Neuland Laboratories Limited (NEULANDLAB.NS) Bundle
Step into the world of Neuland Laboratories Limited-founded in 1984 and headquartered in Hyderabad-where a publicly listed CDMO combines a network of three regulatory-approved manufacturing facilities, a cutting-edge R&D center and a bench strength of over 300 scientists to serve more than 500 clients across 80+ countries; with a portfolio spanning APIs, advanced intermediates and peptide APIs, a track record of developing 300+ processes and 100+ APIs and filing over 950 regulatory submissions globally, Neuland's mission to improve patient outcomes through innovation, integrity and collaborative, sustainable partnerships maps directly onto a vision built on Transparency, Agility, Empathy and Accountability, positioning the company-listed on the BSE and NSE-as a resilient partner for cost-effective access to essential medicines across the US, Europe, Japan and Latin America.
Neuland Laboratories Limited (NEULANDLAB.NS) - Intro
Neuland Laboratories Limited (NEULANDLAB.NS), founded in 1984 and headquartered in Hyderabad, India, is a publicly listed contract development and manufacturing organization (CDMO) focused on active pharmaceutical ingredients (APIs), advanced intermediates, and peptide APIs. The company combines regulatory-approved manufacturing assets and a scientific workforce to serve global pharmaceutical customers across innovator, generic and OTC segments.- Founded: 1984 (Hyderabad, India)
- Business model: CDMO - APIs, advanced intermediates, peptide APIs, generic & OTC products
- Regulatory footprint: Listed on Bombay Stock Exchange (BSE) and National Stock Exchange (NSE)
- Client reach: >500 clients in 80+ countries (including US, EU, Japan, Latin America)
- Deliver high-quality, regulatory-compliant APIs and peptide solutions that enable global access to safe and affordable medicines.
- Drive innovation in process development, scale-up and regulatory support while maintaining responsible environmental and safety standards.
- Be a trusted global partner for pharmaceutical innovators and generics manufacturers by offering integrated CDMO capabilities, scientific excellence and compliant manufacturing across regulated markets.
- Quality & Compliance - maintaining regulatory approvals and robust quality systems across facilities.
- Scientific Excellence - continuous investment in R&D and technology to develop scalable, cost-effective processes.
- Customer Focus - partnership-oriented engagement with over 500 clients worldwide.
- Integrity & Safety - ethical conduct, product safety, and environmental responsibility.
- Innovation & Agility - developing new processes and expanding capability sets (including peptides).
- Manufacturing: Three regulatory-approved manufacturing facilities in India.
- R&D: State-of-the-art R&D center in Hyderabad with a scientific team of 300+ scientists.
- Process & filings: >300 developed processes, ~100 APIs and 950+ regulatory filings across the US, EU and other geographies.
| Metric | Value |
|---|---|
| Year Established | 1984 |
| Headquarters | Hyderabad, India |
| Manufacturing Facilities | 3 (regulatory-approved) |
| R&D Scientists | 300+ |
| Clients | 500+ |
| Countries Served | 80+ |
| Processes Developed | 300+ |
| APIs Developed | ~100 |
| Regulatory Filings | 950+ (US, EU, other) |
| Stock Exchanges | Bombay Stock Exchange (BSE), National Stock Exchange (NSE) |
Neuland Laboratories Limited (NEULANDLAB.NS) - Overview
Neuland Laboratories Limited's mission is to support its customers in advancing healthcare and improving patient outcomes. The company aims to be a reliable and trusted partner, delivering impactful solutions with a tenacious spirit that drives continuous improvement. Neuland's mission emphasizes innovation, integrity, collaboration, and progress. The company is committed to agility, ethical practices, partnerships, and sustainable growth. Neuland's mission reflects its dedication to creating a healthier world through sustainable practices, trusted partnerships, and agile collaboration. The company's mission aligns with its transformation journey, focusing on creating a healthier world not just today, but for decades to come.- Customer-centricity: partnering with global pharmaceutical innovators to co-develop and reliably supply Active Pharmaceutical Ingredients (APIs) and intermediates.
- Innovation-led growth: investing in process chemistry, scale-up capabilities, and niche complex APIs to move up the value chain.
- Ethical compliance: maintaining global regulatory standards (cGMP, USFDA/EDQM/EU expectations) as a baseline for all facilities and operations.
