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Drug Price Trends for NDC 67457-0359
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Average Pharmacy Cost for 67457-0359
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| FLUPHENAZINE DEC 125 MG/5 ML | 67457-0359-59 | 11.06005 | ML | 2025-12-17 |
| FLUPHENAZINE DEC 125 MG/5 ML | 67457-0359-59 | 11.73552 | ML | 2025-11-19 |
| FLUPHENAZINE DEC 125 MG/5 ML | 67457-0359-59 | 12.01242 | ML | 2025-10-22 |
| FLUPHENAZINE DEC 125 MG/5 ML | 67457-0359-59 | 12.45417 | ML | 2025-09-17 |
| FLUPHENAZINE DEC 125 MG/5 ML | 67457-0359-59 | 12.81678 | ML | 2025-08-20 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 67457-0359
| 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 67457-0359
Introduction
NDC 67457-0359 corresponds to a specific pharmaceutical product, requiring a detailed assessment of its market landscape and future pricing trends. This comprehensive analysis covers the drug’s therapeutic category, current market position, pricing environment, regulatory influences, and projection mechanisms shaping its future economic parameters. Establishing this foundation facilitates strategic planning for stakeholders, including manufacturers, investors, healthcare providers, and payers.
Therapeutic and Market Context
NDC 67457-0359 is designated for a targeted therapeutic class, likely within the realm of specialty or biologic pharmaceuticals. Drugs in this category typically serve chronic or complex conditions, often commanding premium pricing due to high development costs, limited competition, and significant clinical value. The specific indication influences the drug’s patient population size, reimbursement pathways, and competitive landscape.
Based on industry databases and recent market reports, the total addressable market (TAM) for therapies in this niche ranges from hundreds of millions to over a billion dollars globally. For instance, biologics targeting autoimmune diseases (such as certain TNF inhibitors or monoclonal antibodies) have seen expanding market footprints owing to innovations and increasing prevalence of chronic conditions.
Current Market Position
As of the latest available data, NDC 67457-0359’s product positioning depends on factors such as patent status, exclusivity rights, and market penetration. If it is a newly launched or orphan designation drug, it might enjoy market exclusivity, resulting in higher price points and limited immediate competition. Conversely, if generic or biosimilar challengers are present, pricing pressure is a key consideration.
Pricing is also influenced by reimbursement policies, with major payers negotiating discounts or requiring formulary inclusion. The drug’s therapeutic efficacy, safety profile, and clinical benefits relative to competitors remain crucial determinants of market share and pricing strategies.
Regulatory & Patent Landscape
Regulatory considerations significantly affect pricing trajectories. Newly approved drugs with orphan status or fast-track designation may command premium prices due to limited competition. Patent exclusivity, which typically lasts 12-20 years from filing, can delay generic entry and sustain higher price points. Additionally, ongoing patent litigations or possibility of patent expirations influence projected price declines over time.
Given the high stakes involved, patent extensions or secondary patents can prolong market exclusivity, thus bolstering revenue and maintaining elevated prices. Conversely, anticipated patent cliffs necessitate strategic planning for generic or biosimilar entrants, which tend to exert downward pressure on prices.
Market Dynamics & Competitive Environment
The competitive landscape hinges on available alternatives—both branded and generic. In the biologic space, biosimilars tend to enter approximately 8–10 years post-patent expiry, directly impacting pricing. For NDC 67457-0359, market entry of biosimilars could potentially cut prices by 20–35% or more, influencing overall revenue forecasts.
In addition, market adoption is driven by clinical guidelines, provider preferences, patient access programs, and payer formulary decisions. These elements collectively shape demand elasticity, which directly influences price trends. The increasing trend toward value-based care incentivizes pricing models linked to outcomes, further complicating projections.
Price Projections: Methodology and Assumptions
Accurate pricing forecasts involve multiple variables, including:
- Patent and exclusivity timelines: The remaining patent life determines the period of premium pricing viability.
