제네릭 의약품 시장 - 세계 산업 규모, 점유율, 동향, 기회, 예측, 유형별, 용도별, 약물전달별, 형태별, 공급원별, 유통 채널별, 지역별, 경쟁별 예측(2020-2030년)
Generic Drugs Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, Segmented By Type, By Application, By Drug Delivery, By Form, By Source, By Distribution Channel, By Region and Competition, 2020-2030F
상품코드:1778884
리서치사:TechSci Research
발행일:2025년 07월
페이지 정보:영문 185 Pages
라이선스 & 가격 (부가세 별도)
ㅁ Add-on 가능: 고객의 요청에 따라 일정한 범위 내에서 Customization이 가능합니다. 자세한 사항은 문의해 주시기 바랍니다.
한글목차
제네릭 의약품 세계 시장 규모는 2024년에 4,434억 4,000만 달러로 평가되었고, 예측 기간으로는 2030년까지 연평균 복합 성장률(CAGR) 6.27%로 안정된 성장이 예측됩니다.
세계 제네릭 의약품 시장은 만성 질환 증가, 의료비 증가, 저렴한 치료 옵션의 필요성 등 몇 가지 주요 요인에 의해 주도되고 있습니다. 제네릭 의약품은 오리지널 의약품을 대체할 수 있는 비용 효율적인 대안을 제공하여 더 많은 사람들이 이용할 수 있도록 합니다. 오리지널 의약품의 특허가 만료되면 제네릭 제약사가 시장에 진입할 수 있는 기회가 생기고, 경쟁이 치열해져 가격이 하락합니다. 의료비 절감을 위해 제네릭 의약품 사용을 장려하는 정부의 이니셔티브는 시장 성장을 더욱 촉진할 것입니다. 생물학적 제제의 제네릭 의약품에 대한 수요 증가와 신흥 시장의 제네릭 의약품 생산 능력 확대도 시장 확대에 기여하고 있습니다. 세계 제네릭 의약품 시장은 저렴한 가격, 접근성, 시장 경쟁으로 인해 지속적인 성장이 예상됩니다. 제네릭 의약품과 바이오시밀러가 미국 전체 의료비 지출에서 차지하는 비중은 1.2%에 불과해 비용 대비 효율성이 뛰어납니다.
시장 개요
예측 기간
2026-2030년
시장 규모 : 2024년
4,434억 4,000만 달러
시장 규모 : 2030년
6,408억 8,000만 달러
CAGR : 2025-2030년
6.27%
급성장 부문
저분자 제네릭 의약품
최대 시장
북미
시장 성장 촉진요인
비용 효율적이고 저렴한 가격
시장 과제
규제 장애물 및 승인 절차
주요 시장 동향
제네릭 생물학적 제제(바이오시밀러)의 진보
목차
제1장 개요
제2장 조사 방법
제3장 주요 요약
제4장 고객의 소리
제5장 세계의 제네릭 의약품 시장 전망
시장 규모와 예측
금액별
시장 점유율과 예측
유형별(저분자 제네릭 의약품, 바이오시밀러)
용도별(심혈관질환, 당뇨병, 신경학, 종양학, 항염증 질환, 기타)
약물전달(경구, 국소, 비경구, 기타)
형태별(정제, 캡슐, 주사제, 기타)
공급원별(사내, 계약 제조 조직)
유통 채널별(병원 약국, 소매 약국, 온라인 약국, 기타)
지역별
기업별(2024년)
시장 맵
제6장 북미의 제네릭 의약품 시장 전망
시장 규모와 예측
시장 점유율과 예측
북미 : 국가별 분석
미국
캐나다
멕시코
제7장 유럽의 제네릭 의약품 시장 전망
시장 규모와 예측
시장 점유율과 예측
유럽 : 국가별 분석
독일
영국
이탈리아
프랑스
스페인
제8장 아시아태평양의 제네릭 의약품 시장 전망
시장 규모와 예측
시장 점유율과 예측
아시아태평양 : 국가별 분석
중국
인도
일본
한국
호주
제9장 남미의 제네릭 의약품 시장 전망
시장 규모와 예측
시장 점유율과 예측
남미 : 국가별 분석
브라질
아르헨티나
콜롬비아
제10장 중동 및 아프리카의 제네릭 의약품 시장 전망
시장 규모와 예측
시장 점유율과 예측
중동 및 아프리카 : 국가별 분석
남아프리카공화국
사우디아라비아
아랍에미리트(UAE)
제11장 시장 역학
성장 촉진요인
과제
제12장 시장 동향과 발전
인수합병(M&A)
제품 출시
제13장 Porter의 Five Forces 분석
산업내 경쟁
신규 참여 가능성
공급업체의 힘
고객의 힘
대체품의 위협
제14장 경쟁 구도
Teva Pharmaceutical Industries Ltd.
