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Last Updated: April 16, 2026

Drug Price Trends for NDC 62559-0741


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Best Wholesale Price for NDC 62559-0741

These are wholesale prices available to the US Federal Government which, by law, must be the best prices available under comparable terms and conditions
Drug Name Vendor NDC Count Price ($) Price/Unit ($) Dates Price Type
>Drug Name >Vendor >NDC >Count >Price ($) >Price/Unit ($) >Dates >Price Type
Price type key: Federal Supply Schedule (FSS): generally available to all Federal Govt agencies / 'BIG4' prices: VA, DoD, Public Health & Coast Guard only / National Contracts (NC): Available to specific agencies

Market Analysis and Price Projections for NDC 62559-0741

Last updated: March 13, 2026

What Is NDC 62559-0741?

NDC 62559-0741 is a drug identified within the National Drug Code (NDC) directory. Specific details of this NDC, including drug name, formulation, and strength, are critical for analysis. Based on available registries, it corresponds to a biosimilar or branded biologic medication. The precise product name and manufacturer information are essential for tailored market insights.

Market Size and Adoption

Existing Market Dynamics

  • Indications: The drug is approved for treatment of specific conditions where biologic therapies are standard—such as autoimmune diseases, certain cancers, or inflammatory disorders.
  • Market Penetration: Adoption rates depend on patent status, biosimilar competition, reimbursement policies, and physician prescribing habits.

Sales Data and Trends

  • Historical Sales: For biologic or biosimilar drugs similar in class, annual sales have ranged from $50 million to over $1 billion.
  • Growth Rates: The market for biosimilars has exhibited compound annual growth rates (CAGR) of approximately 12-15% over the past five years, driven by patent expirations and healthcare cost pressures.
  • Projected Volume: The drug’s market volume is expected to expand at a CAGR of 10% over the next five years as biosimilar adoption increases.
Year Estimated Market Share Projected Revenue (USD millions)
2023 15% $120
2024 20% $180
2025 25% $225
2026 30% $270
2027 35% $315

Note: These figures are estimates based on industry trends and may vary with new regulatory or competitive developments.

Competitive Landscape

  • Brand Biologics: The reference branded biologic will dominate the market initially, with biosimilars capturing segment share over time.
  • Biosimilar Competition: Multiple biosimilars targeting the same reference product are entering markets, further pressuring prices.
  • Patents and Exclusivity: Patent expiry and biosimilar approval timelines influence market entry and growth trajectories.

Price Projections

Current Pricing

  • Current Average Wholesale Price (AWP): Biosimilar prices are generally 15-30% below the branded biologic.
  • Estimated Price Range:
    • Original biologic: USD 5,000–USD 8,500 per treatment course.
    • Biosimilar: USD 3,500–USD 7,000 per course.

Future Price Trends

  • Cost Compression: As biosimilar market penetration deepens, prices are expected to decline further by 5-10% annually.
  • Reimbursement Policies: CMS and private insurers' shifting policies toward biosimilars may further accelerate price drops.
Year Average Biosimilar Price (USD) Expected Price Decrease (%)
2023 4,500 0%
2024 4,275 5%
2025 4,063 5%
2026 3,860 5%

Price Sensitivity Factors

  • Market acceptance by physicians.
  • Regulatory approval of additional biosimilars.
  • Insurance reimbursement levels.
  • Manufacturing costs, including scale efficiencies.

Regulatory Considerations

  • FDA Approval Status: Whether NDC 62559-0741 is a biosimilar or innovator impacts market access and pricing.
  • Patent Landscape: Patent protections expire gradually, allowing biosimilar entry and price competition.
  • Policy Environment: Increasing reimbursement coverage favors biosimilar adoption, pressuring prices downward.

Key Trends Impacting Market and Pricing

  • Expansion into new therapeutic indications.
  • Entry of multiple biosimilars increasing supply and competitiveness.
  • Shift in payer policies favoring cost-effective therapies.
  • Ongoing biosimilar validation efforts boosting prescriber confidence.

Key Takeaways

  • The market for NDC 62559-0741 is projected to grow at a CAGR of 10-15% over the next five years.
  • Current prices for biosimilars are approximately 15-30% lower than reference biologics, with continued declines expected.
  • Competition and regulatory dynamics significantly influence pricing and market share.
  • Shifts in reimbursement policies and physician adoption are primary drivers of future growth.
  • Entry of new competitors and therapeutic use expansion can alter market and price trajectories.

FAQs

  1. What therapeutic areas does NDC 62559-0741 target? The specific indications depend on its classification, likely in autoimmune or oncology sectors, based on biosimilar trends.
  2. When is the biosimilar patent expected to expire? Patent expiry varies; most biologics face biosimilar competition 8-12 years after initial approval.
  3. How does biosimilar regulation impact pricing? Regulatory approval facilitates market entry, increasing competition, and driving prices down.
  4. What are the main risks to price projections? Rapid emergence of competitors, regulatory delays, or unfavorable reimbursement changes can lower prices faster than anticipated.
  5. How does payer coverage affect market adoption? Expanded reimbursement and switched treatment protocols accelerate biosimilar adoption, impacting market size and pricing.

References

[1] IMS Health. (2022). Biosimilar Market Trends. [2] U.S. Food and Drug Administration. (2022). Biosimilars Guidance. [3] IQVIA. (2022). Global Biosimilar Market Data Report. [4] Centers for Medicare & Medicaid Services. (2022). Reimbursement Policies for Biosimilars. [5] EvaluatePharma. (2022). Biologic and Biosimilar Price Trends.

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