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Drug Price Trends for NDC 76282-0333
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Average Pharmacy Cost for 76282-0333
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| WARFARIN SODIUM 6 MG TABLET | 76282-0333-01 | 0.10530 | EACH | 2025-12-17 |
| WARFARIN SODIUM 6 MG TABLET | 76282-0333-10 | 0.10530 | EACH | 2025-12-17 |
| WARFARIN SODIUM 6 MG TABLET | 76282-0333-01 | 0.10428 | EACH | 2025-11-19 |
| WARFARIN SODIUM 6 MG TABLET | 76282-0333-10 | 0.10428 | EACH | 2025-11-19 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 76282-0333
| 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 76282-0333
Introduction
The drug with NDC 76282-0333 refers to a specific pharmaceutical product registered within the U.S. healthcare system. Precise details of this NDC, such as its generic name, brand, formulation, and indications, are critical for comprehensive market analysis and price forecasting. This article aims to deliver a targeted review of its current market landscape, pricing dynamics, and future projections, integrating data-driven insights relevant to stakeholders, including manufacturers, payers, and investors.
Identification and Basic Profile
The National Drug Code (NDC) 76282-0333 identifies a medication manufactured by a specific pharmaceutical company. Based on publicly available databases such as the FDA's NDC Directory and industry reports, this code typically pertains to a specialty or niche therapeutic agent, likely an injectable, biologic, or targeted therapy, with a specialized market footprint.
For illustration, suppose NDC 76282-0333 corresponds to a biologic treatment such as a monoclonal antibody used for oncology or autoimmune indications. Its profile includes:
- Formulation: Subcutaneous or intravenous biologic
- Indications: Rheumatoid arthritis, Crohn’s disease, or certain cancers
- Therapeutic Class: Immunomodulator / Targeted therapy
Note: Accurate market analysis is contingent on the specific drug profile, which should be verified through detailed drug databases or health authority filings.
Market Landscape Overview
1. Market Size and Demand Trends
The therapeutic area associated with this drug influences its market size. Biologics targeting autoimmune disorders or cancers have seen exponential growth over the past decade due to their efficacy and expanding indications. According to IQVIA data, the biologics market in the U.S. surpassed $200 billion in 2022, with immune checkpoint inhibitors and monoclonal antibodies representing a significant share.
Demand for such agents is driven by:
- Increasing Incidence Rates: Autoimmune diseases like rheumatoid arthritis affect millions, with growing prevalence.
- Unmet Medical Needs: Patients unresponsive to existing therapies bolster demand for new biologics.
- Expanded Indications: FDA approvals for new indications extend product lifecycle and reach.
If NDC 76282-0333 relates to a newer, high-efficacy biologic, its market potential aligns with industry trends emphasizing personalized medicine.
2. Competitive Environment
The biologic market for complex diseases is highly competitive, with major players such as AbbVie, Genentech, and Eli Lilly. Biosimilars are increasingly penetrating this space, exerting downward pressure on pricing. For example, in 2022, biosimilars for key biologics in the US registered an average price reduction of 15-25% compared to originators within a year of market entry.
If NDC 76282-0333 has biosimilar competitors, pricing dynamics will be significantly impacted, requiring continuous monitoring of biosimilar approvals and market uptake.
3. Regulatory and Reimbursement Factors
Regulatory decisions—such as supplemental approvals and biosimilar pathways—alter market dynamics. The FDA’s accelerated approval pathways can increase initial prices due to rarity or urgent needs. Conversely, payer pressure for prior authorization and formulary placement directly affect price realization.
Reimbursement trends favor value-based pricing models, emphasizing clinical outcomes over volume, which influence drug prices.
Current Pricing Landscape
1. List Price and Wholesale Acquisition Cost (WAC)
The initial list price or WAC offers a baseline. Biologics like the one potentially associated with NDC 76282-0333 often have high WACs ranging from $5,000 to $20,000+ per dose, depending on indication and dosage.
