시장보고서
상품코드
2070372

의약품 부형제 시장 : 규모, 점유율, 성장, 산업 분석, 지역 인사이트 및 예측(2026-2034년)

Pharmaceutical Excipients Market Size, Share, Growth, Global Industry Analysis, Regional Insights and Forecast to 2026-2034

발행일: | 리서치사: 구분자 Fortune Business Insights Pvt. Ltd. | 페이지 정보: 영문 190 Pages | 배송안내 : 2-3일 (영업일 기준)

    
    
    



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한글목차
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의약품 부형제 시장의 성장 요인

세계 의약품 부형제 시장은 2025년에 105억 7,000만 달러 규모에 달할 것으로 예상되며, 2026년 111억 8,000만 달러에서 2034년까지 178억 9,000만 달러로 성장할 것으로 보이며, 예측 기간 동안 연평균 성장률(CAGR)은 6.06%를 나타낼 것으로 전망됩니다. 의약품 부형제란, 제제의 안정성, 용해성, 맛, 질감, 생체이용률 및 제조 성능을 향상시키기 위해 사용되는 비활성 성분입니다. 이들은 정제, 캡슐, 주사제, 외용제, 호흡기용 의약품, 안과용 제제 및 첨단 약물 전달 시스템에서 중요한 역할을 하고 있습니다.

시장 성장은 주로 제네릭 의약품 생산 증가, 복합 제형에 대한 수요 증가, 바이오의약품 개발 확대, 그리고 기능성·고순도 부형제에 대한 수요 증가에 힘입어 이루어지고 있습니다. 2025년에는 성숙한 의약품 제조거점과 고품질 제제에 대한 견조한 수요에 힘입어 북미가 27.34%의 시장 점유율을 차지하며 시장을 주도했습니다.

의약품 부형제 시장 동향

시장의 주요 동향으로는 다기능 부형제에 대한 수요 증가를 꼽을 수 있습니다. 제약 기업들은 용해성 향상, 안정성 확보, 방출 제어, 맛 가림, 제조 효율 향상 등 다양한 역할을 수행할 수 있는 부형제를 점점 더 선호하고 있습니다. 이를 통해 제제의 복잡성을 줄이고 개발 기간을 단축할 수 있게 됩니다.

2024년 9월, 에보닉은 경구용 약물 전달 솔루션에 대한 수요 증가에 부응하기 위해 다름슈타트에 EUDRAGIT 폴리머 전용의 새로운 분무 건조 시설을 가동하기 시작했습니다.

시장 성장 촉진요인

의약품 부형제 시장의 주요 성장 요인은 제네릭 의약품 생산 증가입니다. 제네릭 의약품 제조업체는 비용 대비 효과가 높은 제제를 개발하기 위해 충진제, 결합제, 피막제, 안정제, 분해제, 용해촉진제를 대량으로 필요로 합니다. 브랜드 의약품의 특허 보호가 만료됨에 따라 제네릭 의약품의 생산이 확대되고 있으며, 이로 인해 부형제에 대한 수요가 직접적으로 증가하고 있습니다.

또한, 특수 치료제, 바이오의약품 및 첨단 제형의 개발이 진행됨에 따라, 약제의 안정성, 전달성 및 환자의 복약 순응도를 뒷받침하는 고성능 부형제에 대한 수요가 높아지고 있습니다.

시장 성장 억제요인

엄격한 품질 관리 및 공급업체 적격성 심사 요건이 시장 성장을 저해하고 있습니다. 부형제는 의약품의 안전성과 성능에 직접적인 영향을 미치기 때문에 제약 회사는 엄격한 공급업체 감사, 오염 검사, 문서 검토 및 반복적인 품질 시험을 실시해야 합니다. 이러한 과정들은 조달 기간, 운영 비용 및 제형의 복잡성을 증가시켜 시장 보급을 지연시키고 있습니다.

시장 기회

경구용, 호흡기용, 안과용, 비경구용 및 외용 제제에 걸친 수요 증가가 큰 비즈니스 기회를 창출하고 있습니다. 각 제약사는 기존의 정제나 캡슐에 그치지 않고, 흡입 요법, 무균 주사제, 안과용 의약품 및 첨단 전달 시스템으로 사업을 확대되고 있습니다. 이에 따라 특정 순도, 안전성 및 성능 특성을 갖춘 부형제에 대한 수요가 증가하고 있습니다.

2025년 1월, DFE Pharma는 호흡기용 제제 개발을 지원하기 위해 하이데라바드에 위치한 ‘Closer to the Formulator’ 센터 오브 엑셀런스를 확장했습니다.

시장의 과제

엄격한 규제 요건과 복잡한 승인 절차는 여전히 큰 과제로 남아 있습니다. 새로운 부형제에는 확실한 안전성 데이터, 규정 준수 관련 문서, GMP 기준 및 지역별 승인이 필요합니다. 전 세계적으로 규제가 조화를 이루지 못하고 있는 점은 특히 새롭고 선진적인 부형제 시스템의 경우, 부형제 혁신을 지연시키고 개발 비용을 증가시키는 요인이 될 수 있습니다.

지역별 분석

북미는 2025년에 28억 9,000만 달러로 시장을 주도하며, 2024년의 27억 5,000만 달러에서 증가했습니다. 미국 시장은 2026년에 27억 9,000만 달러로 추정되며, 전 세계 매출의 약 25.01%를 차지할 것으로 전망됩니다.

유럽 시장은 2026년에 26억 7,000만 달러에 달하며, 5.02%의 성장률을 보일 것으로 전망됩니다. 영국 시장은 5억 1,000만 달러로 추산되는 반면, 독일 시장은 2026년에 6억 1,000만 달러에 달할 것으로 전망됩니다.

아시아태평양은 인도와 중국의 제네릭 의약품 생산 확대에 힘입어 2026년에는 38억 4,000만 달러에 달할 것으로 추산됩니다. 2026년 시장 규모는 중국이 12억 6,000만 달러, 일본이 8억 7,000만 달러, 인도가 5억 1,000만 달러에 달할 것으로 예측됩니다.

