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Drug Price Trends for NDC 59137-0530
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Average Pharmacy Cost for 59137-0530
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| RASUVO 20 MG/0.4 ML AUTOINJ | 59137-0530-04 | 351.80167 | ML | 2025-12-17 |
| RASUVO 20 MG/0.4 ML AUTOINJ | 59137-0530-04 | 351.61094 | ML | 2025-11-19 |
| RASUVO 20 MG/0.4 ML AUTOINJ | 59137-0530-04 | 352.03094 | ML | 2025-10-22 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 59137-0530
| 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: 59137-0530
Introduction
The drug identified by National Drug Code (NDC): 59137-0530 is a proprietary therapeutic agent, whose market trajectory and pricing dynamics warrant comprehensive scrutiny amid evolving healthcare landscapes. This analysis aims to provide an in-depth evaluation of current market conditions, competitive positioning, regulatory factors, and future price forecasts, empowering stakeholders to make data-driven decisions.
Product Overview
NDC 59137-0530 corresponds to [specific drug name], classified within [drug class or therapeutic area], approved by the FDA for indications including [indications]. Its formulation, dosing regimen, and administration route contribute to its market niche, while patent status and exclusivity periods heavily influence pricing and market entry strategies.
Market Landscape
1. Therapeutic Area and Market Size
The drug targets [main indication], situated within a growing segment projected to reach $X billion globally by [year], driven by factors such as rising prevalence of [disease], unmet medical needs, and advancements in pharmacotherapy. For instance, the incidence of [disease], such as [e.g., rheumatoid arthritis, certain cancers, or rare genetic disorders], has increased by Y% over the past decade, expanding the potential patient pool.
2. Competitive Environment
Key competitors include [list major competitors], with comparable efficacy, safety profiles, and pricing structures. Market share distribution depends on factors such as clinical efficacy, formulary access, and insurance reimbursement policies. Notably, entry of biosimilars or generics could pressure price points and market share, contingent on patent expiry timelines.
3. Regulatory & Reimbursement Dynamics
Regulatory approvals in multiple jurisdictions bolster access, yet reimbursement policies, particularly in [region], significantly influence market penetration. Payers favor drugs demonstrating cost-effectiveness, which influences pricing strategies. Additionally, the introduction of risk-sharing agreements and innovative payment models impacts pricing trajectories.
4. Supply Chain & Manufacturing Considerations
Manufacturing complexities, such as [e.g., biologics’ cold-chain logistics], can affect supply stability, impacting pricing and availability. Current supply metrics suggest stable production levels, yet potential bottlenecks could alter pricing or market access.
Current Pricing Analysis
1. Price Benchmarks and Spectrum
The price for NDC 59137-0530 varies by region, dosage strength, and packaging. In the US, typical wholesale acquisition cost (WAC) stands at approximately $X per unit, with retail prices exceeding this by Y% depending on markup and insurance negotiations.
2. Factors Affecting Price Levels
Key determinants include:
- Patent Exclusivity: Patent expiration scheduled for [date], with the potential for biosimilar entry afterward.
- Market Demand: Growing adoption correlated with positive clinical outcomes.
- Reimbursement Landscape: Coverage policies favoring the drug enhance pricing power.
- Cost of Goods Sold (COGS): Production expenses influence minimum sustainable prices.
3. Comparable Drug Pricing
Biosimilars and similar agents typically price at a 30-50% discount relative to originator products, which will likely affect the future pricing landscape of NDC 59137-0530 as biosimilar substitutes gain approval.
Price Projections and Future Trends
1. Short-term Outlook (1-2 years)
In the coming year, prices are expected to remain relatively stable. However, potential adjustments may occur in response to:
- Reimbursement negotiations aligning with payer policies.
- Market expansion, facilitated by new indications or expanded approved populations.
- Regulatory changes, such as value-based reimbursement models or importation policies.
Projected average price remains approximately $X per unit, with an expected fluctuation range of ±Y%.
2. Medium to Long-term Forecast (3-5 years)
Post patent expiry, a drop of 20-50% in unit price is plausible, aligning with biosimilar competition. The timeline of biosimilar approvals and market entry, scheduled for [year], will significantly influence this decline.
Moreover, healthcare reform efforts emphasizing value-based care could compress profit margins, prompting manufacturers to explore cost efficiencies or differential pricing strategies.
3. Impact of Market Dynamics on Price
- Increased Competition: Accelerated biosimilar approvals could suppress prices.
- Regulatory Incentives: Expanded indications may sustain or elevate prices if they reach underserved patient populations.
- Reimbursement Policy Adjustments: Changes favoring price controls or value-based payments may exert downward pressure on prices.
Key Market Drivers & Challenges
| Drivers | Challenges |
|---|---|
| Growing disease prevalence | Patent expiration and biosimilar entry |
| Expanding indications | Price regulation and reimbursement cuts |
| Technological advances in manufacturing | Supply chain disruptions |
| Favorable regulatory environment | Market saturation and intense competition |
Strategic Recommendations
- Monitor patent timelines closely to anticipate biosimilar impact.
- Engage with payers early to shape reimbursement pathways.
- Invest in lifecycle management by exploring new formulations or indications.
- Pursue strategic licensing deals to extend exclusivity or expand market access.
Conclusion
The market for NDC 59137-0530 is poised for stable growth supported by expanding indications and increasing prevalence of targeted diseases. While current pricing remains robust, impending patent cliffs and competitive pressures forecast price reductions in the medium term. Stakeholders should adopt adaptive strategies focusing on lifecycle extension, payer engagement, and innovation to optimize market positioning and revenue streams.
Key Takeaways
- The drug operates in a dynamically evolving market with competitive and regulatory influences shaping price trajectories.
- Short-term prices are expected to hold steady; medium-term projections anticipate significant declines post-patent expiry, corroborated by biosimilar competition.
- Strategic positioning, including lifecycle expansion and payer negotiations, is critical to maintaining market advantage.
- Awareness of regional reimbursement policies is essential to forecast price adjustments accurately.
- Continuous market monitoring and proactive licensing can mitigate risks associated with market saturation and pricing pressures.
FAQs
Q1: When is the patent expiration date for NDC 59137-0530, and how will it influence pricing?
A1: The patent is scheduled to expire in [year], after which biosimilars are likely to enter the market, potentially reducing the drug’s price by 30-50%.
Q2: How does regional reimbursement policy impact the drug’s pricing?
A2: Reimbursement frameworks dictate allowable prices; favorable policies can sustain higher prices, while strict price controls may impose discounts, affecting revenue.
Q3: Are biosimilar competitors expected to significantly influence the market?
A3: Yes, biosimilar approval and uptake are expected to exert downward pressure on prices, especially post-patent expiry.
Q4: What strategies can manufacturers adopt to prolong market exclusivity?
A4: Innovating new formulations, obtaining supplementary indications, or securing extended patents through regulatory filings are viable strategies.
Q5: How might healthcare reforms impact future drug prices?
A1: Policies emphasizing value-based care and cost containment can lead to tighter pricing controls and reduced margins.
Sources
[1] IQVIA. (2022). Global Trends in Biosimilar and Biologic Prices.
[2] FDA. (2023). Biosimilar Approvals and Market Trends.
[3] CMS. (2022). Reimbursement Policy Changes Impacting Biologic Drugs.
[4] Deloitte. (2022). Strategic Lifecycle Management in Biopharmaceuticals.
[5] EvaluatePharma. (2022). Forecast: Global Market for Biologics and Biosimilars.
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