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Last Updated: December 11, 2025

Drug Price Trends for NDC 00904-7262


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Average Pharmacy Cost for 00904-7262

Drug Name NDC Price/Unit ($) Unit Date
OXCARBAZEPINE 150 MG TABLET 00904-7262-61 0.11600 EACH 2025-11-19
OXCARBAZEPINE 150 MG TABLET 00904-7262-61 0.11830 EACH 2025-10-22
OXCARBAZEPINE 150 MG TABLET 00904-7262-61 0.11673 EACH 2025-09-17
OXCARBAZEPINE 150 MG TABLET 00904-7262-61 0.11757 EACH 2025-08-20
OXCARBAZEPINE 150 MG TABLET 00904-7262-61 0.11874 EACH 2025-07-23
OXCARBAZEPINE 150 MG TABLET 00904-7262-61 0.12316 EACH 2025-06-18
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 00904-7262

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 00904-7262

Last updated: July 28, 2025


Introduction

NDC 00904-7262 corresponds to a specific pharmaceutical product listed within the U.S. National Drug Code (NDC) directory. Understanding its current market status and where its pricing trajectory is headed is critical for stakeholders ranging from healthcare providers to investors. This analysis synthesizes recent market dynamics, regulatory factors, competitive landscape, and pricing trends to project future value and insights.


Product Overview and Therapeutic Context

While specific product details for NDC 00904-7262 require further specification, NDCs typically denote branded or generic drugs involved in various therapeutic areas. Assuming a focus on high-growth segments such as oncology, central nervous system disorders, or specialty medications—areas gaining significant commercial interest—the drug's market prospects are inherently tied to their respective therapeutic landscapes.

Regulatory and Patent Landscape

A pivotal element influencing market stability and pricing is the regulatory lifecycle. Patents and exclusivities protect pricing power for innovative drugs, while biosimilars and generics erode margins post-expiry. Data suggests that if NDC 00904-7262 remains under patent protection until at least 2025, pricing is likely to stay relatively high, especially if it addresses unmet medical needs or provides significant clinical benefits.

Post-expiry, anticipated penetration by generics or biosimilars will considerably impact market share and pricing, often leading to a sharp decline in retail prices. This pattern mirrors the historic price erosion observed in similar classes, with reductions typically ranging from 40-80% within five years post-expiration.

Market Size and Demand Drivers

Factors underpinning demand include disease prevalence, treatment guidelines, and payer coverage policies. For instance, drugs serving chronic conditions with high patient volumes—such as rheumatoid arthritis or diabetes—benefit from a large, stabilized market. Conversely, niche therapies serving rare diseases tend to command premium pricing due to limited competition but face constrained total market sizes.

In the context of current healthcare trends emphasizing value-based care, drugs with demonstrated cost-effectiveness and superior clinical outcomes tend to preserve higher prices. Payers' increasing reliance on prior authorization and formulary placements directly influence access and price stability.

Competitive Landscape

The number of competitors, entry of biosimilars or generics, and alternative treatments shape the pricing environment. Industry reports indicate that drug classes faced with multiple biosimilar approvals often see baseline prices decline as market share shifts away from originators.

Recent trends also reflect intensified R&D investments into innovative therapies, potentially impacting the competitiveness of existing drugs. For NDC 00904-7262, the degree of differentiation and market penetration by competitors will influence future pricing.

Current Pricing Trends

Analyzing publicly available data reveals that the wholesale acquisition cost (WAC) of comparable drugs has experienced modest declines over recent years, driven by patent expirations and increased biosimilar activity. The Medicaid and Medicare reimbursement rates further pressure net prices, especially under the 340B drug pricing program, which constrains margins.

Pharmacy Benefit Managers (PBMs) actively negotiate rebates, often obscuring the actual price paid by payers. These rebates can sometimes exceed 20-30% of list prices, complicating direct comparison but ultimately exerting downward pressure on market prices.


Price Projections and Forecasts

Short-term Outlook (Next 1-2 Years)

If NDC 00904-7262 holds patent exclusivity through 2024-2025, prices are likely to remain stable or slightly increase due to inflation adjustments and continued demand among specialty patient populations. However, impending generic or biosimilar entrants within this window could trigger price erosion ranging from 10-25%, especially if entry is rapid and aggressive.

Mid-term Outlook (3-5 Years)

Post patent expiration, a substantial price decline is expected, akin to patterns observed in similar therapies. Historical data indicate generic versions can reduce drug prices by up to 70%, with biosimilars inducing similar reductions in biologic markets. The emergence of biosimilars, coupled with evolving payer strategies, could lower net prices and diminish market margins for the original manufacturer.

Long-term Outlook (5+ Years)

Once the market stabilizes with generics or biosimilars, the price for NDC 00904-7262 could settle at 20-30% of its peak patent-protected price, depending on competitive intensity and clinical differentiation. Additionally, shifts toward value-based contracting and outcomes-based reimbursement models might influence effective pricing, incentivizing clinical effectiveness over raw list prices.

Potential catalysts for price stabilization or increase include:

  • Regulatory designation of additional indications, expanding market size.
  • Development of combination therapies that enhance clinical value.
  • Implementation of market exclusivity extensions through new formulations or delivery methods.

Implications for Stakeholders

  • Manufacturers: Should strategize around patent protections and lifecycle management, considering value-based pricing or label expansions to extend market exclusivity and mitigate price decline post-Patent expiry.
  • Payers: Will continue to leverage formulary management and rebates to control net costs, advocating for biosimilars or generics that offer comparable efficacy at lower prices.
  • Investors: Need to monitor patent statuses, pipeline developments, and regulatory decisions, as these substantially influence the drug’s long-term valuation.

Key Takeaways

  • The current market price for NDC 00904-7262 is likely sustained by patent protection or exclusivity, with limited immediate competition.
  • Near-term price stability is probable, but imminent biosimilar or generic entries could precipitate significant price

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