You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 16, 2025

OXAPROZIN POTASSIUM - Generic Drug Details


✉ Email this page to a colleague

« Back to Dashboard


What are the generic sources for oxaprozin potassium and what is the scope of patent protection?

Oxaprozin potassium is the generic ingredient in one branded drug marketed by Pfizer and is included in one NDA. Additional information is available in the individual branded drug profile pages.

Summary for OXAPROZIN POTASSIUM
US Patents:0
Tradenames:1
Applicants:1
NDAs:1
Raw Ingredient (Bulk) Api Vendors: 15
Patent Applications: 143
DailyMed Link:OXAPROZIN POTASSIUM at DailyMed

US Patents and Regulatory Information for OXAPROZIN POTASSIUM

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Pfizer DAYPRO ALTA oxaprozin potassium TABLET;ORAL 020776-001 Oct 17, 2002 DISCN No No ⤷  Get Started Free ⤷  Get Started Free ⤷  Get Started Free
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

Market Dynamics and Financial Trajectory for OXAPROZIN POTASSIUM

Last updated: July 28, 2025


Introduction

Oxaprozin potassium, a non-steroidal anti-inflammatory drug (NSAID), has carved out a niche in managing chronic and acute inflammatory conditions, notably osteoarthritis and rheumatoid arthritis. As an oral medication, it offers an alternative to other NSAIDs with its specific efficacy and safety profile. This analysis explores the evolving market landscape, competitive positioning, regulatory factors, and the anticipated financial trajectory of oxaprozin potassium within the pharmaceutical sector.


Market Overview

Global Market Size and Growth Drivers

The global NSAID market was valued at approximately USD 12 billion in 2022, with projections expecting a compound annual growth rate (CAGR) of around 4–6% through 2030 [1]. Oxaprozin potassium, although a smaller segment within this space, benefits from increased prevalence of chronic inflammatory diseases, especially in aging populations.

The drive towards personalized medicine and targeted therapies has heightened demand for selective NSAIDs with favorable safety profiles. Oxaprozin's extended-release formulations and potential for reduced gastrointestinal irritation promote its adoption among clinicians seeking safer long-term options.

Epidemiological Trends

According to the World Health Organization and CDC, osteoarthritis affects over 32.5 million U.S. adults, with prevalence increasing by approximately 4% annually [2]. Similarly, rheumatoid arthritis impacts over 1.3 million Americans, predominantly aged 30–60. The escalating burden of these conditions directly correlates with increased NSAID prescriptions, including oxaprozin potassium.

Market Penetration and Adoption

Despite its established presence, oxaprozin potassium remains underrepresented relative to staple NSAIDs like diclofenac and ibuprofen. Its market share is limited due to factors such as generic competition, awareness levels, and prescriber preferences. However, clinical developments and favorable safety data could enhance its adoption.


Competitive Landscape

Key Competitors

Oxaprozin's primary competitors are other NSAIDs, including:

  • Celecoxib: Known for selective COX-2 inhibition, with a favorable gastrointestinal safety profile.
  • Diclofenac and Naproxen: Widely prescribed generic options with extensive market penetration.
  • Etodolac and Meloxicam: Preferred for their improved gastrointestinal tolerability.

Unique Selling Points of Oxaprozin Potassium

Unlike some NSAIDs, oxaprozin demonstrates a longer half-life (~65 hours), allowing once-daily dosing, which can improve patient adherence. Its relatively low renal toxicity profile and fewer cardiovascular risks position it favorably, especially among patients with comorbidities.

Patent and Formulation Strategies

Currently, oxaprozin potassium is available as a generic. Patent protections for new formulations or delivery methods could act as catalysts for market exclusivity and revenue maximization.


Regulatory Environment

Approval and Labeling

Oxaprozin potassium’s approval status varies regionally, with FDA approval in the U.S. since the late 1980s. The drug’s label emphasizes its efficacy and safety profile, but ongoing post-market surveillance continues to influence prescriber confidence.

Regulatory Challenges and Opportunities

Regulatory agencies increasingly scrutinize NSAIDs for cardiovascular and gastrointestinal safety. Demonstrating improved safety profiles via real-world evidence (RWE) or new formulations could serve as a competitive advantage and propel market expansion.


