Dirithromycin Market by Type (Branded, Generic), Formulation (Capsule, Suspension, Tablet), Distribution Channel, Application, End User - Global Forecast 2026-2032
Description
The Dirithromycin Market was valued at USD 133.86 million in 2025 and is projected to grow to USD 141.46 million in 2026, with a CAGR of 4.37%, reaching USD 180.67 million by 2032.
A concise orientation to dirithromycin’s evolving role in therapeutic protocols driven by adherence, tolerability, and shifting outpatient antibiotic strategies
Dirithromycin has re-emerged as a molecule of clinical and commercial interest owing to evolving antimicrobial stewardship priorities, differentiated formulation strategies, and renewed clinical evidence in select indications. The therapeutic profile of dirithromycin, an azalide antibiotic, positions it at the intersection of outpatient respiratory care and targeted anti-infective regimens where tolerability and dosing convenience influence prescribing patterns. As healthcare systems globally emphasize shorter courses, oral alternatives to intravenous therapy, and improved adherence, dirithromycin’s clinical attributes are being reassessed by clinicians and formulary committees.
In this context, product developers and commercial teams are recalibrating strategies to address physician expectations, payer requirements, and patient preferences. This introductory overview outlines the compound’s clinical relevance, prevailing regulatory considerations, and the competitive landscape dynamics that will shape investment and commercialization decisions over the coming years. It sets the stage for deeper analysis of product segmentation, distribution pathways, end-user adoption, and regional drivers that follow in this executive summary.
How shifting clinical priorities, regulatory expectations, and distribution innovations are collectively redefining opportunity and strategy for dirithromycin
The landscape for dirithromycin is being reshaped by several transformative shifts that extend beyond simple product launch activity. Clinically, there is a growing emphasis on agents that reduce treatment complexity and support outpatient management of respiratory and select bacterial infections; this shift is accelerating interest in oral azalide options that combine efficacy with simplified dosing. Concurrently, regulatory pathways and formulary processes are evolving to prioritize real-world evidence and pharmacoeconomic value, prompting sponsors to invest in post-approval studies and health economics dossiers to support inclusion in standard treatment algorithms.
Commercially, disruption is occurring across the value chain as digital channels and specialty distribution models alter how physicians access information and how patients obtain therapy. Manufacturing and supply resilience have also moved to the forefront, with firms diversifying supply bases and investing in quality oversight to mitigate disruptions. Finally, antimicrobial stewardship imperatives are redefining appropriate use, meaning that product positioning must reconcile commercial ambitions with stewardship-aligned messaging and evidence generation to ensure accepted place-in-therapy.
Assessing the cumulative operational and strategic consequences of United States tariff actions in 2025 on procurement, supply chains, and formulary dynamics
United States tariff decisions announced in recent trade policy cycles have introduced new cost variables for pharmaceutical ingredients and packaging components that feed into oral antibiotic production. For dirithromycin, cumulative tariff effects in 2025 will influence upstream procurement strategies, with manufacturers assessing alternative sourcing, long-term contracts, and domestic capacity enhancements to preserve margin structures. The tariff environment has also heightened sensitivity among purchasers and procurement teams to landed costs, leading to more rigorous supplier evaluations and greater emphasis on total cost of ownership rather than unit price alone.
Consequently, supply chain reconfiguration is emerging as a near-term operational priority. Manufacturers and distributors are accelerating localization of critical inputs where feasible and renegotiating logistics arrangements to absorb or offset tariff-driven cost increases. At the same time, payers and hospital procurement groups are monitoring these changes and may respond by tightening formulary negotiation positions or prioritizing therapeutics with stable supply economics. These developments underscore the need for proactive commercial planning that incorporates scenario analysis for various tariff and trade contingencies.
Segmented assessment revealing how formulation choices, distribution pathways, clinical indications, and end-user settings dictate differentiated commercialization strategies
A nuanced segmentation framework clarifies where dirithromycin may gain traction and where targeted investment will be necessary. Based on Type, market is studied across Branded and Generic, which influences pricing expectations, promotional approaches, and formulary negotiation tactics; branded presentations typically require a value narrative tied to clinical differentiation whereas generics compete primarily on cost and supply reliability. Based on Formulation, market is studied across Capsule, Suspension, and Tablet, with the Tablet further studied across Extended Release and Immediate Release; formulation choice affects patient adherence, dosing convenience, and manufacturing complexity, so product teams must align formulation strategy with the intended treatment setting and target patient population.
