Alizapride Market by Route Of Administration (Intramuscular, Intravenous, Oral), Therapeutic Indication (Chemotherapy Induced Nausea, Postoperative Nausea, Pregnancy Related Nausea), Distribution Channel, End User - Global Forecast 2025-2032
Description
The Alizapride Market was valued at USD 412.60 million in 2024 and is projected to grow to USD 438.82 million in 2025, with a CAGR of 7.30%, reaching USD 725.44 million by 2032.
A strategic overview detailing how clinical utility, regulatory pathways, and commercial dynamics converge to shape adoption of alizapride across care settings
Alizapride occupies a distinct niche in antiemetic therapy with a pharmacological mechanism that complements commonly used alternatives and informs clinical decision pathways. The compound’s antiemetic efficacy, dosing flexibility across multiple routes of administration, and tolerability profile have driven adoption in settings that prioritize rapid onset of symptom control and predictable outcomes. Clinical stakeholders evaluate alizapride not only against efficacy metrics but also for its capacity to integrate into multimodal care protocols that address nausea driven by chemotherapy, surgical procedures, and pregnancy.
Concurrently, regulatory trajectories and evolving labeling considerations influence formulary decisions and hospital protocols. Payors and procurement teams factor in formulary tiering and practicalities such as storage, preparation time, and compatibility with existing administration infrastructure. From a commercial perspective, manufacturers and distributors are responding to these clinical and regulatory signals by optimizing packaging formats, expanding distribution pathways, and investing in targeted educational outreach to prescribers and nursing teams. As a result, the clinical utility of alizapride is increasingly evaluated through the prism of system-level adoption barriers and enablers rather than purely by isolated efficacy outcomes.
How evolving patient-centric care models, regulatory emphasis on real-world outcomes, and distribution innovations are reshaping antiemetic treatment paradigms
The therapeutic landscape surrounding antiemetics has undergone transformative shifts driven by advances in personalized care, novel administration approaches, and changing expectations for patient experience. Clinicians are placing greater emphasis on tailoring antiemetic regimens to patient phenotypes, procedural risks, and concurrent therapies, which has elevated the importance of agents that offer flexible dosing and rapid onset. Technological improvements in outpatient infusion devices and the maturation of home care services have broadened where and how antiemetics are delivered, encouraging formulations and packaging optimized for those environments.
At the same time, regulatory frameworks are adapting to evidence that prioritizes patient-reported outcomes and real-world effectiveness. This has prompted manufacturers to align development strategies with pragmatic trials and post-market evidence generation. Commercially, payors and hospital systems are incentivizing therapies that reduce downstream resource utilization, such as shortened stays and reduced readmissions associated with poorly controlled nausea. Together, these shifts are reshaping procurement criteria, clinical guidelines, and the competitive differentiation playbook for alizapride and its therapeutic peers.
Assessing the operational and strategic repercussions of 2025 United States tariff measures on pharmaceutical sourcing, supply resilience, and procurement choices
The announcement and implementation of tariff measures in the United States for 2025 introduced a layer of commercial complexity for stakeholders across pharmaceutical supply chains. Manufacturers, distributors, and procurement teams must now operate with heightened sensitivity to cross-border cost drivers and the potential for supply routing adjustments. In response, several organizations have revisited sourcing strategies, prioritized near-shoring where feasible, and accelerated supplier diversification to mitigate tariff exposure. This recalibration affects not only landed cost calculations but also timing, as lead times and customs processes may be adjusted to smooth continuity of supply.
Moreover, the tariff environment has prompted downstream purchasers to re-evaluate contractual terms and to explore strategic purchasing pools or longer-term purchase agreements that can provide pricing stability. Regulatory compliance teams have expanded scrutiny of classification and valuation practices at customs to ensure defensible tariff positions. Clinicians and hospital supply managers, while focused on clinical outcomes, are increasingly involved in discussions about product variants and packaging formats that may be less affected by import duties. Looking ahead, many market participants are investing in enhanced scenario planning and stress-testing commercial models to preserve access and maintain therapeutic continuity under variable trade conditions.
