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Last Updated: November 6, 2025

Drug Price Trends for NDC 51407-0115


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Best Wholesale Price for NDC 51407-0115

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
FUROSEMIDE 80MG TAB Golden State Medical Supply, Inc. 51407-0115-01 100 5.72 0.05720 2023-12-15 - 2028-06-14 FSS
FUROSEMIDE 80MG TAB Golden State Medical Supply, Inc. 51407-0115-05 500 27.22 0.05444 2023-12-15 - 2028-06-14 FSS
>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 51407-0115

Last updated: July 31, 2025


Introduction

The drug identified by NDC 51407-0115 refers to a specific pharmaceutical product with distinct market dynamics, competitive landscape, and pricing trends. Analyzing this drug’s market involves understanding its therapeutic application, regulatory status, supply chain factors, competitive environment, and economic trends influencing its valuation.

This report provides a comprehensive market analysis and price projection, aiding stakeholders such as pharmaceutical manufacturers, healthcare providers, payers, and investors in making informed decisions.


Product Overview

NDC 51407-0115 corresponds to [Insert Drug Name], marketed primarily for [indications, e.g., oncology, autoimmune diseases, rare conditions]. It is manufactured by [Manufacturer Name] and has received [FDA approval date and regulatory status]. The drug’s formulation includes [active ingredients, dosage forms].

Its commercial application focuses on [primary patient demographic, such as adult or pediatric patients], with claims emphasizing [efficacy, safety profile, unique mechanism of action].


Market Dynamics and Drivers

Therapeutic Area and Patient Demand

The drug operates within the [specific therapeutic area], which has experienced a compound annual growth rate (CAGR) of [X]% over the past [Y] years, driven by [e.g., rising prevalence, advancements in treatment protocols, unmet medical needs]. For example, the increasing incidence of [disease] directly impacts demand, especially as new treatment guidelines favor this drug’s mechanism.

Regulatory and Reimbursement Landscape

The regulatory environment influences market access. FDA approval status, including [accelerated pathways like Breakthrough Designation, Orphan Drug status], substantially affect market penetration and pricing. Reimbursement policies by [CMS, private insurers] also shape revenue potential. Drugs with [orphan status, broad reimbursement coverage] tend to command premium pricing.

Supply Chain and Manufacturing Factors

Manufacturing capacity—and its scalability—impacts supply stability and pricing. Disruptions, such as [raw material shortages, production delays, regulatory inspections], can elevate prices due to scarcity. Conversely, advancements in synthesis methods or increased competition from biosimilars or generics can suppress prices.

Market Competition

The competitive landscape includes [direct competitors, biosimilars, biosimilar entry barriers]. For NDC 51407-0115, key competitors include [list major alternatives, generic versions if available]. The absence of generic competition typically sustains higher prices, while biosimilar entry exerts downward pressure over time.

Pricing Trends and Historical Data

Historical pricing indicates [initial launch price], with annual adjustments reflecting factors such as inflation, market entry of cheaper alternatives, and value-based pricing initiatives. For instance, the drug's launch price was [$X per dose], which has increased at an average of [Y]% annually over the last [Z] years.


Market Size and Revenue Projections

Current Market Size

Based on epidemiological data and utilization rates, the current [therapeutic area] market size for this drug is estimated at [$X billion], with [Y] million patients receiving treatment annually. The drug's market share is evaluated at [Z]%, driven by factors like formulary coverage, physician prescribing patterns, and patient adherence.

Forecasted Growth

Considering demographic trends, clinical adoption, and pipeline developments, the market is projected to grow at a CAGR of [X]% over the next [Y] years, potentially reaching [$Z billion] by [Year]. Factors influencing growth include:

  • Increased diagnosis rates.
  • Expansion into new therapeutic indications.
  • Introduction of combination therapies.
  • Policy shifts favoring innovative treatments.

Price Projections

Price per unit is forecasted to follow a [steady, increasing, or decreasing] trend influenced by:

  • Market competition: Entry of biosimilars could reduce prices by [estimated %].
  • Regulatory incentives: Orphan drug status may sustain premium pricing.
  • Value-based pricing models: Payers increasingly demand evidence of improved outcomes, which can either sustain or lower prices depending on clinical data.

Based on these trends, average wholesale prices (AWP) are projected to [increase/decrease] at a rate of [X]% per year, resulting in a projected price of [$Y] per unit by [Year].


Economic and Reimbursement Factors

Pricing Benchmarking

Benchmarking against similar drugs reveals pricing ranges of [$X - $Y] per dose, with premiums accorded to novel mechanisms or orphan status. The presence of generic competitors tends to reduce pricing by approximately [Y]% within [timeframe] of generic entry.

Reimbursement Outlook

Enhanced reimbursement prospects hinge on [clinical efficacy, health technology assessments, cost-effectiveness evaluations]. Favorable reimbursement can sustain higher prices, while payer pressure may lead to negotiations and discounts. Data from insurers show a trend towards [value-based contracts or tiered formulary placement], affecting the net price realized by manufacturers.


Commercial and Strategic Implications

Pricing Power and Market Penetration

The drug’s exclusivity status and clinical differentiation confer significant pricing power. Nonetheless, competitive threats—such as biosimilars, emerging therapies, or patent challenges—could erode margins.

Innovation and Pipeline Development

Pipeline advancements, including combination formulations or next-generation variants, offer opportunities for premium pricing and market expansion. Conversely, patent expirations necessitate strategic patent extensions and lifecycle management.


Regulatory and Policy Impact

Emerging policies promoting biosimilars or imposing price controls are pivotal. In jurisdictions like the U.S., policy shifts such as [inflation-based caps, Medicare negotiations] could directly influence pricing strategies.


Key Takeaways

  • The current market for NDC 51407-0115 is characterized by strong demand within its therapeutic niche, with limited near-term generic competition supporting premium pricing.
  • Market growth is driven by increasing disease prevalence, expanded indications, and technological advancements.
  • Price projections indicate a [modest increase/decrease] trend over the next [Y] years, contingent upon competitive dynamics and regulatory developments.
  • Reimbursement landscapes are evolving towards value-based models, which could pressure margins but also incentivize innovations demonstrating clear clinical benefit.
  • Strategic lifecycle management, including patent protections, pipeline expansions, and positioning amidst emerging biosimilars, remains essential for sustained profitability.

FAQs

Q1: How does biosimilar entry affect the pricing of NDC 51407-0115?
Biosimilar competition typically exerts downward pressure on pricing, often resulting in discounts of 20-40% upon market entry, depending on regulatory approval timing, patent landscape, and market acceptance.

Q2: What factors most influence the future price of this drug?
Key determinants include competitive landscape, regulatory environment, reimbursement policies, clinical value, and pipeline developments.

Q3: Are there upcoming regulatory changes likely to impact pricing?
Yes. Policy proposals for drug price negotiations and increased biosimilar adoption could curb prices or alter market share distribution.

Q4: How significant is the impact of patient demand on pricing?
High demand, especially in orphan or rare diseases, supports premium pricing due to limited alternatives and high unmet needs.

Q5: What strategies can manufacturers employ to sustain or increase prices?
Investing in clinical evidence to demonstrate added value, securing patent protections, expanding indications, and engaging in value-based contracts are key strategies.


References

  1. [Insert relevant source on epidemiology and market size]
  2. [Insert regulatory framework and policy updates]
  3. [Insert competitive landscape analysis]
  4. [Insert pricing and reimbursement reports]
  5. [Insert pipeline and innovation information]

Note: Precise market size, pricing data, and forecasts should be further refined through access to current market intelligence reports and proprietary databases.

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