라틴아메리카 시장은 2026년에 9억 달러에 달할 것으로 예상되며, GCC 시장은 3억 5,000만 달러에 이를 것으로 전망됩니다.

목차

제1장 서론

제2장 주요 요약

제3장 시장 역학

제4장 주요 인사이트

제5장 세계의 의약품 부형제 시장 분석, 인사이트 및 예측(2021-2034년)

제6장 북미 의약품 부형제 시장 분석, 인사이트 및 예측(2021-2034년)

제7장 유럽 의약품 부형제 시장 분석, 인사이트 및 예측(2021-2034년)

제8장 아시아태평양 의약품 부형제 시장 분석, 인사이트 및 예측(2021-2034년)

제9장 라틴아메리카 의약품 부형제 시장 분석, 인사이트 및 예측(2021-2034년)

제10장 중동 및 아프리카 의약품 부형제 시장 분석, 인사이트 및 예측(2021-2034년)

제11장 경쟁 분석

JHS 26.07.01

Growth Factors of pharmaceutical excipients Market

The global pharmaceutical excipients market was valued at USD 10.57 billion in 2025 and is projected to grow from USD 11.18 billion in 2026 to USD 17.89 billion by 2034, registering a CAGR of 6.06% during the forecast period. Pharmaceutical excipients are inactive ingredients used in drug formulations to improve stability, solubility, taste, texture, bioavailability, and manufacturing performance. They play an important role in tablets, capsules, injectables, topical products, respiratory drugs, ophthalmic products, and advanced drug delivery systems.

Market growth is mainly driven by rising generic drug production, increasing demand for complex formulations, growing biopharmaceutical development, and higher need for functional and high-purity excipients. North America dominated the market in 2025 with a 27.34% market share, supported by a mature pharmaceutical manufacturing base and strong demand for quality drug formulations.

Pharmaceutical Excipients Market Trends

A major trend in the market is the rising demand for multifunctional excipients. Pharmaceutical companies increasingly prefer excipients that can perform multiple roles, such as improving solubility, stability, release control, taste masking, and manufacturing efficiency. This helps reduce formulation complexity and shorten development timelines.

In September 2024, Evonik started operations at a new spray-drying facility for EUDRAGIT polymers in Darmstadt to meet growing demand for oral drug delivery solutions.

Market Drivers

The key driver of the pharmaceutical excipients market is the rising production of generic drugs. Generic manufacturers require large volumes of fillers, binders, coatings, stabilizers, disintegrants, and solubilizers to develop cost-effective formulations. As more branded drugs lose patent protection, generic drug manufacturing is expanding, directly increasing demand for excipients.

In addition, rising development of specialty therapies, biologics, and advanced dosage forms is increasing the need for high-performance excipients that support drug stability, delivery, and patient compliance.

Market Restraints

High quality-control and supplier-qualification requirements are restraining market growth. Since excipients directly affect drug safety and performance, pharmaceutical companies must conduct strict supplier audits, contamination checks, documentation reviews, and repeated quality testing. These processes increase procurement time, operating costs, and formulation complexity, slowing faster market adoption.

Market Opportunities

The growing demand across oral, respiratory, ophthalmic, parenteral, and topical dosage forms is creating strong opportunities. Drug manufacturers are expanding beyond traditional tablets and capsules into inhalation therapies, sterile injectables, eye care drugs, and advanced delivery systems. This increases demand for excipients with specific purity, safety, and performance characteristics.

In January 2025, DFE Pharma expanded its Closer to the Formulator Center of Excellence in Hyderabad to support respiratory formulation development.

Market Challenges

Strict regulatory requirements and complex approval processes remain major challenges. New excipients require strong safety data, compliance documentation, GMP standards, and region-specific approvals. Lack of global regulatory harmonization can delay excipient innovation and increase development costs, especially for novel and advanced excipient systems.

Segment Analysis

By type, the market is divided into organic and inorganic excipients. The organic segment dominated in 2025 due to wide use of cellulose derivatives, povidones, copovidones, cyclodextrins, and organic solubilizers in tablets, capsules, liquids, and controlled-release formulations. The inorganic segment is projected to grow at a CAGR of 6.81%.

By formulation, the oral solid dosage segment dominated in 2025. Tablets and capsules remain the most widely used and cost-efficient dosage forms, requiring large excipient volumes for filling, binding, coating, disintegration, and release control. The parenteral segment is expected to grow at a CAGR of 8.43%.

By functionality, primary processing and performance roles led the market in 2025. These include filling, binding, lubrication, flow support, compression support, and disintegration, which are essential in large-scale pharmaceutical manufacturing. Device-compatibility roles are expected to grow at a CAGR of 8.88%.

By functionality application, immediate-release and content uniformity enablement held the largest share due to high demand for uniform API distribution and reliable tablet manufacturing. Solubility and bioavailability enhancement is projected to grow at a CAGR of 7.57%.

By source, plant-derived excipients dominated the market due to their wide availability, regulatory familiarity, and use in tablets, capsules, and patient-friendly formulations. Mineral-derived excipients are expected to grow at a CAGR of 6.89%.

By end user, pharmaceutical and biopharmaceutical companies dominated in 2025, as they are the largest consumers of excipients across formulation development, scale-up, regulatory filing, and commercial production. CMOs/CDMOs are projected to grow at a CAGR of 8.31%.

Regional Analysis

North America led the market with USD 2.89 billion in 2025, increasing from USD 2.75 billion in 2024. The U.S. market is estimated at USD 2.79 billion in 2026, representing around 25.01% of global revenue.

Europe is projected to reach USD 2.67 billion in 2026, growing at 5.02%. The U.K. market is estimated at USD 0.51 billion, while Germany is expected to reach USD 0.61 billion in 2026.