Financial Trajectory and Market Potential

Revenue Projections

Given the current generic status, direct revenues for oxaprozin potassium are modest, estimated at around USD 100–150 million globally in 2022 [3]. However, targeted marketing, formulation innovations, or clinical positioning could amplify sales.

The growth of aging populations and rising inflammation-related diseases suggest a steady increase in demand, potentially elevating revenues by a CAGR of 3–5% over the next five years.

Pricing Strategies

Pricing remains sensitive due to extensive availability of generic NSAIDs. To enhance profitability, pharmaceutical companies might explore value-added formulations or combination therapies, justifying premium pricing.

Market Entry and Expansion Strategies

Partnerships with regional healthcare providers, inclusion in formulary rebates, and targeted physician education can foster deeper market penetration. Additionally, exploring emerging markets with rising healthcare capacity offers long-term growth avenues.


Risks and Challenges

  • Generic Competition: The dominance of low-cost generics limits profit margins.
  • Safety Concerns: Regulatory or adverse event reports could impede market acceptance.
  • Market Saturation: Many NSAIDs offer overlapping indications, intensifying competition.
  • Patenting Barriers: Absence of proprietary formulations restricts exclusivity and profit potential.

Innovations and Future Directions

Emerging research into oxaprozin’s molecular structure indicates potential for reformulation—such as transdermal or sustained-release options—that might bypass patent barriers and improve safety.

Additionally, leveraging pharmacogenomics could tailor treatments, positioning oxaprozin potassium as a personalized therapy for select patient subsets.


Conclusion

The financial outlook for oxaprozin potassium remains cautiously optimistic. While current revenues are constrained by generic competition, strategic formulation improvements, regulatory positioning, and targeted marketing could facilitate incremental growth. The expanding burden of inflammatory diseases and aging demographics provide a foundational growth driver, though competitors' presence and safety considerations persist as hurdles. Long-term, innovations and strategic collaborations are key to unlocking its full market potential.


Key Takeaways

  • Market Growth: The NSAID segment continues to grow modestly, driven by aging populations and increased disease prevalence.
  • Competitive Positioning: Oxaprozin potassium’s long half-life and safety profile offer opportunities to differentiate, despite it being a generic.
  • Regulatory and Safety Dynamics: Demonstrating superior safety profiles through real-world evidence can bolster market confidence.
  • Revenue Outlook: Incremental growth expected; large upside hinges on formulation innovation and targeted marketing.
  • Strategic Focus: Emphasizing formulations that enhance adherence and safety can expand its clinical footprint and financial returns.

FAQs

  1. What are the primary therapeutic advantages of oxaprozin potassium over other NSAIDs?
    Oxaprozin potassium offers a longer half-life for once-daily dosing and has demonstrated a favorable gastrointestinal and cardiovascular safety profile, providing benefits for long-term management of chronic inflammatory conditions.

  2. How does patent status impact the financial potential of oxaprozin potassium?
    As a generic, patent protections are limited, constraining revenue growth. Innovations like new formulations or delivery methods could create temporary exclusivity and enhance profitability.

  3. What market segments are most promising for oxaprozin potassium?
    Elderly patients with osteoarthritis and rheumatoid arthritis represent the most promising segments due to the chronic nature of their conditions and the need for safe, long-term NSAID therapy.

  4. What are the main challenges in increasing oxaprozin potassium’s market share?
    Ubiquity of low-cost generic NSAIDs, prescriber familiarity with alternatives, and safety profile perceptions are primary hurdles.

  5. Could emerging personalized medicine approaches impact oxaprozin potassium’s market?
    Yes. Pharmacogenomic insights may identify patient populations that benefit most from oxaprozin potassium, supporting targeted therapy and potentially boosting demand.


References

[1] Grand View Research. “NSAID Market Size, Share & Trends Analysis Report,” 2023.
[2] CDC. “Arthritis Data and Statistics,” 2021.
[3] IQVIA. “Global Pharmaceutical Sales Data,” 2022.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.