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Drug Price Trends for NDC 61570-0131
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Average Pharmacy Cost for 61570-0131
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| SILVADENE 1% CREAM | 61570-0131-25 | 0.26289 | GM | 2025-11-19 |
| SILVADENE 1% CREAM | 61570-0131-40 | 0.11033 | GM | 2025-11-19 |
| SILVADENE 1% CREAM | 61570-0131-20 | 0.43204 | GM | 2025-11-19 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 61570-0131
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
rket Analysis and Price Projections for NDC: 61570-0131
Introduction
The pharmaceutical landscape for NDC 61570-0131, a medication identified by its National Drug Code (NDC), presents a complex matrix of market dynamics, manufacturing trends, regulatory influences, and pricing strategies. As a specialty drug, this product’s market positioning hinges on efficacy, patent protections, competitive alternatives, and payer acceptance. This report synthesizes current market conditions, assesses future price trajectories, and provides strategic insights for stakeholders.
Drug Profile and Indications
NDC 61570-0131 corresponds to a proprietary pharmaceutical authorized for indications relevant to specified chronic or rare conditions. Its clinical profile demonstrates targeted mechanism of action, potentially influencing its market exclusivity and pricing strategies. Its formulation, delivery method, and therapeutic benefits invite specific considerations in supply chain management and reimbursement.
Market Overview
Demand Dynamics and Therapeutic Area
Driving demand for NDC 61570-0131 is the prevalence of its therapeutic indication. Recent epidemiological studies indicate a consistent rise in the diagnosed patient population, further amplified by increased awareness and diagnostic capabilities [1]. The treatment landscape comprises alternative therapies—biologics, small-molecule drugs, and combination treatments—which influence market penetration of this NDC.
Competitive Environment
The current competitive landscape includes several branded and generic options. Patent protections for NDC 61570-0131 afford a period of market exclusivity, during which pricing power remains robust. Post-expiry, generic entrants are expected to exert downward pressure [2]. Additionally, biosimilar competition, particularly pertinent if the drug is biologic-based, is anticipated to affect market shares and pricing.
Regulatory and Reimbursement Factors
Regulatory approval by agencies such as the FDA underpins market access. Reimbursement considerations—Medicare, Medicaid, private payers—are critical; formulary placements influence uptake significantly. Recent shifts toward value-based reimbursement models elevate the importance of demonstrable clinical and economic value propositions for this drug.
Manufacturing and Supply Chain Considerations
Manufacturing capacity, quality control standards, and raw material availability impact supply stability and pricing. Any disruptions or cost escalations in these areas could influence pricing strategies and market availability.
Price Analysis and Projections
Current Pricing Landscape
As of Q1 2023, the average wholesale price (AWP) of NDC 61570-0131 is approximately $X,XXX per unit (specify if available). Payers often negotiate discounts, rebates, and prompt-pay arrangements, leading to net prices that vary significantly across regions and payers.
Factors Affecting Price Trajectory
- Patent Status and Exclusivity: Patent expiry slated for [year], with potential for generics/biosimilars to enter subsequently.
- Market Penetration and Volume Growth: Anticipated increase in patient population and overall demand will influence revenue streams.
- Competitive Pricing Pressure: Entry of generics or biosimilars will pressure list prices post-patent expiry [3].
- Health Technology Assessments (HTAs): Favorable HTA outcomes may validate premium pricing, whereas negative assessments could necessitate price reductions.
- Reimbursement Policies: Shifts toward capitated or value-based payment models could limit pricing freedom but enhance volume.
Price Projection Scenarios
- Baseline Scenario (Continue Current Trend): Price maintains around current levels, adjusted annually for inflation (~3%), potentially reaching $X,XXX per unit by 2027.
- Optimistic Scenario: Demonstrable superior efficacy and favorable reimbursement facilitate a pricing premium, with prices increasing by 5–7% annually.
- Pessimistic Scenario: Patent expiry and robust generic competition lead to price erosion of 20–30% within two years post-expiry.
- Post-Patent Scenario: Entry of biosimilar/generic options reduces list price significantly, with potential discounts exceeding 50%.
Forecast Summary
| Scenario | Price Change (Annual) | Projected Price (2027) | Key Drivers | Risks |
|---|---|---|---|---|
| Baseline | 3% inflation | $X,XXX per unit | Market expansion, controlled competition | Patent expiry, market saturation |
| Optimistic | 5–7% gain | $X,XXX per unit | Superior clinical outcomes | Regulatory delays |
| Pessimistic | 20–30% decline (post-expiry) | $XXX per unit | Generic entry, payer pressure | Patent litigation, market share loss |
Strategic Considerations
- Patent and Exclusivity Management: Protecting data exclusivities and pursuing supplementary indications can prolong market exclusivity.
- Value-Based Agreements: Collaborating with payers for outcomes-based contracts can enhance pricing power and market access.
- Cost Optimization: Innovations in manufacturing and supply chain efficiency could sustain margins amidst increasing competition.
- Market Expansion: Licensing or expanding indications can boost volume and offset potential price decreases post-patent expiration.
Key Takeaways
- The current pricing of NDC 61570-0131 reflects its monopolistic position during patent protection, with premiums supported by clinical efficacy and market demand.
- Patent expiry remains the most significant event influencing price trajectory, with a typical decline of 20–50%, contingent upon competitive pressures.
- Strategic investment in lifecycle management, including new indications and value-based contracting, is critical for sustaining profitability.
- Regulatory developments and payer policies will continue to influence pricing strategies and market share.
- Market growth is driven by increasing prevalence of targeted indications and expanding global access, but competitive threats necessitate proactive management.
Conclusion
The commercial outlook for NDC 61570-0131 hinges on timely patent protection, market acceptance, and strategic positioning. While current prices reflect strong market power, impending patent expiry and competitive innovations will necessitate adaptive pricing and market strategies to optimize revenue streams and market share.
FAQs
-
When is the patent expiry for NDC 61570-0131, and how will it affect prices?
The patent expiry is projected for [year], after which generic or biosimilar competitors are expected to enter the market, significantly reducing prices through increased competition. -
What factors influence the pricing of biologic drugs like NDC 61570-0131?
Factors include manufacturing costs, clinical efficacy, patent status, regulatory exclusivities, payer negotiations, and market competition. -
How do reimbursement policies impact the drug's market price?
Reimbursement policies influence net prices via negotiated discounts, rebates, and formulary positioning, which can either support premium pricing or necessitate reductions. -
Will increasing adoption of biosimilars impact the future price of NDC 61570-0131?
Yes; biosimilar competition typically drives down prices, especially post-patent expiry, impacting revenue potential and market share. -
What strategies can manufacturers deploy to sustain pricing power?
They can pursue new indications, enhance clinical value, develop cost-effective manufacturing processes, and engage in value-based contracting.
Sources
[1] Epidemiological data on therapeutic indications and demand trends.
[2] Patent protection and market exclusivity analysis.
[3] Industry reports on biosimilar competition and pricing trends.
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