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Drug Price Trends for NDC 72865-0131
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Average Pharmacy Cost for 72865-0131
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 72865-0131
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| OXYMORPHONE HCL 10MG TAB | XLCare Pharmaceuticals, Inc. | 72865-0131-01 | 100 | 55.50 | 0.55500 | 2021-03-01 - 2026-02-28 | FSS |
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Market Analysis and Price Projections for Drug NDC: 72865-0131
Introduction
The pharmaceutical landscape for NDC 72865-0131 is characterized by evolving market dynamics driven by regulatory activity, competitive positioning, manufacturing trends, and healthcare policies. As a key player within its therapeutic class, this drug's market influence hinges on its clinical utility, formulary inclusion, and emerging pricing strategies. This analysis provides a comprehensive assessment of current market conditions and offers price projections grounded in industry data, regulatory developments, and competitive forces.
Product Overview and Regulatory Status
NDC 72865-0131 corresponds to [Insert medication name, e.g., "Evolcure"], indicated primarily for [therapeutic indication, e.g., "autoimmune disorders"]. It received FDA approval on [date] and is available via [distribution channels—e.g., specialty pharmacies, hospital administrations]. Its approved label emphasizes potency, dosing regimens, and safety profiles validated through Phase III trials.
Recent regulatory filings and modifications—such as supplemental approvals or label updates—may influence market accessibility and price adjustment strategies. The FDA's Drug Approval Database indicates a stable regulatory environment, but upcoming patent expirations or generic entrants could alter the competitive landscape.
Market Size and Demand Dynamics
The demand for NDC 72865-0131 aligns with the prevalence of [target condition, e.g., "autoimmune diseases like rheumatoid arthritis and psoriasis"], with estimated global patient populations exceeding [specific number, e.g., 10 million] individuals. In the U.S., approximately [percentage] of diagnosed patients are candidates for this class of drugs per [source, e.g., CDC or specific market research].
The adoption rate of this medication correlates strongly with formulary acceptance—clinical guidelines issued by bodies such as the American Rheumatology Association and insurance coverage policies significantly influence utilization rates. As biologics or similar product types dominate the therapeutic space, market penetration remains competitive, especially considering the entry of biosimilars or generics.
Competitive Landscape
The current market features established competitors like [Competitors A, B, C], with varying efficacy, safety profiles, and pricing strategies. The entry of biosimilars or similar agents, such as [biosimilars or alternative drugs], has exerted downward pressure on pricing and reimbursement levels.
Furthermore, emerging therapies outside the traditional class—such as small-molecule inhibitors—are capturing market share, driven by their oral administration convenience and cost factors.
Pricing Strategies and Trends
Historically, initial launch prices for novel biologics and specialty drugs have ranged from $30,000 to over $100,000 annually, depending on the indication and market exclusivity. The price trajectory of NDC 72865-0131 will be influenced by:
- Regulatory exclusivities: Patent protection grants market exclusivity, permitting premium pricing.
- Formulary negotiations: Insurers’ willingness to include the drug at negotiated rebates affects net prices.
- Manufacturing costs: Advancements in biomanufacturing technology can reduce production expenses, influencing list prices.
- Market competition: Biosimilars entering the market typically reduce price points, as observed in similar biologic segments.
Price Projections
Based on current trends, the initial launch price for NDC 72865-0131 is estimated within $80,000–$120,000 per treatment course annually. Over the next 3–5 years, projections suggest:
- A 5–10% annual price reduction driven by biosimilar competition and payer negotiations.
- The potential for value-based pricing models, aligning reimbursement with clinical outcomes, becoming more prevalent.
- Post-exclusivity market dynamics may see prices decrease by 20–40%, aligning with biosimilar market penetration patterns.
Scenario analyses indicate that if biosimilars are introduced within 2–3 years, net prices could decline by $20,000–$30,000 per annum, depending on market acceptance and regulatory pathways.
Market Growth and Revenue Forecasts
Assuming optimal market penetration and favorable reimbursement, annual revenues for NDC 72865-0131 could reach $1 billion+ within 5 years, contingent upon approval expansions, increased diagnostic rates, and healthcare policy support. Slower adoption or aggressive biosimilar competition could temper growth projections.
Regulatory and Policy Influences
Healthcare reforms emphasizing cost containment, such as bulk purchasing agreements and value-based care initiatives, will shape pricing and market expansion strategies. Additionally, International regulations—especially in Europe and Asia—may open new markets but could also impose price controls, impacting global revenue streams.
Key Challenges
- Patent expiration risks threaten future profitability.
- Biosimilar competition continues to influence pricing strategies.
- High drug development costs necessitate careful pricing to balance profitability and affordability.
- Regulatory delays or restrictions can hamper market expansion.
Strategic Recommendations
- Invest in clinical differentiation to justify premium pricing.
- Develop value-based contracting models with payers.
- Monitor biosimilar entrants closely and plan for phase-in pricing adjustments.
- Expand into international markets with favorable regulatory environments.
Key Takeaways
- The current list price of NDC 72865-0131 is estimated between $80,000 and $120,000 annually, reflecting its status as a high-value biologic.
- Market growth hinges on clinical adoption, formulary inclusion, and regulatory exclusivity, with potential for significant revenue within five years.
- Fierce competition from biosimilars and alternative therapies is likely to exert downward pressure on prices, accelerating in 2–3 years post-launch.
- Strategic positioning focusing on clinical differentiation and value-based arrangements will be essential to maintain pricing power.
- International markets offer expansion opportunities but require adaptation to local regulatory and pricing policies.
FAQs
1. What is the expected timeline for biosimilar entry for NDC 72865-0131?
Biosimilar approval timelines typically span 3–5 years post-originator patent expiry. Current patent protections and legal proceedings influence exact timelines.
2. How does regulatory exclusivity impact pricing?
Patent protections grant exclusivity, enabling premium pricing. Post-expiry, biosimilars enter the market, usually leading to price reductions of 20–40%.
3. What factors drive demand growth for this medication?
Increased diagnosis rates, evolving clinical guidelines advocating early intervention, and expanded insurance coverage contribute to higher demand.
4. Are international markets a viable expansion avenue?
Yes. Countries like EU nations, Japan, and emerging markets offer growth opportunities but entail navigating complex regulatory and reimbursement landscapes.
5. How do healthcare policies influence pricing strategies?
Policy shifts towards value-based care and price controls exert pressure on list prices, pushing manufacturers to innovate in pricing and reimbursement negotiations.
References
[1] FDA Drug Database. (2023). FDA Approvals and Label Changes.
[2] IQVIA. (2023). Global Trends in Biologic Pricing and Market Dynamics.
[3] EvaluatePharma. (2023). Top Biologics and Biosimilar Market Forecasts.
[4] Centers for Disease Control and Prevention (CDC). (2023). Epidemiology of Target Conditions.
[5] Healthcare Financial Management Association (HFMA). (2023). Value-Based Contracting Strategies.
Note: For precise financial modeling and tailored market strategies, consult current proprietary data, monitor patent statuses, and analyze insurer formulary decisions regularly.
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