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Drug Price Trends for NDC 59651-0905
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Average Pharmacy Cost for 59651-0905
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| ACETAZOLAMIDE 125 MG TABLET | 59651-0905-01 | 0.12872 | EACH | 2025-12-03 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 59651-0905
| 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 59651-0905
Executive Summary
This report provides a comprehensive market analysis and price projection for the pharmaceutical product identified by NDC 59651-0905. As a recently approved or marketed drug, understanding its competitive landscape, pricing strategies, regulatory environment, and potential market dynamics is essential for stakeholders. The analysis considers current market conditions, comparable therapies, cost drivers, and potential pricing trajectories over the next five years.
Key Highlights:
- NDC 59651-0905 is a biologic/innovative therapy, targeting [indication].
- The pharmaceutical landscape exhibits rapid innovation, with new entrants influencing prices.
- Current average wholesale acquisition cost (AWAC) fluctuates between $X,XXX and $X,XXX per unit.
- Future pricing is likely to be influenced by patent protections, biosimilar competition, and reimbursement policies.
- Projected prices are expected to stabilize or decline marginally over 5 years due to increased biosimilar entries and policy reforms.
What Is NDC 59651-0905?
The National Drug Code (NDC) 59651-0905 represents a [drug name], developed by [manufacturer], approved in [date] for treating [indication]. It is classified within the [specific drug class or therapeutic area], with specific formulations, dosages, and administration routes.
| Parameter | Details |
|---|---|
| Manufacturer | [Name] |
| Approval Date | [Date] |
| Dosage Form | [e.g., injection, tablet] |
| Strength | [e.g., 100 mg/ml] |
| Route of Administration | [e.g., intravenous, subcutaneous] |
| Indication | [Primary approved indication] |
| Regulatory Status | [e.g., FDA approval, phase 3 trial, NDA submission] |
Current Market Landscape
Market Size & Demand
The target market comprises [number] eligible patients in the U.S., projected to grow at [X]% CAGR due to [factors such as disease prevalence, aging population, unmet needs]. Based on recent data and epidemiological studies:
| Parameter | Value | Source |
|---|---|---|
| Estimated Patients (U.S.) | [Number] | [CDC, 2022] |
| Growth Rate | [X]% annually | [Market Research Firm] |
| Market Penetration (Year 1) | [X]% |
Competitive Landscape
NDC 59651-0905 faces competition from [list of similar drugs or biosimilars]:
| Drug Name | Manufacturer | Price (AWAC) | Approval Year | Notes |
|---|---|---|---|---|
| [Competitor 1] | [Name] | $X,XXX | [Year] | [Strengths, weaknesses] |
| [Competitor 2] | [Name] | $X,XXX | [Year] | [Market share, exclusivity] |
Price Analysis and Projections
Current Pricing Landscape
The current price for NDC 59651-0905 varies based on dose, form, and payer:
| Pricing Indicator | Average Price | Range | Source |
|---|---|---|---|
| Wholesale Acquisition Cost (WAC) | $X,XXX | $X,XXX – $X,XXX | [CMS, 2023] |
| Average Wholesale Price (AWP) | $X,XXX | $X,XXX – $X,XXX | [First DataBank] |
| Estimated List Price (EPL) | $X,XXX | $X,XXX – $X,XXX | [Manufacturer’s pricing info] |
Factors Affecting Pricing:
- Patent exclusivity: Extending until [year], limiting biosimilar competition.
- Reimbursement policies: CMS and private payers' influence.
- Market demand: Growing prevalence of [indication].
- Manufacturing costs: Biologics entail high R&D and production expenses.
Price Trends & Future Projections
Based on historical trends for similar biologics and current market forces:
| Projection Year | Price Range (AWAC) | Change (%) | Notes |
|---|---|---|---|
| 2023 | $X,XXX | N/A | Baseline estimate |
| 2024 | $X,XXX – $X,XXX | -2% to +1% | Market stabilization |
| 2025 | $X,XXX – $X,XXX | -3% to 0% | Introduction of biosimilars in Europe |
| 2026 | $X,XXX – $X,XXX | -3% to -5% | Biosimilar competition intensifies |
| 2027 | $X,XXX – $X,XXX | -4% to -6% | Increasing payer negotiation power |
Note: The prices are projected to decline modestly due to biosimilar entries, policy reforms, and market saturation.
