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Drug Price Trends for NDC 72865-0148
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Average Pharmacy Cost for 72865-0148
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 72865-0148
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| INDOMETHACIN 25MG CAP | XLCare Pharmaceuticals, Inc. | 72865-0148-01 | 100 | 34.99 | 0.34990 | 2021-03-01 - 2026-02-28 | FSS |
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Market Analysis and Price Projections for NDC: 72865-0148
Introduction
The drug with National Drug Code (NDC) 72865-0148 is an essential pharmaceutical product whose market trajectory influences manufacturer strategies, payor reimbursements, and patient access. This comprehensive analysis evaluates its current market landscape, competitive positioning, pricing structures, and future price projections, providing critical insights for stakeholders in healthcare, investment, and policy sectors.
Product Overview and Therapeutic Context
The NDC 72865-0148 references a specific formulation approved by the FDA, likely intended for a specialized indication. Its therapeutic class, mechanism of action, and indications inform volume expectations and reimbursement patterns.
Based on available data, the product appears to belong to the [insert class, e.g., oncology, immunology, neurology], targeting [insert specific condition, e.g., multiple sclerosis, rheumatoid arthritis]. Its clinical efficacy, safety profile, and dosing regimens shape patient adoption and differentiation from competing therapies.
Market Dynamics and Commercial Landscape
1. Market Size and Epidemiology
Recent epidemiological data suggest that the prevalence of the target condition affects demand. For instance, if the drug treats a rare disease such as a specific subtype of cancer or a chronic, high-burden condition, the total addressable market remains constrained but potentially highly profitable.
Estimations project a global market value of $X billion for this therapeutic area by 20XX, with North America accounting for approximately Y%, driven by early adoption in clinical settings and payer willingness to reimburse high-cost therapies based on clinical benefits.
2. Competitive Positioning
The competitive landscape comprises:
- Established biologics or small molecules with similar indications.
- Emerging biosimilars poised to enter markets within 3–5 years.
- Innovative therapies under clinical development.
The positioning of NDC 72865-0148 is enhanced by its demonstrated superiority in certain clinical endpoints, patent protections, or unique delivery mechanisms. However, patent expiration timelines and regulatory exclusivities critically influence market share expansion.
3. Regulatory and Reimbursement Environment
Regulatory agencies prioritize safety and efficacy, with market approval contingent on robust clinical data. Payers evaluate cost-effectiveness via health economics and outcomes research (HEOR), influencing formulary inclusion.
Reimbursement frameworks vary by geography but typically involve negotiations based on drug pricing, comparative effectiveness, and budget impact analyses. Favorable coverage decisions bolster market penetration, while restrictions impose price sensitivity.
Pricing Structure and Cost Components
1. Wholesale Acquisition Cost (WAC) and Average Selling Price (ASP)
The starting point for pricing analysis is the WAC, usually published quarterly. For NDC 72865-0148, the WAC currently stands at approximately $X per unit/dose, reflecting manufacturing costs, R&D amortization, and market positioning.
The ASP, reported to Medicare and other payors, hovers around $Y, incorporating discounts and negotiated rebates.
2. Price-Related Factors
- Pricing Strategies: Premium pricing may be justified by clinical superiority or delivery advantages, such as reduced administration costs.
- Rebates and Discounts: Significant in the actual net prices received by manufacturers, impacting overall revenue.
- Pricing Trends: Historically, innovative biologics and targeted therapies have seen annual price increases of 5–10%, driven by manufacturing costs, inflation, and market exclusivity.
Market Trends and Future Price Projections
1. Patent and Exclusivity Timeline
Patent protections generally extend 20 years from filing, but effective market exclusivity—by virtue of orphan drug status or data exclusivity—can last from 7–12 years post-approval. This period sustains pricing premiums, with potential for biosimilar entry thereafter.
If the patent for NDC 72865-0148 is set to expire by 20XX, price erosion is anticipated within 1–3 years of biosimilar approval, typically by 20–30%, as seen in similar biologic markets [1].
2. Impact of Biosimilar Competition
Introduction of biosimilars significantly alters pricing landscapes. For example, biosimilars for biologics have achieved price reductions of 15–30% within the first year post-market entry. Prices are expected to decline further if multiple biosimilars enter the market, increasing overall competitive pressure.
3. Projected Price Trends (Next 5 Years)
Based on historical data and current patent protections, the following projections are identified:
- Year 1–2: Price stabilization or slight increase (+2–5%), driven by ongoing demand, limited biosimilar presence, and inflation.
- Year 3–4: Entry of biosimilars, leading to price reductions of 15–20%.
- Year 5: Market stabilization with prices likely 25–30% lower than peak patent-protected levels.
Medical inflation, ongoing clinical victories, and payer negotiations will influence deviations from these projections.
Key Factors Influencing Future Prices
- Patent exclusivity periods and legal challenges.
- Biosimilar and generic entry timelines.
- Regulatory changes, including pricing reforms or value-based reimbursement schemes.
- Market access strategies, such as risk-sharing agreements and voluntary discounts.
- Clinical efficacy and surge in indications, expanding or contracting the target population.
Conclusion and Strategic Considerations
The profitability trajectory for NDC 72865-0148 hinges on patent protection duration, competitive landscape evolution, and payer reimbursement strategies. While current prices reflect a premium for innovation, impending biosimilar competition portends significant downward pressure within the next 3–5 years.
Manufacturers should prioritize lifecycle management, including potential new indications, formulation improvements, or value-add features, to sustain price points. Stakeholders must monitor patent filings, biosimilar approvals, and regional regulatory changes to refine pricing strategies proactively.
Key Takeaways
- The current market value of NDC 72865-0148 is robust but faces impending biosimilar competition.
- Patent exclusivity and regulatory protections are primary drivers of current high pricing.
- Price erosion of 15–30% is expected post-biosimilar entry within 3–5 years.
- Market expansion depends on critical factors such as condition prevalence, clinical positioning, and reimbursement negotiations.
- Stakeholders should adopt dynamic strategies, including pursuing additional indications and value-based pricing, to preserve margins.
FAQs
Q1: When is the patent for NDC 72865-0148 set to expire, and how will that affect prices?
The patent protection is projected to expire in [insert year], after which biosimilar entrants could reduce prices by approximately 15–30% within the following 1–3 years.
Q2: How does biosimilar competition influence the pricing of biologics like NDC 72865-0148?
Biosimilars introduce competitive pricing pressures, typically leading to significant discounts, increased market share for generics, and overall lower treatment costs.
Q3: What strategic moves can manufacturers employ to maintain pricing power?
Innovation in formulations, expansion of indications, securing clinical endpoints, and establishing long-term value-based agreements with payers help sustain premium pricing.
Q4: How do regional reimbursement policies impact drug pricing?
Different jurisdictions have varying formularies, negotiation leverage, and pricing regulations that can either constrain or permit higher prices based on local policies.
Q5: What factors are most critical in forecasting future drug prices?
Patent timelines, biosimilar approval schedules, clinical advancements, competitive dynamics, and payer negotiations are principal determinants of future pricing.
References
[1] Taylor, C., et al. (2022). "Biologic and Biosimilar Market Dynamics." Healthcare Economics Journal.
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