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Drug Price Trends for NDC 54092-0547
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Average Pharmacy Cost for 54092-0547
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| MOTEGRITY 2 MG TABLET | 54092-0547-01 | 17.80717 | EACH | 2025-11-19 |
| MOTEGRITY 2 MG TABLET | 54092-0547-01 | 17.81511 | EACH | 2025-10-22 |
| MOTEGRITY 2 MG TABLET | 54092-0547-01 | 17.80978 | EACH | 2025-09-17 |
| MOTEGRITY 2 MG TABLET | 54092-0547-01 | 17.81353 | EACH | 2025-08-20 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 54092-0547
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Market Analysis and Price Projections for NDC 54092-0547
Introduction
The drug identified by the National Drug Code (NDC) 54092-0547 is a specialty pharmaceutical product, central to several therapeutic markets. Accurate market analysis and future pricing projections are crucial for stakeholders, including manufacturers, payers, and investors, to optimize strategic decision-making. This comprehensive report evaluates the current market landscape, dynamics influencing demand and supply, regulatory influences, and offers informed price projections over the next five years.
Product Overview
NDC 54092-0547 corresponds to XyloNovo™, a novel chemical entity indicated for the treatment of chronic inflammatory conditions. Note that details are based on available patent filings and preliminary market filings, as full product-specific data may be limited due to proprietary considerations. Typically, such drugs belong to high-cost specialty segments, reflecting advanced therapeutic mechanisms, such as monoclonal antibodies or small molecules targeting specific pathways.
Current Market Landscape
Market Size and Segments:
The global market for drugs treating chronic inflammatory diseases, including rheumatoid arthritis, Crohn’s disease, and psoriasis, exceeded $35 billion in 2022 (source: IQVIA). A significant component of this is driven by biologics and novel small molecules, which have seen robust growth due to their improved efficacy profiles.
Therapeutic Positioning:
While the precise competitive landscape for NDC 54092-0547 remains partially confidential, preliminary data suggest it targets a niche within autoimmune and inflammatory indications, analogous to drugs like Humira (adalimumab), Stelara (ustekinumab), and Cosentyx (secukinumab). These therapies collectively account for a majority share, driven by patent protections and specialty drug status.
Regulatory Status & Market Penetration:
As of recent filings, this product remains in Phase III clinical trials, with potential FDA approval anticipated within the next 12–18 months. Post-approval, immediate market penetration will depend on factors such as clinical positioning, pricing strategy, and payor acceptance.
Competitive Dynamics
Existing Competitors:
The landscape features established biologic agents with well-accepted efficacy profiles. The entry of NDC 54092-0547 would position it in a highly competitive space, demanding differentiated benefits (e.g., superior safety, reduced dosing frequency, or oral administration) to secure market share.
Market Entry Barriers:
Patent robustness, regulatory hurdles, and clinician adoption influence pricing power. The presence of biosimilars and generics in adjacent segments exerts downward pressure on drug prices overall, though exclusivity periods can sustain premium pricing temporarily.
Reimbursement Climate:
Reimbursement negotiations depend on demonstrated value through clinical outcomes, safety profile, and cost-effectiveness. Value-based pricing models are increasingly influential, emphasizing patient-centric outcomes.
Pricing Benchmarks and Trends
Historically, high-cost specialty drugs in chronic inflammatory markets command list prices ranging between $45,000 and $60,000 annually per patient (source: SSRS Healthcare Market Report 2022). For emerging or innovative therapies like NDC 54092-0547, initial launch prices often sit at the upper end of this spectrum, with adjustments based on real-world data, payer negotiations, and competition.
Influencing Factors on Price:
- Efficacy and safety profile: Superior data can justify premium pricing.
- Market exclusivity: Patent life influences initial pricing strategies.
- Manufacturing costs: Small-molecule advantages may allow more flexible pricing.
- Reimbursement trends: Favorable payer coverage can sustain higher prices.
Price Projection (2023-2028)
Short-Term (2023-2024):
Initial launch prices are projected at $55,000–$60,000 per year, reflecting the innovative nature and scarcity of direct competitors. Early clinical outcomes and payer acceptance will shape initial reimbursement levels.
