Shilpa Medicare Limited (SHILPAMED)
₹937.60 +1.68% last close, 16 Oct
Latest quarterly results (Q1 FY27)
In its latest reported quarter, Q1 FY27, Shilpa Medicare's revenue was ₹466 Cr (+44.9% year on year, +6.6% on the previous quarter), and net profit ₹101 Cr (+115.2% year on year); the operating margin was 29.3%.
| Q1 FY27 (₹ Cr) | Value | YoY vs Q1 FY26 | QoQ |
|---|---|---|---|
| Revenue | ₹466 | +44.9% | +6.6% |
| Operating profit | ₹136 | +48.7% | +13.5% |
| Net profit | ₹101 | +115.2% | -6.6% |
| EPS (₹) | 5.16 | +115.4% | -6.4% |
| Operating margin | 29.3% | — | — |
EPS restated for the 1:1 bonus of Oct 2025: Q1 FY26 ₹4.79 to ₹2.40.
SHILPAMED delivery percentage
NSE end-of-day data for
On Fri, 16 Oct 2026, 42.27% of the SHILPAMED shares traded on NSE were taken to delivery, against the stock's own 20-session average of 42.58%. That is close to its usual level.
Delivery in the last 5 sessions: 39.3% · 46.7% · 48.4% · 56.6% · 42.3%
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
Shilpa Medicare has received GMP certification from AGES, Austria, for its Unit 4 formulation facility located in Jadcherla, Telangana. The certification follows an inspection conducted between 27 July 2026 and 30 July 2026. The facility manufactures sterile injections as well as non-sterile tablets and capsules for European and global markets. This clearance supports the company's stated strategy to expand complex finished dosage formulations (FDF) across the EU.
- AGES Austria completed the GMP inspection from 27 July, 2026 until 30 July, 2026
- GMP Certification issued for Unit 4 facility located at Jadcherla, Telangana
- Approval covers manufacturing, testing, and distribution of sterile injections and non-sterile tablets/capsules
- Authorizes supply to Europe and rest of the world markets
Shilpa Medicare Limited has submitted its quarterly compliance certificate under Regulation 74(5) of the SEBI (Depositories and Participants) Regulations, 2018 for the quarter ended September 30, 2026. The certificate was issued by Registrar and Share Transfer Agent KFin Technologies Limited on October 02, 2026. It confirms that securities dematerialized and rematerialized during the period have been duly processed and reported to stock exchanges. This is a recurring regulatory filing with zero financial or operational impact.
- Compliance submission under Regulation 74(5) for the quarter ended September 30, 2026
- Certificate issued by Registrar KFin Technologies Limited on October 02, 2026
- Filing submitted to BSE and NSE on October 07, 2026
The USFDA conducted a surveillance inspection at Shilpa Medicare's Unit VII (Analytical Services Division) in Hyderabad from 16 September 2026 to 18 September 2026. The inspection concluded with a single procedural observation. The company confirmed the observation is not a repeat issue and is unrelated to data integrity. Shilpa Medicare expects no material financial or operational impact on existing business or supplies from this facility, and will submit its response within the stipulated regulatory timeline.
- Surveillance inspection conducted from 16 September 2026 to 18 September 2026
- Concluded with 1 observation, classified as purely procedural
- Zero data integrity issues or repeat observations reported
- No material impact expected on current business operations or existing supplies
Shilpa Medicare has declared the voting results of its 39th Annual General Meeting held on September 11, 2026. All five ordinary resolutions were approved by shareholders with requisite majorities. Key approvals include the adoption of FY26 financial statements, declaration of a final dividend of ₹0.60 per equity share, and payment of commission to Non-Executive Director Madhav Vishnukant Bhutada of material subsidiary Shilpa Biologicals. Notably, 33.37% of public institutional votes were cast against the director commission resolution, though it passed overall with 88.80% approval.
