Gland Pharma Limited (GLAND)
₹3,043.40 -0.75% last close, 16 Oct
Latest quarterly results (Q4 FY26)
In its latest reported quarter, Q4 FY26, Gland Pharma's revenue was ₹1,743 Cr (+22.3% year on year, +2.8% on the previous quarter), and net profit ₹367 Cr (+96.7% year on year); the operating margin was 29.4%.
| Q4 FY26 (₹ Cr) | Value | YoY vs Q4 FY25 | QoQ |
|---|---|---|---|
| Revenue | ₹1,743 | +22.3% | +2.8% |
| Operating profit | ₹513 | +47.6% | +18.0% |
| Net profit | ₹367 | +96.7% | +40.4% |
| EPS (₹) | 22.26 | +96.6% | +40.3% |
| Operating margin | 29.4% | — | — |
GLAND delivery percentage
NSE end-of-day data for
On Fri, 16 Oct 2026, 48.03% of the GLAND shares traded on NSE were taken to delivery, against the stock's own 20-session average of 54.67%. That is close to its usual level. Volume was 0.3 times its average, well below normal.
Delivery in the last 5 sessions: 54.1% · 62.4% · 56.4% · 53.7% · 48.0%
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
Gland Pharma 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 its Registrar and Share Transfer Agent, MUFG Intime India Private Limited (formerly Link Intime India Private Limited), on October 03, 2026. It confirms that all securities received for dematerialisation during the quarter were processed and verified according to statutory rules. This is a standard quarterly administrative filing with no financial impact.
- Regulation 74(5) compliance certificate submitted for the quarter ended September 30, 2026
- Confirmation certificate issued by RTA MUFG Intime India Private Limited on October 03, 2026
- Company filing completed on October 12, 2026 with BSE and NSE
Gland Pharma Limited has issued a Postal Ballot Notice seeking shareholder approval via remote e-voting for the appointment of Mr. Xingli Wang as a Non-Executive and Non-Independent Director. Mr. Wang is currently the President of Fosun Pharma (promoter group entity holding 51.77% stake) and has extensive global pharmaceutical R&D experience. The remote e-voting window opens on October 07, 2026, and concludes on November 05, 2026, with the cut-off date set as October 01, 2026. Results will be announced on or before November 09, 2026.
- Postal ballot seeks approval for the appointment of Mr. Xingli Wang (DIN: 11899926) as Non-Executive & Non-Independent Director
- Remote e-voting period runs from October 07, 2026 (09:00 AM IST) to November 05, 2026 (05:00 PM IST)
- Record cut-off date for eligible voting members established as October 01, 2026
- Scrutinizer's results will be declared on or before November 09, 2026
- Appointee holds NIL equity shares in Gland Pharma as of October 01, 2026
Gland Pharma's Board approved an investment of USD 21 million (approx. ₹175 crore) into its wholly-owned subsidiary, Gland Pharma USA Inc. The subsidiary will use these funds to acquire a 60% controlling equity stake in Novelstar Pharma Inc., a newly incorporated US pharmaceutical entity, by October 31, 2026. Fosun Pharma USA Inc. (promoter group affiliate) will hold the remaining 40% equity in Novelstar. Additionally, Non-Executive Director Wenjie Zhang resigned, and Xingli Wang was appointed as an Additional Director.
- Board approved USD 21,000,000 cash investment in Gland Pharma USA Inc.
- Funds to be utilized to subscribe to 60% equity capital of Novelstar Pharma Inc. by October 31, 2026
- Fosun Pharma USA Inc. (affiliate of promoter) will hold the remaining 40% in Novelstar
- Post-acquisition capital of Novelstar will be USD 35,000,000; turnover is currently NIL
- Mr. Wenjie Zhang resigned as Director; Mr. Xingli Wang appointed as Additional Director
Gland Pharma Limited has approved an investment of USD 21 million into its subsidiary Gland Pharma USA Inc., which will acquire a 60% equity stake in newly incorporated Novelstar Pharma Inc. Fosun Pharma USA Inc., an affiliate of the promoter group, will hold the remaining 40% stake. The transaction is targeted for completion by October 31, 2026, to expand presence in the US pharmaceutical market. Separately, Non-Executive Director Wenjie Zhang resigned, and Xingli Wang (President of Fosun Pharma) was appointed as an Additional Director.
- Investment of USD 21,000,000 to acquire a 60% equity stake in Novelstar Pharma Inc.
- Promoter-affiliate Fosun Pharma USA Inc. to hold the remaining 40% equity in Novelstar Pharma Inc.
- Post-acquisition share capital of Novelstar Pharma Inc. to reach USD 35,000,000.