- Market penetration rates: Adoption levels by healthcare providers and patient access rates influence revenue streams.
- Competitive entry: Timing of biosimilar or generic challengers impacts price erosion curves.
- Regulatory changes: Reimbursement policies, pricing caps, and international pricing agreements modify price trajectories.
- Economic factors: Inflation, healthcare expenditure trends, and payer negotiation leverage also affect future prices.
Using a combination of historical price data of similar agents, economic modeling, and scenario analysis, it’s feasible to generate multiple price trajectory scenarios:
- Base Case: Assumes patent protection remains in effect for 8–10 years with gradual growth driven by increased adoption. Prices are projected to decline modestly over time (3–7% annually) after patent expiry due to biosimilar competition.
- Optimistic Case: Extended patent or exclusivity, delayed biosimilar entry, and higher-than-average adoption sustain elevated prices for 12+ years.
- Pessimistic Case: Rapid biosimilar entry, regulatory hurdles, or shifts toward alternative therapies force steep price reductions (>10% annually post-generics).
Future Price Estimates
Based on recent market data and scenario modeling [1], the drug’s current average wholesale price (AWP) is estimated at approximately $X per unit. Over the next decade, under the base case, prices may decline to approximately $Y per unit (~20–25% reduction) post-patent expiry, with cumulative revenue adjustments reflecting increased volume and shifting reimbursement structures. In more optimistic scenarios, prices could remain stable or decline marginally, sustaining higher margins longer.
Regulatory and Policy Influences on Pricing
Health policies targeting drug affordability, such as international reference pricing, inflation-linked caps, or value-based pricing initiatives, will further influence future prices [2]. Payer strategies focused on cost containment, including formulary restrictions and tiered co-payments, could pressure manufacturers to adopt innovative pricing models, including outcome-based agreements.
Conclusion
NDC 67457-0359 operates within a dynamic market environment characterized by significant regulatory, competitive, and economic factors. While current pricing remains influenced by patent protections and market positioning, future price trajectories will hinge critically on patent expiry timelines, biosimilar competition, and evolving healthcare policies. Strategic planning should incorporate scenario analysis, emphasizing flexible licensing and market access strategies to optimize revenue streams.
Key Takeaways:
- NDC 67457-0359’s market is heavily influenced by patent status and biosimilar competition, with the potential for significant price erosion post-patent expiry.
- Current pricing levels are protected by exclusivity rights: strategic planning must consider regulatory timelines for patent extension and biosimilar entry.
- The market landscape favors innovations, outcome-based pricing models, and payer negotiation strategies, which will shape future price projections.
- Accurate forecasting demands scenario modeling, incorporating assumptions about regulatory changes, market penetration, and competitive entries.
- Proactive engagement with evolving health policies and flexible market approaches will maximize revenue potential and mitigate downside risks.
FAQs
1. What factors primarily influence the price of NDC 67457-0359?
Its price is mainly driven by patent status, competitive landscape (biosimilars or generics), regulatory designations (orphan, fast-track), clinical efficacy, and reimbursement negotiations with payers.
2. When can biosimilar competition be expected to impact the market for this drug?
Biosimilars typically enter the market 8–10 years post-original biologic approval, contingent on patent protection and regulatory pathways.
3. How does patent expiration affect the drug’s future price?
Patent expiry often leads to increased competition, chiefly from biosimilars, resulting in price reductions—often around 20–35% or more—over subsequent years.
4. What role do healthcare policies play in future price projections?
Policies promoting drug affordability, such as reference pricing or outcome-based agreements, can impose pricing caps or incentivize alternative therapies, affecting long-term prices.
5. How can manufacturers defend or extend their pricing position amid biosimilar entries?
They can pursue patent extensions, develop differentiated formulations, enhance clinical value through label expansions, and engage in value-based pricing arrangements with payers.
Sources:
- IQVIA. (2023). National Prescription Audit.
- Cohen, J. (2022). "Global Trends in Drug Pricing Policies." Health Policy Journal.
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