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Last Updated: December 12, 2025

Drug Price Trends for NDC 51407-0603


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Best Wholesale Price for NDC 51407-0603

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
CAPTOPRIL 100MG TAB Golden State Medical Supply, Inc. 51407-0603-01 100 184.41 1.84410 2023-06-15 - 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 51407-0603

Last updated: July 27, 2025

Introduction

The drug identified by the National Drug Code (NDC) 51407-0603 represents a pharmaceutical product widely recognized within clinical and commercial landscapes. Understanding its market positioning, competitive environment, pricing strategies, and future trends is essential for healthcare providers, payers, and investors seeking informed decision-making.

This analysis offers a comprehensive overview of the current market dynamics surrounding NDC 51407-0603, encompassing supply chain considerations, regulatory context, competitive analysis, and future pricing outlook.


Product Profile and Therapeutic Area

NDC 51407-0603 corresponds to [Specific product name and formulation], approved for treating [indicate approved indications]. Its active pharmaceutical ingredient (API) is [name], positioned within [therapeutic class]. Its clinical value lies in [briefly describe benefits, such as efficacy, safety profile, or unique mechanisms], driving its utilization in [hospital, outpatient, specialty clinics].


Market Overview and Demand Drivers

The demand for NDC 51407-0603 is primarily driven by increasing prevalence rates of [relevant disease areas]. For example, burgeoning cases of [disease] in [geographies] augment market size, with projections indicating compounded annual growth rates (CAGR) of [percent] over the next five years.

Innovations within the therapeutic area, expanding indications, and approval of new combination regimens bolster future demand. Additionally, demographic shifts such as aging populations contribute to sustained market momentum.


Supply Chain and Manufacturing Landscape

Manufacturing of NDC 51407-0603 involves [major manufacturers or generic suppliers], with production aligning to strict regulatory standards, including FDA and international GMP protocols. Recent supply chain disruptions—such as raw material shortages or logistical bottlenecks—have intermittently impacted distribution, but overall supply remains robust.

Patent statuses and exclusivity periods influence manufacturing strategies. Once patents expire, a surge in generic competition can significantly affect pricing and market share.


Competitive Environment

The competitive landscape includes:

  • Branded equivalents: Market leaders hold proprietary rights, leveraging clinical data and brand recognition.
  • Generic competitors: Post-patent expiration, generic versions emerge, often offering substantial price discounts.
  • Biosimilars and novel therapies: In some segments, biosimilars threaten branded products, compelling price adjustments.

Competitive intensity varies regionally; the U.S. market demonstrates fierce price competition among generics, impacting profit margins. International markets may present different dynamics based on regulatory and payer policies.


Regulatory and Reimbursement Context

Regulatory pathways influence drug accessibility and pricing. The product's approval status affects market penetration, especially in countries with incremental approval processes. Reimbursement policies and formulary placements determine patient access and influence pricing strategy.

Medicare, Medicaid, and private insurers typically negotiate discounts or set reimbursement rates based on the drug's formulary status. Value-based agreements and outcomes-based contracts are gaining traction to align pricing with clinical efficacy.


Current Pricing Dynamics

As of [latest available data, e.g., Q1 2023], the average wholesale price (AWP) for NDC 51407-0603 ranges between $[low range] and $[high range] per unit, with variability influenced by dosage form, packaging, and market factors. Manufacturer list prices often exceed net prices after negotiations, rebates, and discounts.

In the U.S., pharmacy benefit managers (PBMs) and payers exert significant influence, often negotiating rebates that can reduce the actual transaction price by [estimated percentage]. This dynamic underscores the importance of understanding net pricing rather than list prices alone.


Price Projections and Future Trends

Short-Term Outlook (1-2 years):
Expect price stabilization or modest declines driven by increased generic competition and payer negotiations. Price erosion of [percent]% annually is typical post-patent expiry, depending on the therapeutic class and regional market conditions.

Medium to Long-Term Outlook (3-5 years):
Potential price reductions of [percent]% are anticipated as more competitors enter the market and biosimilars or alternative therapies gain approval. However, innovative formulations, improved delivery mechanisms, or expanded indications may sustain or even elevate pricing.

Emerging Trends Influencing Pricing:

  • Value-based pricing models emphasize outcomes, potentially leading to price adjustments aligned with real-world efficacy.
  • Market consolidation among manufacturers could influence pricing strategies, either enabling premium pricing or fostering intense price competition.
  • Regulatory incentives and policy reforms, particularly in countries adopting value-based healthcare models, will shape future pricing landscapes.

Implications for Stakeholders

  • Manufacturers should consider timing for patent expirations and engagement in biosimilar development to maintain market share.
  • Payers and providers should negotiate rebates and formulary placements to optimize total cost of care.
  • Investors benefit from understanding the lifecycle stage of NDC 51407-0603, assessing risks associated with patent cliffs and competitive pressures.

Key Takeaways

  • The market for NDC 51407-0603 is poised for moderate price declines in the immediate future due to increasing generic competition.
  • Demand drivers remain robust given the disease prevalence and ongoing R&D efforts, supporting a resilient market environment.
  • Supply chain stability is generally maintained, but vigilance is necessary amid geopolitical and logistical uncertainties.
  • Adaptive pricing strategies incorporating value-based approaches are becoming standard, influencing future price trajectories.
  • Stakeholders should closely monitor patent timelines and regulatory developments to optimize market positioning and pricing.

FAQs

  1. What is the patent status of NDC 51407-0603, and how does it impact pricing?
    The patent protecting NDC 51407-0603 is set to expire in [year], after which generic manufacturers are expected to enter the market, exerting downward pressure on prices.

  2. How does the introduction of biosimilars affect the price of NDC 51407-0603?
    Biosimilars generally lead to significant price reductions, often between [percent]% and [percent]%, depending on market acceptance and regulatory pathways.

  3. What are the primary factors influencing future price projections for this drug?
    Key factors include patent expirations, competitive landscape, demand elasticity, regulatory policies, and emerging value-based reimbursement models.

  4. How do regional differences influence the pricing of NDC 51407-0603?
    Pricing varies widely by region due to differing regulatory environments, negotiation leverage of payers, and market maturity, with U.S. prices typically higher than international markets.

  5. What strategies can manufacturers adopt to sustain profitability amidst declining prices?
    Strategies include innovating new formulations, expanding indications, engaging in risk-sharing agreements, optimizing supply chains, and strengthening brand value.


Sources

[1] U.S. Food and Drug Administration (FDA) - Drug Approval and Regulatory Data
[2] IQVIA. (2023). Healthcare Market Reports.
[3] CMS.gov. (2023). Medicare and Medicaid reimbursement policies.
[4] EvaluatePharma. (2023). Price and Market Share Forecasts.
[5] Pharmaceutical Marketplace Analyses, Industry Reports 2022-2023.

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