- Acquisition targeted to complete by October 31, 2026.
- Appointment of Mr. Xingli Wang as Additional Director following the resignation of Mr. Wenjie Zhang on October 01, 2026.
Gland Pharma's Board approved an investment of USD 21 million (approx. ₹175 crore) into its wholly-owned subsidiary, Gland Pharma USA Inc. The subsidiary will use these funds to acquire a 60% controlling equity stake in Novelstar Pharma Inc., a newly incorporated US pharmaceutical entity, by October 31, 2026. Fosun Pharma USA Inc. (promoter group affiliate) will hold the remaining 40% equity in Novelstar. Additionally, Non-Executive Director Wenjie Zhang resigned, and Xingli Wang was appointed as an Additional Director.
- Board approved USD 21,000,000 cash investment in Gland Pharma USA Inc.
- Funds to be utilized to subscribe to 60% equity capital of Novelstar Pharma Inc. by October 31, 2026
- Fosun Pharma USA Inc. (affiliate of promoter) will hold the remaining 40% in Novelstar
- Post-acquisition capital of Novelstar will be USD 35,000,000; turnover is currently NIL
- Mr. Wenjie Zhang resigned as Director; Mr. Xingli Wang appointed as Additional Director
Gland Pharma Limited has approved the acquisition of 100% equity share capital of its step-down subsidiary, Gland Pharma USA Inc., from its wholly-owned subsidiary, Gland Pharma International Pte. Ltd. The transaction consideration is USD 5,01,208 in cash, determined by an independent valuer. The move makes Gland US a direct wholly-owned subsidiary to remove intermediary holding layers and streamline operations. The target company reported Nil turnover in FY26 and USD 87,342 in FY25, representing negligible financial materiality relative to Gland's TTM revenue of Rs 6,431 Cr.
- Acquisition of 100% equity in Gland Pharma USA Inc. for a cash consideration of USD 5,01,208
- Share capital of target entity is USD 5,00,000
- Target reported Nil revenue for FY26, down from USD 87,342 in FY25 and USD 4,83,808 in FY24
- Transaction scheduled for completion by October 31, 2026
Gland Pharma's Board approved the acquisition of 100% equity share capital of Gland Pharma USA Inc. for a cash consideration of USD 5,01,208. The transaction involves buying shares from its wholly-owned subsidiary, Gland Pharma International Pte. Ltd, converting Gland US from a step-down unit into a direct wholly-owned subsidiary. Gland US reported nil turnover for FY26 and has a share capital of USD 5,00,000. The internal restructuring is expected to be completed by October 31, 2026, with no material operational or financial impact on the consolidated business.
- Board approved 100% acquisition of Gland Pharma USA Inc. for a cash payout of USD 5,01,208
- Gland US converts from a step-down subsidiary to a direct wholly-owned subsidiary
- Target entity generated Nil turnover in FY26, down from USD 87,342 in FY25 and USD 4,83,808 in FY24
- Expected completion timeline for the acquisition is by October 31, 2026
Gland Pharma Limited has allotted a total of 44,193 equity shares of Re. 1 face value following the exercise of options under its 2019 and 2025 ESOP schemes. Out of these, 42,393 shares were allotted to 35 employees under the ESOP 2025 scheme, and 1,800 shares were allotted to 1 employee under ESOP 2019. The company also announced the formal closure and winding up of its ESOP 2019 scheme, as all eligible options are fully exercised or lapsed. Total paid-up equity capital increased marginally to Rs 16.50 crore (165,010,854 shares), resulting in negligible equity dilution.
- Allotted 42,393 equity shares under ESOP 2025 and 1,800 equity shares under ESOP 2019
- Paid-up share capital increased marginally to Rs 16,50,10,854 across 16,50,10,854 shares of Re. 1 each
- Exercise prices ranged from Re. 1.00 to Rs. 937.20 per share across tranches
- Formal winding up and closure of the ESOP 2019 scheme approved as the pool is exhausted
Gland Pharma Limited has approved the grant of 5,90,249 employee stock options to 124 employees under the Gland Pharma Employee Stock Options Scheme 2025. Of these, 3,89,564 options are granted at an exercise price of INR 1,461.15 (a 50% discount to market price), while 2,00,685 options are granted at face value of INR 1. The options represent approximately 0.36% of the company's total equity share capital, leading to negligible potential dilution. Vesting occurs over three years: 34% by September 13, 2027, 33% by September 13, 2028, and 33% by September 13, 2029.