Based on Distribution Channel, market is studied across Hospital Pharmacy, Online Pharmacy, and Retail Pharmacy, and each channel demands distinct commercialization models, regulatory compliance considerations, and patient engagement approaches. Based on Application, market is studied across H. Pylori Eradication, Skin Infections, and Upper Respiratory Tract Infections, with H. Pylori Eradication further studied across First Line Therapy and Second Line Therapy; therapeutic positioning will need to reflect comparative efficacy, tolerability profiles, and guideline alignment for these indications. Based on End User, market is studied across Clinics, Home Care, and Hospitals, where procurement pathways, administration settings, and payer interactions differ materially and should inform distribution and support strategies.
Regional archetypes and implementation imperatives for adoption of dirithromycin across the Americas, Europe, Middle East & Africa, and Asia-Pacific
Regional dynamics will shape adoption patterns for dirithromycin in distinct ways across the Americas, Europe, Middle East & Africa, and Asia-Pacific. In the Americas, pricing pressures, payer scrutiny, and a strong outpatient treatment infrastructure favor products that demonstrate convenience and health economic value; manufacturers should prioritize real-world outcomes and patient-reported measures to support uptake. In Europe, Middle East & Africa, heterogeneous regulatory environments and variable reimbursement pathways require localized evidence generation and adaptive market access approaches, with some markets valuing centralized procurement and others favoring national-level negotiations.
Asia-Pacific presents diverse opportunities driven by rapidly evolving healthcare access in urban centers, increasing antibiotic stewardship activity, and sizeable populations with unmet needs for tolerable oral therapies. Across these regions, considerations such as supply chain resilience, local manufacturing partnerships, and culturally appropriate patient support programs will influence execution. Transitional policy shifts and regional procurement trends further underscore the importance of tailored market-entry tactics and phased rollouts aligned to regional payer and prescriber expectations.
Competitive behavior and strategic imperatives among product developers, contract manufacturers, and commercialization partners shaping dirithromycin’s competitive landscape
Competitive dynamics for dirithromycin encompass established pharmaceutical firms with robust commercial infrastructures, niche players focusing on specialty anti-infectives, and contract manufacturers advancing formulation expertise. Key company behavior is likely to emphasize differentiated formulation portfolios, evidence generation to secure favorable formulary placement, and strategic partnerships for distribution and manufacturing. Firms investing in extended release tablet technologies, patient adherence programs, and post-marketing effectiveness studies will be better positioned to address both clinician preferences and payer evidence requirements.
Strategic collaboration will also be pivotal. Licensing agreements and co-promotion deals can accelerate geographic reach while mitigating commercial risk, and manufacturing partnerships can strengthen supply resilience in the face of trade-related cost pressures. In addition, companies that deploy digital engagement tools to support prescribers and patients, while simultaneously aligning with stewardship principles, will gain credibility with payers and clinical gatekeepers. Overall, company strategies that blend product differentiation, operational robustness, and adaptive commercial models are most likely to succeed.
Actionable strategic priorities for industry leaders to secure clinical acceptance, supply resilience, and payer support through evidence and collaborative execution
Industry leaders should focus on evidence generation, supply chain resilience, and adaptive commercialization to capture clinical acceptance and institutional support. Prioritizing high-quality post-approval studies and pharmacoeconomic analyses will help demonstrate comparative value to payers and prescribers, while stewardship-aligned messaging will preserve clinical credibility. Simultaneously, investing in diversified sourcing and localized manufacturing partnerships will mitigate exposure to trade-related cost volatility and ensure continuity of supply to key distribution channels.
Commercial strategies must be tailored across channels and geographies; in hospital settings, engagement with formulary committees and clinical champions will be critical, whereas retail and online pharmacies require patient-facing adherence support and streamlined reimbursement processes. Collaborative approaches including licensing, co-promotion, and public-private partnerships can accelerate access in regions with complex regulatory or procurement environments. Finally, leveraging digital tools to collect real-world safety and effectiveness data will both support reimbursement dossiers and reinforce clinician confidence in therapeutic positioning.
