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Last Updated: December 31, 2025

Drug Price Trends for NDC 60505-4716


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Best Wholesale Price for NDC 60505-4716

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 60505-4716: A Comprehensive Overview

Last updated: September 28, 2025

Introduction

The pharmaceutical landscape surrounding the drug with NDC 60505-4716 demands rigorous analysis to inform stakeholders—including manufacturers, investors, healthcare providers, and policymakers—about its market potential and future pricing trajectory. This detailed assessment synthesizes market dynamics, competitive positioning, regulatory environment, and economic factors influencing the drug's future valuation.

Product Profile and Therapeutic Area

NDC 60505-4716 corresponds to [Insert specific drug name], a medication targeting [Specify disease/condition, e.g., rheumatoid arthritis, multiple sclerosis, etc.]. Its active ingredients, dosing, delivery mechanism, and current indications are pivotal for understanding its market positioning and competitive edge.

The drug’s therapeutic class and mechanism of action influence both patient demand and clinical adoption. Its patent status, exclusivity provisions, and whether it is a biosimilar or novel compound further shape its market lifecycle.

Key Point: The uniqueness of the formulation, combined with clinical efficacy and safety profile, directly impacts its market penetration and pricing strategies.

Market Landscape and Demand Dynamics

Current Market Size

The global market for [therapeutic area] pharmaceuticals was valued at approximately USD [X] billion in 2022, with an expected compound annual growth rate (CAGR) of [Y]% over the next five years (Source: [1]). In North America alone, the market exceeds USD [Z] billion, driven by high prevalence rates and healthcare system adoption.

Prevalence and Incidence Rates

For the targeted condition, prevalence estimates suggest [X] million affected patients globally, with a significant proportion eligible for pharmacotherapy. The US, as a leading market, accounts for roughly [Y]% of total demand, influenced by demographic factors such as aging populations and disease awareness initiatives.

Competitive Landscape

Major competitors include [List of comparable drugs], with market shares spanning from [specific %] to [specific %]. The entry of biosimilars or generics, patent expirations, and healthcare reimbursement policies influence the competitive intensity and pricing.

Market Drivers:

  • Increasing diagnoses due to improved diagnostics
  • Expanding indication approvals
  • Favorable reimbursement policies for innovative therapies
  • Patient advocacy and awareness campaigns

Market Barriers:

  • High development and manufacturing costs
  • Stringent regulatory approvals
  • Pricing pressures from payers
  • Competition from alternative therapies and biosimilars

Regulatory Environment and Patents

The patent protection for NDC 60505-4716 grants exclusivity until approximately [year], after which biosimilar or generic entrants could enter, exerting downward pressure on prices.

Regulatory pathways, including data exclusivity periods, orphan drug status, or accelerated approvals, dictate launch timelines and potential market exclusivity extensions.

Key Consideration: The expiration of patent rights will markedly influence future pricing projections and market share dynamics.

Pricing Analysis and Trends

Current Price Benchmarks

Current list and net prices for NDC 60505-4716 vary by region and dispensing setting. In the US, average wholesale prices (AWP) for similar drugs range between USD [X] and USD [Y] per dose or treatment course, depending on formulation and dosing.

Pricing Strategies

Manufacturers often employ value-based pricing, considering factors such as clinical benefits, patient quality of life improvements, and healthcare system savings. List prices tend to be higher initially, with discounts, rebates, and pay-for-performance agreements influencing net prices.

Reimbursement Environment

Reimbursement levels hinge on payer policies, formulary placements, and negotiated discounts. The adoption rate correlates with the drug’s perceived value, side effect profile, and comparative effectiveness.

Price Projection Outlook (Next 5-10 Years)

Short-term (0-3 years)

  • Prices are expected to remain stable or increase modestly, influenced by inflation, manufacturing costs, and initial market share growth.
  • Limited impact from biosimilar competition until patent expiry.

Medium-term (3-7 years)

  • Price reductions anticipated post-patent expiration due to biosimilar entries.
  • Increasing competition could reduce prices by approximately 20-40%, depending on market penetration and regulatory approvals.

Long-term (7-10 years and beyond)

  • Potential for significant price declines, especially if biosimilars or alternative therapies achieve broad adoption.
  • Price stabilization might occur through negotiated discounts, value-based contracts, or new combination therapies.

Forecasting Models: Utilizing current pricing data, historical patent expiry trends, and competitive analyses, future prices could average USD [X] per dose, reflecting a decline of approximately [Y]% over the next decade.

Market Risks and Opportunities

Risks:

  • Regulatory delays or rejections
  • Emergence of superior or more cost-effective therapies
  • Reimbursement reductions and increased price sensitivity
  • Healthcare policy shifts affecting market access

Opportunities:

  • Expanding indications to broader patient populations
  • Strategic partnerships for global distribution
  • Investing in biosimilar development post-patent expiry
  • Leveraging data exclusivity and orphan designations for sustained market presence

Conclusion

The market for NDC 60505-4716 is poised for growth driven by rising disease prevalence and ongoing clinical innovation. However, impending patent expirations pose significant pricing and market share challenges. Strategic positioning, differentiated value propositions, and adaptive pricing approaches will be essential for optimizing revenue streams in this evolving landscape.


Key Takeaways

  • The current market size for the drug is substantial, with future growth contingent upon regulatory approvals and therapeutic adoption.
  • Patent expiration around [year] is likely to precipitate significant price reductions due to biosimilar competition.
  • Short-term pricing stability offers opportunities for revenue maximization, while medium-to-long-term strategies should focus on diversification and cost management.
  • Reimbursement policies and healthcare provider preferences considerably influence the actual realized prices.
  • Continuous monitoring of regulatory developments, competitor activity, and market penetration metrics is critical for accurate forecasting.

FAQs

Q1: When is patent expiration expected for NDC 60505-4716?
A1: Patent expiration is projected around [specific year], post which biosimilars or generics could enter the market, impacting prices.

Q2: How does biosimilar entry affect pricing for this drug?
A2: Biosimilar competition typically leads to a 20-40% reduction in prices, driven by increased market competition and payer negotiations.

Q3: What are the primary factors influencing the drug’s future price?
A3: Patent status, regulatory approvals, competitive landscape, reimbursement policies, and clinical efficacy data.

Q4: Are there opportunities for expanding the drug’s indications?
A4: Yes, regulatory agencies often approve additional indications based on new clinical trial data, which can accelerate revenue growth and offset price declines.

Q5: How do reimbursement policies impact the actual price received by manufacturers?
A5: Reimbursement negotiations, formulary placements, and payer discounts can substantially lower net prices relative to list prices, affecting overall profitability.


Sources:

[1] MarketResearch.com, "Global Pharma Market Trends," 2022.

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