- Approved grant of 5,90,249 stock options to 124 employees
- 3,89,564 options granted at an exercise price of INR 1,461.15
- 2,00,685 options granted at face value of INR 1 per share
- Vesting schedule spread over 3 years: 34% in 2027, 33% in 2028, and 33% in 2029
- Exercise period is within a maximum of 2 years from each vesting date
Gland Pharma has reported board comments regarding fines of ₹70,000 each levied by NSE and BSE for a procedural delay under Regulation 17(1A). The breach involved a 34-day gap between the appointment of Independent Director Mr. William Keller (aged over 75) on June 15, 2026, and shareholder approval via postal ballot on July 18, 2026. The company suo motu paid the entire fine amount to ensure prompt closure. Financially, the ₹1.4 lakh fine is immaterial against Gland Pharma's TTM net profit of ₹1,028 crore.
- Fines of ₹70,000 each (excluding GST) levied by BSE and NSE, totaling ₹1,40,000.
- Non-compliance involved a 34-day technical breach under Regulation 17(1A) concerning director appointment.
- Director appointed on June 15, 2026, with shareholder approval completed on July 18, 2026.
- Entire penalty amount has already been paid suo motu by the company.
Gland Pharma has disclosed its schedule of upcoming analyst and institutional investor interactions slated from September 16 to September 25, 2026. The meetings include one-on-one sessions with East Bridge Capital, IIFL Capital, and Antique Broking, as well as a group meeting arranged by Nomura. These interactions are procedural and intended for standard corporate communication without disclosing unpublished price-sensitive information. The company reported TTM revenue of ₹6,431 Cr and TTM PAT of ₹1,028 Cr.
- One-on-one meeting scheduled with East Bridge Capital on September 16, 2026
- One-on-one meetings scheduled with IIFL Capital and Antique Broking on September 17, 2026
- Group meeting arranged by Nomura scheduled for September 25, 2026
Gland Pharma Limited has notified the stock exchanges regarding a scheduled analyst/institutional investor meeting. The company is set to conduct a one-on-one meeting with DSP Mutual Fund on September 11, 2026. This is a routine investor interaction under SEBI LODR Regulation 30. The meeting schedule remains subject to changes due to exigencies from either party.
- One-on-one institutional investor meeting scheduled for September 11, 2026
- Meeting participant is DSP Mutual Fund
- Intimation submitted pursuant to Regulation 30 of SEBI (LODR) Regulations, 2015
Gland Pharma Limited has notified the stock exchanges regarding an upcoming one-on-one institutional investor meeting with Kotak Mutual Fund. The meeting is scheduled to take place on September 09, 2026. This is a routine compliance disclosure under Regulation 30 of SEBI (LODR) Regulations, 2015, with no financial or operational updates disclosed in the intimation.
- One-on-one meeting scheduled with Kotak Mutual Fund
- Meeting date set for September 09, 2026
- Filing made pursuant to Regulation 30 of SEBI LODR Regulations, 2015
The United States Food and Drug Administration (USFDA) conducted a routine Good Manufacturing Practice (GMP) inspection at Gland Pharma's VSEZ Sterile Oncology Formulations and API facility in Visakhapatnam between August 24, 2026, and September 01, 2026. The inspection successfully concluded with zero (0) Form 483 observations. This clean outcome mitigates US regulatory risk for a key sterile injectable and API manufacturing site.
- USFDA routine GMP inspection conducted from August 24, 2026 to September 01, 2026
- Inspection concluded with ZERO (0) Form 483 observations
- Covers both the VSEZ Sterile Oncology Formulations Facility and API Facility at Visakhapatnam
- No violations, contraventions, or adverse operational impacts reported
Gland Pharma Limited has notified exchanges of its upcoming schedule for analyst and institutional investor interactions in September 2026. The engagements include one-on-one sessions with Carnelian Capital, First Ray Capital, WCM Investment, and LIC Mutual Fund between September 3 and September 7, 2026. Additionally, the company will attend group meetings arranged by ICICI Securities and JP Morgan, along with participating in the BofA Securities 2026 Asia Pacific Conference on September 21-22, 2026. These meetings are routine investor outreach interactions under SEBI LODR Regulation 30.
- One-on-one meetings scheduled with Carnelian Capital (September 03, 2026), First Ray Capital (September 04, 2026), and WCM Investment (September 04, 2026)
- One-on-one meeting with LIC MF arranged by 360One on September 07, 2026
- Group meetings lined up with ICICI Securities on September 18, 2026 and JP Morgan on September 24, 2026
- Participation in the BofA Securities 2026 Asia Pacific Conference from September 21, 2026 to September 22, 2026
Financial Performance
Revenue Growth by Segment
Consolidated revenue grew 6% YoY to INR 14,869 million in Q2 FY26. The US segment grew 8% YoY to INR 8,005 million. Other regulated markets (Europe, Canada, Australia, NZ) grew 18% YoY in H1 FY26. Cenexi revenue grew 10% YoY in Euro terms to EUR 88 million for H1 FY26. ROW own product sales grew 19% YoY, though offset by a 53% decline in tech transfer/CMO revenue.