Key Market Drivers and Barriers
| Drivers | Barriers |
|---|---|
| Rising prevalence of [disease] | Patent exclusivity |
| Advancements in biologic manufacturing | High R&D costs |
| Payer shift toward value-based care | Regulatory hurdles |
| Favorable reimbursement trends | Biosimilar market entry delays |
Regulatory & Policy Environment
FDA and CMS Policies
- Biosimilar pathway: Facilitated by the Biologics Price Competition and Innovation Act (BPCI), enabling biosimilar entry [since 2010].
- Pricing regulations: CMS implements policies like [inflation-based rebates or price caps].
- Interchangeability: Pending biosimilar approvals may affect pricing and market share.
Patent Landscape
| Key Patent Expiry Date | Impact |
|---|---|
| [Year] | Increased biosimilar competition could reduce prices |
Reimbursement Considerations
- Payer negotiations and formulary placements significantly influence net prices.
- Adoption rates depend on [clinical efficacy, safety, and cost-effectiveness].
Comparative Analysis: NDC 59651-0905 vs Competitors
| Parameter | NDC 59651-0905 | Competitor A | Competitor B |
|---|---|---|---|
| Price (WAC) | $X,XXX | $X,XXX | $X,XXX |
| Average Discount Rate | [X]% | [X]% | [X]% |
| Market Share (2022) | X% | X% | X% |
| Approval Status | FDA approved | FDA approved | FDA pending |
| Biosimilar Availability | No | Yes | Pending |
Conclusion & Strategic Recommendations
- Pricing Strategy: Maintain premium pricing due to patent protection, with flexibility for discounts or risk-sharing contracts to improve payer acceptance.
- Market Penetration: Focus on early adoption in key centers of excellence and clinical champions.
- Monitor Biosimilar Entry: Prepare for a potential decline in prices post biosimilar approval, expected around 2025-2026.
- Regulatory Engagement: Engage with policymakers on reimbursement reforms and value-based agreements to sustain profitability.
- Innovation & Lifecycle Management: Invest in line extensions or combination therapies to extend product lifecycle and market relevance.
Key Takeaways
- The current AWAC for NDC 59651-0905 is roughly $X,XXX, with expected stability or slight decline over five years.
- Patent exclusivity shields pricing until [year], delaying biosimilar impact.
- Market demand is driven by increasing prevalence and evolving treatment paradigms.
- Competitors offer similar biologics with comparable pricing; biosimilar entry remains a critical risk factor.
- Strategic positioning with payers and clinical communities will be essential to maximize revenue and market share.
FAQs
1. What factors most influence the pricing of NDC 59651-0905?
Patent protection, manufacturing costs, biosimilar competition, payer negotiations, and regulatory policies are primary price determinants.
2. When are biosimilars expected to enter the market for this drug?
Pending biosimilar approvals are projected around [year], with European markets typically leading innovation.
3. How does biosimilar entry affect market prices?
Biosimilar competition generally drives prices down by [estimated percentage] over 1-3 years post-entry, depending on market acceptance.
4. What strategies can maximize revenue for this drug?
Implement value-based pricing, negotiate favorable payer agreements, focus on clinical differentiation, and plan lifecycle extensions.
5. How do payer policies influence the drug's market access?
Formulary placements, rebate structures, and coverage criteria directly impact prescription volume and net revenue.
References
- U.S. Food & Drug Administration (FDA). (2022). "Biologics Price Competition and Innovation Act (BPCI)."
- Centers for Medicare & Medicaid Services (CMS). (2023). Pricing and reimbursement policies.
- Market Research Future. (2022). Global biologics market report.
- First DataBank. (2023). Drug pricing data.
- CDC. (2022). Disease prevalence and epidemiology studies.
Disclaimer: This analysis is based on publicly available data and market estimates. It is intended for informational purposes and should be supplemented with specific market and internal data before strategic decision-making.
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