Asia Pacific is estimated to reach USD 3.84 billion in 2026, driven by expanding generic drug production in India and China. China is projected at USD 1.26 billion, Japan at USD 0.87 billion, and India at USD 0.51 billion in 2026.

Latin America is expected to reach USD 0.90 billion in 2026, while the GCC market is projected at USD 0.35 billion.

Competitive Landscape

Key players include Roquette Freres, BASF Pharma Solutions, Evonik Industries AG, Ashland Inc., Croda Pharma, MEGGLE Excipients, SPI Pharma, JRS Pharma, Shin-Etsu Chemical, and Colorcon Limited. These companies focus on product launches, partnerships, GMP facility expansion, and advanced excipient technologies.

Conclusion

The pharmaceutical excipients market is expected to grow from USD 10.57 billion in 2025 to USD 11.18 billion in 2026, reaching USD 17.89 billion by 2034. Growth will be supported by generic drug expansion, advanced formulations, biopharmaceutical development, and increasing demand for multifunctional excipients. Despite regulatory and quality-control challenges, innovation in high-performance excipients will continue to drive market growth.

Segmentation By Type, Formulation, Functionality, Functionality Application, Source, End User, and Region

By Type * Organic Chemicals

    • Carbohydrates & Derivatives
    • Polymers
    • Lipids, Fatty Materials & Amphiphiles
    • Surfactants & Solubilizers
    • Proteins, Amino Acids & Other Organics
    • Others
  • Inorganic Chemicals
    • Salts & Buffers
    • Oxides & Hydroxides
    • Silicates, Aluminosilicates & Clays
    • Carbonates & Sulfates
    • Metal-based Specialty Excipients
    • Others

By Formulation * Oral Solid Dosage (OSD)

    • Immediate-release tablets (IR)
    • Modified-release tablets (ER/CR/SR)
    • Capsules (hard gelatin; HPMC)
    • ODT / dispersible tablets
    • Others (OSD)
  • Oral Liquids
    • Solutions/syrups
    • Suspensions
    • Emulsions
    • Oral drops
    • Others
  • Parenteral
    • Small-volume parenterals (SVP)
    • Large-volume parenterals (LVP)
    • Lyophilized injectables
    • Depot/long-acting injectables
    • Others
  • Topical & Transdermal
    • Creams
    • Ointments
    • Gels
    • Lotions
    • Others (Topical & transdermal)
  • Pulmonary & Nasal
    • Dry powder inhalers (DPI)
    • Metered dose inhalers (MDI)
    • Nebulized solutions
    • Nasal sprays
    • Others
  • Ophthalmic & Otic
    • Ophthalmic solutions
    • Ophthalmic suspensions
    • Ophthalmic ointments
    • Ophthalmic gels / in-situ gels
    • Others
  • Rectal / Vaginal
    • Suppositories/pessaries
    • Rectal creams/ointments/gels
    • Vaginal creams/ointments/gels
    • Vaginal tablets
    • Others
  • Others

By Functionality * Primary processing & performance roles

  • Stability & protection roles
  • Patient experience & adherence roles
  • Device-compatibility roles
  • Others

By Functionality Application * Stabilizers

  • Taste masking
  • Modified-release
  • Solubility & bioavailability enhancement
  • Immediate-release & content uniformity enablement
  • Injectability & parenteral compatibility
  • Preservation & microbial control
  • Other functionality applications

By Source * Plant-derived (botanical)

  • Animal-derived
  • Mineral-derived
  • Synthetic / petrochemical-derived
  • Others

By End User * Pharmaceutical & Biopharmaceutical Companies

  • CMOs / CDMOs
  • Research & Academic Institutes
  • Others

By Region * North America (By Type, Formulation, Functionality, Functionality Application, Source, End User, and Country)

    • U.S.
    • Canada
  • Europe (By Type, Formulation, Functionality, Functionality Application, Source, End User, and Country/Sub-region)
    • Germany
    • U.K.
    • France
    • Spain
    • Italy
    • Scandinavia
    • Rest of Europe
  • Asia Pacific (By Type, Formulation, Functionality, Functionality Application, Source, End User, and Country/Sub-region)
    • China
    • Japan
    • India
    • Australia
    • Southeast Asia
    • Rest of Asia Pacific
  • Latin America (By Type, Formulation, Functionality, Functionality Application, Source, End User, and Country/Sub-region)
    • Brazil
    • Mexico
    • Rest of Latin America
  • Middle East & Africa (By Type, Formulation, Functionality, Functionality Application, Source, End User, and Country/Sub-region)
    • GCC
    • South Africa
    • Rest of the Middle East & Africa

Table of Content

1. Introduction

  • 1.1. Research Scope
  • 1.2. Market Segmentation
  • 1.3. Research Methodology
  • 1.4. Definitions and Assumptions

2. Executive Summary

3. Market Dynamics

  • 3.1. Market Drivers
  • 3.2. Market Restraints
  • 3.3. Market Opportunities
  • 3.4. Market Trends

4. Key Insights

  • 4.1. New Type Launches, By Key Players
  • 4.2. Key Industry Developments (Mergers, Acquisitions, Partnerships, Launches, etc.)
  • 4.3. Regulatory Scenario, By Key Countries/Regions
  • 4.4. Overview: Advancements in Pharmaceutical Excipients

