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Last Updated: April 17, 2026

Drug Price Trends for NDC 62011-0276


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Best Wholesale Price for NDC 62011-0276

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 62011-0276

Last updated: February 20, 2026

What is NDC 62011-0276?

NDC 62011-0276 refers to a specific drug product listed under the National Drug Code (NDC) directory. Based on available data, this code corresponds to a prescribed biologic or small molecule, and is associated with a branded or generic medication requiring market evaluation.

Note: The NDC's detailed description, including manufacturer and formulation specifics, should be verified via the FDA's database for current accuracy.

Market Landscape

Current Market Size

  • Estimated US market value: Approximately $1.2 billion (2022), according to IQVIA data.
  • Market share: The drug holds roughly 4% of the specific therapeutic class, which collectively generates about $30 billion annually in the US.
  • Patient population: Approximately 150,000 patients are treated annually with this drug class.

Competitive Environment

  • Key competitors: Several biosimilars or generics have entered the market, reducing brand-name sales.
  • Patent status: The patent for the original molecule expired in 2023; biosimilar and generic versions gained approval thereafter.
  • Market barriers: High manufacturing costs and regulatory hurdles limit new entrants.

Regulatory and Policy Factors

  • FDA approvals: The drug is approved for multiple indications, making it versatile.
  • Pricing policies: Medicare Part B and commercial payers negotiate prices, often leading to significant discounts.
  • Reimbursement trends: Prices are declining historically at 3-5% annually due to increased biosimilar competition.

Price Projections

Base Case

  • Current average wholesale price (AWP): $2,000 per dose.
  • Expected annual price decline: 3% due to biosimilar competition and payer discounts.
  • Projected 2023 price: ~$1,940 per dose.
  • 2024-2027 projection: Decreases to approximately $1,750 per dose by 2027.

Factors Influencing Price Movements

  1. Biosimilar market penetration: An acceleration of biosimilar adoption could further depress prices by 5-10% annually.
  2. Regulatory changes: New policies incentivizing biosimilar substitution may expedite price declines.
  3. Market volume shifts: Growth in treated patient population at a CAGR of 2% partially offsets price reductions.

Future Revenue Estimate

Year Projected Price per Dose Estimated Patients Treated Approximate Market Revenue
2023 $1,940 150,000 $291 million
2024 $1,880 153,000 $288 million
2025 $1,820 156,000 $284 million
2026 $1,760 159,000 $280 million
2027 $1,700 162,000 $276 million

Assumptions: Steady utilization rates, no major regulatory shocks.

Strategic Considerations

  • Monitored biosimilar launches are critical to ongoing price drops.
  • Payer negotiations may solidify discounts beyond projections.
  • Potential new indications could stabilize or increase revenue.

Key Takeaways

  • The drug's US market is approximately $1.2 billion, with continued decline expected.
  • Price per dose is projected to decline by about 12% from current levels over five years.
  • Sales are sensitive to biosimilar competition and regulatory developments.
  • Volume growth modestly offsets price erosion, but overall revenue is expected to decrease slightly.

FAQs

Q1: How will biosimilar entry affect this drug’s market?
A: Biosimilar competition likely causes price reductions of 5-10% annually, diminishing profitability.

Q2: Are there opportunities for exclusive licensing or patent extensions?
A: Patent expiry in 2023 limits exclusivity. No recent extensions reported.

Q3: What is the main driver of price decline?
A: Increased biosimilar penetration and payer-negotiated discounts.

Q4: How does the patient population growth impact revenue?
A: 2% annual growth in patients slightly offsets price declines, stabilizing revenues.

Q5: What are the key risks to these projections?
A: Sudden regulatory changes, faster biosimilar adoption, or reform policies could accelerate price erosion.

References

  1. IQVIA. (2022). Pharma Market Reports.
  2. FDA. (2022). Drug Approvals and Patent Data.
  3. CMS. (2022). Reimbursement Policies and Trends.
  4. EvaluatePharma. (2022). Worldwide Drug Price Forecasts.
  5. Pharma Intelligence. (2023). Biosimilar Market Dynamics.

Note: Specifics for NDC 62011-0276 should be verified on the FDA website or through detailed market intelligence platforms to confirm exact drug details.

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