Robust mixed-methods research design combining primary stakeholder engagement, secondary evidence synthesis, and scenario modeling to underpin strategic conclusions
The analytical approach underpinning this executive summary combined structured evidence review, stakeholder interviews, and comparative product analysis to create a balanced perspective on therapeutic, commercial, and operational dynamics. Primary research included qualitative interviews with clinicians, formulary decision-makers, procurement specialists, and distribution partners to surface real-world considerations affecting prescribing, purchasing, and supply. Secondary research involved peer-reviewed literature, regulatory filings, clinical trial registries, and publicly available guidance documents to triangulate findings and ensure consistency with prevailing clinical standards.
In addition, scenario analysis was used to explore the implications of trade and tariff volatility, supply chain disruption, and changes in stewardship policies. Cross-functional synthesis enabled alignment of clinical positioning with commercial pathways and operational readiness. Throughout the methodology, emphasis was placed on transparency of assumptions and the use of multiple independent sources to validate conclusions and reduce bias in strategic recommendations.
Concise synthesis of strategic imperatives and operational priorities that determine the pathway to clinical adoption and sustainable program execution for dirithromycin
Dirithromycin occupies a niche of renewed clinical and commercial relevance where formulation convenience, tolerability, and alignment with outpatient care preferences intersect with evolving procurement and stewardship imperatives. The path to successful adoption requires integrated planning across evidence generation, regulatory positioning, and supply chain management. Firms that harmonize clinical value narratives with pragmatic operational execution and targeted regional approaches will be better equipped to navigate payer scrutiny and prescriber expectations.
In summary, realizing potential will hinge on credible real-world evidence, resilient sourcing strategies, and tailored commercialization that respects both clinical stewardship and local payer dynamics. Organizations that adopt a phased, data-driven approach-combining rigorous post-marketing research with adaptive distribution partnerships-can meaningfully improve the probability of sustained clinical uptake and institutional acceptance.
Note: PDF & Excel + Online Access - 1 Year
A concise orientation to dirithromycin’s evolving role in therapeutic protocols driven by adherence, tolerability, and shifting outpatient antibiotic strategies
Dirithromycin has re-emerged as a molecule of clinical and commercial interest owing to evolving antimicrobial stewardship priorities, differentiated formulation strategies, and renewed clinical evidence in select indications. The therapeutic profile of dirithromycin, an azalide antibiotic, positions it at the intersection of outpatient respiratory care and targeted anti-infective regimens where tolerability and dosing convenience influence prescribing patterns. As healthcare systems globally emphasize shorter courses, oral alternatives to intravenous therapy, and improved adherence, dirithromycin’s clinical attributes are being reassessed by clinicians and formulary committees.
In this context, product developers and commercial teams are recalibrating strategies to address physician expectations, payer requirements, and patient preferences. This introductory overview outlines the compound’s clinical relevance, prevailing regulatory considerations, and the competitive landscape dynamics that will shape investment and commercialization decisions over the coming years. It sets the stage for deeper analysis of product segmentation, distribution pathways, end-user adoption, and regional drivers that follow in this executive summary.
How shifting clinical priorities, regulatory expectations, and distribution innovations are collectively redefining opportunity and strategy for dirithromycin
The landscape for dirithromycin is being reshaped by several transformative shifts that extend beyond simple product launch activity. Clinically, there is a growing emphasis on agents that reduce treatment complexity and support outpatient management of respiratory and select bacterial infections; this shift is accelerating interest in oral azalide options that combine efficacy with simplified dosing. Concurrently, regulatory pathways and formulary processes are evolving to prioritize real-world evidence and pharmacoeconomic value, prompting sponsors to invest in post-approval studies and health economics dossiers to support inclusion in standard treatment algorithms.
Commercially, disruption is occurring across the value chain as digital channels and specialty distribution models alter how physicians access information and how patients obtain therapy. Manufacturing and supply resilience have also moved to the forefront, with firms diversifying supply bases and investing in quality oversight to mitigate disruptions. Finally, antimicrobial stewardship imperatives are redefining appropriate use, meaning that product positioning must reconcile commercial ambitions with stewardship-aligned messaging and evidence generation to ensure accepted place-in-therapy.