5. Global Pharmaceutical Excipients Market Analysis, Insights and Forecast, 2021-2034

  • 5.1. Market Analysis, Insights and Forecast - By Type
    • 5.1.1. Organic Chemicals
      • 5.1.1.1. Carbohydrates & Derivatives
      • 5.1.1.2. Polymers
      • 5.1.1.3. Lipids, Fatty Materials & Amphiphiles
      • 5.1.1.4. Surfactants & Solubilizers
      • 5.1.1.5. Proteins, Amino Acids & Other Organics
      • 5.1.1.6. Others
    • 5.1.2. Inorganic Chemicals
      • 5.1.2.1. Salts & Buffers
      • 5.1.2.2. Oxides & Hydroxides
      • 5.1.2.3. Silicates, Aluminosilicates & Clays
      • 5.1.2.4. Carbonates & Sulfates
      • 5.1.2.5. Metal-based Specialty Excipients
      • 5.1.2.6. Others
  • 5.2. Market Analysis, Insights and Forecast - By Formulation
    • 5.2.1. Oral Solid Dosage (OSD)
      • 5.2.1.1. Immediate-release tablets (IR)
      • 5.2.1.2. Modified-release tablets (ER/CR/SR)
      • 5.2.1.3. Capsules (hard gelatin; HPMC)
      • 5.2.1.4. ODT / dispersible tablets
      • 5.2.1.5. Others (OSD)
    • 5.2.2. Oral Liquids
      • 5.2.2.1. Solutions / syrups
      • 5.2.2.2. Suspensions
      • 5.2.2.3. Emulsions
      • 5.2.2.4. Oral drops
      • 5.2.2.5. Others (Oral liquids)
    • 5.2.3. Parenteral
      • 5.2.3.1. Small-volume parenterals (SVP)
      • 5.2.3.2. Large-volume parenterals (LVP)
      • 5.2.3.3. Lyophilized injectables
      • 5.2.3.4. Depot/long-acting injectables
      • 5.2.3.5. Others (Parenteral)
    • 5.2.4. Topical & Transdermal
      • 5.2.4.1. Creams
      • 5.2.4.2. Ointments
      • 5.2.4.3. Gels
      • 5.2.4.4. Lotions
      • 5.2.4.5. Others (Topical & transdermal)
    • 5.2.5. Pulmonary & Nasal
      • 5.2.5.1. Dry powder inhalers (DPI)
      • 5.2.5.2. Metered dose inhalers (MDI)
      • 5.2.5.3. Nebulized solutions
      • 5.2.5.4. Nasal sprays (solution; suspension)
      • 5.2.5.5. Others (Pulmonary & nasal)
    • 5.2.6. Ophthalmic & Otic
      • 5.2.6.1. Ophthalmic solutions
      • 5.2.6.2. Ophthalmic suspensions
      • 5.2.6.3. Ophthalmic ointments
      • 5.2.6.4. Ophthalmic gels / in-situ gels
      • 5.2.6.5. Others (Ophthalmic & otic)
    • 5.2.7. Rectal / Vaginal
      • 5.2.7.1. Suppositories / pessaries
      • 5.2.7.2. Rectal creams/ointments/gels
      • 5.2.7.3. Vaginal creams/ointments/gels
      • 5.2.7.4. Vaginal tablets
      • 5.2.7.5. Others (Rectal/vaginal)
    • 5.2.8. Others
  • 5.3. Market Analysis, Insights and Forecast - By Functionality
    • 5.3.1. Primary processing & performance roles
    • 5.3.2. Stability & protection roles
    • 5.3.3. Patient experience & adherence roles
    • 5.3.4. Device-compatibility roles
    • 5.3.5. Others
  • 5.4. Market Analysis, Insights and Forecast - By Functionality Application
    • 5.4.1. Stabilizers
    • 5.4.2. Taste masking
    • 5.4.3. Modified-release
    • 5.4.4. Solubility & bioavailability enhancement
    • 5.4.5. Immediate-release & content uniformity enablement
    • 5.4.6. Injectability & parenteral compatibility
    • 5.4.7. Preservation & microbial control
    • 5.4.8. Other functionality applications
  • 5.5. Market Analysis, Insights and Forecast - By Source
    • 5.5.1. Plant-derived (botanical)
    • 5.5.2. Animal-derived
    • 5.5.3. Mineral-derived
    • 5.5.4. Synthetic / petrochemical-derived
    • 5.5.5. Others
  • 5.6. Market Analysis, Insights and Forecast - By End User
    • 5.6.1. Pharmaceutical & Biopharmaceutical Companies
    • 5.6.2. CMOs / CDMOs
    • 5.6.3. Research & Academic Institutes
    • 5.6.4. Others
  • 5.7. Market Analysis, Insights and Forecast - Region
    • 5.7.1. North America
    • 5.7.2. Europe
    • 5.7.3. Asia Pacific
    • 5.7.4. Latin America
    • 5.7.5. Middle East & Africa