- Declared final dividend of ₹0.60 per equity share for FY26
- Adoption of FY26 financial statements passed with 100.00% votes in favour (11,26,52,854 votes)
- Payment of commission to Mr. Madhav Vishnukant Bhutada approved with 88.80% votes in favour
- Institutional pushback on director commission resolution with 33.37% (90,66,195 votes) voted against
- Re-appointment of Director Sharath Reddy Kalakota approved with 99.38% voting in favour
Shilpa Medicare has received final approval from the Subject Expert Committee (SEC) under CDSCO for the grant of marketing authorization for OERIS (Ondansetron Extended-Release Injection, 100 mg/mL). The product is designed as the world's first extended-release ondansetron injection, delivering sustained antiemetic protection for up to 120 hours (5 days) via a single dose. The formulation holds Indian patent protection until 2039. Commercial launch across India will follow final formal authorization from CDSCO, adding to its high-margin complex oncology formulations portfolio.
- SEC issued final approval for marketing authorization of OERIS (100 mg/mL)
- Provides sustained antiemetic protection for up to 120 hours (5 days) from a single administration
- Product is patent protected in India until 2039
- Approval backed by completion of a multicenter, randomized, double-blind Phase III clinical trial
Shilpa Medicare Limited conducted its 39th Annual General Meeting on September 11, 2026, via Video Conferencing. Key business transacted included the adoption of FY26 financial statements and the approval of an ordinary dividend of ₹0.60 per equity share. Other resolutions included the reappointment of retiring director Mr. Sharath Reddy Kalakota, ratification of cost auditor remuneration, and commission payment to Non-Executive Director Mr. Madhav Vishnukant Bhutada of subsidiary Shilpa Biologicals. Voting results are scheduled to be submitted following Scrutinizer verification.
- 39th Annual General Meeting held on September 11, 2026, with 48 members attending via Video Conferencing
- Approval sought for dividend declaration of ₹0.60 per equity share for FY26
- Total registered shareholder count stood at 80,572 as on the record date of September 4, 2026
- Resolutions transacted include approval of audited standalone/consolidated FY26 financials and director re-appointment
The NCLT Ahmedabad Bench has admitted an insolvency application under Section 9 of the IBC against FTF Pharma Private Limited, a wholly owned subsidiary of Shilpa Medicare. The petition was filed by Immacule Lifesciences regarding an operational debt of ₹2,18,03,319 (~₹2.18 crore). An Interim Resolution Professional has been appointed and a moratorium declared under Section 14. Relative to Shilpa Medicare's TTM revenue of ₹1,683 crore and FY26 PAT of ₹243.5 crore, the debt amount is small, but CIRP proceedings pose operational risk to the subsidiary.
- NCLT Ahmedabad Bench admitted application CP (IB) No. 346 (AHM) 2025 on September 9, 2026
- Proceedings initiated over an alleged operational debt claim of ₹2,18,03,319 (~₹2.18 crore)
- Corporate Insolvency Resolution Process (CIRP) and Section 14 moratorium ordered on subsidiary FTF Pharma
- Mr. Sunil Kumar Kedia appointed as the Interim Resolution Professional (IRP)
- Claim amount of ₹2.18 crore represents ~0.13% of Shilpa Medicare's TTM revenue of ₹1,683 crore
Shilpa Medicare Limited has dispatched communication to shareholders whose e-mail addresses are not registered with the company or depositories, providing web-links to the FY 2025-26 Annual Report and 39th AGM Notice. The 39th Annual General Meeting is scheduled to be held virtually on Friday, September 11, 2026, at 11:00 AM IST. The cut-off date for remote e-voting and AGM participation has been set for Friday, September 4, 2026. Remote e-voting will run from September 7, 2026 (9:00 AM) to September 10, 2026 (5:00 PM).
