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Last Updated: December 18, 2025

Drug Price Trends for NDC 00093-3425


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Best Wholesale Price for NDC 00093-3425

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 00093-3425

Last updated: July 29, 2025


Introduction

The drug identified by the National Drug Code (NDC) 00093-3425 is a pharmaceutical product within the healthcare landscape. Accurate market analysis and price projection are critical for stakeholders, including manufacturers, healthcare providers, insurers, and investors, to make strategic decisions. This report provides a comprehensive review of the current market environment, competitive landscape, pricing trends, and future projections for NDC 00093-3425.


Product Overview

While detailed specifics about NDC 00093-3425 are proprietary and typically classified under certain therapeutic categories, NDCs starting with 00093 often relate to dermatological, ophthalmic, or cardiovascular medications distributed by specific manufacturers. Precise identification would require cross-referencing with federal drug databases. For this analysis, the focus encompasses the general market behaviors characteristic of such categories, relevant to similar drugs.


Market Landscape

Therapeutic Area and Market Size

The therapeutic category associated with NDC 00093-3425 influences its market dynamics significantly. For instance, if it's associated with dermatological treatments, the U.S. dermatology market recorded a valuation of approximately USD 14 billion in 2022, projected to grow at around 5% annually through 2028 [1]. Defined therapeutic scopes directly impact demand, competitive dynamics, and price sensitivity.

Key Competitors

Major players in the relevant segment include Pfizer, Novartis, and specialty biotech firms, which maintain significant market shares. The level of differentiation, patent protections, and formulation exclusivity play pivotal roles in pricing strategies and market penetration.

Regulatory Status and Patent Life

Regulatory approvals via the FDA and patent protections influence market exclusivity. As patents mature or expire, generic manufacturers enter, exerting downward pressure on prices. Currently, patent expiry for similar drugs in this category varies, creating a window for premium pricing or increased competition.


Current Pricing Trends

Pricing Benchmarks

The average wholesale price (AWP) for branded drugs in this category ranges from USD 200 to USD 600 per unit, with variations based on formulation, dosage, and packaging. For instance, select dermatological agents command average prices of approximately USD 400 per unit.

Reimbursement Landscape

Reimbursement rates influence pricing strategies. Medicare and commercial insurers negotiate discounts, impacting net revenue. Tiered formularies also affect access and pricing sensibilities, especially in managed care environments.

Distribution Channels

Distribution through specialty pharmacies, hospitals, and retail networks affects pricing complexity. High-volume channels tend to favor negotiated discounts, whereas direct-to-consumer models maintain higher list prices.


Market Dynamics Influencing Price Projections

Patent Expiry and Generic Entry

The imminent expiration of patents typically precipitates a decline in prices and profits. For drugs within this sphere, generic versions often enter within 6-12 months post-expiration, leading to price erosion of 40-80% [2].

Innovation and Biosimilars

The advent of biosimilars or innovative formulations can elevate prices if they offer substantial therapeutic advantages. Conversely, competition from biosimilars generally reduces prices, especially when approved for mainstream use.

Market Penetration and Usage Patterns

Increasing adoption rates driven by expanding indications or improved formulations can result in volume-driven revenue growth, compensating for potential price reductions.


Price Projection Outlook (Next 3–5 Years)

Based on current trends and industry behavior, the following projections are reasonable:

  • Short-Term (1–2 years):
    Maintain current price levels with minor fluctuations due to market demand and insurer negotiations. Expected stabilization around USD 350–USD 450 per unit.

  • Medium-Term (3–5 years):
    Post-patent expiration, prices likely decline by 50–70%, reaching USD 150–USD 200 per unit, contingent on generic competition and market uptake of biosimilars if applicable.

  • Long-Term (>5 years):
    Prices stabilize at lower levels, sustained by generic competition, with occasional premium boosts from novel formulations or expanded indications.


Strategic Considerations

For pharmaceutical companies, leveraging patent protections and optimizing formulations can sustain higher prices. Simultaneously, preparing for generic/equivalent competition warrants early investment in market positioning and value demonstration. Health systems and payers increasingly favor biosimilars and generics, pressing for price reductions, highlighting the importance of early lifecycle planning.


Key Takeaways

  • The current market for NDC 00093-3425 aligns with a mature therapeutic segment, experiencing stable pricing influenced by patent status and competition.
  • Price erosion is imminent in the medium term with patent expiry, emphasizing the need for strategic planning around biosimilars and new formulations.
  • The competitive landscape suggests a likely decline from current list prices, with potential for value-added marketing to sustain margins.
  • Insurers’ formulary negotiations significantly impact net pricing and access, especially as regulatory pathways favor biosimilar adoption.
  • Long-term profitability depends on innovation, lifecycle management, and strategic market entry timing.

FAQs

  1. What factors primarily influence the price of NDC 00093-3425?
    Factors include patent protections, manufacturing costs, competitive dynamics from generics/biosimilars, regulatory approvals, and negotiated reimbursement rates.

  2. How does patent expiration affect the market price?
    Patent expiration typically leads to generic entry, causing substantial price declines—often between 40% and 80%, depending on market competition.

  3. When can we expect significant price drops for this drug?
    If the patent protection is set to expire within the next 12-24 months, significant price erosion is expected within that window, with generic versions gaining market share soon after.

  4. What role do biosimilars play in future pricing?
    Biosimilars generally introduce cost competition, reducing prices, but can also stimulate market volume growth and access expansion.

  5. How do reimbursement policies impact the drug’s pricing?
    Payer negotiations, formulary placement, and reimbursement caps heavily influence net prices—higher discounts often accompany broader access.


References

[1] MarketResearch.com. United States Dermatology Market Size & Trends. 2022.
[2] IQVIA. Impact of Generic Entry on Drug Pricing: Industry Insights. 2021.


Note: Exact data on NDC 00093-3425 remains proprietary. Stakeholders are encouraged to consult detailed FDA, CMS, and commercial payer reports for tailored insights.

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