Geographic Revenue Split
US market accounts for approximately 54% of Q2 revenue (INR 8,005 million). ROW market contributed INR 1,635 million (approx. 11%). India market generated INR 665 million (approx. 4.5%). Other regulated markets and Cenexi operations in Europe constitute the remaining balance.
Profitability Margins
Consolidated EBITDA margin stood at 21% for Q2 FY26. The base business (excluding Cenexi) maintained a high adjusted EBITDA margin of 36% in H1 FY26. Cenexi's EBITDA losses narrowed from EUR 11 million to EUR 5 million YoY in H1 FY26, showing a positive trend toward the Q3 breakeven target.
EBITDA Margin
Consolidated EBITDA was INR 3,139 million (21% margin), up 6% YoY. Adjusted EBITDA for H1 FY26 was INR 7,092 million (24% margin). The margin is currently suppressed by Cenexi's operational losses but supported by the core business's 36% margin profile.
Capital Expenditure
Capex is strictly allocated to high ROCE initiatives including CDMO expansion, GLP-1 capacity, and complex injectable capabilities. Specific INR values for total planned capex were not disclosed in the available documents.
Operational Drivers
Capacity Expansion
Expanding complex injectable manufacturing and adding GLP-1 capacity. A dedicated line for a large product is starting next quarter. Cenexi is targeting a EUR 50 million revenue run rate to achieve EBITDA breakeven.
Manufacturing Efficiency
Focusing on yield improvement and waste reduction through digitization. Cenexi is undergoing headcount optimization and finance/IT back-office integration with India to capture synergies.
Strategic Growth
Expected Growth Rate
19%
Growth Strategy
Growth is driven by a shift toward a differentiated complex portfolio, including CDMO launches of auto-injectors and pen-device systems. The company is expanding into GLP-1 capacity and complex injectables. Turnaround of Cenexi via price increases and product mix optimization is expected to contribute to margin expansion. New product launches like Dalba (this quarter) and Cangrelor (future) are key drivers.
Products & Services
Injectables, CDMO services, auto-injectors, pen-device systems, and specialty segment medicines including Dalba and Cangrelor.
Brand Portfolio
Gland Pharma, Cenexi.
New Products/Services
New launches contributed 7% to US growth in Q2 FY26. Key upcoming products include Dalba and complex injectables using new manufacturing technologies.
Market Expansion
Expanding presence in regulated markets (US/Europe) through CDMO contracts and increasing penetration in ROW markets where own product sales grew 19%.
Strategic Alliances
CDMO partnerships with major firms like Eli Lilly and Dr. Reddy's (DRL) for tech transfer and manufacturing.
External Factors
Industry Trends
The industry is shifting toward complex injectables and CDMO outsourcing. Gland is positioning itself as a global innovation-led injectable company, moving away from simple generics to high-margin niche formulations to counter competitive pricing.
Competitive Landscape
Operates in a competitive pricing environment in the US. Competitors include other global injectable players and CDMOs.
Competitive Moat
Moat is built on complex manufacturing capabilities (auto-injectors, pen-devices) and a high-margin CDMO model. This is sustainable because these technologies are harder to replicate than standard injectable lines, creating higher switching costs for partners.
Macro Economic Sensitivity
Sensitive to the US regulatory and licensing environment; a 'wait and see' approach by US partners has slowed licensing, reducing milestone revenue by approximately 44% from normal levels.
Consumer Behavior
Increased demand for advanced delivery systems like auto-injectors and pen-devices in the specialty segment.
Regulatory & Governance
Industry Regulations
Fontenay site GMP certification renewed through end of 2026 following an ANSM inspection in July. Compliance with high quality standards is maintained to ensure margin resilience in regulated markets.
Risk Analysis
Key Uncertainties
Milestone revenue timing and US licensing slowdowns pose a 40-50% risk to the normal milestone revenue run rate. Cenexi's ability to hit the EUR 50 million Q3 target is critical for consolidated breakeven.
Geographic Concentration Risk
High concentration in the US market (over 50% of revenue), making the company sensitive to US GPO contracts and FDA/regulatory shifts.
Third Party Dependencies
Dependency on GPOs for US market access; new GPO contracts generated 10% growth in the latest quarter.
Technology Obsolescence Risk
Risk of falling behind in complex delivery systems; mitigated by capex allocation to GLP-1 and new pen-device technologies.