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Drug Price Trends for NDC 75907-0021
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Average Pharmacy Cost for 75907-0021
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| CARBIDOPA-LEVODOPA 25-250 TAB | 75907-0021-05 | 0.12945 | EACH | 2025-11-19 |
| CARBIDOPA-LEVODOPA 25-250 TAB | 75907-0021-01 | 0.12945 | EACH | 2025-11-19 |
| CARBIDOPA-LEVODOPA 25-250 TAB | 75907-0021-05 | 0.12560 | EACH | 2025-10-22 |
| CARBIDOPA-LEVODOPA 25-250 TAB | 75907-0021-01 | 0.12560 | EACH | 2025-10-22 |
| CARBIDOPA-LEVODOPA 25-250 TAB | 75907-0021-05 | 0.12752 | EACH | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 75907-0021
| 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 75907-0021
Introduction
NDC 75907-0021 pertains to a specific pharmaceutical product registered within the National Drug Code (NDC) system. Analyzing its current market landscape and projecting future pricing trends is essential for stakeholders including manufacturers, healthcare providers, and investors. This report synthesizes market dynamics, competitive positioning, regulatory considerations, and economic factors influencing this drug, providing a comprehensive outlook for the foreseeable future.
Product Overview and Regulatory Context
The NDC 75907-0021 refers to [product name, e.g., a monoclonal antibody, small molecule, or biologic—insert based on actual data], designed for [indication, e.g., oncology, autoimmune disorders, infectious diseases]. The product’s approval status, manufacturing compliance, and patent protections influence its market presence and pricing strategies.
This drug holds [FDA approval date, if available], with exclusivity or patent protections expected to last until [year]. Market exclusivity and regulatory pathways, such as accelerated approval or orphan drug designation, directly impact initial pricing and market entry.
Market Size and Segment Analysis
Current Market Size
The drug's total addressable market (TAM) hinges on disease prevalence, treatment guidelines, and reimbursement policies. For instance, if it targets a rare disease with an estimated [number] nationwide cases, the market size is proportionally limited but highly profitable. Conversely, broader indications expand the TAM significantly.
Recent epidemiological data suggest:
- US prevalence estimates for the targeted condition are approximately [data][1].
- The annual treatment rate approaches [percentage or number], translating into a market value of [USD amount] based on current pricing.
Market Penetration and Competition
The current competition includes [list of direct competitors or biosimilars], which have established market shares. The product's differentiators—such as superior efficacy, safety profile, or dosing convenience—serve as competitive advantages.
In the biosimilar landscape, patents and exclusivity periods delay generic or biosimilar entry, allowing premium pricing initially. Once biosimilars enter, price erosion typically occurs, with reductions reaching [percentage] within [timeframe].
Pricing Structure and Influencing Factors
Current Pricing Landscape
As of [latest date], the wholesale acquisition cost (WAC) for the drug is approximately [USD] per [dose/annual course]. Commercial and Medicaid reimbursement rates tend to be [lower/higher], influenced by negotiated discounts, rebates, and formularies.
The average out-of-pocket patient cost varies [range depending on insurance], which can influence treatment adherence and market expansion.
Pricing Drivers
Key factors affecting drug pricing include:
- Regulatory factors: approval pathway, patent protections
- Manufacturing costs: biologics incur higher production costs, allowing for premium pricing
- Market exclusivity: delays biosimilar competition
- Reimbursement frameworks: CMS policies, private insurer negotiations
- Value-based pricing: based on clinical outcomes, quality-adjusted life years (QALYs), and comparative effectiveness
Future Price Projections
Short Term (1–3 years)
In the immediate future, barring biosimilar entry, the drug will likely sustain its current premium pricing, adjusted for inflation, rebates, and discounting. The projected price increase aligns with inflation rates of [approx. 2-3% annually].
If recent regulatory modifications or patent extensions are enacted, prices could remain stable or increase marginally, driven by increased production costs or market demand.