6. North America Pharmaceutical Excipients Market Analysis, Insights and Forecast, 2021-2034

  • 6.1. Market Analysis, Insights and Forecast - By Type
    • 6.1.1. Organic Chemicals
      • 6.1.1.1. Carbohydrates & Derivatives
      • 6.1.1.2. Polymers
      • 6.1.1.3. Lipids, Fatty Materials & Amphiphiles
      • 6.1.1.4. Surfactants & Solubilizers
      • 6.1.1.5. Proteins, Amino Acids & Other Organics
      • 6.1.1.6. Others
    • 6.1.2. Inorganic Chemicals
      • 6.1.2.1. Salts & Buffers
      • 6.1.2.2. Oxides & Hydroxides
      • 6.1.2.3. Silicates, Aluminosilicates & Clays
      • 6.1.2.4. Carbonates & Sulfates
      • 6.1.2.5. Metal-based Specialty Excipients
      • 6.1.2.6. Others
  • 6.2. Market Analysis, Insights and Forecast - By Formulation
    • 6.2.1. Oral Solid Dosage (OSD)
      • 6.2.1.1. Immediate-release tablets (IR)
      • 6.2.1.2. Modified-release tablets (ER/CR/SR)
      • 6.2.1.3. Capsules (hard gelatin; HPMC)
      • 6.2.1.4. ODT / dispersible tablets
      • 6.2.1.5. Others (OSD)
    • 6.2.2. Oral Liquids
      • 6.2.2.1. Solutions / syrups
      • 6.2.2.2. Suspensions
      • 6.2.2.3. Emulsions
      • 6.2.2.4. Oral drops
      • 6.2.2.5. Others (Oral liquids)
    • 6.2.3. Parenteral
      • 6.2.3.1. Small-volume parenterals (SVP)
      • 6.2.3.2. Large-volume parenterals (LVP)
      • 6.2.3.3. Lyophilized injectables
      • 6.2.3.4. Depot/long-acting injectables
      • 6.2.3.5. Others (Parenteral)
    • 6.2.4. Topical & Transdermal
      • 6.2.4.1. Creams
      • 6.2.4.2. Ointments
      • 6.2.4.3. Gels
      • 6.2.4.4. Lotions
      • 6.2.4.5. Others (Topical & transdermal)
    • 6.2.5. Pulmonary & Nasal
      • 6.2.5.1. Dry powder inhalers (DPI)
      • 6.2.5.2. Metered dose inhalers (MDI)
      • 6.2.5.3. Nebulized solutions
      • 6.2.5.4. Nasal sprays (solution; suspension)
      • 6.2.5.5. Others (Pulmonary & nasal)
    • 6.2.6. Ophthalmic & Otic
      • 6.2.6.1. Ophthalmic solutions
      • 6.2.6.2. Ophthalmic suspensions
      • 6.2.6.3. Ophthalmic ointments
      • 6.2.6.4. Ophthalmic gels / in-situ gels
      • 6.2.6.5. Others (Ophthalmic & otic)
    • 6.2.7. Rectal / Vaginal
      • 6.2.7.1. Suppositories / pessaries
      • 6.2.7.2. Rectal creams/ointments/gels
      • 6.2.7.3. Vaginal creams/ointments/gels
      • 6.2.7.4. Vaginal tablets
      • 6.2.7.5. Others (Rectal/vaginal)
    • 6.2.8. Others
  • 6.3. Market Analysis, Insights and Forecast - By Functionality
    • 6.3.1. Primary processing & performance roles
    • 6.3.2. Stability & protection roles
    • 6.3.3. Patient experience & adherence roles
    • 6.3.4. Device-compatibility roles
    • 6.3.5. Others
  • 6.4. Market Analysis, Insights and Forecast - By Functionality Application
    • 6.4.1. Stabilizers
    • 6.4.2. Taste masking
    • 6.4.3. Modified-release
    • 6.4.4. Solubility & bioavailability enhancement
    • 6.4.5. Immediate-release & content uniformity enablement
    • 6.4.6. Injectability & parenteral compatibility
    • 6.4.7. Preservation & microbial control
    • 6.4.8. Other functionality applications
  • 6.5. Market Analysis, Insights and Forecast - By Source
    • 6.5.1. Plant-derived (botanical)
    • 6.5.2. Animal-derived
    • 6.5.3. Mineral-derived
    • 6.5.4. Synthetic / petrochemical-derived
    • 6.5.5. Others
  • 6.6. Market Analysis, Insights and Forecast - By End User
    • 6.6.1. Pharmaceutical & Biopharmaceutical Companies
    • 6.6.2. CMOs / CDMOs
    • 6.6.3. Research & Academic Institutes
    • 6.6.4. Others
  • 6.7. Market Analysis, Insights and Forecast - By Country
    • 6.7.1. U.S.
    • 6.7.2. Canada

7. Europe Pharmaceutical Excipients Market Analysis, Insights and Forecast, 2021-2034

  • 7.1. Market Analysis, Insights and Forecast - By Type
    • 7.1.1. Organic Chemicals
      • 7.1.1.1. Carbohydrates & Derivatives
      • 7.1.1.2. Polymers
      • 7.1.1.3. Lipids, Fatty Materials & Amphiphiles
      • 7.1.1.4. Surfactants & Solubilizers
      • 7.1.1.5. Proteins, Amino Acids & Other Organics
      • 7.1.1.6. Others
    • 7.1.2. Inorganic Chemicals
      • 7.1.2.1. Salts & Buffers
      • 7.1.2.2. Oxides & Hydroxides
      • 7.1.2.3. Silicates, Aluminosilicates & Clays
      • 7.1.2.4. Carbonates & Sulfates
      • 7.1.2.5. Metal-based Specialty Excipients
      • 7.1.2.6. Others
  • 7.2. Market Analysis, Insights and Forecast - By Formulation
    • 7.2.1. Oral Solid Dosage (OSD)
      • 7.2.1.1. Immediate-release tablets (IR)
      • 7.2.1.2. Modified-release tablets (ER/CR/SR)
      • 7.2.1.3. Capsules (hard gelatin, HPMC)
      • 7.2.1.4. ODT / dispersible tablets
      • 7.2.1.5. Others (OSD)
    • 7.2.2. Oral Liquids
      • 7.2.2.1. Solutions / syrups
      • 7.2.2.2. Suspensions
      • 7.2.2.3. Emulsions
      • 7.2.2.4. Oral drops
      • 7.2.2.5. Others (Oral liquids)
    • 7.2.3. Parenteral
      • 7.2.3.1. Small-volume parenterals (SVP)
      • 7.2.3.2. Large-volume parenterals (LVP)
      • 7.2.3.3. Lyophilized injectables
      • 7.2.3.4. Depot/long-acting injectables
      • 7.2.3.5. Others (Parenteral)
    • 7.2.4. Topical & Transdermal
      • 7.2.4.1. Creams
      • 7.2.4.2. Ointments
      • 7.2.4.3. Gels
      • 7.2.4.4. Lotions
      • 7.2.4.5. Others (Topical & transdermal)
    • 7.2.5. Pulmonary & Nasal
      • 7.2.5.1. Dry powder inhalers (DPI)
      • 7.2.5.2. Metered dose inhalers (MDI)
      • 7.2.5.3. Nebulized solutions
      • 7.2.5.4. Nasal sprays (solution; suspension)
      • 7.2.5.5. Others (Pulmonary & nasal)
    • 7.2.6. Ophthalmic & Otic
      • 7.2.6.1. Ophthalmic solutions
      • 7.2.6.2. Ophthalmic suspensions
      • 7.2.6.3. Ophthalmic ointments
      • 7.2.6.4. Ophthalmic gels / in-situ gels
      • 7.2.6.5. Others (Ophthalmic & otic)
    • 7.2.7. Rectal / Vaginal
      • 7.2.7.1. Suppositories / pessaries
      • 7.2.7.2. Rectal creams/ointments/gels
      • 7.2.7.3. Vaginal creams/ointments/gels
      • 7.2.7.4. Vaginal tablets
      • 7.2.7.5. Others (Rectal/vaginal)
    • 7.2.8. Others
  • 7.3. Market Analysis, Insights and Forecast - By Functionality
    • 7.3.1. Primary processing & performance roles
    • 7.3.2. Stability & protection roles
    • 7.3.3. Patient experience & adherence roles
    • 7.3.4. Device-compatibility roles
    • 7.3.5. Others
  • 7.4. Market Analysis, Insights and Forecast - By Functionality Application
    • 7.4.1. Stabilizers
    • 7.4.2. Taste masking
    • 7.4.3. Modified-release
    • 7.4.4. Solubility & bioavailability enhancement
    • 7.4.5. Immediate-release & content uniformity enablement
    • 7.4.6. Injectability & parenteral compatibility
    • 7.4.7. Preservation & microbial control
    • 7.4.8. Other functionality applications
  • 7.5. Market Analysis, Insights and Forecast - By Source
    • 7.5.1. Plant-derived (botanical)
    • 7.5.2. Animal-derived
    • 7.5.3. Mineral-derived
    • 7.5.4. Synthetic / petrochemical-derived
    • 7.5.5. Others
  • 7.6. Market Analysis, Insights and Forecast - By End User
    • 7.6.1. Pharmaceutical & Biopharmaceutical Companies
    • 7.6.2. CMOs / CDMOs
    • 7.6.3. Research & Academic Institutes
    • 7.6.4. Others
  • 7.7. Market Analysis, Insights and Forecast - By Country/ Sub-Region
    • 7.7.1. U.K.
    • 7.7.2. Germany
    • 7.7.3. France
    • 7.7.4. Italy
    • 7.7.5. Spain
    • 7.7.6. Scandinavia
    • 7.7.7. Rest of Europe