In-depth segmentation synthesis revealing how administration routes, distribution channels, end-user types, and therapeutic indications interact to direct clinical and commercial strategies
A granular segmentation lens reveals how route, distribution, end-user, and therapeutic indication considerations collectively shape clinical adoption and commercial strategy for alizapride. Route of administration considerations encompass intramuscular options, differentiated by multi-dose and single-dose formats, intravenous delivery that includes both bolus infusion and continuous infusion approaches, and oral modalities offered as solutions or tablets; each of these choices carries implications for dosing convenience, nursing time, and formulary placement. Distribution channel dynamics map to hospital pharmacies, which separate private and public hospital procurement practices; online pharmacies, which operate through direct-to-patient models or third-party marketplaces; and retail pharmacies where chain versus independent operators follow distinct inventory and stocking logics.
From the end-user perspective, demand signals vary across clinics that serve general or oncology populations, home care that relies on nurse-administered or self-administered protocols, and hospitals that differentiate between private and public settings in purchasing behavior and clinical pathways. Therapeutic indication segmentation further refines clinical prioritization: chemotherapy-induced nausea affects both adult and pediatric cohorts with distinct dosing and monitoring needs; postoperative nausea spans day surgery and inpatient surgery pathways with differing rapidity and duration of symptom control required; and pregnancy-related nausea ranges from morning sickness to hyperemesis gravidarum with divergent safety and administration considerations. Integrating these intersecting segmentation layers enables more targeted product development, tailored messaging, and distribution strategies that align with real-world care delivery models.
Regional strategic perspectives explaining how Americas, Europe Middle East & Africa, and Asia-Pacific market features influence adoption, distribution, and policy decisions
Regional dynamics exert a powerful influence on policy decisions, reimbursement structures, and clinical practice patterns that affect alizapride utilization across the Americas, Europe, Middle East & Africa, and Asia-Pacific. In the Americas, payer fragmentation and hospital purchasing autonomy create divergent adoption pathways that favor flexible contract terms and strong local sales engagement. Transitional reimbursement models and emphasis on outcomes are driving procurement decisions that incorporate clinician preference and real-world tolerability.
In Europe, Middle East & Africa, centralized procurement in some markets and heterogenous regulatory frameworks in others shape distribution approaches and the importance of regulatory harmonization. Stakeholders in these regions often prioritize products with established safety records and proven integration into existing clinical pathways. Meanwhile, Asia-Pacific markets display rapid adoption of outpatient care innovations and expanding home care services, prompting manufacturers to invest in localized formulation and packaging solutions. Across all regions, geopolitical influences, trade policies, and regional supply chain infrastructures continue to dictate timelines for product launch and scale-up, making region-specific go-to-market strategies essential for sustained access and uptake.
Corporate and competitive insights capturing how strategic partnerships, formulation innovation, and distribution specialization are shaping commercial leadership in the alizapride space
Competitive dynamics in the alizapride landscape are characterized by a mix of established pharmaceutical players, evolving generics manufacturers, and specialty distributors focusing on hospital and home care channels. Leading organizations are differentiating through investments in clinical education, optimized packaging for varied administration routes, and partnerships that extend reach into outpatient and home infusion services. Strategic alliances between manufacturers and logistics providers are enhancing cold chain resilience and ensuring alignment with stringent hospital procurement requirements.
Intellectual property lifecycles and regulatory exclusivities affect R&D prioritization, prompting some companies to pursue formulation improvements or delivery innovations to sustain differentiation. Meanwhile, contract manufacturers and regional suppliers have emerged as crucial enablers for market entry, offering scalable production and localized regulatory support. Competitive success increasingly depends on a coordinated approach that aligns clinical evidence generation, targeted distribution strategies, and commercial models that accommodate institutional buyers as well as retail and online pharmacy channels.
Actionable multi-dimensional recommendations that align evidence generation, supply chain resilience, and channel-specific commercialization to accelerate adoption and reduce operational risk
Industry leaders should prioritize a multi-pronged strategy that balances clinical evidence, supply resilience, and targeted commercialization to capitalize on therapeutic demand while mitigating operational risks. First, investment in real-world evidence and clinician-facing education will strengthen clinical positioning and support integration into guideline-driven care pathways. Demonstrating improvements in patient experience and care efficiency is increasingly persuasive for hospital formularies and payor discussions.
