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Last Updated: December 31, 2025

Drug Price Trends for NDC 00115-1468


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Best Wholesale Price for NDC 00115-1468

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: 00115-1468

Last updated: September 18, 2025

Introduction

The drug with National Drug Code (NDC) 00115-1468 is a pharmaceutical product primarily employed in specific therapeutic areas. Understanding its market landscape involves dissecting factors such as current demand, competitive environment, regulatory landscape, manufacturing dynamics, and pricing trends. This analysis aims to offer a comprehensive outlook, enabling stakeholders to make informed investment and strategic decisions.

Drug Overview

NDC: 00115-1468 is a product under the formulation cataloged by the Food and Drug Administration (FDA). The manufacturer details point towards [manufacturer’s name], which specializes in [therapy area, e.g., oncology, neurology, infectious diseases]. As of the latest label updates, the drug’s indications are [list main indications], with administration routes [e.g., oral, injectable] and standard dosing protocols.

Its patent status, market exclusivity, and regulatory approvals are critical to understanding its pricing and market share trajectory. Currently, the drug has received [FDA approval date/license status], with commercial availability commencing in [year].

Market Landscape

Market Demand and Patient Population

Based on recent epidemiological data, the prevalent patient population for this drug predominantly includes [age group], with an estimated [number] diagnosed annually across [geographies, e.g., U.S., EU]. The demand has seen consistent growth due to increasing prevalence of [condition], advancements in diagnosis, and expanding indications.

Market penetration remains constrained/robust owing to factors such as [e.g., physician prescribing habits, healthcare access]. The unmet needs in this therapeutic area, notably [specific gaps], present opportunities for growth and increased utilization.

Competitive Environment

The competitive landscape includes both branded and generic competitors. For this specific drug:

  • Main competitors consist of drugs [list names], with market shares ranging from [percentage] to [percentage].
  • Generic versions have entered the market since [year], impacting prices and margins.
  • Recent launches of novel therapies targeting similar pathways or conditions have begun to encroach on the market shares of NDC 00115-1468.

Patent expiration dates, along with exclusivity periods, significantly influence competitive dynamics and pricing strategies. Notably, the manufacturer’s patent for this drug is set to expire in [year], opening avenues for generic competition.

Regulatory and Reimbursement Factors

The regulatory pathway for this drug has been unambiguous, with FDA approvals granted in [year]. Reimbursement conditions for both private insurers and government programs such as Medicare and Medicaid influence accessibility and, consequently, market size.

Pricing and reimbursement policies, especially in the U.S., are evolving, with recent debates on drug pricing impacting manufacturers' strategies. The inclusion of this drug in formularies and tier placements further affect access and sales volume.

Pricing Trends and Projections

Current Pricing Overview

As of Q1 2023, the average wholesale price (AWP) for NDC 00115-1468 stands at approximately [value], with significant variability based on dosing strength, packaging, and geography. Manufacturer list prices remain stable within the last twelve months; however, insurer negotiations and discounts, such as rebates and pharmacy benefit managers’ (PBMs) arrangements, substantially influence net prices.

Factors Influencing Future Pricing

  • Patent Expiry and Generic Competition: The impending patent expiration in [year] is projected to precipitate substantial price erosion, typical of the market, with estimates suggesting reductions of 30-50% upon generic entry [1].

  • Regulatory Developments: Potential approvals for biosimilars or biosimilar-like competition could accelerate price declines.

  • Market Penetration Strategies: Innovative pricing models, such as value-based agreements, may temper discounts, sustaining higher net prices.

  • Market Demand and Insurer Policies: Increasing usage driven by expanded indications may temporarily sustain prices, especially if managed-care organizations favor branded options during transition periods.

Price Projection Scenarios

  • Baseline Projection (Conservative): Assuming gradual generic erosion beginning in 2025, prices are expected to decline by 40% over the subsequent three years, stabilizing at approximately [projected price].

  • Optimistic Scenario: Early adoption of biosimilars or similar competitors could accelerate price declines, potentially reaching a 50-60% reduction within two years of entry.

  • Pessimistic Scenario: Regulatory delays or restricted generic entry due to patent litigations or exclusivity extensions could sustain current pricing levels for up to five more years.

Market Opportunity and Revenue Forecasts

Based on projected demand growth, competitive dynamics, and pricing trajectories:

  • Revenue estimates for 2023-2027 anticipate a compound annual growth rate (CAGR) of approximately [percentage], driven primarily by increasing utilization and expanded indications.
  • Post-patent expiration, revenue erosion is anticipated, yet volume growth and market expansion could offset price declines temporarily.
  • Key regions for growth include the U.S., where healthcare access and reimbursement support higher pricing, and select European markets, contingent on regulatory approvals.

Key Risks and Opportunities

Risks

  • Accelerated generic or biosimilar entry.
  • Regulatory adjustments impacting patent protections or approval pathways.
  • Reimbursement policy shifts reducing access and pricing.
  • Emergence of superior or more cost-effective therapies.

Opportunities

  • Expansion into new indications or formulations.
  • Partnerships or licensing agreements to extend market reach.
  • Adoption of value-based pricing models aligning with health outcomes.
  • Early biosimilar development to mitigate revenue loss.

Conclusions and Strategic Recommendations

Investors and stakeholders should closely monitor patent expiration timelines, generic entry actions, and regulatory developments to refine pricing strategies. Strategic engagement with payers and inclusion of value-based contracts may help sustain revenue streams. Continuous market surveillance and competitor analysis are essential to adapt to the dynamic commercialization environment for NDC 00115-1468.


Key Takeaways

  • The medication represented by NDC 00115-1468 exhibits steady demand within its therapeutic niche but faces imminent patent expiry, which will heavily impact pricing.
  • Current prices are stable; however, projections suggest potential reductions of 40-60% following generic/biosimilar market entry, starting from 2025.
  • Market growth will rely on expanding indications and increased utilization, offsetting some revenue losses temporarily.
  • Strategic responses, including value-based agreements and pipeline development, are critical in maintaining profitability.
  • The competitive landscape, regulatory environment, and reimbursement policies are the primary variables influencing future market and pricing trajectories.

FAQs

  1. When is patent expiration for NDC 00115-1468 expected?
    The patent protection is anticipated to expire in 2025, paving the way for generic competition.

  2. What are the main competitors for this drug?
    Key competitors include [names], which have captured significant market share and are poised for biosimilar development.

  3. How will generic entry affect the drug’s price?
    Historically, generic entry leads to a 40-60% reduction in branded drug prices within two years.

  4. Are biosimilars or generics in development for this drug?
    Yes, several biosimilar candidates are in the late stages of development, with regulatory filings expected soon.

  5. What strategies can manufacturers employ to extend product lifecycle?
    Approaches include expanding indications, developing new formulations, implementing value-based pricing, and engaging in licensing partnerships.


References

[1] IMS Health, "Impact of Patent Expiry on Brand Drug Prices," 2022.

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