Sandoz International GmbH
Viatris Inc.
Sun Pharmaceutical Industries Ltd.
Fresenius Kabi AG
STADA Arzneimittel AG
Aurobindo Pharma Limited
Dr Reddy's Laboratories Ltd.
Cipla Ltd.
Novo Nordisk A/S
Abbott Laboratories Inc.
Endo International plc
Sanofi S.A.
Aspen Pharmacare Holdings Limited
Lupin Limited
제15장 전략적 제안
제16장 회사 소개 및 면책조항
LSH
영문 목차
영문목차
Global Generic Drugs Market was valued at USD 443.44 Billion in 2024 and is anticipated to project steady growth in the forecast period with a CAGR of 6.27% through 2030. The Global Generic Drugs Market is primarily driven by several key factors, including the rising prevalence of chronic diseases, increasing healthcare costs, and the need for affordable treatment options. Generic drugs offer a cost-effective alternative to brand-name medications, making them accessible to a broader population. Patent expirations of branded drugs create opportunities for generic manufacturers to enter the market, leading to increased competition and lower prices. Government initiatives promoting the use of generic drugs to reduce healthcare expenditures further fuel market growth. The growing demand for generic versions of biologic drugs and the expansion of generic drug manufacturing capabilities in emerging markets also contribute to the market's expansion. The Global Generic Drugs Market is poised for sustained growth driven by affordability, accessibility, and market competition. Generics and biosimilars represent just 1.2% of total U.S. healthcare spending, underscoring their cost-effectiveness.
Market Overview
Forecast Period
2026-2030
Market Size 2024
USD 443.44 Billion
Market Size 2030
USD 640.88 Billion
CAGR 2025-2030
6.27%
Fastest Growing Segment
Small Molecule Generics
Largest Market
North America
Key Market Drivers
Cost-effectiveness and Affordability
The affordability and accessibility of generic drugs compared to their brand-name counterparts constitute a pivotal factor driving their widespread adoption and market expansion on a global scale. Generic medications, renowned for their lower price points, serve as indispensable alternatives for patients and healthcare systems grappling with constrained budgets or exorbitant out-of-pocket expenses associated with branded pharmaceuticals. In regions where healthcare resources are scarce or where patients bear a substantial burden of medication costs, the cost-effectiveness of generic drugs emerges as a cornerstone of healthcare provision. The considerable price differentials between generic and brand-name medications facilitate broader access to essential treatments, ensuring that individuals can afford the medications they need to manage their health conditions effectively.
A fundamental driver of the cost-effectiveness of generic drugs lies in the expiration of patents on brand-name medications. Upon patent expiry, generic manufacturers gain the legal right to produce and distribute equivalent versions of the drug, igniting competition within the pharmaceutical market. This competitive landscape fosters price reductions as generic manufacturers leverage economies of scale, streamlined production processes, and reduced research and development costs to offer their products at significantly lower prices.
Key Market Challenges
Regulatory Hurdles and Approval Processes
One of the primary challenges confronting the Global Generic Drugs Market is navigating the complex regulatory landscape governing generic drug approval processes. Regulatory agencies worldwide, including the U.S. Food and Drug Administration (FDA), the European Medicines Agency (EMA), and others, enforce stringent standards and requirements for the approval of generic medications. Generic manufacturers must demonstrate bioequivalence, pharmaceutical equivalence, and therapeutic equivalence to the reference brand-name drug through comprehensive analytical and clinical studies. The regulatory pathway for generic drug approval often entails navigating intricate legal frameworks, conducting extensive pharmacokinetic and pharmacodynamic studies, and adhering to stringent quality assurance standards, all of which pose formidable barriers to entry for manufacturers. Disparities in regulatory requirements between different regions and countries necessitate meticulous compliance with diverse regulatory mandates, adding complexity and uncertainty to the generic drug approval process.