Second, supply chain diversification and near-shore manufacturing options will reduce exposure to tariff-driven cost volatility and customs delays. Establishing redundant sourcing lanes and strategic inventory buffers in critical regions will safeguard continuity of care. Third, tailoring distribution models to match the needs of hospital pharmacies, online channels, and retail outlets will improve availability and speed of access; this requires differentiated packaging, administration training, and digital support for direct-to-patient channels. Finally, engage with health systems to pilot value-based contracting arrangements and to co-develop care pathways that illustrate measurable clinical and operational benefits. These actions together will strengthen market position and reduce execution risk across diverse healthcare environments.
A rigorous mixed-methods research framework combining primary expert engagement and structured secondary analysis to produce validated, actionable insights
The research methodology underpinning this executive summary integrates a mix of primary and secondary approaches designed to ensure data validity, triangulation, and practical relevance. Primary inputs included structured interviews with clinical experts, hospital procurement leaders, and distribution partners to capture operational realities, clinical preferences, and procurement drivers. These qualitative insights were complemented by targeted surveys of end users to identify prevailing care pathways and administration preferences.
Secondary research involved systematic review of regulatory documentation, clinical literature, and publicly available policy statements to contextualize practice patterns and regulatory trends. Data synthesis employed cross-validation techniques that compared stakeholder-reported behaviors with documented practice guidelines and supply chain indicators. Throughout the process, analysis was guided by a rigorous framework that prioritized reproducibility, clarity of assumptions, and transparency in sources. Quality assurance steps included expert panel review and iterative validation of emerging findings against real-world practice to enhance the reliability and applicability of conclusions.
Conclusive synthesis emphasizing the imperative to combine clinical evidence, supply resilience, and outcome-focused commercial approaches to secure therapeutic access and value
In sum, alizapride’s role within modern antiemetic therapy is being redefined by converging clinical, regulatory, and commercial forces that prioritize patient-centred outcomes and system-level efficiencies. Flexibility in administration routes, alignment with evolving practice settings such as home care, and responsiveness to regional procurement dynamics are central to strategic success. Tariff-related pressures and supply chain considerations further underscore the importance of proactive sourcing strategies and scenario planning.
For stakeholders seeking to navigate this environment, the imperative is clear: integrate robust clinical evidence with adaptive supply and distribution models while engaging payors and health systems in outcomes-focused conversations. Doing so will enable sustained access and clear differentiation in a market where operational resilience and demonstrable clinical value are increasingly decisive. These findings should inform near-term prioritization and longer-term investment decisions that enhance both patient care and organizational performance.
Note: PDF & Excel + Online Access - 1 Year
A strategic overview detailing how clinical utility, regulatory pathways, and commercial dynamics converge to shape adoption of alizapride across care settings
Alizapride occupies a distinct niche in antiemetic therapy with a pharmacological mechanism that complements commonly used alternatives and informs clinical decision pathways. The compound’s antiemetic efficacy, dosing flexibility across multiple routes of administration, and tolerability profile have driven adoption in settings that prioritize rapid onset of symptom control and predictable outcomes. Clinical stakeholders evaluate alizapride not only against efficacy metrics but also for its capacity to integrate into multimodal care protocols that address nausea driven by chemotherapy, surgical procedures, and pregnancy.
Concurrently, regulatory trajectories and evolving labeling considerations influence formulary decisions and hospital protocols. Payors and procurement teams factor in formulary tiering and practicalities such as storage, preparation time, and compatibility with existing administration infrastructure. From a commercial perspective, manufacturers and distributors are responding to these clinical and regulatory signals by optimizing packaging formats, expanding distribution pathways, and investing in targeted educational outreach to prescribers and nursing teams. As a result, the clinical utility of alizapride is increasingly evaluated through the prism of system-level adoption barriers and enablers rather than purely by isolated efficacy outcomes.
How evolving patient-centric care models, regulatory emphasis on real-world outcomes, and distribution innovations are reshaping antiemetic treatment paradigms
The therapeutic landscape surrounding antiemetics has undergone transformative shifts driven by advances in personalized care, novel administration approaches, and changing expectations for patient experience. Clinicians are placing greater emphasis on tailoring antiemetic regimens to patient phenotypes, procedural risks, and concurrent therapies, which has elevated the importance of agents that offer flexible dosing and rapid onset. Technological improvements in outpatient infusion devices and the maturation of home care services have broadened where and how antiemetics are delivered, encouraging formulations and packaging optimized for those environments.