- Sustainability & safety: embedding environmental stewardship and employee safety in manufacturing processes and capital projects.
- Agility & collaboration: rapid technical responsiveness and long-term strategic alliances with customers and suppliers.
- To be a globally trusted CDMO and API partner known for complex chemistries, reliable supply continuity, and sustainable operations.
- To transform into a higher-margin, innovation-focused organization that balances scale with specialized capabilities.
- Integrity - transparent, ethical conduct across markets and partnerships.
- Excellence - rigorous quality, continuous improvement and operational discipline.
- Customer Success - aligning R&D, manufacturing and service to improve patient outcomes.
- Accountability - ownership from lab to plant to customer delivery.
- Respect & Inclusion - valuing people, safety and environmental responsibility.
| Metric | Approx. Value / Status |
|---|---|
| Annual Revenue (latest FY, approximate) | INR 1,100 crore (≈) |
| Net Profit (latest FY, approximate) | INR 120 crore (≈) |
| EBITDA Margin | ~18% (≈) |
| Export Contribution | ~80-85% of revenue (global CDMO/API clients) |
| R&D / Innovation Spend | ~3-5% of revenue (targeting complex chemistries) |
| Employees (approx.) | ~2,000-2,500 |
| Manufacturing footprint | Multiple facilities in India with cGMP-compliant plants and scaling capacity for commercial API manufacture |
| Market capitalization (approx.) | INR 3,000-3,800 crore (varies with market) |
- Quality & Compliance: sustain high regulatory-readiness to protect patient safety and secure long-term customer contracts.
- Portfolio Upgradation: shift toward higher-margin, complex APIs and CDMO services through targeted R&D investment (~4% of revenue).
- Supply Chain Resilience: diversify raw material sourcing and expand scale to provide continuity for global pharma partners (exports ~80% of sales).
- Sustainable Growth: reduce waste, improve energy efficiency and embed environmental metrics in capital projects to align with global ESG expectations.
- Partnership & Commercialization: deepen strategic alliances to convert development programs into multi-year manufacturing contracts, improving revenue visibility.
Neuland Laboratories Limited (NEULANDLAB.NS) - Mission Statement
Neuland Laboratories Limited's mission is to advance human health by developing and delivering high-quality active pharmaceutical ingredients (APIs) and integrated solutions through sustainable practices, trusted partnerships, and agile collaboration. The company aligns operational decisions with five core values-Transparency, Innovation, Agility, Empathy, and Accountability-so that scientific rigor and ethical conduct drive every stage from R&D to global supply.- Transparency: Open communication with partners, regulators, employees, and communities to build trust across the value chain.
- Innovation: Continuous investment in process chemistry, green chemistry, and formulation pathways to address unmet medical needs.
- Agility: Rapid, flexible responses to partner requirements, regulatory shifts, and supply-chain disruptions.
- Empathy: Prioritizing patient-centric outcomes and workforce wellbeing in decision-making.
- Accountability: Measurable commitments on quality, compliance, environmental stewardship, and social responsibility.
- Partnering with leading innovators to co-develop breakthrough molecules and scale commercial APIs that target unmet medical needs.
- Improving access and reducing cost of essential medicines through optimized manufacturing and collaborative licensing/contract models.
- Embedding sustainability across operations to benefit employees, suppliers, communities, and the environment-aiming for long-term health impacts over decades.
| Metric | Figure / Status |
|---|---|
| Years in operation | 40+ years |
| Manufacturing facilities | 4 facilities (API & intermediates; multi-site model) |
| Global reach | 70+ countries served (export-oriented business) |
| Employee base | ~2,000+ employees (R&D, manufacturing, quality, and commercial) |
| R&D workforce | 200+ scientists and technical staff |
| Strategic partnerships | Multiple long-term alliances with innovators, CMOs, and biotech firms |
- Quality & Compliance: Continuous investment in regulatory readiness (e.g., US FDA, EU, and other major regulatory frameworks) to ensure uninterrupted patient access.
- Capacity & Cost Efficiency: Scaling flexible manufacturing to lower per-unit costs for essential APIs and support generic and specialty pipelines.
- Sustainability: Initiatives to reduce waste, energy intensity, and carbon footprint while improving supplier sustainability practices.
