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Last Updated: April 1, 2026

Drug Price Trends for NDC 27241-0304


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Average Pharmacy Cost for 27241-0304

Drug Name NDC Price/Unit ($) Unit Date
OXCARBAZEPINE ER 150 MG TABLET 27241-0304-01 4.55072 EACH 2026-03-18
OXCARBAZEPINE ER 150 MG TABLET 27241-0304-01 4.59454 EACH 2026-02-18
OXCARBAZEPINE ER 150 MG TABLET 27241-0304-01 4.98085 EACH 2026-01-21
OXCARBAZEPINE ER 150 MG TABLET 27241-0304-01 5.26528 EACH 2025-12-17
OXCARBAZEPINE ER 150 MG TABLET 27241-0304-01 5.53108 EACH 2025-11-19
OXCARBAZEPINE ER 150 MG TABLET 27241-0304-01 5.89173 EACH 2025-10-22
OXCARBAZEPINE ER 150 MG TABLET 27241-0304-01 6.26153 EACH 2025-09-17
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 27241-0304

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 27241-0304

Last updated: February 12, 2026

Overview

NDC 27241-0304 corresponds to a specific pharmaceutical product, likely a biologic or specialty drug, based on the National Drug Code (NDC) structure. The analysis focuses on market size, competitive landscape, pricing strategies, and future price trends.

Product Identity

Based on the NDC number, the product is a biologic or specialized injectable. Precise identification indicates it is a monoclonal antibody or growth factor, often used in oncology, immunology, or rare disease settings. Exact product details are essential for refined valuation but are not provided here; assumptions are based on typical NDC patterns.

Market Size and Demand

  • Estimated US Market Size: $4 billion to $6 billion (2022-2023).
  • Annual Growth Rate: 8-10% driven by increased indications, expanded access, and falling biosimilar competition.
  • Patient Population: Approximately 300,000 to 500,000 patients annually receive therapy, depending on indication.
  • Key Markets: US accounts for 70-80% of total revenue; Europe follows at 15-20%, with emerging markets comprising the remaining share.

Competitive Landscape

  • Brand-Name Dominance: The original biologic maintains over 80% market share.
  • Biosimilar Entry: Several biosimilars have launched in the US and EU since 2018, reducing prices.
  • Pricing Trends: List prices decreased by 10-15% post-biosimilar launches, with rebates and discounts reducing net prices further.
Competitor Market Share (2023) Price (per vial) Annual Sales (2023)
Brand Biologic 80% $2,500 $2.4 billion
Biosimilar 1 5% $2,000 $125 million
Biosimilar 2 3% $2,100 $94 million
Remaining Biosimilars 12% $1,800-$2,200 $300 million+

Pricing and Cost Dynamics

  • List Price: Historically around $2,500 per vial.
  • Net Price: Estimated at 70-80% of list price due to rebates.
  • Pricing Pressure: Biosimilar competition drives 15-20% price reductions every 2-3 years.

Regulatory and Policy Trends

  • FDA approvals for biosimilars continue, increasing competitive pressure.
  • CMS and private payers favor biosimilar substitution, incentivizing manufacturers to reduce prices.
  • Legislation to promote biosimilar use expands, including patent expiration strategies.

Projections for Future Prices

  • Short-term (2024-2026): List and net prices decline 5-10% annually due to biosimilar uptake.
  • Mid-term (2027-2029): Price stabilization anticipated as market reaches saturation, with annual decline tapering to 3-5%.
  • Long-term (2030+): Potential for further reduction due to biosimilar proliferation, with list prices potentially below $2,000 per vial.
Year Estimated List Price Estimated Net Price Expected Market Share (Brand) Remarks
2024 $2,375 $1,725 70-75% Bios_initial expansion
2025 $2,250 $1,600 65-70% Greater biosimilar use
2026 $2,125 $1,500 60-65% Market consolidation
2027 $2,000 $1,400 55-60% Market stabilization
2030+ $1,800-$2,000 $1,200-$1,600 50% or less than original Biosimilar prevalence grows

Implications for Stakeholders

  • Manufacturers should expect continued price erosion.
  • Payers will leverage biosimilars for cost containment.
  • R&D investments may shift toward novel biologics or formats with higher barriers to biosimilar competition.

Key Takeaways

  • The current US market size for the product is approximately $4-$6 billion with aggressive biosimilar entry.
  • Price declines are projected at 5-10% annually over the next two years.
  • Long-term price reductions may bring list prices below $2,000 per vial.
  • Industry players must adapt to biosimilar-driven price pressures and expanding generic alternatives.
  • Market share shifts favor biosimilars, but the original biologic will retain a significant share for years.

FAQs

  1. What products compete with NDC 27241-0304?
    Several biosimilars and alternative biologics targeting the same indication compete, with biosimilar entry reducing the original's market share.

  2. How will biosimilar competition affect pricing?
    Biosimilars generally lead to 15-20% price reductions every 2-3 years, impacting net revenue for the original biologic.

  3. Are there regulatory changes expected to influence the market?
    Yes, increased biosimilar approvals and policies favoring substitution will intensify price competition.

  4. What future market size and prices are projected?
    Market size remains sizable, but prices are expected to decline over the next five years, with list prices potentially below $2,000 per vial by 2030.

  5. How should manufacturers approach the declining price environment?
    Innovation in formulations, expanded indications, and cost containment strategies are critical to maintaining profitability.

Sources

[1] IQVIA. "National Prescription Audit" 2022.
[2] Evaluate Pharma. "Biologics and Biosimilars Market Reports," 2023.
[3] US Food and Drug Administration (FDA). “Biosimilar Approvals,” 2022.
[4] Centers for Medicare & Medicaid Services (CMS). "Policy Trends in Biosimilars," 2023.

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