At the same time, regulatory frameworks are adapting to evidence that prioritizes patient-reported outcomes and real-world effectiveness. This has prompted manufacturers to align development strategies with pragmatic trials and post-market evidence generation. Commercially, payors and hospital systems are incentivizing therapies that reduce downstream resource utilization, such as shortened stays and reduced readmissions associated with poorly controlled nausea. Together, these shifts are reshaping procurement criteria, clinical guidelines, and the competitive differentiation playbook for alizapride and its therapeutic peers.
Assessing the operational and strategic repercussions of 2025 United States tariff measures on pharmaceutical sourcing, supply resilience, and procurement choices
The announcement and implementation of tariff measures in the United States for 2025 introduced a layer of commercial complexity for stakeholders across pharmaceutical supply chains. Manufacturers, distributors, and procurement teams must now operate with heightened sensitivity to cross-border cost drivers and the potential for supply routing adjustments. In response, several organizations have revisited sourcing strategies, prioritized near-shoring where feasible, and accelerated supplier diversification to mitigate tariff exposure. This recalibration affects not only landed cost calculations but also timing, as lead times and customs processes may be adjusted to smooth continuity of supply.
Moreover, the tariff environment has prompted downstream purchasers to re-evaluate contractual terms and to explore strategic purchasing pools or longer-term purchase agreements that can provide pricing stability. Regulatory compliance teams have expanded scrutiny of classification and valuation practices at customs to ensure defensible tariff positions. Clinicians and hospital supply managers, while focused on clinical outcomes, are increasingly involved in discussions about product variants and packaging formats that may be less affected by import duties. Looking ahead, many market participants are investing in enhanced scenario planning and stress-testing commercial models to preserve access and maintain therapeutic continuity under variable trade conditions.
In-depth segmentation synthesis revealing how administration routes, distribution channels, end-user types, and therapeutic indications interact to direct clinical and commercial strategies
A granular segmentation lens reveals how route, distribution, end-user, and therapeutic indication considerations collectively shape clinical adoption and commercial strategy for alizapride. Route of administration considerations encompass intramuscular options, differentiated by multi-dose and single-dose formats, intravenous delivery that includes both bolus infusion and continuous infusion approaches, and oral modalities offered as solutions or tablets; each of these choices carries implications for dosing convenience, nursing time, and formulary placement. Distribution channel dynamics map to hospital pharmacies, which separate private and public hospital procurement practices; online pharmacies, which operate through direct-to-patient models or third-party marketplaces; and retail pharmacies where chain versus independent operators follow distinct inventory and stocking logics.
From the end-user perspective, demand signals vary across clinics that serve general or oncology populations, home care that relies on nurse-administered or self-administered protocols, and hospitals that differentiate between private and public settings in purchasing behavior and clinical pathways. Therapeutic indication segmentation further refines clinical prioritization: chemotherapy-induced nausea affects both adult and pediatric cohorts with distinct dosing and monitoring needs; postoperative nausea spans day surgery and inpatient surgery pathways with differing rapidity and duration of symptom control required; and pregnancy-related nausea ranges from morning sickness to hyperemesis gravidarum with divergent safety and administration considerations. Integrating these intersecting segmentation layers enables more targeted product development, tailored messaging, and distribution strategies that align with real-world care delivery models.
Regional strategic perspectives explaining how Americas, Europe Middle East & Africa, and Asia-Pacific market features influence adoption, distribution, and policy decisions
Regional dynamics exert a powerful influence on policy decisions, reimbursement structures, and clinical practice patterns that affect alizapride utilization across the Americas, Europe, Middle East & Africa, and Asia-Pacific. In the Americas, payer fragmentation and hospital purchasing autonomy create divergent adoption pathways that favor flexible contract terms and strong local sales engagement. Transitional reimbursement models and emphasis on outcomes are driving procurement decisions that incorporate clinician preference and real-world tolerability.
In Europe, Middle East & Africa, centralized procurement in some markets and heterogenous regulatory frameworks in others shape distribution approaches and the importance of regulatory harmonization. Stakeholders in these regions often prioritize products with established safety records and proven integration into existing clinical pathways. Meanwhile, Asia-Pacific markets display rapid adoption of outpatient care innovations and expanding home care services, prompting manufacturers to invest in localized formulation and packaging solutions. Across all regions, geopolitical influences, trade policies, and regional supply chain infrastructures continue to dictate timelines for product launch and scale-up, making region-specific go-to-market strategies essential for sustained access and uptake.