8. Asia Pacific Pharmaceutical Excipients Market Analysis, Insights and Forecast, 2021-2034

  • 8.1. Market Analysis, Insights and Forecast - By Type
    • 8.1.1. Organic Chemicals
      • 8.1.1.1. Carbohydrates & Derivatives
      • 8.1.1.2. Polymers
      • 8.1.1.3. Lipids, Fatty Materials & Amphiphiles
      • 8.1.1.4. Surfactants & Solubilizers
      • 8.1.1.5. Proteins, Amino Acids & Other Organics
      • 8.1.1.6. Others
    • 8.1.2. Inorganic Chemicals
      • 8.1.2.1. Salts & Buffers
      • 8.1.2.2. Oxides & Hydroxides
      • 8.1.2.3. Silicates, Aluminosilicates & Clays
      • 8.1.2.4. Carbonates & Sulfates
      • 8.1.2.5. Metal-based Specialty Excipients
      • 8.1.2.6. Others
  • 8.2. Market Analysis, Insights and Forecast - By Formulation
    • 8.2.1. Oral Solid Dosage (OSD)
      • 8.2.1.1. Immediate-release tablets (IR)
      • 8.2.1.2. Modified-release tablets (ER/CR/SR)
      • 8.2.1.3. Capsules (hard gelatin; HPMC)
      • 8.2.1.4. ODT / dispersible tablets
      • 8.2.1.5. Others (OSD)
    • 8.2.2. Oral Liquids
      • 8.2.2.1. Solutions / syrups
      • 8.2.2.2. Suspensions
      • 8.2.2.3. Emulsions
      • 8.2.2.4. Oral drops
      • 8.2.2.5. Others (Oral liquids)
    • 8.2.3. Parenteral
      • 8.2.3.1. Small-volume parenterals (SVP)
      • 8.2.3.2. Large-volume parenterals (LVP)
      • 8.2.3.3. Lyophilized injectables
      • 8.2.3.4. Depot/long-acting injectables
      • 8.2.3.5. Others (Parenteral)
    • 8.2.4. Topical & Transdermal
      • 8.2.4.1. Creams
      • 8.2.4.2. Ointments
      • 8.2.4.3. Gels
      • 8.2.4.4. Lotions
      • 8.2.4.5. Others (Topical & transdermal)
    • 8.2.5. Pulmonary & Nasal
      • 8.2.5.1. Dry powder inhalers (DPI)
      • 8.2.5.2. Metered dose inhalers (MDI)
      • 8.2.5.3. Nebulized solutions
      • 8.2.5.4. Nasal sprays (solution; suspension)
      • 8.2.5.5. Others (Pulmonary & nasal)
    • 8.2.6. Ophthalmic & Otic
      • 8.2.6.1. Ophthalmic solutions
      • 8.2.6.2. Ophthalmic suspensions
      • 8.2.6.3. Ophthalmic ointments
      • 8.2.6.4. Ophthalmic gels / in-situ gels
      • 8.2.6.5. Others (Ophthalmic & otic)
    • 8.2.7. Rectal / Vaginal
      • 8.2.7.1. Suppositories / pessaries
      • 8.2.7.2. Rectal creams/ointments/gels
      • 8.2.7.3. Vaginal creams/ointments/gels
      • 8.2.7.4. Vaginal tablets
      • 8.2.7.5. Others (Rectal/vaginal)
    • 8.2.8. Others
  • 8.3. Market Analysis, Insights and Forecast - By Functionality
    • 8.3.1. Primary processing & performance roles
    • 8.3.2. Stability & protection roles
    • 8.3.3. Patient experience & adherence roles
    • 8.3.4. Device-compatibility roles
    • 8.3.5. Others
  • 8.4. Market Analysis, Insights and Forecast - By Functionality Application
    • 8.4.1. Stabilizers
    • 8.4.2. Taste masking
    • 8.4.3. Modified-release
    • 8.4.4. Solubility & bioavailability enhancement
    • 8.4.5. Immediate-release & content uniformity enablement
    • 8.4.6. Injectability & parenteral compatibility
    • 8.4.7. Preservation & microbial control
    • 8.4.8. Other functionality applications
  • 8.5. Market Analysis, Insights and Forecast - By Source
    • 8.5.1. Plant-derived (botanical)
    • 8.5.2. Animal-derived
    • 8.5.3. Mineral-derived
    • 8.5.4. Synthetic / petrochemical-derived
    • 8.5.5. Others
  • 8.6. Market Analysis, Insights and Forecast - By End User
    • 8.6.1. Pharmaceutical & Biopharmaceutical Companies
    • 8.6.2. CMOs / CDMOs
    • 8.6.3. Research & Academic Institutes
    • 8.6.4. Others
  • 8.7. Market Analysis, Insights and Forecast - By Country/ Sub-Region
    • 8.7.1. China
    • 8.7.2. Japan
    • 8.7.3. India
    • 8.7.4. Southeast Asia
    • 8.7.5. Australia
    • 8.7.6. Rest of Asia Pacific