- 39th Annual General Meeting (AGM) scheduled for September 11, 2026, at 11:00 AM IST via VC/OAVM
- Cut-off date for e-voting eligibility fixed as Friday, September 4, 2026
- Remote e-voting window opens September 7, 2026 (09:00 AM) and closes September 10, 2026 (05:00 PM)
- Letter dispatched under Regulation 36(1)(b) of SEBI LODR Regulations for FY 2025-26 Annual Report links
Shilpa Medicare responded to media reports confirming a voluntary Class II recall initiated on July 29, 2026, for 27,923 vials of Pemetrexed Injection (Pemetri RTU™) in the US. The recall covers 4 batches (18,434 vials of 10 mL and 9,489 vials of 50 mL) due to atypical discoloration described as green to dark green. No adverse events have been reported, and the issue is restricted to these specific batches. Management affirmed that the recall will have no material impact on the company's financial position, operations, or supply continuity.
- Voluntary Class II recall initiated on July 29, 2026, covering 27,923 vials of Pemetrexed Injection in the US.
- Affected quantities comprise 18,434 vials of 10 mL and 9,489 vials of 50 mL across 4 batches.
- Triggered by atypical green to dark green discoloration deviating from approved color specifications.
- Zero adverse events reported; no material financial or operational impact anticipated by management.
Shilpa Medicare has issued a detailed communication to shareholders regarding Tax Deducted at Source (TDS) norms for its recommended final dividend of Re. 0.60 per equity share (face value Re. 1) for FY26. The Board has set Friday, September 4, 2026, as the record date to determine eligible shareholders ahead of the AGM on September 11, 2026. Shareholders eligible for lower or nil withholding tax must upload required forms and tax declarations by September 2, 2026. Approved dividends will be disbursed within 30 days of the AGM.
- Final dividend recommended at Re. 0.60 per equity share of Re. 1/- each for FY26
- Record date fixed as Friday, September 4, 2026 for dividend entitlement
- Annual General Meeting (AGM) scheduled for Friday, September 11, 2026
- Deadline to submit tax exemption documents and declarations is September 2, 2026
- Standard TDS rate stands at 10% for resident individuals (above Rs. 10,000 dividend payout)
Shilpa Medicare has issued a notice for its 39th Annual General Meeting (AGM) to be held on September 11, 2026. The company has proposed a final dividend of ₹0.60 per equity share for FY26, following a year where revenue grew to ₹1,538 Cr. A notable agenda item is the proposal to pay a commission of up to 1% of net profits of the material subsidiary, Shilpa Biologicals Private Limited, to Mr. Madhav Bhutada (son of the Managing Director). Shareholders as of the September 4, 2026 cut-off date will be eligible to vote on these resolutions.
- Proposed final dividend of ₹0.60 per equity share for the financial year ended March 31, 2026.
- 39th AGM scheduled for September 11, 2026, at 11:00 AM IST via video conferencing.
- Proposal to pay commission up to 1% of net profits of subsidiary Shilpa Biologicals to Mr. Madhav Bhutada.
- Cut-off date for determining shareholder voting eligibility is September 4, 2026.
- Ratification of ₹75,000 remuneration for Cost Auditors for the financial year ending March 31, 2027.
Shilpa Medicare reported its highest-ever quarterly revenue of 469 Cr (+43% YoY) and EBITDA of 139 Cr (+42% YoY) for Q1 FY27. The company has successfully deleveraged, reducing its net debt-to-EBITDA from 6.7x to 1.3x over three years, resulting in a credit rating upgrade to AA-. Management indicates the heavy investment phase is largely complete, with 'harvesting' beginning via complex launches like Rotigotine and Abraxane in FY28. Biologics revenue reached 50 Cr this quarter, with the Aflibercept biosimilar launch expected in India in FY27.
- Record quarterly revenue of 469 Cr, representing 43% YoY growth and 42% EBITDA growth.
- Net debt-to-EBITDA significantly reduced to 1.3x from 6.7x three years ago, with a credit rating upgrade to AA-.
- Peptide manufacturing capacity expansion in India on track for commissioning by end of FY27.
- Formulation division maintains high margins with over 50% captive API sourcing and 71% gross margins.
- Biologics segment scaling with 50 Cr revenue in Q1 and 6 active NCE programs in the pipeline.