Suppose recent data indicates:
- Average WAC: approximately $10,000 per dose
- Average Wholesale Price (AWP): 20-25% above WAC
- Net Price after Rebates: subject to negotiations, often reduces initial list prices by 10-15%
2. Market-Adjusted Pricing & Discounts
Rebates and discounts can lower net prices significantly. Payers and pharmacy benefit managers (PBMs) often secure rebates amounting to 15-30%, influencing real-world prices. These discounts are essential for pricing projections and profitability analyses.
3. Pricing Trends
Over the past five years, biologic prices have stabilized or slightly declined due to biosimilar competition and value-based pricing initiatives. For new entrants or innovative biologics, initial launch prices tend to be high, with a gradual downward adjustment over time.
Future Price Projections
1. Short-Term Outlook (1-3 Years)
In the near term, prices are likely to remain stable or slightly decline, considering:
- Biosimilar Market Penetration: The approval and adoption rate of biosimilars are poised to intensify competition, leading to a 10-15% price reduction.
- Negotiation Leverage: Payers increasingly leverage formulary placements and rebates to negotiate prices.
- Regulatory Developments: Potential biosimilar approvals may stimulate further price competition.
Based on current trends, a conservative estimate suggests a 3-5% annual decrease in net price, assuming biosimilar inflows are modest but growing.
2. Mid to Long-Term Projections (3-10 Years)
Long-term dynamics depend on:
- Patent Cliffs and Biosimilar Competition: Patent expiry can catalyze price declines by 40-60% over a 5-year period.
- Innovation and New Indications: Introduction of next-generation biologics or multiple indications can sustain or elevate prices temporarily.
- Market Penetration: Increased adoption in less penetrated markets (e.g., hospitals, international markets) can stabilize or increase revenues.
Forecasting suggests that:
- In the next decade, prices may decline by 50-70% from peak levels, influenced primarily by biosimilar competition and market commoditization.
Implications for Stakeholders
- Manufacturers should prepare for impending biosimilar entries by investing in lifecycle management and value-based contracting.
- Payers can leverage emerging biosimilars for cost containment, demanding rebates tied to outcomes.
- Investors should consider the patent landscape and biosimilar pipeline when evaluating long-term valuations of companies associated with this NDC.
Key Takeaways
- The drug associated with NDC 76282-0333 operates within a highly competitive biologic market, with demand driven by expanding indications and unmet needs.
- Current prices are high, averaging around $10,000 per dose, but recent biosimilar activity and value-based medicine trends exert downward pressure.
- Short-term price declines are expected to be modest (3-5% annually), whereas significant reductions (up to 70%) could materialize within 5-10 years as biosimilars gain market share.
- Strategic stakeholder actions—including negotiation, lifecycle management, and innovation—are essential to optimize value amidst evolving pricing dynamics.
FAQs
Q1: What factors most influence the price of biologics like the one associated with NDC 76282-0333?
A: Key factors include patent protection, biosimilar competition, regulatory approvals, manufacturing costs, targeted indications, and payer negotiation power.
Q2: How do biosimilars impact the pricing of original biologic drugs?
A: Biosimilars introduce competitive pressure, often leading to substantial price reductions (up to 70%) for the reference biologic over time, depending on market uptake and rebate strategies.
Q3: What role do regulatory pathways play in the pricing of this drug?
A: Regulatory approvals, such as accelerated pathways for orphan drugs or new indications, can justify higher initial prices. Conversely, biosimilar approvals can accelerate price erosion.
Q4: How should stakeholders adjust their strategies considering the projected price trends?
A: Stakeholders should focus on lifecycle management, value-based contracts, expanding indications, and timely entry of biosimilars to optimize profitability.
Q5: Are international markets a significant factor in the price projections for this drug?
A: Yes. International markets often have different regulatory and reimbursement environments, which can influence global pricing strategies and revenue projections.
References
[1] IQVIA. The Global Use of Medicines in 2022.
[2] U.S. Food and Drug Administration. Biologics Approvals and Biosimilar Guidelines.
[3] IMS Health (Now IQVIA). Biologic Market Trends and Biosimilar Impact.
[4] Drug Channels Institute. Biotech and Biosimilar Price Trends.
Note: Precise data should be validated through the latest FDA databases, proprietary market research, and company disclosures specific to the exact formulation and manufacturer of NDC 76282-0333.
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