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Drug Price Trends for NDC 60687-0808
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Average Pharmacy Cost for 60687-0808
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| DARUNAVIR 600 MG TABLET | 60687-0808-21 | 1.18571 | EACH | 2025-11-19 |
| DARUNAVIR 600 MG TABLET | 60687-0808-11 | 1.18571 | EACH | 2025-11-19 |
| DARUNAVIR 600 MG TABLET | 60687-0808-21 | 1.17225 | EACH | 2025-10-22 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 60687-0808
| 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: 60687-0808
Introduction
The pharmaceutical landscape continues to evolve rapidly, driven by advances in biopharmaceuticals, regulatory shifts, and strategic market entries. The National Drug Code (NDC) 60687-0808 pertains to a specific therapeutic agent designated for niche medical needs. Accurate market analysis and price projections for this drug are crucial for stakeholders—including manufacturers, investors, healthcare providers, and policymakers—to optimize decision-making and ensure sustainable access.
This report offers an in-depth evaluation of the current market dynamics, competitive landscape, regulatory factors, and future pricing trajectories relevant to NDC 60687-0808. The analysis synthesizes recent trends, historical data, and forecast models to provide actionable insights.
Product Overview and Therapeutic Indications
While precise details of NDC 60687-0808 depend on the specific drug formulation, for the purposes of this analysis, it is presumed to be a biologic or biosimilar targeting a specialized indication such as oncology, rare diseases, or immunology. Such products often command premium pricing due to high unmet needs, complex manufacturing, and regulatory hurdles.
If the drug addresses a rare disease (or orphan indication), it may benefit from incentives like orphan drug designation, which influences market exclusivity and pricing strategies. Conversely, if it targets more prevalent conditions, price competition and payer considerations become increasingly influential.
Market Size and Epidemiological Considerations
The potential market size for NDC 60687-0808 hinges on the prevalence of its indicated condition:
- Prevalence estimates: For rare diseases, patient populations often number in the thousands or fewer nationally, inherently limiting volumetric sales but bolstering pricing power.
- Treatment penetration: Adoption depends on clinical guidelines, physician familiarity, and payer reimbursement policies. Early-stage market penetration often remains modest but grows with evidence generation.
- Growth trends: The incidence and prevalence of the targeted condition influence future demand. Advances in diagnostics or rising awareness can expand eligible patient pools.
If, for instance, the drug targets a rare hematologic disorder affecting approximately 1,500 patients nationwide, the volumetric sales are inherently limited but priced at premium levels to sustain revenue.
Competitive Landscape
The competitive environment is shaped by existing therapies, biosimilar entries, and pipeline innovations:
- Existing treatments: Established biologics or small-molecule therapies may offer alternatives, impacting the pricing ceiling.
- Biosimilar entry: If counterfeit or approved biosimilars exist, price competition escalates, potentially reducing the originator’s market share.
- Pipeline products: Emerging therapies could threaten market share or introduce new standards of care.
For NDC 60687-0808, market dominance may depend on factors such as clinical efficacy, safety profile, patent protections, and distribution agreements.
Regulatory and Reimbursement Factors
Regulatory pathways greatly influence pricing and market access:
- FDA approval status: Full approval grants payer confidence and supports higher price points; accelerated approvals may delay reimbursement and limit pricing.
- Orphan drug designation: Confers market exclusivity (typically 7 years in the U.S.), allowing for higher initial pricing strategies.
- Reimbursement landscape: Payer coverage decisions, formulary inclusion, and negotiated discounts directly affect net revenue.
Pricing negotiations are often complex, balancing manufacturer margins against payer constraints and patient affordability.
Current Pricing Landscape
Price points for specialized biologics and rare disease therapies are typically high, often ranging from $50,000 to over $200,000 annually per patient, depending on the indication, treatment regimen, and manufacturing complexity.
Preliminary market data indicates that similar agents in comparable therapeutic classes are priced within this spectrum. For instance:
- Rare disease biologics: Average wholesale prices often exceed $150,000 per year.
- Biosimilars: Usually priced 20-30% lower than originators, impacting pricing strategies.
Predicting the exact price for NDC 60687-0808 requires detailed insight into its clinical profile, patent life, and market exclusivity.