Assessing the cumulative operational and strategic consequences of United States tariff actions in 2025 on procurement, supply chains, and formulary dynamics
United States tariff decisions announced in recent trade policy cycles have introduced new cost variables for pharmaceutical ingredients and packaging components that feed into oral antibiotic production. For dirithromycin, cumulative tariff effects in 2025 will influence upstream procurement strategies, with manufacturers assessing alternative sourcing, long-term contracts, and domestic capacity enhancements to preserve margin structures. The tariff environment has also heightened sensitivity among purchasers and procurement teams to landed costs, leading to more rigorous supplier evaluations and greater emphasis on total cost of ownership rather than unit price alone.
Consequently, supply chain reconfiguration is emerging as a near-term operational priority. Manufacturers and distributors are accelerating localization of critical inputs where feasible and renegotiating logistics arrangements to absorb or offset tariff-driven cost increases. At the same time, payers and hospital procurement groups are monitoring these changes and may respond by tightening formulary negotiation positions or prioritizing therapeutics with stable supply economics. These developments underscore the need for proactive commercial planning that incorporates scenario analysis for various tariff and trade contingencies.
Segmented assessment revealing how formulation choices, distribution pathways, clinical indications, and end-user settings dictate differentiated commercialization strategies
A nuanced segmentation framework clarifies where dirithromycin may gain traction and where targeted investment will be necessary. Based on Type, market is studied across Branded and Generic, which influences pricing expectations, promotional approaches, and formulary negotiation tactics; branded presentations typically require a value narrative tied to clinical differentiation whereas generics compete primarily on cost and supply reliability. Based on Formulation, market is studied across Capsule, Suspension, and Tablet, with the Tablet further studied across Extended Release and Immediate Release; formulation choice affects patient adherence, dosing convenience, and manufacturing complexity, so product teams must align formulation strategy with the intended treatment setting and target patient population.
Based on Distribution Channel, market is studied across Hospital Pharmacy, Online Pharmacy, and Retail Pharmacy, and each channel demands distinct commercialization models, regulatory compliance considerations, and patient engagement approaches. Based on Application, market is studied across H. Pylori Eradication, Skin Infections, and Upper Respiratory Tract Infections, with H. Pylori Eradication further studied across First Line Therapy and Second Line Therapy; therapeutic positioning will need to reflect comparative efficacy, tolerability profiles, and guideline alignment for these indications. Based on End User, market is studied across Clinics, Home Care, and Hospitals, where procurement pathways, administration settings, and payer interactions differ materially and should inform distribution and support strategies.
Regional archetypes and implementation imperatives for adoption of dirithromycin across the Americas, Europe, Middle East & Africa, and Asia-Pacific
Regional dynamics will shape adoption patterns for dirithromycin in distinct ways across the Americas, Europe, Middle East & Africa, and Asia-Pacific. In the Americas, pricing pressures, payer scrutiny, and a strong outpatient treatment infrastructure favor products that demonstrate convenience and health economic value; manufacturers should prioritize real-world outcomes and patient-reported measures to support uptake. In Europe, Middle East & Africa, heterogeneous regulatory environments and variable reimbursement pathways require localized evidence generation and adaptive market access approaches, with some markets valuing centralized procurement and others favoring national-level negotiations.
Asia-Pacific presents diverse opportunities driven by rapidly evolving healthcare access in urban centers, increasing antibiotic stewardship activity, and sizeable populations with unmet needs for tolerable oral therapies. Across these regions, considerations such as supply chain resilience, local manufacturing partnerships, and culturally appropriate patient support programs will influence execution. Transitional policy shifts and regional procurement trends further underscore the importance of tailored market-entry tactics and phased rollouts aligned to regional payer and prescriber expectations.
Competitive behavior and strategic imperatives among product developers, contract manufacturers, and commercialization partners shaping dirithromycin’s competitive landscape
Competitive dynamics for dirithromycin encompass established pharmaceutical firms with robust commercial infrastructures, niche players focusing on specialty anti-infectives, and contract manufacturers advancing formulation expertise. Key company behavior is likely to emphasize differentiated formulation portfolios, evidence generation to secure favorable formulary placement, and strategic partnerships for distribution and manufacturing. Firms investing in extended release tablet technologies, patient adherence programs, and post-marketing effectiveness studies will be better positioned to address both clinician preferences and payer evidence requirements.
Strategic collaboration will also be pivotal. Licensing agreements and co-promotion deals can accelerate geographic reach while mitigating commercial risk, and manufacturing partnerships can strengthen supply resilience in the face of trade-related cost pressures. In addition, companies that deploy digital engagement tools to support prescribers and patients, while simultaneously aligning with stewardship principles, will gain credibility with payers and clinical gatekeepers. Overall, company strategies that blend product differentiation, operational robustness, and adaptive commercial models are most likely to succeed.
