Global Oral Solid Dosage Pharmaceutical Formulation Market to Reach US$818.6 Million by 2030
The global market for Oral Solid Dosage Pharmaceutical Formulation estimated at US$668.0 Million in the year 2024, is expected to reach US$818.6 Million by 2030, growing at a CAGR of 3.4% over the analysis period 2024-2030. Tablets, one of the segments analyzed in the report, is expected to record a 2.9% CAGR and reach US$280.1 Million by the end of the analysis period. Growth in the Capsules segment is estimated at 4.6% CAGR over the analysis period.
The U.S. Market is Estimated at US$182.0 Million While China is Forecast to Grow at 6.3% CAGR
The Oral Solid Dosage Pharmaceutical Formulation market in the U.S. is estimated at US$182.0 Million in the year 2024. China, the world`s second largest economy, is forecast to reach a projected market size of US$161.8 Million by the year 2030 trailing a CAGR of 6.3% over the analysis period 2024-2030. Among the other noteworthy geographic markets are Japan and Canada, each forecast to grow at a CAGR of 1.4% and 2.6% respectively over the analysis period. Within Europe, Germany is forecast to grow at approximately 2.0% CAGR.
Global Oral Solid Dosage Pharmaceutical Formulation Market – Key Trends & Drivers Summarized
Why Do Oral Solid Dosage Forms Remain the Cornerstone of Pharmaceutical Drug Delivery Systems?
Oral Solid Dosage (OSD) forms—primarily tablets, capsules, and powders—continue to dominate global pharmaceutical formulations due to their ease of administration, cost-effectiveness, high patient compliance, and manufacturing scalability. Despite growing interest in biologics and parenterals, OSDs account for over 50% of global pharmaceutical prescriptions. Their stability, controlled-release potential, and long shelf life make them especially advantageous for chronic therapy regimens and large-scale distribution, particularly in low- and middle-income markets.
The versatility of OSD formats supports an expansive range of therapeutic categories including cardiovascular, anti-infective, CNS, oncology, and gastrointestinal treatments. The rise in chronic disease prevalence, geriatric population, and demand for personalized medicine further reinforces the relevance of OSDs. Recent innovations—such as orally disintegrating tablets (ODTs), abuse-deterrent formulations, and multi-particulate capsules—are addressing challenges related to pediatric and geriatric adherence, dosage titration, and bioavailability, ensuring that OSDs remain the foundation of global drug delivery systems.
How Are Formulation Science and Manufacturing Technologies Enhancing the Efficiency of OSD Development?
Advancements in formulation technologies have significantly improved the performance, stability, and release profiles of oral solid dosage drugs. Hot melt extrusion, spray drying, and nano-milling are enabling the development of OSDs for poorly soluble Active Pharmaceutical Ingredients (APIs), addressing the growing Biopharmaceutics Classification System (BCS) class II and IV drug portfolios. Modified-release technologies, including extended-release, delayed-release, and pulsatile systems, are being deployed to improve therapeutic windows and reduce dosing frequency.
Manufacturers are increasingly adopting continuous manufacturing, Process Analytical Technology (PAT), and Quality by Design (QbD) principles to enhance production efficiency, reduce cycle times, and ensure consistent quality. Automated tablet compression, real-time monitoring, and advanced granulation methods are improving batch-to-batch reproducibility and reducing material wastage. Moreover, 3D printing is being explored for patient-specific dosage customization and multi-drug combinations. These innovations are not only expanding formulation flexibility but also streamlining regulatory approvals and accelerating time-to-market.
Which Therapeutic Areas and Regional Markets Are Driving Demand for OSD Pharmaceutical Formulations?
OSDs are extensively used across a wide array of therapeutic segments, but their dominance is particularly pronounced in chronic disease management. Hypertension, diabetes, depression, epilepsy, and infectious diseases are among the top drivers of volume-based OSD production globally. Oncology and autoimmune segments are also increasingly utilizing oral targeted therapies and kinase inhibitors in solid dosage formats, improving outpatient treatment protocols.
North America and Europe remain the leading markets, supported by advanced manufacturing facilities, regulatory expertise, and high prescription drug usage. The Asia-Pacific region, led by India and China, is experiencing the fastest growth in OSD production due to rising healthcare access, domestic pharmaceutical industry expansion, and strong export infrastructure. Latin America, the Middle East, and Africa are seeing growing adoption through public health initiatives, generics penetration, and increased domestic manufacturing capacity. These regions represent high potential for volume growth, especially for essential medicines in tablet or capsule form.
What Is Powering Long-Term Growth and Strategic Innovation in the OSD Formulations Market?
The growth in the oral solid dosage pharmaceutical formulation market is driven by increasing demand for cost-effective therapies, generics substitution, and long-term treatment adherence in chronic conditions. With payers and governments pushing for affordable healthcare solutions, OSDs remain the preferred format for formulary inclusion and reimbursement. Patent expiries are also creating robust opportunities for generic and branded-generic OSD products across global markets.
Strategic innovation is focused on fixed-dose combinations (FDCs), taste-masked pediatric formulations, and patient-centric packaging. Companies are developing multi-layer tablets, multiparticulate delivery systems, and film-coated formats to enhance swallowing, stability, and drug release dynamics. Sustainability is emerging as a priority, with biodegradable packaging and greener synthesis methods gaining traction. As pharmacogenomics and individualized dosing evolve, OSDs are expected to adapt through modular dosing platforms and digital integration, ensuring their continued dominance in the global pharmaceutical landscape.
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