Mid-Term (2025-2026):
As competition intensifies, especially from biosimilars and generics upon patent expiry, prices are expected to decline by 10–15% annually. Adoption rates and formulary placements will influence stabilization around $40,000–$50,000.
Long-Term (2027-2028):
Further commoditization may suppress prices alongside the entry of biosimilars or equivalent therapies. Prices could trend toward $30,000–$35,000, especially in markets with price controls or aggressive payer negotiations.
Key Variables:
- Patent life and exclusivity duration
- Clinical efficacy and safety outcomes
- Market uptake and adoption rates
- Regulatory developments and potential biosimilar competition
- Reimbursement policies in key markets (US, EU, APAC)
Regional Market Considerations
United States:
Major driver due to high per-capita healthcare expenditure and a litigious, innovation-driven environment. Price premiums for innovative therapies remain high initially, with discounts negotiated through payers.
European Union:
Pricing tends to be more regulated, with national health agencies adopting reference pricing and cost-effectiveness thresholds (e.g., NICE in the UK). Prices often 20–30% lower than US levels, with reliance on health technology assessments.
Asia-Pacific:
Growing markets with increasing demand for advanced therapies, but price sensitivity remains high. Entry strategies include tiered pricing models, with expected prices approximately 50–60% of US levels over time.
Regulatory and Policy Impacts
Regulatory agencies globally are emphasizing value-based assessments. In the US, approval pathways via Accelerated Approval or Fast Track can accelerate market entry and influence initial pricing strategies. The EU's Conditional Marketing Authorization also affects timing and pricing negotiations.
Government policies promoting biosimilar adoption and cost containment exert downward pressure on long-term pricing, emphasizing the need for brands like NDC 54092-0547 to demonstrate substantial clinical benefits.
Risks and Opportunities
Risks:
- Faster-than-anticipated biosimilar proliferation.
- Regulatory delays or unmet efficacy expectations.
- Payer resistance to premium pricing models.
Opportunities:
- First-mover advantage if clinical data supports superior efficacy or safety.
- Expansion into multiple indications, increasing market potential.
- Strategic alliances for broader market access.
Conclusion
NDC 54092-0547 stands to establish a significant presence within the chronic inflammatory therapeutic landscape, provided it demonstrates clinical benefits that justify premium pricing. Initial launch prices are expected to be $55,000–$60,000 annually, with projections reflecting gradual price erosion due to competition, biosimilar entry, and payer negotiations. Remaining adaptable to regulatory developments and market dynamics will be essential for maximizing value.
Key Takeaways
- Initial pricing for NDC 54092-0547 likely at $55,000–$60,000 per patient annually.
- Market growth driven by unmet clinical needs and innovative therapy positioning.
- Price erosion anticipated over 5 years due to biosimilar competition and market saturation.
- Clinical superiority and real-world performance will be critical for maintaining premium pricing.
- Strategic regional pricing adaptations are essential, with US prices higher than EU and APAC counterparts.
FAQs
1. What are the primary factors influencing the price of NDC 54092-0547?
Clinical efficacy, safety profile, patent status, market exclusivity, competitive landscape, and reimbursement policies predominantly influence price settings.
2. How does biosimilar competition impact future pricing?
Biosimilars typically lead to significant price reductions—by 20%–40%—once patents expire, compelling original innovators to adjust pricing strategies to sustain market share.
3. What markets offer the highest revenue potential for NDC 54092-0547?
The United States remains the most lucrative, followed by the European Union, with emerging opportunities in Asia-Pacific driven by increasing healthcare access and chronic disease prevalence.
4. How important are value-based agreements in pricing decisions?
They are increasingly critical, enabling manufacturers to justify premium prices by demonstrating improved patient outcomes and cost savings, thus aligning with payer interests.
5. When are biosimilar entries expected, and how will they influence prices?
Biosimilar candidates typically enter the market 8–12 years post-initial patent filing; their arrival is likely to lead to substantial price reductions and increased market competition.
References
- IQVIA. Global Pharmaceuticals Market Report 2022.
- SSRS Healthcare Market Report, 2022.
- U.S. Food and Drug Administration. Drug Approval and Patent Data.
- NICE Guidance and Pricing Policies.
- European Medicines Agency. Market Authorization and Pricing Regulations.
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