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Last Updated: April 16, 2026

Drug Price Trends for NDC 60505-6146


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Best Wholesale Price for NDC 60505-6146

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 60505-6146

Last updated: April 5, 2026

What is the drug associated with NDC 60505-6146?

NDC 60505-6146 identifies Lenvatinib Mesylate, marketed under the brand name Lenvima. It is a tyrosine kinase inhibitor approved for the treatment of various cancers including thyroid carcinoma, hepatocellular carcinoma, and renal cell carcinoma.

Market Overview

Commercial Landscape

  • Indications: Lenvatinib's primary approved uses cover differentiated thyroid carcinoma, hepatocellular carcinoma, renal cell carcinoma, and certain endometrial cancers.
  • Market Players: Prime competitors include sorafenib, sunitinib, pazopanib, and cabozantinib.
  • Market Size (2022): Estimated global sales of Lenvatinib approximated $1.2 billion, with North America accounting for roughly 60%.

Regulatory and Patent Status

  • Patent Expirations: Patent protection originally extended to 2025; patent litigation and exclusivity periods may influence market entry.
  • Regulatory Approvals: Initially approved by FDA in 2015; indications expanded post-approval, influencing sales dynamics.

Key Market Drivers

  • Incidence of targeted cancers is rising globally.
  • Growing awareness and acceptance of oral targeted therapies.
  • Expansion of indication approvals.

Market Challenges

  • High treatment costs.
  • Competitive landscape with established TKIs.
  • Patent challenges and biosimilar development.

Price Projections (2023-2028)

Current Pricing (2023)

  • Average Wholesale Price (AWP): Approximately $11,820 per 30-count, 4 mg tablets (~$295 per tablet).
  • Per Treatment Course: Varies by indication and dosage; average treatment course ranges from 3 to 6 months.

Projected Trends

Year Estimated Wholesale Price (per 30-count) Key Factors
2023 $11,820 Current pricing; high cost due to innovation.
2024 $11,200 – $12,000 Slight price decrease anticipated with patent challenges and biosimilar entry.
2025 $10,500 – $11,500 Possible price reductions due to biosimilar approvals and increased competition.
2026 $9,800 – $11,000 Market stabilization; biosimilars gain market share.
2027 $9,200 – $10,500 Continued biosimilar penetration; pricing pressure persists.
2028 $8,500 – $10,000 Further biosimilar entry; potential for price stabilization at lower levels.

Influencing Factors

  1. Biosimilar Development: Biosimilar versions expected to enter the market by 2025-2026, exerting downward pressure on prices.
  2. Market Penetration: Increased adoption in combination therapies could maintain higher prices.
  3. Reimbursement Policies: Changes in insurance strategies and payer negotiations may influence net prices.
  4. Regulatory Changes: Additional indications or expanded approvals may temporarily increase demand and price points.

Competitive and Market Share Analysis

Competitor Market Share (2022) Indications Price Range (per month)
Sorafenib (Nexavar) 30% Liver, renal, thyroid cancers ~$10,300
Sunitinib (Sutent) 25% Renal, gastrointestinal tumors ~$10,700
Pazopanib (Votrient) 15% Renal, soft tissue sarcoma ~$8,800
Cabozantinib (Cabometyx) 10% Renal, liver, thyroid cancers ~$12,000
Lenvatinib (Lenvima) 20% Thyroid, liver, renal ~$11,800

Key Takeaways

  • The global market for Lenvatinib is mature, with a current value near $1.2 billion.
  • Price projections indicate a gradual decline driven by biosimilar competition and market saturation.
  • Patent expiry and biosimilar approvals forecast significant price reductions starting in 2025.
  • Continued innovation and expanded indications could sustain higher prices temporarily.
  • Competition from other TKIs remains stiff, influencing pricing strategies and market share.

FAQs

1. When are biosimilars for Lenvatinib expected to be approved?
Expected approvals are around 2025-2026, considering development timelines and regulatory review periods.

2. How does biosimilar competition impact pricing?
Biosimilar entry typically causes a 20-40% decrease in list prices, depending on market conditions and adoption rates.

3. What are the primary indications for Lenvatinib that influence its market?
Differentiated thyroid carcinoma, hepatocellular carcinoma, renal cell carcinoma, and some endometrial cancers.

4. How does Lenvatinib's price compare with other TKIs?
It is priced similarly to sunitinib and cabozantinib, generally between $10,000 and $12,000 per month.

5. Are there upcoming regulatory changes that could influence market dynamics?
Potential approval of new indications and biosimilar competitors could reshape the competitive landscape and pricing.


Sources:
[1] IQVIA. (2022). Global Oncology Market Data.
[2] U.S. Food and Drug Administration. (2015). Lenvatinib (Lenvima) approval documentation.
[3] Evaluated price listings from Red Book and CMS pricing databases.
[4] Market research reports from MedTrack and EvaluatePharma.

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