly in the specialty and generic segments. While specific YoY cost changes for raw materials are not detailed, the gross margin of 79.3% suggests high value-add over base material costs.
Manufacturing Efficiency
The company focuses on vertical integration to ensure supply chain reliability. Efficiency is also driven by a dedicated sales force of over 2,900 representatives in emerging markets to maximize brand adoption.
Logistics & Distribution
The company utilizes a dedicated sales force and local manufacturing in key regions like Romania and Nigeria to reduce distribution lead times and manage costs.
Strategic Growth
Expected Growth Rate
7-9%
Growth Strategy
Growth will be achieved through the ramp-up of the global specialty portfolio (currently 20% of sales), new product launches in India (9 launched in Q2 FY26), and the INR 3,000 Cr greenfield expansion in Madhya Pradesh. Strategic acquisitions like Taro and Checkpoint, along with alliances like the AstraZeneca partnership for Hyperkalaemia, are key to expanding market reach.
Products & Services
Specialty and generic medicines in dermatology, ophthalmology, onco-dermatology, and chronic segments; bulk drugs (APIs); and consumer healthcare products.
Brand Portfolio
Sun Pharma, Taro, Checkpoint, and various chronic segment formulation brands.
New Products/Services
Launched 9 new products in India in Q2 FY26. The specialty portfolio, including innovative medicines, now accounts for 20% of total sales.
Market Expansion
Focusing on gaining critical mass in Emerging Markets and Western Europe. The company is expanding its specialty basket in these regions to move away from low-margin generics.
Market Share & Ranking
Ranked No. 1 in the Indian pharmaceutical market with an 8.1% market share as of September 2024.
Strategic Alliances
Partnered with AstraZeneca Pharma India Limited to distribute medicines for Hyperkalaemia in India.
External Factors
Industry Trends
The industry is shifting toward specialty and innovative medicines to counter generic pricing erosion. Sun Pharma is positioned as a leader in this shift, with specialty products growing to 20% of sales. The Indian market remains a high-growth area driven by chronic therapies.
Competitive Landscape
Faces intense competition in the US from authorized generics and customer consolidation. In India, it competes with local and international firms but maintains the top position in prescription volume.
Competitive Moat
The moat is built on a leadership position in the domestic chronic segment (8.1% share), a vertically integrated manufacturing model, and a growing portfolio of patented specialty products which are harder for competitors to replicate than standard generics.
Macro Economic Sensitivity
Highly sensitive to foreign exchange fluctuations; reported a forex gain of INR 430.5 Cr in Q2 FY26 compared to INR 128.1 Cr in the previous year.
Consumer Behavior
Demand is driven by healthcare professionals; Sun Pharma is the most prescribed company across 13 doctor categories, reflecting strong brand trust and medical representative reach.
Geopolitical Risks
Geopolitical tensions are cited as a primary risk to the global supply chain, potentially impacting manufacturing sites in regions like Russia and Egypt.
Regulatory & Governance
Industry Regulations
Subject to stringent US FDA inspections. Current import alerts are active for facilities in Halol (Gujarat), Toansa (Punjab), Dewas (MP), and Poanta Sahib (HP), which restrict US supply.
Environmental Compliance
The company has reduced Scope 1 and 2 emissions by 22% and water consumption by 31% as of FY24 against a 2020 baseline. 45% of energy is sourced from renewables.
Taxation Policy Impact
Effective Tax Rate (ETR) was 24.7% in Q2 FY26, up from 15.8% in Q2 FY25.
Legal Contingencies
Settled the GxMDL putative class action case for INR 1,711.2 Cr. Other ongoing litigations and disputed tax liabilities exist, though the impact is not fully ascertainable.
Risk Analysis
Key Uncertainties
Regulatory outcomes from the US FDA remain the primary uncertainty; adverse observations can lead to significant revenue loss (e.g., Halol's 3% impact). Litigation payouts, like the INR 1,711.2 Cr settlement, also impact liquidity.
Geographic Concentration Risk
High concentration in India (33% of revenue) and the US market. Any regulatory or policy change in these two regions significantly impacts the financial profile.
Third Party Dependencies
Not disclosed, but vertical integration in APIs reduces dependency on external suppliers for key products.
Technology Obsolescence Risk
The company manages technology risks through an ERM framework and focuses on upskilling its workforce (92% male, 8% female) to handle complex manufacturing processes.
Credit & Counterparty Risk
Credit risk is low given the 'Superior' liquidity rating and net cash position of over INR 25,000 Cr.