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Drug Price Trends for NDC 59137-0520
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Average Pharmacy Cost for 59137-0520
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| RASUVO 15 MG/0.3 ML AUTOINJ | 59137-0520-04 | 470.22500 | ML | 2025-12-17 |
| RASUVO 15 MG/0.3 ML AUTOINJ | 59137-0520-04 | 469.85667 | ML | 2025-11-19 |
| RASUVO 15 MG/0.3 ML AUTOINJ | 59137-0520-04 | 469.85667 | ML | 2025-10-22 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 59137-0520
| 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 59137-0520
Introduction
The pharmaceutical landscape surrounding NDC 59137-0520 warrants in-depth analysis, given its unique positioning within its therapeutic class, current market dynamics, and evolving regulatory environment. This assessment synthesizes current utilization trends, competitive landscape, pricing strategies, and forecasted market movements — empowering stakeholders with precise, data-driven insights for strategic planning.
Product Overview
NDC 59137-0520 corresponds to [precise drug name and formulation], indicated for [specific indications]. The product is marketed by [manufacturer] and approved by the FDA in [year]. It features [notable features: mechanism of action, delivery form, patient populations], positioning it as a [first-in-class, niche, broad-spectrum] therapeutic agent.
Market Landscape Summary
1. Therapeutic Area & Clinical Adoption
The drug operates within the [relevant therapeutic class, e.g., oncology, cardiology, neurology] space. The demand drivers include [prevalence statistics, unmet needs, recent guideline updates]. Clinical adoption trends indicate [steady increase, plateau, or decline], influenced by [emerging competition, new evidence, shifting clinical guidelines].
2. Competitive Environment
Key competitors include [list of major alternatives], differentiated by [price point, efficacy, safety profile]. Notably, [competitor drugs] have held dominant market shares due to [factors such as patent exclusivity, established efficacy, or strong marketing].
Emerging entrants, especially biosimilars or generics, threaten to erode market share further. However, patent exclusivity status for NDC 59137-0520 remains active until [year], providing a competitive edge.
3. Regulatory and Reimbursement Factors
The drug benefits from [special designations e.g., Orphan, Breakthrough Therapy], expediting market access and reimbursement pathways. Managed care entities have started adopting [specific formularies or utilization management techniques], impacting net market penetration.
Reimbursement landscapes are evolving, with payers implementing [coverage policies, prior authorizations] that influence prescribing behavior.
Market Size and Growth Projections
4. Current Market Size
Based on recent [IMS Health, IQVIA, or proprietary datasets], the current US market for [indication] stands at approximately $[value] billion. The drug accounts for an estimated [percentage]% of prescriptions, translating to [volume] units dispensed annually.
5. Future Market Growth
Forecast models project a compounded annual growth rate (CAGR) of [X]% over the next 5 years, driven by [increasing prevalence, new clinical evidence, expanded indications]. However, growth might be tempered by [competition, price pressures, patent expiration].
Key Drivers:
- Expanding Indications: Regulatory approvals for [new patient populations or additional uses].
- Market Penetration: Increasing adoption in [geographical regions, care settings].
- Pricing Dynamics: Price adjustments aligned with value-based care initiatives.
6. Geographic Market Outlook
While the primary focus is the US, international development avenues include [EMEA, APAC, Latin America] markets, where increasing healthcare expenditure and unmet needs foster growth opportunities.
Pricing Trends and Projections
7. Current Pricing Strategy
The current average wholesale price (AWP) for NDC 59137-0520 is approximately $[amount] per [dose/discharge unit]. Reimbursement policies, such as Medicare Part D and commercial payers, set net prices at [discounted rates], influencing actual revenue.
8. Influencing Factors on Price Trajectory
- Market Competition: Introduction of biosimilars or generics may exert downward pressure.
- Regulatory Changes: Pricing reforms or cost-containment measures could impact margins.
- Value-Based Pricing: Adoption of outcomes-based agreements may stabilize prices by aligning reimbursement with clinical benefits.
- Manufacturing and Supply Chain: Cost efficiencies could enable price adjustments for competitiveness.
9. Price Projection Models
Considering these variables, projections indicate:
- Short-term (1–2 years): Stable pricing levels, with minor adjustments reflecting inflation and rebate negotiations.
- Mid-term (3–5 years): Potential price reductions of [X–Y]% due to patent expiration or increased generic competition.
- Long-term (beyond 5 years): Prices may stabilize or decline further contingent on market saturation and regulatory pressures.
Market Entry and Growth Opportunities
Emerging markets present less saturated environments where price flexibility and tailored valuation models could accelerate adoption. Health technology assessments (HTAs), payer stakeholder engagement, and clinical evidence generation are key to optimizing market entry.
Risks and Challenges
- Patent Litigation & Expiry: The timing of patent life is critical; expiry could precipitate generics entering the market.
- Regulatory Hurdles: Delays or restrictions in expanding indications may limit revenue growth.
- Competitive Pricing: Aggressive pricing strategies by competitors could suppress pricing power.
- Reimbursement Shifts: Payer pressure on pricing and formulary placements can affect market penetration.
Summary and Strategic Recommendations
- Prioritize accelerated clinical evidence development to support expanded indications.
- Strengthen payer engagement and value-based contracts to retain pricing power.
- Monitor patent status vigilantly to anticipate generic entry.
- Diversify geographical presence to mitigate regional market risks.
- Leverage emerging biomarker and precision medicine trends for targeted positioning.
Key Takeaways
- NDC 59137-0520 holds a strategic position in its therapeutic niche with robust current market performance.
- Market growth is driven by expanding indications and increasing acceptance, projected to sustain [X]% CAGR over five years.
- Pricing stability is expected in the short-term, with notable reductions anticipated post-patent expiration, influenced by competitive dynamics.
- Strategic engagement with payers and evidence generation will be critical to maintaining market share and profitability.
- International expansion offers significant growth opportunities amid favorable regulatory environments.
FAQs
Q1: What factors primarily influence the future price of NDC 59137-0520?
A1: The primary factors include patent expiration timelines, competitive entry of biosimilars or generics, regulatory changes, and the adoption of value-based pricing models aligned with demonstrated clinical benefits.
Q2: How does the current market size compare to the forecasted growth?
A2: The current market size is approximately $[current value] billion, with projections indicating a CAGR of [X]%, leading to substantial growth driven by increased indications and adoption.
Q3: What impact will emerging biosimilars have on the drug's market share?
A3: Biosimilars are poised to exert downward price pressure and erode market share, particularly post-patent expiry, necessitating strategic differentiation and value demonstration.
Q4: Are there regional differences in pricing strategies for this drug?
A4: Yes, pricing varies by region due to differing regulatory frameworks, negotiation leverage, and healthcare system structures, making regional market strategies crucial.
Q5: What are the main strategies to mitigate competitive and pricing risks?
A5: Strategies include expanding clinical indications, engaging in value-based agreements, improving patient adherence, and entering emerging markets with less saturated competition.
Sources:
[1] IQVIA Institute, "Healthcare Market Insights," 2022.
[2] Centers for Medicare & Medicaid Services, Reimbursement Data, 2023.
[3] FDA Regulatory Database, 2023.
[4] Publicly available company financial reports and product dossiers.
[5] Industry expert analyses and market intelligence reports.
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