Corporate and competitive insights capturing how strategic partnerships, formulation innovation, and distribution specialization are shaping commercial leadership in the alizapride space
Competitive dynamics in the alizapride landscape are characterized by a mix of established pharmaceutical players, evolving generics manufacturers, and specialty distributors focusing on hospital and home care channels. Leading organizations are differentiating through investments in clinical education, optimized packaging for varied administration routes, and partnerships that extend reach into outpatient and home infusion services. Strategic alliances between manufacturers and logistics providers are enhancing cold chain resilience and ensuring alignment with stringent hospital procurement requirements.
Intellectual property lifecycles and regulatory exclusivities affect R&D prioritization, prompting some companies to pursue formulation improvements or delivery innovations to sustain differentiation. Meanwhile, contract manufacturers and regional suppliers have emerged as crucial enablers for market entry, offering scalable production and localized regulatory support. Competitive success increasingly depends on a coordinated approach that aligns clinical evidence generation, targeted distribution strategies, and commercial models that accommodate institutional buyers as well as retail and online pharmacy channels.
Actionable multi-dimensional recommendations that align evidence generation, supply chain resilience, and channel-specific commercialization to accelerate adoption and reduce operational risk
Industry leaders should prioritize a multi-pronged strategy that balances clinical evidence, supply resilience, and targeted commercialization to capitalize on therapeutic demand while mitigating operational risks. First, investment in real-world evidence and clinician-facing education will strengthen clinical positioning and support integration into guideline-driven care pathways. Demonstrating improvements in patient experience and care efficiency is increasingly persuasive for hospital formularies and payor discussions.
Second, supply chain diversification and near-shore manufacturing options will reduce exposure to tariff-driven cost volatility and customs delays. Establishing redundant sourcing lanes and strategic inventory buffers in critical regions will safeguard continuity of care. Third, tailoring distribution models to match the needs of hospital pharmacies, online channels, and retail outlets will improve availability and speed of access; this requires differentiated packaging, administration training, and digital support for direct-to-patient channels. Finally, engage with health systems to pilot value-based contracting arrangements and to co-develop care pathways that illustrate measurable clinical and operational benefits. These actions together will strengthen market position and reduce execution risk across diverse healthcare environments.
A rigorous mixed-methods research framework combining primary expert engagement and structured secondary analysis to produce validated, actionable insights
The research methodology underpinning this executive summary integrates a mix of primary and secondary approaches designed to ensure data validity, triangulation, and practical relevance. Primary inputs included structured interviews with clinical experts, hospital procurement leaders, and distribution partners to capture operational realities, clinical preferences, and procurement drivers. These qualitative insights were complemented by targeted surveys of end users to identify prevailing care pathways and administration preferences.
Secondary research involved systematic review of regulatory documentation, clinical literature, and publicly available policy statements to contextualize practice patterns and regulatory trends. Data synthesis employed cross-validation techniques that compared stakeholder-reported behaviors with documented practice guidelines and supply chain indicators. Throughout the process, analysis was guided by a rigorous framework that prioritized reproducibility, clarity of assumptions, and transparency in sources. Quality assurance steps included expert panel review and iterative validation of emerging findings against real-world practice to enhance the reliability and applicability of conclusions.
Conclusive synthesis emphasizing the imperative to combine clinical evidence, supply resilience, and outcome-focused commercial approaches to secure therapeutic access and value
In sum, alizapride’s role within modern antiemetic therapy is being redefined by converging clinical, regulatory, and commercial forces that prioritize patient-centred outcomes and system-level efficiencies. Flexibility in administration routes, alignment with evolving practice settings such as home care, and responsiveness to regional procurement dynamics are central to strategic success. Tariff-related pressures and supply chain considerations further underscore the importance of proactive sourcing strategies and scenario planning.
For stakeholders seeking to navigate this environment, the imperative is clear: integrate robust clinical evidence with adaptive supply and distribution models while engaging payors and health systems in outcomes-focused conversations. Doing so will enable sustained access and clear differentiation in a market where operational resilience and demonstrable clinical value are increasingly decisive. These findings should inform near-term prioritization and longer-term investment decisions that enhance both patient care and organizational performance.
