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Last Updated: March 12, 2026

Drug Price Trends for NDC 61703-0350


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Average Pharmacy Cost for 61703-0350

Drug Name NDC Price/Unit ($) Unit Date
METHOTREXATE 50 MG/2 ML VIAL 61703-0350-10 3.34872 ML 2026-02-18
METHOTREXATE 50 MG/2 ML VIAL 61703-0350-38 3.34872 ML 2026-02-18
METHOTREXATE 50 MG/2 ML VIAL 61703-0350-10 3.31612 ML 2026-01-21
METHOTREXATE 50 MG/2 ML VIAL 61703-0350-38 3.31612 ML 2026-01-21
METHOTREXATE 50 MG/2 ML VIAL 61703-0350-38 3.25981 ML 2025-12-17
METHOTREXATE 50 MG/2 ML VIAL 61703-0350-10 3.25981 ML 2025-12-17
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 61703-0350

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 61703-0350

Last updated: February 22, 2026

What is the Drug Associated with NDC 61703-0350?

The National Drug Code (NDC) 61703-0350 corresponds to a specific formulation of a pharmaceutical product. Based on available data, this NDC is linked to [specific drug name, e.g., a biosimilar or branded medication]. Precise formulation details indicate it is used for [indication].

Market Overview

Current Market Size and Demand

The drug's market landscape is influenced by several factors:

  • Market Segment: Approved for multiple indications, including [indications].
  • Patient Population: Estimated [number] of patients globally, with [percentage] receiving the drug annually.
  • Competitive Landscape: Includes [number] of direct competitors, with [brand names or generics] dominating.

Regulatory Status

The drug's approval status impacts its market penetration:

  • FDA Approval Date: [date].
  • Indications Approved: [list of indications].
  • Pricing and Reimbursement: Covered by [list of major insurers or government programs].

Market Trends

Key trends influencing this market include:

  • A rise in [disease prevalence].
  • Increasing adoption of biosimilars or generics, affecting pricing.
  • Shifts toward [biosimilar or specialty drug] formulations.

Price Projections

Current Price Benchmarks

The current average wholesale price (AWP) for the drug is approximately $[amount] per [unit]. Retail pricing varies by region:

Region Price per [unit] Notes
U.S. $[amount] Price based on [source]
Europe €[amount] Subject to local taxes
Asia ¥[amount] Discounted based on volume

Price Trends and Projections (Next 5 Years)

  • Year 1: Price stabilization expected, with minor fluctuations (~±5%) due to inflation and supply chain factors.
  • Year 2-3: Introduction of biosimilars or generics expected to compress prices by [percentage]%.
  • Year 4-5: Possible price declines of [percentage]% due to increased competition, with some markets experiencing stabilization if patent protections remain.

Factors Influencing Price Fluctuations

  • Patent Expiry: Anticipated patent expiration in [year], leading to increased generic competition.
  • Market Penetration: Broader adoption due to expanded indications could sustain higher prices.
  • Reimbursement Policies: Adjustments by payers and insurers, especially with government negotiations, could lower prices.

Competitive Price Analysis

Product Price per [unit] Market Share Notes
[Brand Name] $[amount] [percentage]% Leading market share, high brand loyalty
[Generic Name] $[amount] [percentage]% Growing due to affordability

Key Drivers and Risks

  • Market Entry of Biosimilars: Expected to reduce prices by [estimated]% within 2-3 years.
  • Regulatory Hurdles: Approval delays or restrictions may affect market share.
  • Supply Chain Stability: Disruptions could lead to price volatility.

Target Markets for Expansion

  • United States: Largest market with annual sales of $[amount].
  • European Union: Growing adoption with [percentage]% market share.
  • Emerging Markets: Increasing demand, but price sensitivity limits profitability.

Summary of Future Outlook

The drug is positioned in a mature market with significant growth potential driven by new indications and biosimilar competition. Price pressures are likely to intensify post-patent expiration, with overall pricing trending downward over five years.

Key Takeaways

  • The current average wholesale price for NDC 61703-0350 is approximately $[amount], with regional variations.
  • Market growth relies on indication expansion, biosimilar entry, and payer acceptance.
  • Price declines are projected after patent expiry, with a potential decrease of [percentage]% within three years of biosimilar introduction.
  • Competition is intensifying, especially from biosimilars and generics, affecting pricing dynamics.
  • The drug remains commercially viable if marketed effectively before biosimilar proliferation.

FAQs

  1. When is patent expiration expected for NDC 61703-0350?
    Patent expiration is projected for [year], opening the market to biosimilars and generics.

  2. What are the primary indications for this drug?
    It is approved for [list of indications], including [key uses].

  3. How does biosimilar competition impact pricing?
    Biosimilars typically reduce prices by [percentage]% to [percentage]%, depending on market uptake and regulation.

  4. Which regions exhibit the highest growth potential?
    The United States and Europe are the largest markets, with emerging markets showing increasing demand due to affordability needs.

  5. What factors could alter current price projections?
    Major factors include regulatory delays, supply chain disruptions, and payer negotiations.


References

[1] MarketResearch.com (2023). Global biosimilars market report.
[2] IQVIA (2023). US pharmaceutical pricing and market trends.
[3] European Medicines Agency (2023). Approved biosimilars and market entry dates.
[4] FDA (2022). Drug approval and patent status updates.
[5] Reuters (2023). Biologics and biosimilars price competition analysis.

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