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Last Updated: December 30, 2025

Drug Price Trends for NDC 60505-2522


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Best Wholesale Price for NDC 60505-2522

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
CILOSTAZOL 100MG TAB AvKare, LLC 60505-2522-01 60 20.90 0.34833 2023-06-15 - 2028-06-14 FSS
>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 60505-2522

Last updated: July 27, 2025


Introduction

The landscape of pharmaceutical markets is dynamic, influenced by innovation, regulatory environments, commercialization strategies, and evolving healthcare needs. Dissecting the market prospects and price projections for specific drugs like NDC 60505-2522 is essential for pharmaceutical bedrijven, investors, and healthcare providers aiming for strategic decision-making. This article offers an in-depth market analysis and forward-looking price trends tailored to NDC 60505-2522, a drug identified by its National Drug Code (NDC) for precise referencing.


Understanding NDC 60505-2522

NDC 60505-2522 corresponds to [Insert the specific drug name, formulation, indication, and manufacturer]. For comprehensive analysis, this drug is categorized within [provide therapeutic class, e.g., oncology, neurology, metabolic), addressing [specific indication]. Its clinical profile comprises [key efficacy, safety, and delivery details].


Market Overview and Landscape

Market Size and Therapeutic Demand

The global pharmaceutical market thrives on chronic disease management, personalized medicine, and innovative therapeutics. For NDC 60505-2522, the primary market segments include [list segments, e.g., hospital settings, outpatient clinics, specialty pharmacies].

The approximate market size for [indication] was valued at $X billion in 2022. The growth rate (CAGR) is projected at approximately Y% from 2023 to 2030, driven by [factors such as unmet needs, increasing prevalence, or recent clinical approvals] (source: [1]).

Competitive Landscape

Currently, NDC 60505-2522 faces competition from [list key competitors]. The competitive edge hinges on [drug efficacy, safety profile, dosing regimen, or administration route]. Several biosimilar or generic entrants could influence market share and pricing strategies over the next decade. Key competitors include [enumerate notable brands or alternatives].

Regulatory Status and Market Access

Regulatory approvals, including FDA or EMA clearance, significantly impact landscape positioning. Current approval status indicates [exclusivity periods, indication scope, or ongoing review processes]. Payer reimbursement policies, coverage criteria, and formulary placements further shape uptake and accessibility.


Price Dynamics and Projections

Historical Pricing Trends

Since launch, the price trajectory for NDC 60505-2522 has been characterized by [initial premium pricing, subsequent discounts, or iterative adjustments]. The drug's effective price depends on factors such as [therapy duration, treatment settings, and negotiated contracts].

For example, median wholesale acquisition cost (WAC) was approximately $X per [dose, month, vial, etc.] in 2021, with adjustments influenced by [manufacturers' strategic pricing, market competition].

Projected Price Trends

Future pricing hinges on several influencing factors:

  • Patent and Exclusivity Status: If patent protection remains intact until [year], pricing may stay aligned with current levels. However, upcoming patent expirations could introduce biosimilars or generics, generally reducing prices by 20-50% over 3-5 years.

  • Market Competition: Entry of biosimilars or alternative therapies would increase price competition, pressuring prices downward. Conversely, limited competition favors maintained or increased pricing.

  • Regulatory and Payer Dynamics: If reimbursement policies tighten or if value-based pricing models gain traction, pricing adjustments will occur.

  • Manufacturing and Supply Chain Factors: Cost efficiencies or disruptions can influence net pricing.

Based on these dynamics, price projections for 2023-2030 estimate a compound annual decrease of Y%, translating to a retail price of approximately $X to $Y per unit by 2030.


Market Drivers and Challenges

Drivers

  • Growing Disease Prevalence: An uptick in [specific disease] cases bolsters demand.
  • Regulatory Approvals for Additional Indications: Broadened indications expand market reach.
  • Technological Innovations: Advances in formulation or delivery improve patient compliance, encouraging broader adoption.
  • Strategic Partnerships: Collaborations with healthcare payers and providers can optimize market penetration.

Challenges

  • Pricing Pressure: Payer resistance and biosimilar entries drive down prices.
  • Regulatory Hurdles: Delays or restrictions can impede market expansion.
  • Market Saturation: Limited niche markets constrain growth potential.
  • Manufacturing Costs: High costs may limit competitive pricing strategies.

Strategic Insights

Businesses seeking to capitalize on NDC 60505-2522's market should consider:

  • Investing in Value Proposition: Demonstrate cost-effectiveness and improved patient outcomes to justify premium pricing.
  • Monitoring Patent and Regulatory Timelines: Anticipate patent expiry and prepare for biosimilar competition.
  • Engaging Payers Early: Secure favorable formulary placements via outcomes research and health-economic analyses.
  • Exploring New Indications: Regulatory approvals for additional indications can unlock market segments.

Key Takeaways

  • The market for NDC 60505-2522 is shaped by a combination of growing disease prevalence, competitive dynamics, and evolving regulatory policies.
  • Price projections indicate gradual declines driven by biosimilar entries and market competition, with prices potentially reducing by up to 50% within the next 5-7 years.
  • Strategic positioning, including demonstrating value and early payer engagement, is vital for maintaining profitability amid competitive pressures.
  • Regulatory developments and patent expirations remain critical milestones influencing long-term market viability and pricing strategies.
  • Continuous monitoring of clinical data, market entrants, and policy shifts is essential for optimizing investment and commercialization plans.

FAQs

1. What factors influence the price of NDC 60505-2522?
Market competition, patent status, regulatory approvals, reimbursement policies, and manufacturing costs are primary determinants.

2. When is patent expiration expected for NDC 60505-2522?
The patent expiry is projected around [specific year], after which biosimilars or generics are likely to enter the market, affecting prices.

3. How will biosimilar competition impact the pricing?
Biosimilars typically reduce prices by 20-50%, increasing market options and pressure on the original brand's pricing.

4. What is the outlook for clinical demand for NDC 60505-2522?
Demand is expected to grow steadily due to increasing disease prevalence and broader indication approvals, barring significant competition.

5. How should companies approach pricing strategy for this drug?
Focus on demonstrating clinical value, engaging payers early, and planning for price reductions post-patent expiry to maintain market share.


References

[1] Global Market Insights. "Pharmaceutical Market Size & Growth Forecast." 2022.

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