Key Market Trends
Advancements in Generic Biologics (Biosimilars)
The emergence of biosimilars heralds a transformative paradigm shift within the pharmaceutical landscape, ushering in a new era of accessibility, affordability, and innovation in biologic drug therapy. Biosimilars, colloquially referred to as generic versions of biologic drugs, constitute a rapidly burgeoning segment of the generic drugs market, poised to revolutionize the treatment landscape across a diverse array of therapeutic domains. This paradigmatic evolution is underpinned by significant advancements in biotechnology and regulatory frameworks governing biosimilar approval, which collectively catalyze the development, commercialization, and widespread adoption of biosimilar therapies as compelling alternatives to their costly brand-name counterparts. In 2023, the average out-of-pocket cost for a generic drug was USD 7.05, compared to $27.10 for a brand-name drug.
The ascendancy of biosimilars as a burgeoning force within the generic drugs market is predicated upon the intricate interplay between scientific innovation and regulatory harmonization. Pioneering breakthroughs in biotechnological methodologies have empowered manufacturers to elucidate the complex structural and functional attributes of biologic drugs with unparalleled precision and fidelity, thereby facilitating the rational design and engineering of biosimilar formulations that closely mimic the reference biologic products. Leveraging state-of-the-art analytical techniques, manufacturers can meticulously characterize the physicochemical properties, pharmacokinetic profiles, and immunogenicity profiles of biosimilars, ensuring their comparability to the reference biologic drugs with utmost rigor and scientific rigor.
Key Market Players
Teva Pharmaceutical Industries Ltd.
Sandoz International GmbH
Viatris Inc.
Sun Pharmaceutical Industries Ltd.
Fresenius Kabi AG
STADA Arzneimittel AG
Aurobindo Pharma Limited
Dr Reddy's Laboratories Ltd.
Cipla Ltd.
Novo Nordisk A/S
Abbott Laboratories Inc.
Endo International plc
Sanofi S.A.
Aspen Pharmacare Holdings Limited
Lupin Limited
Report Scope:
In this report, the Global Generic Drugs Market has been segmented into the following categories, in addition to the industry trends which have also been detailed below:
Generic Drugs Market, By Type:
Small Molecule Generics
Biosimilars
Generic Drugs Market, By Application:
Cardiovascular Diseases
Diabetes
Neurology
Oncology
Anti-Inflammatory Diseases
Others
Generic Drugs Market, By Drug Delivery:
Oral
Topical
Parenteral
Others
Generic Drugs Market, By Form:
Tablet
Capsule
Injection
Others
Generic Drugs Market, By Source:
In House
Contract Manufacturing Organizations
Generic Drugs Market, By Distribution Channel:
Hospital Pharmacies
Retail Pharmacies
Online Pharmacies
Others
Generic Drugs Market, By Region:
North America
United States
Canada
Mexico
Europe
France
United Kingdom
Italy
Germany
Spain
Asia-Pacific
China
India
Japan
Australia
South Korea
South America
Brazil
Argentina
Colombia
Middle East & Africa
South Africa
Saudi Arabia
UAE
Competitive Landscape
Company Profiles: Detailed analysis of the major companies present in the Global Generic Drugs Market.
Available Customizations:
Global Generic Drugs market report with the given market data, TechSci Research offers customizations according to a company's specific needs. The following customization options are available for the report:
Company Information
Detailed analysis and profiling of additional market players (up to five).
Table of Contents
1. Product Overview
1.1. Market Definition
1.2. Scope of the Market
1.2.1. Markets Covered
1.2.2. Years Considered for Study
1.2.3. Key Market Segmentations
2. Research Methodology
2.1. Objective of the Study
2.2. Baseline Methodology
2.3. Key Industry Partners
2.4. Major Association and Secondary Sources
2.5. Forecasting Methodology
2.6. Data Triangulation & Validations
2.7. Assumptions and Limitations
3. Executive Summary
3.1. Overview of the Market
3.2. Overview of Key Market Segmentations
3.3. Overview of Key Market Players
3.4. Overview of Key Regions/Countries
3.5. Overview of Market Drivers, Challenges, Trends
4. Voice of Customer
5. Global Generic Drugs Market Outlook
5.1. Market Size & Forecast
5.1.1. By Value
5.2. Market Share & Forecast
5.2.1. By Type (Small Molecule Generics and Biosimilars)