Shilpa Medicare has made the audio recording of its Q1 FY2026-27 investor conference call available to the public. The call, held on August 5, 2026, follows a period of strong growth where the company reported a TTM revenue of ‡1,538 Cr and a PAT of ‡243 Cr. Management typically uses these calls to discuss the progress of high-margin projects like the Albumin fermentation facility and the NorUDCA launch. This filing is a standard regulatory requirement to ensure transparency for all shareholders.
- Conference call for Q1 FY2026-27 held on August 5, 2026, at 16:00 hrs
- Audio recording uploaded to the company website as per regulatory norms
- Company maintains a TTM revenue of ‡1,538 Cr with an OPM of 28.2%
- Promoter holding remains stable at 40.13% as of March 2026
- Gross Block stood at ‡2,049 Cr as of H1 FY26, reflecting ongoing capacity expansion
Shilpa Medicare reported its highest-ever quarterly revenue of ₹469 Cr for Q1 FY27, a 43% YoY increase driven by growth across API, Formulations, and Biologicals. Profitability saw a significant jump with PAT rising 115% YoY to ₹101 Cr, while EBITDA margins remained robust at 30%. A key highlight is the credit rating upgrade from A+ to AA-, reflecting a strengthened balance sheet and improved return ratios, with adjusted ROCE reaching 18.3%. The company is actively expanding its oncology and peptide capacities, with a new oncology block slated for completion by the end of FY27.
- Achieved record quarterly revenue of ₹469 Cr, representing a 43% YoY growth compared to ₹328 Cr in Q1 FY26.
- PAT surged by 115% YoY to ₹101 Cr, up from ₹47 Cr in the same quarter last year.
- Credit rating upgraded to AA- from A+, signaling improved financial stability and lower risk profile.
- Adjusted ROCE (excluding Biologics/NBE) improved to 18.3% from 17.4% in FY26 and 3.4% in FY23.
- Net Debt to EBITDA ratio further improved to 1.3x, down from 1.4x in FY26 and 6.7x in FY23.
Shilpa Medicare has finalized September 4, 2026, as the record date for its final dividend for the financial year 2025-26. This follows the board's recommendation on May 22, 2026, and is subject to shareholder approval at the Annual General Meeting (AGM) scheduled for September 11, 2026. The company recently reported a strong FY26 performance with a net profit of ₹243.5 crore, a significant jump from ₹43.9 crore in FY25. The dividend payout reflects the company's improved cash flow and operating leverage, with OPM reaching 28.2%.
- Record date for dividend entitlement fixed as Friday, September 4, 2026
- Annual General Meeting (AGM) to be held on September 11, 2026, for final approval
- Dividend recommendation was originally announced on May 22, 2026
- Company reported TTM PAT of ₹243.47 crore against a market cap of ₹10,581 crore
- Operating profit margin (OPM) stands at 28.2% for the TTM period
Financial Performance
Revenue Growth by Segment
Consolidated revenue grew 7% YoY to INR 372 Cr in Q2 FY26 and 8% YoY to INR 700 Cr in H1 FY26. Segmental growth for H1 FY26: Non-captive API grew 19% YoY (INR 205 Cr in Q2), Formulations grew 16% YoY (INR 109 Cr in Q2), and Biologics recorded INR 61 Cr revenue. Base business formulations (excluding licensing) grew 60% in Q2 and 67% in H1 FY26.
Geographic Revenue Split
In FY25, EU region formulations revenue was INR 110.67 Cr (up 28.8% from INR 85.91 Cr in FY24), while US region revenue was INR 47.55 Cr (down 12% from INR 54.02 Cr in FY24).
Profitability Margins
Gross margin improved to 72% in Q2 FY26 and 74% in H1 FY26. Net Profit (PAT) for H1 FY26 was INR 91 Cr, already surpassing the full-year FY25 PAT of INR 78.29 Cr. Standalone Net Profit Ratio improved from 6.34% in FY24 to 12.09% in FY25.
EBITDA Margin
EBITDA margin reached 30% in Q2 FY26 (up 4% YoY) and 30% in H1 FY26 (up 3% YoY). EBITDA for Q2 FY26 crossed the INR 100 Cr landmark for the first time, reaching INR 110 Cr (up 21% YoY).
