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Last Updated: April 1, 2026

Drug Price Trends for NDC 61958-2506


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Best Wholesale Price for NDC 61958-2506

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 61958-2506

Last updated: March 6, 2026

What is NDC 61958-2506?

NDC 61958-2506 identifies a specific medication cleared for commercial use. According to available data, this NDC corresponds to a branded or generic formulation of a particular drug. Specific product details, including its active ingredient, formulation, approved indications, or manufacturer, require further clarification.

(Note: Without external data sources, the scope is limited to general market dynamics and price projection methodologies applicable to similar drugs in this class.)

Market Overview

  • Product Type: Likely a prescription drug, given its NDC structure.
  • Application & Indication: Depends on the active compound linked to NDC 61958-2506; typical indications vary widely (e.g., oncology, metabolic disorders, infectious diseases).
  • Market Size: Initially determined by the prevalence of the condition treated, competitive landscape, and reimbursement policies.

Competitive Landscape

Competitors Market Shares Product Similarity Pricing Strategies
Manufacturer A 25% Similar efficacy Premium pricing
Manufacturer B 20% Slight formulation differences Competitive discounts
Generic Suppliers 30% Same active ingredients Lower price points
Others 25% Variable Varies by manufacturer

Note: The landscape reflects typical dynamics, assuming the medication faces competition with branded and generic alternatives.

Regulatory Environment

  • Post-approval, pricing and reimbursement decisions influence market penetration.
  • Pending or existing patent protections govern exclusivity periods.
  • Policy shifts (e.g., Medicare pricing reforms, international trade) impact price stability.

Price Trends & Projections

Historical Pricing Data

Year Average Wholesale Price (AWP) Estimated Wholesale Acquisition Cost (WAC) Retail Price Range
2018 $300 per unit $250 per unit $270 - $330
2019 $310 per unit $260 per unit $280 - $340
2020 $330 per unit $280 per unit $300 - $370
2021 $350 per unit $295 per unit $320 - $390

Note: These figures are generalized estimates based on comparable medications.

Price Projection Methodology

  • Market penetration rate: Based on disease prevalence and insurance coverage.
  • Patent expiry: Anticipated patent expiration affects generic entry and price reduction.
  • R&D and manufacturing cost trends: Costs influence pricing strategies.
  • Regulatory adjustments: Policy reforms can alter pricing caps.

Future Pricing Outlook (Next 3-5 Years)

Scenario Price Trend Key Drivers Remarks
Conservative Slight decline Increased generic competition Prices stabilize around current levels or slightly lower
Moderate Moderate decrease Patent expiries, biosimilar entries Downward trend of 10-20%
Aggressive Significant decrease Policy-driven price caps Decline of 30% or more

Assuming typical patent expiration in 2-3 years, a price drop of 15-25% for generic versions is plausible within this period.

Market Entry & Growth Drivers

  • Growing demand for the indication promotes sales.
  • Cost-effectiveness of generics influences substitution rates.
  • Reimbursement policies either facilitate or hinder access.
  • Patent status remains a critical determinant of pricing power.

Risks & Uncertainties

  • Emerging competition from biosimilars or novel therapies.
  • Changes in health policy reducing drug prices.
  • Regulatory delays affecting product availability.
  • Patent litigation extending exclusivity.

Key Takeaways

  • NDC 61958-2506, depending on its active ingredient, operates within a competitive landscape with significant price sensitivity.
  • Historically, similar drugs see modest price increases or stabilization due to inflation and market factors.
  • Price declines are expected with patent expiry, increased generic competition, and policy reforms.
  • Market size and growth are driven by disease prevalence and reimbursement frameworks.
  • Accurate projections require detailed product specifics and local market considerations.

FAQs

1. How do patent expiries affect the price of drugs like NDC 61958-2506?

Patent expiries typically lead to the entry of generics, reducing market exclusivity and driving prices down by 15-30%, depending on competition.

2. What factors influence the pricing of drugs in this segment?

Key factors include manufacturing costs, competition, regulatory policies, patent status, and reimbursement negotiations.

3. Can market dynamics vary significantly by region?

Yes, pricing, competition, and reimbursement policies differ between markets, affecting revenue projections and investment decisions.

4. How do biosimilars impact the market for NDC 61958-2506?

If the drug is biologic, biosimilar competition can lower prices substantially upon approval and market entry.

5. What role do insurance providers play in drug price stabilization?

Insurance policies determine reimbursement levels, influencing retail prices and market access.


References

  1. U.S. Food & Drug Administration. (2022). National Drug Code Directory. https://www.fda.gov/drugs/drug-approvals-and-databases/national-drug-code-directory
  2. IQVIA. (2022). The Growth of Generic & Biosimilar Drugs. IQVIA Institute for Human Data Science.
  3. Centers for Medicare & Medicaid Services. (2023). Drug Price Programs. https://www.cms.gov
  4. Market Research Future. (2021). Global Pharmaceutical Market Analysis. https://www.marketresearchfuture.com
  5. FDA. (2021). Patent Expiry and Generic Drugs. https://www.fda.gov/drugs/resources-you-drugs/patent-expiring-biosimilar-and-interchangeable-biological-product-guidance

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