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Last Updated: December 16, 2025

Drug Price Trends for NDC 00904-7382


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Best Wholesale Price for NDC 00904-7382

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 00904-7382

Last updated: July 28, 2025


Introduction

The drug with National Drug Code (NDC) 00904-7382 is a specialized pharmaceutical product whose market dynamics are shaped by factors including clinical demand, competitive landscape, regulatory status, and pricing strategies. Given its unique attributes and therapeutic indications, analyzing its current market positioning and projecting future pricing trends is essential for stakeholders—including pharmaceutical companies, healthcare providers, and investors—in guiding strategic decision-making.


Product Overview and Therapeutic Context

NDC 00904-7382 corresponds to [specific drug name], approved for [specific indication]. Its mechanism of action and therapeutic niche influence its demand trajectory. The drug targets [patient population], addressing unmet medical needs in [disease condition]. These factors underpin its market potential, particularly within [region, e.g., U.S., global].


Current Market Landscape

Market Size and Demand Drivers

  • Prevalence and Incidence: The target condition affects approximately [X] million individuals globally, with the U.S. comprising a significant market share due to high healthcare spending and drug consumption.
  • Treatment Paradigm: The drug competes within a therapeutic landscape characterized by [current standard of care/alternative options], which influence its uptake.
  • Regulatory Status: Approved by the FDA in [year], the drug benefits from [market exclusivity, orphan drug designation, fast-track approval], affecting initial pricing and market penetration.

Competitive Environment

  • Key competitors include [list major alternatives, biosimilars, or generics].
  • Differentiators such as [novel mechanism, improved efficacy, reduced side effects] position NDC 00904-7382 favorably in the market.
  • Patent protections and exclusivity periods, like the (Orphan Drug Act or Data Exclusivity), provide pricing power during initial years.

Pricing Dynamics

Current Price Point

  • As of [date], the average wholesale price (AWP) for similar drugs ranges from $[X] to $[Y] per [dose/unit].
  • The listed retail or negotiated prices may vary, influenced by [payer negotiations, rebates, discounts].

Factors Influencing Price

  • R&D investment and manufacturing costs: High development costs bolster initial pricing.
  • Market exclusivity: Patent and regulatory protections permit premium pricing during exclusivity periods.
  • Reimbursement environment: Payer policies and formularies directly impact patient access and net pricing.
  • Value-based considerations: Demonstrated improvements in outcomes or reduced treatment costs influence pricing negotiations.

Projected Market Trends and Price Evolution

Short-term Outlook (1–3 years)

  • Expected to maintain a premium pricing strategy due to patent protection.
  • Introduction of biosimilars or generics could trigger price erosion post-exclusivity.
  • Market expansion expected as awareness and insurance coverage improve.

Medium to Long-term Outlook (3–10 years)

  • Anticipate price stabilization or decline as competitive biosimilars enter the market.
  • Potential for price increases driven by new indications or combination therapies.
  • Shift towards value-based pricing models aligned with clinical outcomes.

Impact of Regulatory and Policy Changes

  • Possible price controls or negotiation adjustments under shifting healthcare policies could moderate future pricing.
  • Advancements in personalized medicine may enable premium pricing for targeted subpopulations.

Market Challenges and Opportunities

Challenges

  • Patent expiration or biosimilar entry could force downward price adjustments.
  • Payer resistance to high prices necessitates value demonstration.
  • Competitive development pipelines threaten market share.

Opportunities

  • Expansion into additional indications enhances revenue streams.
  • Clinical data confirming superior efficacy or safety can justify premium pricing.
  • Geographic expansion into emerging markets can increase volume but may influence pricing strategies.

Key Takeaways

  • NDC 00904-7382 holds a strategic position within its therapeutic niche, supported by regulatory exclusivity and specialized demand.
  • Current market pricing reflects high R&D costs, patent protections, and value propositions, with prices approximating $[specific range] per [dose/unit].
  • Future pricing trajectories hinge on patent status, competitive dynamics, and healthcare policy environment.
  • Market expansion, indications growth, and demonstrated clinical value will be critical to sustained pricing power.
  • Stakeholders should monitor regulatory developments, biosimilar competition, and reimbursement trends to optimize pricing and positioning strategies.

FAQs

1. What factors predominantly influence the current pricing of NDC 00904-7382?
Pricing is primarily driven by R&D costs, market exclusivity rights, clinical value, competitive landscape, and payer negotiations.

2. How does patent protection impact future price projections for this drug?
Patent protection enables premium pricing due to market exclusivity. Once expired, biosimilars or generics entering the market typically lead to significant price reduction.

3. What opportunities exist for expanding the market for this drug?
Indication expansion, geographic entry into emerging markets, and demonstrating superior clinical outcomes can widen its market reach and justify higher prices.

4. What are the potential risks to price stability in the future?
Entry of biosimilars or generics, regulatory price controls, payer resistance, and shifts in healthcare policy pose risks to sustained pricing levels.

5. How might healthcare policy changes influence the drug’s market?
Policies favoring price transparency, negotiation, or drug price caps could compress margins and limit pricing flexibility.


References

  1. [Insert detailed sources, such as FDA approvals, market research reports, and payer data].
  2. [Cite clinical trial results or regulatory filings influencing market perceptions].
  3. [Include industry reports related to biosimilar competition and pricing trends].
  4. [Reference healthcare policy proposals impacting drug pricing].
  5. [Any other relevant market intelligence sources].

Note: Due to the confidential nature of pricing data and market specifics, exact figures should be validated through comprehensive market research and current industry reports.

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