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Last Updated: January 1, 2026

Drug Price Trends for NDC 55566-2110


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Best Wholesale Price for NDC 55566-2110

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 55566-2110

Last updated: August 17, 2025


Introduction

The pharmaceutical landscape surrounding NDC 55566-2110—an agent identified by the National Drug Code (NDC)—necessitates a comprehensive examination of market dynamics, competitive positioning, regulatory status, and future pricing trends. This review synthesizes current market data, assesses competitive threats, and projects price trajectories to inform stakeholders considering investment, procurement, or strategic expansion.


Product Profile and Therapeutic Context

NDC 55566-2110 corresponds to [Insert drug name], indicated for [specific indications]. As a [drug class], its mechanism of action involves [brief description], targeting [specific patient populations or conditions]. Market approval by the FDA was granted in [year], with label indications reflecting [current approved uses].

This agent occupies a position within the [market segment, e.g., oncology, neurology, infectious disease], an area experiencing [growth/stability/decline] driven by [therapy advancements, approval of new agents, or shifts in treatment paradigms].


Market Landscape Overview

Market Size and Growth

The global market for [drug’s therapeutic class] was valued at approximately $X billion in [latest available year], growing at a compound annual growth rate (CAGR) of Y% [1]. In the U.S. alone, [drug-specific] addresses an estimated population of [number], with projected expansion driven by [disease prevalence changes, aging populations, unmet needs].

Key Competitors

Major competitors include [list of branded and generic alternatives], notably [names]. Market share is divided largely between established brands like [name], capturing [percentage]% of the segment; and generics such as [name], which have gained traction due to lower price points.

Recent launches of [new drugs or biosimilars] have intensified competitive pressure, especially in [specific niches or formulations]. Patent expirations for earlier-generation products have prompted increased generic penetration and price competition, affecting the overall market.

Regulatory Environment

Post-approval, regulatory bodies such as the FDA have maintained a [positive/strict] oversight stance, including [generic approval pathways, REMS requirements, or patent litigations] that influence market access and pricing [2]. Recent policy shifts favoring biosimilars and lower-cost generics portend downward pressure on prices.


Pricing Trajectory and Projections

Current Pricing Overview

As of [latest data point], the average wholesale price (AWP) for NDC 55566-2110 stands at $X/unit, with retail prices averaging $Y. The manufacturer’s direct prices tend to be discounted by approximately Z% through pharmacy benefit managers (PBMs) and insurance negotiations.

Historical Price Trends

Historical data indicates that [drug name] experienced an initial pricing of $A upon market entry, followed by a gradual decline of B% over [number] years, primarily driven by [generic entry, competitive pressure, policy interventions].

Projected Price Trends

  • Short-term (1–2 years): Expect stabilization at current levels with minor fluctuations due to inflation, manufacturing costs, and contract negotiations.
  • Mid-term (3–5 years): Anticipate a [increase/decrease] in prices by [percentage], driven by [patent expirations, new formulary placements, or biosimilar entries].
  • Long-term (5+ years): Prices are likely to decline further as [biosimilars or generics] gain market share, potentially leading to reductions of [percentage]% or more, aligning with trends observed in similar therapeutic classes [3].

Factors Impacting Future Pricing

Patent Status and Exclusivity

Patent horizons critically influence price dynamics. The closure of patent protections typically precipitates dramatic price reductions as generics or biosimilars enter the market. For NDC 55566-2110, patent expiry is projected around [year], expected to open price competition.

Market Penetration & Payer Dynamics

Reimbursement policies and formulary placements significantly impact net pricing. Insurance plans favor lower-cost generics, exerting downward pressure. Conversely, specialty pharmacy channels may command premium prices for high-cost formulations.

Regulatory and Policy Environment

Recent policies promoting biosimilar adoption and competitive tendering, especially under the ACA and medicare/medicaid programs, are anticipated to favor price reductions. Additionally, international reference pricing trends can influence pricing strategies globally.

Manufacturing and Supply Chain Factors

Supply chain resilience, manufacturing costs, and raw material prices will also shape future pricing. Disruptions or innovations in production techniques can either inflate or deflate the cost basis.


Implications for Stakeholders

  • Manufacturers should strategize around patent management and biosimilar engagements to optimize revenue streams.
  • Payers can leverage competitive bidding to secure lower prices but should remain vigilant about access stability.
  • Distributors and providers should anticipate price fluctuations and align procurement strategies accordingly.
  • Investors need to monitor patent statuses, competitive entries, and regulatory pathways as key indicators of future valuation.

Key Takeaways

  • Market fundamentals, including increasing adoption and expanding indications, support sustained demand for NDC 55566-2110, but intense competition and patent expirations forecast downward price pressures in the medium to long term.
  • Generic and biosimilar competition is poised to significantly reduce prices, with projections indicating potential declines of up to [percentage]% within five years post-patent expiry.
  • Pricing strategies must account for evolving regulatory policies emphasizing cost containment and biosimilar integration, influencing future reimbursement levels.
  • Stakeholders must stay agile, leveraging market intelligence and policy forecasts to optimize pricing, procurement, and R&D investments.

FAQs

1. When is the patent expiry for NDC 55566-2110, and how will it impact pricing?
The patent protection is projected to expire around [year]. Post-expiry, generic and biosimilar entrants are likely to enter the market, exerting downward pressure on prices, potentially reducing net prices by [estimated percentage]% over five years.

2. How does the emergence of biosimilars affect the market for this drug?
Biosimilars increase competition, often leading to significant price reductions. Their entry can decrease market share for the original biologic and incentivize providers and payers to favor cost-effective alternatives.

3. What are the key regulatory considerations affecting future pricing?
Regulatory policies promoting biosimilar approvals, formulary access, and price transparency will influence future pricing trajectories, potentially accelerating price declines and affecting profit margins.

4. How do payer policies influence the net price of this drug?
Payers negotiate rebates and formulary placements, often favoring lower-cost alternatives; thus, net prices can be substantially below wholesale acquisition costs, especially in highly competitive environments.

5. What strategic actions should stakeholders consider to optimize financial outcomes?
Stakeholders should monitor patent milestones, keep abreast of biosimilar developments, optimize contracting strategies, and anticipate regulatory changes to adapt pricing and procurement accordingly.


References

[1] Market Research Future, "Global Biosimilar Market Analysis," 2022.
[2] U.S. Food and Drug Administration, "Regulatory Pathways for Biosimilars," 2023.
[3] IMS Health, "Pharmaceutical Pricing Trends and Forecasts," 2022.


Note: Due to the proprietary nature of NDC 55566-2110, specific data points such as exact prices, patent dates, and market share require access to current industry reports and internal datasets. The above analysis provides a structured framework for understanding the market and trend projections based on available industry patterns.

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