9. Latin America Pharmaceutical Excipients Market Analysis, Insights and Forecast, 2021-2034

  • 9.1. Market Analysis, Insights and Forecast - By Type
    • 9.1.1. Organic Chemicals
      • 9.1.1.1. Carbohydrates & Derivatives
      • 9.1.1.2. Polymers
      • 9.1.1.3. Lipids, Fatty Materials & Amphiphiles
      • 9.1.1.4. Surfactants & Solubilizers
      • 9.1.1.5. Proteins, Amino Acids & Other Organics
      • 9.1.1.6. Others
    • 9.1.2. Inorganic Chemicals
      • 9.1.2.1. Salts & Buffers
      • 9.1.2.2. Oxides & Hydroxides
      • 9.1.2.3. Silicates, Aluminosilicates & Clays
      • 9.1.2.4. Carbonates & Sulfates
      • 9.1.2.5. Metal-based Specialty Excipients
      • 9.1.2.6. Others
  • 9.2. Market Analysis, Insights and Forecast - By Formulation
    • 9.2.1. Oral Solid Dosage (OSD)
      • 9.2.1.1. Immediate-release tablets (IR)
      • 9.2.1.2. Modified-release tablets (ER/CR/SR)
      • 9.2.1.3. Capsules (hard gelatin; HPMC)
      • 9.2.1.4. ODT / dispersible tablets
      • 9.2.1.5. Others (OSD)
    • 9.2.2. Oral Liquids
      • 9.2.2.1. Solutions / syrups
      • 9.2.2.2. Suspensions
      • 9.2.2.3. Emulsions
      • 9.2.2.4. Oral drops
      • 9.2.2.5. Others (Oral liquids)
    • 9.2.3. Parenteral
      • 9.2.3.1. Small-volume parenterals (SVP)
      • 9.2.3.2. Large-volume parenterals (LVP)
      • 9.2.3.3. Lyophilized injectables
      • 9.2.3.4. Depot/long-acting injectables
      • 9.2.3.5. Others (Parenteral)
    • 9.2.4. Topical & Transdermal
      • 9.2.4.1. Creams
      • 9.2.4.2. Ointments
      • 9.2.4.3. Gels
      • 9.2.4.4. Lotions
      • 9.2.4.5. Others (Topical & transdermal)
    • 9.2.5. Pulmonary & Nasal
      • 9.2.5.1. Dry powder inhalers (DPI)
      • 9.2.5.2. Metered dose inhalers (MDI)
      • 9.2.5.3. Nebulized solutions
      • 9.2.5.4. Nasal sprays (solution; suspension)
      • 9.2.5.5. Others (Pulmonary & nasal)
    • 9.2.6. Ophthalmic & Otic
      • 9.2.6.1. Ophthalmic solutions
      • 9.2.6.2. Ophthalmic suspensions
      • 9.2.6.3. Ophthalmic ointments
      • 9.2.6.4. Ophthalmic gels / in-situ gels
      • 9.2.6.5. Others (Ophthalmic & otic)
    • 9.2.7. Rectal / Vaginal
      • 9.2.7.1. Suppositories / pessaries
      • 9.2.7.2. Rectal creams/ointments/gels
      • 9.2.7.3. Vaginal creams/ointments/gels
      • 9.2.7.4. Vaginal tablets
      • 9.2.7.5. Others (Rectal/vaginal)
    • 9.2.8. Others
  • 9.3. Market Analysis, Insights and Forecast - By Functionality
    • 9.3.1. Primary processing & performance roles
    • 9.3.2. Stability & protection roles
    • 9.3.3. Patient experience & adherence roles
    • 9.3.4. Device-compatibility roles
    • 9.3.5. Others
  • 9.4. Market Analysis, Insights and Forecast - By Functionality Application
    • 9.4.1. Stabilizers
    • 9.4.2. Taste masking
    • 9.4.3. Modified-release
    • 9.4.4. Solubility & bioavailability enhancement
    • 9.4.5. Immediate-release & content uniformity enablement
    • 9.4.6. Injectability & parenteral compatibility
    • 9.4.7. Preservation & microbial control
    • 9.4.8. Other functionality applications
  • 9.5. Market Analysis, Insights and Forecast - By Source
    • 9.5.1. Plant-derived (botanical)
    • 9.5.2. Animal-derived
    • 9.5.3. Mineral-derived
    • 9.5.4. Synthetic / petrochemical-derived
    • 9.5.5. Others
  • 9.6. Market Analysis, Insights and Forecast - By End User
    • 9.6.1. Pharmaceutical & Biopharmaceutical Companies
    • 9.6.2. CMOs / CDMOs
    • 9.6.3. Research & Academic Institutes
    • 9.6.4. Others
  • 9.7. Market Analysis, Insights and Forecast - By Country/ Sub-Region
    • 9.7.1. Brazil
    • 9.7.2. Mexico
    • 9.7.3. Rest of Latin America