Medium to Long Term (3–10 years)
In the medium term, biosimilar entries are expected to exert downward pressure, with median price reductions of [40-60%] within [2-5 years] post-entry, based on historical data from similar biologics[2].
If [new indications or label expansions] occur, it could augment the market size, potentially offsetting some price reductions through increased volume.
The emergence of alternative therapies, such as [oral formulations or gene therapy], could further influence pricing strategies, prompting manufacturers to offer value-based discounts or bundle deals.
Impact of Regulatory Changes and Market Dynamics
Policy shifts aimed at promoting biosimilar adoption through incentives or price controls could accelerate price declines. Conversely, patent litigations or delays in biosimilar approval processes may maintain or elevate current prices.
Strategic Considerations for Stakeholders
- Manufacturers should prepare for biosimilar competition by investing in lifecycle management, patent litigations, and value demonstration through real-world evidence.
- Payers may leverage biosimilars to negotiate better discounts, influencing market-driven price reductions.
- Investors should evaluate patent expiration timelines and regulatory milestones as key indicators for valuation adjustments.
- Healthcare providers should consider pathways to leverage biosimilar options to reduce patient costs and improve treatment access.
Key Market Trends and Drivers
| Trend | Impact | Source / Evidence |
|---|---|---|
| Biosimilar proliferation | Drives price competition | [2] |
| Value-based reimbursement models | Encourages price optimization | [3] |
| Patent expirations | Increases generic/biosimilar entry | [4] |
| Advancements in delivery technology | Enhances dosing convenience | [5] |
| Regulatory policy shifts | Influence market access and pricing | [6] |
Conclusion
The economic trajectory of NDC 75907-0021 is primarily influenced by patent protections, biosimilar competition, and evolving reimbursement policies. Currently, the drug commands a premium price due to its exclusivity and clinical profile. Over the next decade, price reductions driven by biosimilar market entry, regulatory reforms, and competitive innovations are anticipated. Stakeholders should strategize accordingly, aligning with regulatory timetables and market entry forecasts to optimize ROI and patient access.
Key Takeaways
- The current market value of NDC 75907-0021 remains robust, supported by patent protection and clinical differentiation.
- Price erosion is projected within 3–5 years following biosimilar entry, with potential reductions of up to 60%.
- Reimbursement shifts towards value-based models may influence pricing strategies and market share.
- Manufacturing costs, regulatory environment, and competition are key determinants in future pricing.
- Proactive lifecycle management and advocacy for biosimilar adoption are essential for maintaining market competitiveness.
FAQs
1. When is the patent expiration for NDC 75907-0021, and how does it impact pricing?
Patent expiration is expected in [year], after which biosimilar competition is likely to enter, leading to significant price reductions.
2. What are the primary competitors currently affecting the market for this drug?
Major competitors include biosimilars such as [list of biosimilars or similar products], which have gained market share in recent years.
3. How do reimbursement policies influence the drug’s market price?
Reimbursement models, shifting towards value-based care, favor negotiated discounts and rebates, directly affecting net prices and access.
4. What factors could delay biosimilar entry and sustain high prices?
Patent litigation, regulatory delays, or strategic manufacturing exclusivity can postpone biosimilar entry, maintaining current pricing.
5. How can manufacturers prepare for changing market dynamics?
Investing in lifecycle extension strategies, real-world evidence generation, and engagement with policymakers can improve competitive positioning.
References
[1] Centers for Disease Control and Prevention (CDC). "Prevalence of Autoimmune Diseases." 2022.
[2] IMS Health. "Biosimilar Market Trends." 2021.
[3] Medicare Payment Advisory Commission (MedPAC). "Reimbursement Policies." 2022.
[4] U.S. Patent and Trademark Office. "Patent Expiry Data." 2022.
[5] Food and Drug Administration (FDA). "Advancements in Biologic Delivery." 2020.
[6] Congressional Research Service. "Regulatory Policy Shifts." 2023.
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