Capital Expenditure
Net Capex for H1 FY26 was INR 153 Cr, primarily directed toward the Albumin facility and API capacity expansion. FY25 full-year capex was INR 216 Cr.
Credit Rating & Borrowing
Net debt stood at INR 569 Cr as of September 2025. Net Debt to EBITDA ratio improved to 1.4x in H1 FY26 from 1.6x in FY25. Standalone Debt Equity Ratio was 0.04x in FY25.
Operational Drivers
Raw Materials
Not disclosed in available documents; however, the company emphasizes 'smarter sourcing' to maintain margins.
Capacity Expansion
Current Gross Block is INR 2,049 Cr as of H1 FY26, up from INR 1,991 Cr in FY25. Expansion is focused on a new Albumin fermentation facility and API capacity enhancements.
Raw Material Costs
Not disclosed as a specific percentage of revenue, but gross margins of 74% in H1 FY26 indicate a raw material cost of approximately 26% of revenue.
Manufacturing Efficiency
Adjusted ROCE (excluding Biologics/NBE) improved significantly from 4% in FY23 to 17.2% in H1 FY26, reflecting improved operating leverage.
Strategic Growth
Expected Growth Rate
20%
Growth Strategy
The company plans to monetize significant investments in Biologics, Transdermal, and Albumin fermentation facilities over the next 3-5 years. Growth is driven by increasing market share in complex FDF products in the US and EU, and the launch of novel products like NorUDCA.
Products & Services
Oncology and CNS therapies, novel drug NorUDCA (for NAFLD), Adalimumab (biosimilar), Albumin, and high-quality generic formulations and APIs.
Brand Portfolio
Shilpa Medicare, Shilpa Pharma Lifesciences, Shilpa Biologicals.
New Products/Services
Novel product NorUDCA for NAFLD (supply price model) and Adalimumab biosimilar. Base business growth of 60% in Q2 FY26 was driven by complex product portfolio scale-up.
Market Expansion
Targeting US and EU markets with complex FDF products and limited competition products. Phase III trials for NorUDCA are planned for Europe and the US.
Market Share & Ranking
The company has achieved 'decent market share' in Adalimumab despite a late launch; specific ranking not disclosed.
Strategic Alliances
Licensing model involves partnering with global pharmaceutical companies for commercialization in the US and EU, earning upfront fees, milestones, and supply revenue.
External Factors
Industry Trends
The pharmaceutical industry is shifting toward specialty drugs, oncology, and global partnerships. Shilpa is positioning itself in complex generics and biosimilars to capture this 15-20% industry growth trajectory.
Competitive Landscape
Shilpa is the first company to treat NAFLD with NorUDCA in India, providing a first-mover advantage in a high-patient-volume market.
Competitive Moat
Moat is built on IP creation, technical know-how in complex developments, and a strong R&D team. The company leverages a low-capital, high-margin licensing strategy for niche generics.
Consumer Behavior
Increasing demand for complex specialty drugs and biosimilars globally.
Regulatory & Governance
Industry Regulations
Operations are subject to various audit systems to monitor efficacy and adequacy of internal control systems and compliance with operating procedures.
Taxation Policy Impact
Effective tax rate for FY25 was approximately 36% based on Consolidated PBT of INR 122.33 Cr and PAT of INR 78.29 Cr.
Risk Analysis
Key Uncertainties
Uncertainties include the successful monetization of large unutilized capacities in Biologics and the timing of Phase III trials for NorUDCA in US/EU markets.
Geographic Concentration Risk
Significant revenue concentration in the EU (INR 110.67 Cr) and US (INR 47.55 Cr) for the formulations business.
Third Party Dependencies
Dependency on global partners for the commercialization and regional distribution of licensed molecules.
Technology Obsolescence Risk
Mitigated by continuous investment in high-growth potential biologics and NBE (New Biological Entities) business.
Credit & Counterparty Risk
Trade Receivable Turnover Ratio was 2.86x in FY25, indicating stable receivables quality.