Note: PDF & Excel + Online Access - 1 Year
Table of Contents
184 Pages
- 1. Preface
- 1.1. Objectives of the Study
- 1.2. Market Segmentation & Coverage
- 1.3. Years Considered for the Study
- 1.4. Currency
- 1.5. Language
- 1.6. Stakeholders
- 2. Research Methodology
- 3. Executive Summary
- 4. Market Overview
- 5. Market Insights
- 5.1. Increasing off-label use of Alizapride in chemotherapy-induced nausea management driven by updated supportive care guidelines
- 5.2. Expansion of generic Alizapride availability leading to intensified price competition in key emerging markets
- 5.3. Shift toward intravenous Alizapride formulations for hospital-based postoperative nausea protocols to enhance patient recovery
- 5.4. Growing interest in combination therapy of Alizapride with serotonin antagonists to improve control in refractory emesis cases
- 5.5. Regulatory approval processes for Alizapride generics accelerating in Asia-Pacific markets amid rising antiemetic demand
- 5.6. Rising investment in clinical trials assessing Alizapride efficacy in gastroparesis-related nausea symptoms in diabetic populations
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Alizapride Market, by Route Of Administration
- 8.1. Intramuscular
- 8.1.1. Multi Dose
- 8.1.2. Single Dose
- 8.2. Intravenous
- 8.2.1. Bolus Infusion
- 8.2.2. Continuous Infusion
- 8.3. Oral
- 8.3.1. Oral Solution
- 8.3.2. Tablet
- 9. Alizapride Market, by Therapeutic Indication
- 9.1. Chemotherapy Induced Nausea
- 9.1.1. Adult
- 9.1.2. Pediatric
- 9.2. Postoperative Nausea
- 9.2.1. Day Surgery
- 9.2.2. Inpatient Surgery
- 9.3. Pregnancy Related Nausea
- 9.3.1. Hyperemesis Gravidarum
- 9.3.2. Morning Sickness
- 10. Alizapride Market, by Distribution Channel
- 10.1. Hospital Pharmacies
- 10.2. Online Pharmacies
- 10.3. Retail Pharmacies
- 11. Alizapride Market, by End User
- 11.1. Clinics
- 11.1.1. General
- 11.1.2. Oncology
- 11.2. Home Care
- 11.2.1. Nurse Administered
- 11.2.2. Self Administered
- 11.3. Hospitals
- 12. Alizapride Market, by Region
- 12.1. Americas
- 12.1.1. North America
- 12.1.2. Latin America
- 12.2. Europe, Middle East & Africa
- 12.2.1. Europe
- 12.2.2. Middle East
- 12.2.3. Africa
- 12.3. Asia-Pacific
- 13. Alizapride Market, by Group
- 13.1. ASEAN
- 13.2. GCC
- 13.3. European Union
- 13.4. BRICS
- 13.5. G7
- 13.6. NATO
- 14. Alizapride Market, by Country
- 14.1. United States
- 14.2. Canada
- 14.3. Mexico
- 14.4. Brazil
- 14.5. United Kingdom
- 14.6. Germany
- 14.7. France
- 14.8. Russia
- 14.9. Italy
- 14.10. Spain
- 14.11. China
- 14.12. India
- 14.13. Japan
- 14.14. Australia
- 14.15. South Korea
- 15. Competitive Landscape
- 15.1. Market Share Analysis, 2024
- 15.2. FPNV Positioning Matrix, 2024
- 15.3. Competitive Analysis
- 15.3.1. AdvaCare Pharma
- 15.3.2. Alembic Pharmaceuticals Limited
- 15.3.3. BDR Pharmaceuticals
- 15.3.4. BOC Sciences
- 15.3.5. Cadila Pharmaceuticals Limited
- 15.3.6. Cipla Limited
- 15.3.7. Daicel Pharma Standards
- 15.3.8. Dideu Industries Group Limited
- 15.3.9. Dr. Reddy's Laboratories Limited
- 15.3.10. Gland Pharma Limited
- 15.3.11. ICROM S.r.l
- 15.3.12. Lupin Limited
- 15.3.13. Mankind Pharma Limited
- 15.3.14. Neuland Laboratories Limited
- 15.3.15. Simson Pharma Limited
- 15.3.16. Sun Pharmaceutical Industries Limited
- 15.3.17. TargetMol Chemicals Inc
- 15.3.18. Teva Pharmaceutical Industries Limited
- 15.3.19. Viatris Inc
- 15.3.20. Zydus Cadila Healthcare Limited
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