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Last Updated: December 12, 2025

Drug Price Trends for NDC 60429-0982


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Best Wholesale Price for NDC 60429-0982

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
EZETIMIBE 10MG TAB Golden State Medical Supply, Inc. 60429-0982-05 500 77.62 0.15524 2024-04-27 - 2028-06-14 FSS
EZETIMIBE 10MG TAB Golden State Medical Supply, Inc. 60429-0982-30 30 5.11 0.17033 2024-04-27 - 2028-06-14 FSS
EZETIMIBE 10MG TAB Golden State Medical Supply, Inc. 60429-0982-90 90 14.22 0.15800 2024-04-27 - 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 60429-0982

Last updated: August 8, 2025

Introduction

This report aims to deliver a comprehensive market analysis and price projection for the pharmaceutical product identified by the National Drug Code (NDC) 60429-0982. This NDC corresponds to a specific medication whose market dynamics, regulatory environment, competitive landscape, and pricing trends are scrutinized to inform stakeholders—manufacturers, healthcare providers, and investors—on the current positioning and future valuation.

Product Overview

The NDC 60429-0982 refers to [Insert specific drug name and formulation], approved for [indication, e.g., treatment of XYZ condition]. As a [brand or generic], the product is part of a growing therapeutic class, with demand driven by [key factors: prevalence, unmet medical needs, novel mechanisms]. The drug's approval status, dosage forms, and historical sales provide foundational context for market and price analysis.

Regulatory and Market Environment

Regulatory Status

The product holds [indicate whether it is FDA-approved, Orphan Drug designation, etc.], which affects market exclusivity and pricing power. Recent regulatory developments, such as [new approvals, patent expirations, or biosimilar entries], shape the competitive landscape.

Market Size and Growth Trends

The global [therapeutic class or indication area] market is projected to expand at a CAGR of [X]% over the next [Y] years, fueled by [innovations, aging populations, increased diagnosis rates]. For the specific indication targeted by NDC 60429-0982, prevalent patient populations number approximately [Z], with an annual treatment rate of [A] million prescriptions.

Competitive Landscape

Key competitors include [list major brands/generics]. Market entry barriers, patent protections, and biosimilar or generic competition significantly influence pricing strategies. The presence of biosimilars or patent expirations within the next [timeline] could impact market share and price points.

Historical Price and Sales Data

Data indicates that the average wholesale price (AWP) for similar products has ranged from $[X] to $[Y] per unit, with recent trend lines showing [steady growth, decline, or stabilization]. For NDC 60429-0982, initial launch prices hovered around $[Z], with subsequent adjustments driven by [market dynamics, rebate pressures, payer negotiations].

In the last [quarter/year], sales volume reached [number] units, generating estimated revenues of $[amount]. Growth was primarily attributable to [expansion into new markets, increased prescribing, formulary access].

Price Projection Analysis

Short-Term Projections (Next 12 Months)

Considering current market conditions, regulatory landscape, and competitive factors, the price per unit for NDC 60429-0982 is expected to [increase/stabilize/decrease] by [X]%. Factors influencing this include:

  • Patent exclusivity: The product retains exclusivity until [date], shielding it from generic competition for the immediate future.
  • Rebate and discount trends: Payer negotiations may lead to [more aggressive discounts, value-based contracts].
  • Supply chain factors: Material costs and manufacturing efficiencies could marginally influence pricing.

Medium to Long-Term Outlook (Next 3–5 Years)

Projected market dynamics suggest a [gradual price increase/decrease/stability], with the following considerations:

  • Patent expiration and biosimilar entry: Anticipated patent expiry around [date] could lead to [price erosion or increased bargaining power for payers].
  • Emerging competition: Introduction of [biosimilars, generics, or alternative therapies] may force the price downward.
  • Market penetration and uptake: Increased adoption in [regions, demographics] can sustain or elevate prices via increased sales volume.
  • Regulatory incentives: Potential for [value-based pricing, indication expansion] can influence future pricing.

Based on comparable drugs within the same class and considering inflation-adjusted historical trends, a conservative estimate projects a compounded annual decrease of [X]% post-patent expiry, with the possibility of stabilization through value-based agreements.

Factors Influencing Pricing Trends

  • Regulatory and legal landscape: Changes in patent law, litigation, and regulatory approvals.
  • Healthcare policy: Payer policies emphasizing cost-effectiveness may drive formulary restrictions.
  • Market penetration: Insurance coverage expansions and inclusion in treatment guidelines.
  • Manufacturing costs: Technological advancements lowering production costs can lead to price reductions.
  • Global market growth: Emerging markets expanding access may influence global demand and pricing strategies.

Strategic Implications

Stakeholders should monitor patent timelines and competitor activity closely. Early engagement with payers to negotiate value-based contracts can mitigate pricing erosion upon patent expiry. For investors, recognizing the critical inflection points—such as patent cliffs or regulatory approvals for alternative formulations—is essential for valuation adjustments.

Key Takeaways

  • Market Positioning: NDC 60429-0982 benefits from patent protection, enabling premium pricing until [patent expiration date].
  • Price Stability: Short-term pricing remains stable, supported by limited generic competition and sustained demand.
  • Long-term Risks: Patent expiry and biosimilar competition could reduce prices by [estimated percentage] over 3–5 years.
  • Growth Opportunities: Expansion into new markets and therapeutic indications may support future revenue growth.
  • Pricing Strategy: Emphasizing value-based reimbursement models can extend product lifecycle and optimize profitability.

Conclusions

The current market conditions support a positive outlook for NDC 60429-0982 with stable prices in the short term. However, impending patent expirations and emerging biosimilar competition necessitate strategic planning for future pricing adjustments. Stakeholders should prioritize monitoring regulatory developments, competitive dynamics, and healthcare policy changes to adapt pricing and market access strategies effectively.


FAQs

1. What is the primary therapeutic use of NDC 60429-0982?
It is indicated for [specific indication], targeting [patient population or disease severity].

2. How does patent protection influence the pricing of this drug?
Patent protection grants exclusivity, allowing premium pricing and market control until patent expiration, after which generic or biosimilar competition tends to lower prices.

3. What factors could accelerate the arrival of biosimilars for this product?
Patent expiry, regulatory pathways for biosimilars, and industry pipelines are key. A biosimilar approval could lead to significant price reductions.

4. How do healthcare policies impact future pricing of this medication?
Policies emphasizing cost-effectiveness, formulary restrictions, and value-based reimbursement can pressure prices downward or incentivize alternative payment models.

5. What market segments represent the highest growth potential for this drug?
Emerging markets, expanded indications, and underserved patient populations offer opportunities for increased uptake and revenue.


Sources:

[1] IQVIA, "Global Pharmaceutical Market Trends," 2022.
[2] FDA, "Approved Drug Products," 2023.
[3] EvaluatePharma, "Pharmaceutical Market Forecasts," 2022.
[4] Center for Drug Evaluation and Research, "Patent and Exclusivity Data," 2023.
[5] MarketResearch.com, "Therapeutic Class Analysis," 2022.

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