Actionable strategic priorities for industry leaders to secure clinical acceptance, supply resilience, and payer support through evidence and collaborative execution
Industry leaders should focus on evidence generation, supply chain resilience, and adaptive commercialization to capture clinical acceptance and institutional support. Prioritizing high-quality post-approval studies and pharmacoeconomic analyses will help demonstrate comparative value to payers and prescribers, while stewardship-aligned messaging will preserve clinical credibility. Simultaneously, investing in diversified sourcing and localized manufacturing partnerships will mitigate exposure to trade-related cost volatility and ensure continuity of supply to key distribution channels.
Commercial strategies must be tailored across channels and geographies; in hospital settings, engagement with formulary committees and clinical champions will be critical, whereas retail and online pharmacies require patient-facing adherence support and streamlined reimbursement processes. Collaborative approaches including licensing, co-promotion, and public-private partnerships can accelerate access in regions with complex regulatory or procurement environments. Finally, leveraging digital tools to collect real-world safety and effectiveness data will both support reimbursement dossiers and reinforce clinician confidence in therapeutic positioning.
Robust mixed-methods research design combining primary stakeholder engagement, secondary evidence synthesis, and scenario modeling to underpin strategic conclusions
The analytical approach underpinning this executive summary combined structured evidence review, stakeholder interviews, and comparative product analysis to create a balanced perspective on therapeutic, commercial, and operational dynamics. Primary research included qualitative interviews with clinicians, formulary decision-makers, procurement specialists, and distribution partners to surface real-world considerations affecting prescribing, purchasing, and supply. Secondary research involved peer-reviewed literature, regulatory filings, clinical trial registries, and publicly available guidance documents to triangulate findings and ensure consistency with prevailing clinical standards.
In addition, scenario analysis was used to explore the implications of trade and tariff volatility, supply chain disruption, and changes in stewardship policies. Cross-functional synthesis enabled alignment of clinical positioning with commercial pathways and operational readiness. Throughout the methodology, emphasis was placed on transparency of assumptions and the use of multiple independent sources to validate conclusions and reduce bias in strategic recommendations.
Concise synthesis of strategic imperatives and operational priorities that determine the pathway to clinical adoption and sustainable program execution for dirithromycin
Dirithromycin occupies a niche of renewed clinical and commercial relevance where formulation convenience, tolerability, and alignment with outpatient care preferences intersect with evolving procurement and stewardship imperatives. The path to successful adoption requires integrated planning across evidence generation, regulatory positioning, and supply chain management. Firms that harmonize clinical value narratives with pragmatic operational execution and targeted regional approaches will be better equipped to navigate payer scrutiny and prescriber expectations.
In summary, realizing potential will hinge on credible real-world evidence, resilient sourcing strategies, and tailored commercialization that respects both clinical stewardship and local payer dynamics. Organizations that adopt a phased, data-driven approach-combining rigorous post-marketing research with adaptive distribution partnerships-can meaningfully improve the probability of sustained clinical uptake and institutional acceptance.