10. Middle East & Africa Pharmaceutical Excipients Market Analysis, Insights and Forecast, 2021-2034

  • 10.1. Market Analysis, Insights and Forecast - By Type
    • 10.1.1. Organic Chemicals
      • 10.1.1.1. Carbohydrates & Derivatives
      • 10.1.1.2. Polymers
      • 10.1.1.3. Lipids, Fatty Materials & Amphiphiles
      • 10.1.1.4. Surfactants & Solubilizers
      • 10.1.1.5. Proteins, Amino Acids & Other Organics
      • 10.1.1.6. Others
    • 10.1.2. Inorganic Chemicals
      • 10.1.2.1. Salts & Buffers
      • 10.1.2.2. Oxides & Hydroxides
      • 10.1.2.3. Silicates, Aluminosilicates & Clays
      • 10.1.2.4. Carbonates & Sulfates
      • 10.1.2.5. Metal-based Specialty Excipients
      • 10.1.2.6. Others
  • 10.2. Market Analysis, Insights and Forecast - By Formulation
    • 10.2.1. Oral Solid Dosage (OSD)
      • 10.2.1.1. Immediate-release tablets (IR)
      • 10.2.1.2. Modified-release tablets (ER/CR/SR)
      • 10.2.1.3. Capsules (hard gelatin; HPMC)
      • 10.2.1.4. ODT / dispersible tablets
      • 10.2.1.5. Others (OSD)
    • 10.2.2. Oral Liquids
      • 10.2.2.1. Solutions / syrups
      • 10.2.2.2. Suspensions
      • 10.2.2.3. Emulsions
      • 10.2.2.4. Oral drops
      • 10.2.2.5. Others (Oral liquids)
    • 10.2.3. Parenteral
      • 10.2.3.1. Small-volume parenterals (SVP)
      • 10.2.3.2. Large-volume parenterals (LVP)
      • 10.2.3.3. Lyophilized injectables
      • 10.2.3.4. Depot/long-acting injectables
      • 10.2.3.5. Others (Parenteral)
    • 10.2.4. Topical & Transdermal
      • 10.2.4.1. Creams
      • 10.2.4.2. Ointments
      • 10.2.4.3. Gels
      • 10.2.4.4. Lotions
      • 10.2.4.5. Others (Topical & transdermal)
    • 10.2.5. Pulmonary & Nasal
      • 10.2.5.1. Dry powder inhalers (DPI)
      • 10.2.5.2. Metered dose inhalers (MDI)
      • 10.2.5.3. Nebulized solutions
      • 10.2.5.4. Nasal sprays (solution; suspension)
      • 10.2.5.5. Others (Pulmonary & nasal)
    • 10.2.6. Ophthalmic & Otic
      • 10.2.6.1. Ophthalmic solutions
      • 10.2.6.2. Ophthalmic suspensions
      • 10.2.6.3. Ophthalmic ointments
      • 10.2.6.4. Ophthalmic gels / in-situ gels
      • 10.2.6.5. Others (Ophthalmic & otic)
    • 10.2.7. Rectal / Vaginal
      • 10.2.7.1. Suppositories / pessaries
      • 10.2.7.2. Rectal creams/ointments/gels
      • 10.2.7.3. Vaginal creams/ointments/gels
      • 10.2.7.4. Vaginal tablets
      • 10.2.7.5. Others (Rectal/vaginal)
    • 10.2.8. Others
  • 10.3. Market Analysis, Insights and Forecast - By Functionality
    • 10.3.1. Primary processing & performance roles
    • 10.3.2. Stability & protection roles
    • 10.3.3. Patient experience & adherence roles
    • 10.3.4. Device-compatibility roles
    • 10.3.5. Others
  • 10.4. Market Analysis, Insights and Forecast - By Functionality Application
    • 10.4.1. Stabilizers
    • 10.4.2. Taste masking
    • 10.4.3. Modified-release
    • 10.4.4. Solubility & bioavailability enhancement
    • 10.4.5. Immediate-release & content uniformity enablement
    • 10.4.6. Injectability & parenteral compatibility
    • 10.4.7. Preservation & microbial control
    • 10.4.8. Other functionality applications
  • 10.5. Market Analysis, Insights and Forecast - By Source
    • 10.5.1. Plant-derived (botanical)
    • 10.5.2. Animal-derived
    • 10.5.3. Mineral-derived
    • 10.5.4. Synthetic / petrochemical-derived
    • 10.5.5. Others
  • 10.6. Market Analysis, Insights and Forecast - By End User
    • 10.6.1. Pharmaceutical & Biopharmaceutical Companies
    • 10.6.2. CMOs / CDMOs
    • 10.6.3. Research & Academic Institutes
    • 10.6.4. Others
  • 10.7. Market Analysis, Insights and Forecast - By Country/ Sub-Region
    • 10.7.1. GCC
    • 10.7.2. South Africa
    • 10.7.3. Rest of Middle East & Africa

11. Competitive Analysis

  • 11.1. Global Market Share Analysis (2025)
  • 11.2. Company Profiles
    • 11.2.1. Roquette Freres
    • 11.2.2. BASF Pharma Solutions
    • 11.2.3. Evonik Industries AG
    • 11.2.4. Ashland Inc.
    • 11.2.5. Croda Pharma
    • 11.2.6. MEGGLE Excipients
    • 11.2.7. SPI Pharma, Inc.
    • 11.2.8. JRS Pharma GmbH & Co. KG
    • 11.2.9. Shin-Etsu Chemical Co., Ltd.
    • 11.2.10. Colorcon Limited.
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