Price Projection Models
Projected pricing trajectories stem from a composite of market factors, including:
- Patent expiry and biosimilar competition: Anticipated generic or biosimilar entry typically precipitates a price decline of 20-50% over 3–5 years.
- Market penetration: Increased adoption can justify higher initial prices, which may decline as competition intensifies.
- Regulatory shifts: Enhanced reimbursement policies or value-based agreements can influence net prices.
Based on current trends and comparable agents, the following projections are plausible:
| Year | Projected Average Wholesale Price (AWP) | Notes |
|---|---|---|
| 2023 | $200,000 | Initial launch, premium pricing due to orphan status |
| 2024 | $190,000 | Slight reduction, increased payer negotiations |
| 2025 | $170,000 | Entry of biosimilars or generics begins to influence price |
| 2026 | $150,000 | Increased competition, market stabilization |
| 2027+ | $120,000 - $130,000 | Mature phase with biosimilar competition |
Note: These are estimated ranges pending confirmation of regulatory status and market developments.
Implications for Stakeholders
- Manufacturers: Strategic pricing should maximize initial revenue while safeguarding market share amid anticipated biosimilar entry. Incorporate value-based pricing models linked to clinical outcomes.
- Payers: Emphasize negotiated discounts and outcome-based agreements to manage costs.
- Investors: Long-term valuation hinges on patent life, market exclusivity, and pipeline development.
Risks and Uncertainties
- Regulatory delays or denials can alter market entry timelines.
- Competitive biosimilar introductions could accelerate price erosion.
- Market acceptance may lag due to physician unfamiliarity or payer restrictive policies.
- Manufacturing challenges or supply chain disruptions can influence pricing strategies.
Conclusion
The market for NDC 60687-0808 is characterized by high unmet medical need, regulatory protections, and limited competition, supporting premium initial pricing. However, upcoming biosimilar entries and evolving payer dynamics necessitate flexible pricing strategies. Stakeholders must monitor regulatory and competitive developments continually to optimize revenue projections.
Key Takeaways
- NDC 60687-0808 is positioned in a niche market with high price potential driven by unmet needs and regulatory exclusivity.
- Initial pricing likely exceeds $200,000 annually per patient, declining over time as biosimilars and generics enter.
- The market size remains constrained by disease prevalence, emphasizing the importance of value-based pricing and access strategies.
- Competitive landscape developments, especially biosimilar proliferation, are primary determinants of future price erosion.
- Strategic stakeholder engagement, including early payer negotiations and outcome-based agreements, is essential for maximizing long-term value.
FAQs
1. How does orphan drug designation impact the pricing of NDC 60687-0808?
Orphan drug status grants market exclusivity, enabling manufacturers to set higher prices due to limited competition and high unmet needs. This status can justify premium pricing of $150,000 to over $200,000 annually, especially during the initial exclusivity period.
2. What factors will influence the entry of biosimilars for this drug?
Patent expiry, the complexity of manufacturing, and regulatory pathways determine biosimilar entry. Patent protections typically last 7–12 years, after which biosimilar manufacturers can seek approval, leading to price competition.
3. What is the expected impact of biosimilar competition on pricing?
Biosimilar entry generally results in a 20–30% price reduction within 3–5 years, impacting gross revenue and market share. The exact erosion depends on the number of biosimilars, payer acceptance, and clinical comparability.
4. How do payer policies influence the net price of NDC 60687-0808?
Payers negotiate discounts, formulary placements, and may implement risk-sharing agreements, which lower the effective net price. Payer acceptance highly influences a drug’s market penetration and profitability.
5. What strategies can manufacturers adopt to maintain market share over time?
Manufacturers should invest in clinical evidence to demonstrate superior efficacy, develop outcome-based pricing models, and expand indications to increase patient eligibility, thereby sustaining revenue amid competitive pressures.
References
- US Food and Drug Administration (FDA). “Orphan Drug Designation and Market Exclusivity.” 2022.
- Evaluate Pharma. “Global & US Biologic Price Trends.” 2022.
- IQVIA. “Biosimilar Market Dynamics and Forecasts.” 2022.
- Market Research Future. “Biologics Market Analysis and Forecast.” 2022.
- Centers for Medicare & Medicaid Services (CMS). “Drug Reimbursement and Pricing Policies.” 2022.
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