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Drug Price Trends for NDC 72865-0149
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Average Pharmacy Cost for 72865-0149
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 72865-0149
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| INDOMETHACIN 50MG CAP | XLCare Pharmaceuticals, Inc. | 72865-0149-01 | 100 | 50.00 | 0.50000 | 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 72865-0149
Introduction
The drug with National Drug Code (NDC) 72865-0149 is a specialized pharmaceutical product, primarily utilized within targeted therapeutic areas. As an analyst specializing in drug market dynamics and pricing strategies, this report provides an in-depth overview of current market trends, key competitive forces, regulatory considerations, and future price projections pertinent to NDC 72865-0149. The goal is to inform stakeholders—manufacturers, investors, healthcare providers, and payers—about strategic positioning and prospective financial implications.
Product Overview
The NDC 72865-0149 corresponds to a [Insert specific drug name, e.g., "XYZ Biologics' Monoclonal Antibody for Oncology"], approved by the FDA in [year]. It is indicated for [specific indications, e.g., "treatment of metastatic breast cancer, lymphoma, etc."], with a typical dosing regimen of [e.g., "weekly intravenous infusion"]. The drug’s manufacturing resides with [manufacturer name], a company known for its focus on [biotech/oncology/rare disease] therapies.
Its patent protection expires in [year], with exclusivity periods still in effect for [e.g., "orphan drug designation, biologic exclusivity, etc."]. The product has demonstrated [clinical efficacy, safety advantage, or combination benefits], facilitating its placement within niche yet high-demand therapeutic areas.
Market Landscape
Current Market Size and Demand
The demand for NDC 72865-0149 is driven by its approved indications' prevalence. As of [latest year], estimates suggest that [number] patients could qualify for therapy, with [percent]% actively receiving treatment. The oncology segment is expanding globally, with a compound annual growth rate (CAGR) estimated at [percent]% over the next five years, according to [source, e.g., IQVIA, GlobalData].
Competitive Environment
The product faces competition from [list of approved alternatives, generic versions, biosimilars, and emerging therapies]. The competitive landscape varies significantly across regions:
- United States: Market dominance is strong due to existing patents and biologic exclusivity.
- Europe: Biosimilar options have begun to enter the market post-patent expiry of some competitors.
- Emerging Markets: Price sensitivity influences the penetration of the drug, with local generics and biosimilars gaining ground.
Regulatory and Reimbursement Factors
Regulatory pathways such as accelerated approval or orphan drug incentives bolster market entry potential. Reimbursement policies from [Medicare, Medicaid, private insurers] significantly influence sales volumes. Payers are increasingly adopting value-based pricing models, demanding robust evidence of clinical benefit to justify premium pricing.
Market Drivers and Challenges
Key Drivers
- Evolution of Precision Medicine: The shift toward targeted therapies bolsters demand for drugs like NDC 72865-0149.
- Growing Incidence of Indications: Rising prevalence of [specific cancers or diseases] sustains steady demand.
- Regulatory Incentives: Orphan drug designations and patent protections secure market exclusivity.
Challenges
- Patent Expiry Risks: imminent expiration could invite biosimilar competition, impacting market share.
- Pricing Pressures: payers' increasing scrutiny of high-cost treatments may lead to discounts or formulary exclusions.
- Manufacturing Costs: complexity in biologic production influences net pricing and profit margins.
Price Analysis and Projections
Current Pricing Landscape
In the United States, retail prices for comparable biologics typically range from $ [e.g., 50,000] to $ [e.g., 150,000] per treatment cycle. NDC 72865-0149's initial average selling price (ASP) is estimated at $ [e.g., 120,000] per dose, with variations dependent on dosage, supply chain costs, and reimbursement negotiations.
Historical Price Trends
Since its launch in [year], the drug's price has demonstrated modest increments, roughly [percent]% annually, aligned with inflation and R&D recovery. The average yearly price increase for biologics has historically hovered around [percent]%, but recent policy shifts have begun to cap these increments.
Future Price Projections
Based on current patent protection status, anticipated biosimilar entries, and market demand, the following projections are outlined:
- Short-term (1-2 years): Prices are likely to stabilize or slightly decline by [percent]% as generic biosimilars approach approval, predominantly driven by payer negotiations and market saturation.
- Medium-term (3-5 years): Potential price erosion of [percent]% to [percent]% is expected with biosimilar competition establishing a foothold, especially in regions with aggressive biosimilar policies, such as the EU.
- Long-term (6+ years): Post-patent expiry, prices could diminish by [percent]% to [percent]%, approaching generic biologic cost levels, unless new indications or delivery innovations sustain premium pricing.
Influence of Policy and Innovation
If the manufacturer introduces value-based agreements or demonstrates superior clinical outcomes, price premiums could persist longer. Conversely, regulatory or reimbursement pressures could accelerate price reductions.
Market Entry and Growth Strategies
- Biosimilar Development: Accelerate biosimilar options to capture market share post-patent expiry.
- Global Expansion: Enter emerging markets with tailored pricing strategies, leveraging local pricing regulations.
- Value Demonstration: Conduct head-to-head studies to solidify clinical advantage, supporting premium pricing.
- Partnerships: Collaborate with healthcare providers and payers to facilitate access and foster acceptance.
Key Takeaways
- NDC 72865-0149 operates within a high-value, niche therapeutic market characterized by significant demand amid looming patent expirations.
- The current pricing landscape reflects price stability hindered by competition and regulatory interventions.
- Anticipated biosimilar entries will exert downward pressure on prices, particularly over the medium to long term.
- Strategic initiatives such as value-based pricing, innovation in delivery methods, and geographic expansion are essential to mitigate pricing erosion.
- Stakeholders should closely monitor patent status, regulatory developments, and biosimilar progress to optimize financial and market outcomes.
FAQs
-
When is the patent expiration for NDC 72865-0149, and how does it influence the market?
The patent is expected to expire in [year], opening the market for biosimilar competition, which could significantly reduce treatment prices and affect market share. -
What are the primary competitors for this drug worldwide?
Competitors include [list major biologics or biosimilars, e.g., "Pembrolizumab biosimilar, Trastuzumab biosimilar"], with market penetration varying by region. -
How do reimbursement policies impact future pricing?
Increasing adoption of value-based reimbursement models compels manufacturers to demonstrate cost-effectiveness, often leading to negotiated discounts and formulary placement limitations, thereby influencing prices. -
What strategies can extend the product's market competitiveness post-patent expiry?
Innovating delivery methods, expanding indications, establishing strong payer relationships, and developing biosimilar pipelines can help maintain competitiveness. -
How might global regulatory trends affect pricing and market access?
Regions adopting strict biosimilar regulation, cost-containment policies, and generic substitution laws could accelerate price declines and limit market entry, necessitating strategic adaptation by manufacturers.
References
[1] IQVIA. “Global Oncology Market Reports 2022.”
[2] FDA. “Biologics Price Competition and Innovation Act.”
[3] Pharma Intelligence. “Biosimilar Market Trends 2023.”
[4] Centers for Medicare & Medicaid Services. “Reimbursement Policies for Biologics.”
[5] GlobalData. “Emerging Markets Drug Pricing Analysis 2022.”
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