Note: PDF & Excel + Online Access - 1 Year
Table of Contents
188 Pages
- 1. Preface
- 1.1. Objectives of the Study
- 1.2. Market Definition
- 1.3. Market Segmentation & Coverage
- 1.4. Years Considered for the Study
- 1.5. Currency Considered for the Study
- 1.6. Language Considered for the Study
- 1.7. Key Stakeholders
- 2. Research Methodology
- 2.1. Introduction
- 2.2. Research Design
- 2.2.1. Primary Research
- 2.2.2. Secondary Research
- 2.3. Research Framework
- 2.3.1. Qualitative Analysis
- 2.3.2. Quantitative Analysis
- 2.4. Market Size Estimation
- 2.4.1. Top-Down Approach
- 2.4.2. Bottom-Up Approach
- 2.5. Data Triangulation
- 2.6. Research Outcomes
- 2.7. Research Assumptions
- 2.8. Research Limitations
- 3. Executive Summary
- 3.1. Introduction
- 3.2. CXO Perspective
- 3.3. Market Size & Growth Trends
- 3.4. Market Share Analysis, 2025
- 3.5. FPNV Positioning Matrix, 2025
- 3.6. New Revenue Opportunities
- 3.7. Next-Generation Business Models
- 3.8. Industry Roadmap
- 4. Market Overview
- 4.1. Introduction
- 4.2. Industry Ecosystem & Value Chain Analysis
- 4.2.1. Supply-Side Analysis
- 4.2.2. Demand-Side Analysis
- 4.2.3. Stakeholder Analysis
- 4.3. Porter’s Five Forces Analysis
- 4.4. PESTLE Analysis
- 4.5. Market Outlook
- 4.5.1. Near-Term Market Outlook (0–2 Years)
- 4.5.2. Medium-Term Market Outlook (3–5 Years)
- 4.5.3. Long-Term Market Outlook (5–10 Years)
- 4.6. Go-to-Market Strategy
- 5. Market Insights
- 5.1. Consumer Insights & End-User Perspective
- 5.2. Consumer Experience Benchmarking
- 5.3. Opportunity Mapping
- 5.4. Distribution Channel Analysis
- 5.5. Pricing Trend Analysis
- 5.6. Regulatory Compliance & Standards Framework
- 5.7. ESG & Sustainability Analysis
- 5.8. Disruption & Risk Scenarios
- 5.9. Return on Investment & Cost-Benefit Analysis
- 6. Cumulative Impact of United States Tariffs 2025
- 7. Cumulative Impact of Artificial Intelligence 2025
- 8. Dirithromycin Market, by Type
- 8.1. Branded
- 8.2. Generic
- 9. Dirithromycin Market, by Formulation
- 9.1. Capsule
- 9.2. Suspension
- 9.3. Tablet
- 9.3.1. Extended Release
- 9.3.2. Immediate Release
- 10. Dirithromycin Market, by Distribution Channel
- 10.1. Hospital Pharmacy
- 10.2. Online Pharmacy
- 10.3. Retail Pharmacy
- 11. Dirithromycin Market, by Application
- 11.1. H. Pylori Eradication
- 11.1.1. First Line Therapy
- 11.1.2. Second Line Therapy
- 11.2. Skin Infections
- 11.3. Upper Respiratory Tract Infections
- 12. Dirithromycin Market, by End User
- 12.1. Clinics
- 12.2. Home Care
- 12.3. Hospitals
- 13. Dirithromycin Market, by Region
- 13.1. Americas
- 13.1.1. North America
- 13.1.2. Latin America
- 13.2. Europe, Middle East & Africa
- 13.2.1. Europe
- 13.2.2. Middle East
- 13.2.3. Africa
- 13.3. Asia-Pacific
- 14. Dirithromycin Market, by Group
- 14.1. ASEAN
- 14.2. GCC
- 14.3. European Union
- 14.4. BRICS
- 14.5. G7
- 14.6. NATO
- 15. Dirithromycin Market, by Country
- 15.1. United States
- 15.2. Canada
- 15.3. Mexico
- 15.4. Brazil
- 15.5. United Kingdom
- 15.6. Germany
- 15.7. France
- 15.8. Russia
- 15.9. Italy
- 15.10. Spain
- 15.11. China
- 15.12. India
- 15.13. Japan
- 15.14. Australia
- 15.15. South Korea
- 16. United States Dirithromycin Market
- 17. China Dirithromycin Market
- 18. Competitive Landscape
- 18.1. Market Concentration Analysis, 2025
- 18.1.1. Concentration Ratio (CR)
- 18.1.2. Herfindahl Hirschman Index (HHI)
- 18.2. Recent Developments & Impact Analysis, 2025
- 18.3. Product Portfolio Analysis, 2025
- 18.4. Benchmarking Analysis, 2025
- 18.5. Cadila Healthcare Limited
- 18.6. CHEMOS GmbH
- 18.7. Chifeng Arker Pharmaceutical Technology Co., Ltd.
- 18.8. Cipla Limited
- 18.9. Dr. Reddy's Laboratories Limited
- 18.10. Lupin Limited
- 18.11. Pfizer Inc.
- 18.12. Pfizer Inc.
- 18.13. Sandoz International GmbH
- 18.14. Sun Pharmaceutical Industries Limited
- 18.15. Teva Pharmaceutical Industries Ltd.
- 18.16. Torrent Pharmaceuticals Limited
- 18.17. Viatris Inc.
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