- Talent & Culture: Building an empathetic, accountable workplace that fosters innovation and rapid problem-solving.
| Objective | Target / Indicator |
|---|---|
| Enhance access to essential drugs | Expand supply agreements and licensing to increase affordability and widen geographic distribution |
| Reduce environmental impact | Implement process intensification and waste-minimization across sites; continual improvement metrics tracked annually |
| Strengthen partnerships | Increase collaborative R&D projects and co-development agreements with biotech and pharma innovators |
| Employee wellbeing & development | Ongoing training, safety performance metrics, and programs for workforce inclusion and mental health |
Neuland Laboratories Limited (NEULANDLAB.NS) - Vision Statement
Neuland Laboratories Limited (NEULANDLAB.NS) envisions becoming a globally trusted, innovation-driven CDMO and API manufacturer that accelerates accessible therapeutics through chemistry excellence, sustainable operations, and stakeholder-centric performance. Core Values- Transparency - Open reporting, clear regulatory compliance, and consistent investor communication to build external trust and internal alignment.
- Innovation - Continuous refinement of chemical pathways, route scouting, and development of alternative manufacturing processes to reduce costs, increase yields, and de-risk supply chains.
- Agility - Customer-centric collaboration to deliver tailored, first-time-right solutions with accelerated timelines and flexible project execution.
- Empathy - Care for customers, colleagues, suppliers, patients, and the planet; embedding safety, ethics, and sustainability into decision-making.
- Accountability - Clear ownership from corporate strategy to team goals and individual responsibilities to ensure measurable delivery and compliance.
- Transparency: Regular disclosure cadence with quarterly investor communication and public regulatory filings; supplier audit transparency to reduce supply disruptions.
- Innovation: Investment in process chemistry and scalable route design - R&D intensity typically ranges in the mid-single digits of revenue, driving faster tech transfers and lower cost-of-goods.
- Agility: Cross-functional project teams reduce time-to-clinic / time-to-commercial by compressing typical CDMO timelines; customers receive tailored API routes with first-time-right targets.
- Empathy: Programs to ensure patient-centric quality, employee safety metrics, and supplier welfare checkpoints across the value chain.
- Accountability: KPIs cascaded from board-level strategy to shop-floor execution with regular performance reviews and corrective action loops.
| Metric | Data / Indicator |
|---|---|
| Founded | 1984 |
| Headquarters | Hyderabad, India |
| Manufacturing sites | 4 (multiple sites for intermediates, APIs, and dedicated contract manufacturing) |
| Workforce | ~2,500 employees (scientists, engineers, manufacturing & quality personnel) |
| Product breadth | Dozens of APIs and numerous advanced intermediates; broad portfolio serving oncology, CNS, and specialty segments |
| R&D intensity | Mid-single-digit % of revenue (investment in route design, process development, analytical methods) |
| Key markets | North America, Europe, Japan, and emerging markets; mix of captive and CDMO customers |
| Sustainability metrics | Continuous emission/effluent reduction projects; energy-efficiency upgrades and waste-minimization initiatives |
- Transparency enables investor confidence and smoother regulatory interactions: consistent reporting and disclosures reduce perceived risk and support capital-raising when needed.
- Innovation reduces COGS and shortens scale-up timelines: process re-design and alternative chemistries increase margins and protect supply continuity for customers.
- Agility improves customer retention and win rates: customer-focused teams and flexible capacity allocation drive faster time-to-market for partners.
- Empathy strengthens stakeholder relationships: prioritizing patient safety, supplier stability, and employee wellbeing lowers operational and reputational risk.
- Accountability aligns execution with financial and strategic targets: measurable KPIs (safety incidents per 100 employees, on-time delivery %, first-pass quality %) create clear performance expectations.
| Indicator | Representative Value / Target |
|---|---|
| On-time delivery (customer projects) | Target >90% |
| First-pass quality (batch acceptance) | Target >95% |
| R&D spend | ~5-7% of revenues (allocated to route scouting, process development, analytical work) |
| Employee safety | Year-on-year reduction in LTIs; sustained investments in training and EHS systems |
| Customer concentration | Balanced mix with emphasis on diversified CDMO contracts to mitigate single-customer risk |

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