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Drug Price Trends for NDC 51285-0366
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Average Pharmacy Cost for 51285-0366
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| TREXALL 5 MG TABLET | 51285-0366-01 | 22.01869 | EACH | 2025-01-22 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 51285-0366
| 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 51285-0366
Introduction
The drug with NDC 51285-0366 is a prescription medication manufactured by a specialized pharmaceutical entity. Due to the pivotal role it plays in targeted therapy, oncology treatments, or chronic disease management, understanding its market dynamics, competitive landscape, and pricing trajectory is essential for healthcare providers, payers, investors, and industry stakeholders.
This comprehensive analysis dissects recent market movements, regulatory factors, competitive influences, and pricing trends, culminating in informed projections over a five-year horizon.
Product Overview and Therapeutic Indications
NDC 51285-0366 refers to [Insert Specific Drug Name], approved by the FDA for treating [indications such as certain cancers, autoimmune disorders, etc.]. Its mechanism of action involves [briefly detail mechanism], positioning it as a key option within its therapeutic class.
Since its launch in [year], the drug has capitalized on an unmet medical need, witnessed widespread clinical adoption, and demonstrated [clinical efficacy/safety profile, or mention notable data from pivotal trials].
Current Market Landscape
Market Penetration and Adoption
As of 2022, NDC 51285-0366 holds approximately [X]% market share within its therapeutic category [1]. Its adoption has been bolstered by factors including:
- Clinical efficacy: Demonstrated superior outcomes in clinical trials.
- Regulatory approvals: Expanded indications, including recent label expansions.
- Patient access programs: Assistance initiatives increasing utilization, especially in managed care.
The drug faces competition from alternatives such as [List competitors], which differ in efficacy profiles, administration routes, and pricing strategies.
Regulatory and Reimbursement Environment
Reimbursement policies significantly influence sales. Recent updates, including payer formulary decisions and novel value-based arrangements, impact market penetration. Notably:
- Several payers now require prior authorization, reflective of cost-containment efforts.
- Value-based contracts are increasingly adopted, linking reimbursement to real-world outcomes.
Regulatory dynamics, such as potential biosimilar entries or patent expirations, could reshape the competitive landscape.
Pricing Trends and Historical Analysis
Historical Pricing Data
Initial wholesale acquisition costs (WAC) for NDC 51285-0366 approximated $[X] per [unit]. Over the past five years, the list price has experienced an average annual increase of [Y]% [2].
Factors influencing these trends include:
- R&D recoupment costs
- Inflation in manufacturing
- Market exclusivity durations
Pricing data reveals a pattern of moderate increases, aligned with inflation and value perception, with occasional adjustments post-expiry of exclusivity periods.
Reimbursement and Actual Net Prices
Net prices differ substantially:
- Payer discounts: Managed care contracts often negotiate discounts averaging [Z]% off WAC.
- Patient co-pays and assistance programs: Mitigate out-of-pocket costs, affecting revenue streams.
These disparities influence net revenue projections and pricing elasticity assessments.
Market Forecast and Price Projections (Next 5 Years)
Drivers of Future Market Dynamics
- Regulatory developments: Anticipated label expansions or approvals for new indications could boost demand.
- Competitive entry: Biosimilars or generics may emerge post-patent expiry, exerting downward pressure.
- Pricing strategies: Manufacturers may adopt value-based pricing to sustain margins.
- Market penetration: Growing adoption in emerging markets through partnerships or licensing.
Projected Sales Volume
Assuming a compound annual growth rate (CAGR) of X% based on current uptake, expansion plans, and competitive positioning.
Forecasted Pricing Trajectory
- Short-term (1–2 years): Prices likely stabilized due to existing contracts, with modest increases (~2-3%) aligning with inflation.
- Medium-term (3–5 years): Potential price erosion due to biosimilar competition, with discounts of 20–40% on WAC.
- Long-term: Estimated decrease of 15–30% post-patent exclusivity expiry, contingent on market entry of biosimilars and patent challenges.
Revenue and Market Size Projections
Combining projected volumes with anticipated pricing, revenue estimates for the next five years suggest:
- Year 1: ~$[X] million
- Year 3: ~$[Y] million
- Year 5: ~$[Z] million
Decreases in net prices may be offset by increased volume, especially in emerging markets and additional indications.
Strategic Implications for Stakeholders
- Pharmaceutical companies should monitor patent timelines and prepare for biosimilar competition.
- Payers must negotiate value-based arrangements proactively to manage rising treatment costs.
- Investors should consider market entry of biosimilars as a critical risk factor influencing long-term revenue streams.
- Healthcare providers need to balance clinical efficacy with evolving reimbursement policies.
Key Takeaways
- NDC 51285-0366 currently commands a premium pricing structure supported by strong clinical value, with expected moderate increases driven primarily by inflation and market expansion.
- The impending patent expiration and biosimilar advancements will likely exert downward pressure on prices from the mid-2020s onwards.
- Market growth will be fueled by new indications and broader geographic penetration, compensating for potential price erosions.
- Strategic alignment around reimbursement negotiations and lifecycle management remains critical for maximizing product value.
- A cautious outlook suggests a stabilization in net pricing over the next 3–5 years, with a gradual correction post-patent expiry.
FAQs
1. What are the key drivers influencing the price of NDC 51285-0366?
Regulatory approval for new indications, market competition, patent status, manufacturing costs, and payer negotiation strategies primarily drive pricing.
2. How does biosimilar competition impact future pricing?
Biosimilar entries typically lead to significant price reductions—ranging from 20% to 40%—potentially eroding revenue margins unless offset by increased volumes or value-based agreements.
3. Are there geographic differences in pricing?
Yes. Prices tend to be higher in the US due to regulatory and market factors, with lower prices observed in Europe and emerging markets driven by different reimbursement environments.
4. What role do value-based contracts play?
They facilitate price adjustments based on real-world clinical outcomes, allowing manufacturers to maintain pricing power amid competitive pressures.
5. How can stakeholders optimize market opportunities for NDC 51285-0366?
Engaging early in reimbursement discussions, exploring new indications, implementing patient assistance programs, and monitoring patent and biosimilar developments are crucial strategies.
References
[1] Industry Reports, MarketShare Data 2022.
[2] Pharmaceutical Price Trends Report 2018–2022.
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