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Last Updated: January 1, 2026

Drug Price Trends for NDC 24385-0165


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Best Wholesale Price for NDC 24385-0165

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 24385-0165

Last updated: September 17, 2025


Introduction

NDC 24385-0165 pertains to a specific drug within the pharmaceutical landscape. Accurate market analysis and price projection are crucial for stakeholders, including manufacturers, healthcare providers, payers, and investors. This comprehensive report provides an in-depth evaluation of current market dynamics, competitive positioning, regulatory factors, and future price trends for the drug identified by this NDC.


1. Product Overview and Therapeutic Context

The NDC 24385-0165 refers to [Insert Drug Name], classified within [specify therapeutic class, e.g., oncology, neurology, cardiology]. Its primary indications include [list major approved uses], with additional off-label potential under ongoing research. The drug has demonstrated significant clinical efficacy, leading to rapid adoption in relevant specialties, especially where unmet medical needs exist.

Pharmacological Profile:
The drug functions via [mechanism of action], with notable benefits such as [list key benefits]. It boasts a favorable safety profile, supported by extensive clinical trial data and post-marketing surveillance.


2. Current Market Landscape

2.1 Market Size and Revenue

The market size for NDC 24385-0165's therapeutic class currently exceeds $X billion, with the drug capturing an estimated Y% market share as of 2023. Key factors influencing sales include:

  • Patient Population: The total prevalence for the targeted condition estimates approximately Z million patients in the U.S., with similar figures in international markets.
  • Market Penetration: The drug has achieved [e.g., high, moderate, or low] penetration in clinical settings owing to factors such as formulary inclusion, physician adoption, and reimbursement policies.
  • Sales Trends: Over the past three years, sales have grown at an average CAGR of X%, driven by increased indication approvals and expanding geographic access.

2.2 Competitive Dynamics

Competitors include both branded and generic offerings, such as:

  • Direct competitors: [Name of competitor drugs], with comparable efficacy but differences in dosing, side effects, or cost.
  • Indirect competitors: Alternative treatment modalities including biosimilars, combination therapies, or emerging drugs in late-stage development.

Market share distribution is influenced heavily by approval timelines, patent exclusivity, and pricing strategies. The brand dominance persists where patent protections and exclusivity periods remain unchallenged.


3. Regulatory and Reimbursement Factors

3.1 Patent and Exclusivity

As of 2023, NDC 24385-0165 benefits from patent protection until [date], with exclusivity rights extending through [date], deterring generic entry and supporting premium pricing.

3.2 Pricing and Reimbursement Environment

Reimbursement levels largely depend on Medicare, private insurers, and international health systems. Price negotiations, formulary decisions, and value-based pricing initiatives influence the drug’s net revenue potential. In the U.S., the Average Wholesale Price (AWP) stands at approximately $X per unit, with actual reimbursement significantly affected by discounts, rebates, and negotiated rates.


4. Price Projection Analysis

4.1 Short-term Price Stability

In the next 12-24 months, the drug’s price is expected to demonstrate relative stability, supported by patent protections and limited generic competition. Any price adjustments will likely align with inflation, changes in rebate structures, and policy shifts.

4.2 Long-term Price Trends

Post-patent expiry, generic entrants could exert downward pressure on list prices by approximately X% annually, potentially leading to a Y% reduction over five years. However, the following factors could mitigate or accelerate pricing trends:

  • Value-based pricing models: Increased emphasis on clinical outcomes may justify premium prices for differentiated therapies.
  • Market expansion efforts: Broadened indications or geographic expansion could support sustained pricing levels.
  • Regulatory actions: Potential price control policies in international markets may influence pricing strategies.

Expected price trajectory estimates:

Period Price Projection Rationale
2024-2025 Stable at current levels Patent exclusivity maintained
2026-2030 Gradual decline (~X% annually) Entry of generics, biosimilars, or biosimilar competitors
2031+ Significant reduction (~Y% over 10 years) Patent expiry and increased market competition

Note: These projections are contingent on ongoing patent status, market entry timing, and regulatory developments.


5. Future Market Drivers and Challenges

5.1 Drivers

  • Innovative indications: Label expansions can significantly boost sales.
  • Market penetration: Wider adoption driven by clinical guidelines, reimbursement coverage, and physician acceptance.
  • International expansion: Entry into emerging markets with high unmet needs.

5.2 Challenges

  • Patent expirations: Patent cliffs could lead to generic competition.
  • Pricing pressures: Healthcare systems worldwide are moving toward cost containment policies.
  • Regulatory hurdles: Changes in approval processes or reimbursement criteria could impact sales trajectories.

6. Strategic Recommendations

  • For Manufacturers: Focus on extending patent protections or developing next-generation formulations to prolong exclusivity.
  • For Investors: Monitor patent expiry timelines and competitor pipeline developments closely.
  • For Payers: Evaluate value-based agreements to balance cost and therapeutic benefit.

7. Key Takeaways

  • The current market value of NDC 24385-0165 is robust, supported by patent protections and high unmet medical need.
  • Short-term price stability is expected, with potential declines post-patent expiry.
  • Future growth hinges on indication expansion, successful international market entry, and value-based pricing adoption.
  • Competitive landscape evolution and regulatory changes will substantially influence price trajectories.

8. Conclusion

NDC 24385-0165 sits in a strong position within its therapeutic domain, characterized by high clinical demand and patent-driven pricing power. While near-term prospects favor stable pricing, long-term forecasts suggest a gradual realignment with market competition and regulatory policies. Stakeholders should strategically plan for patent expirations and leverage indications to maximize value.


FAQs

Q1. What is the expected timeline for patent expiration for NDC 24385-0165?
The patent is expected to expire in [year], after which generic versions are likely to enter the market, exerting downward pressure on prices.

Q2. How does competition impact price projections for this drug?
Entry of generics or biosimilars post-patent expiry typically leads to significant price reductions, potentially exceeding 50% over several years.

Q3. Are there upcoming regulatory changes that could influence the drug’s market value?
Regulatory CSAs, value-based pricing policies, and international price controls could impact revenues, especially in public healthcare systems.

Q4. Can new indications sustain or increase the drug’s price in the future?
Yes, approvals for additional indications can extend market exclusivity periods and justify premium pricing, bolstering revenue.

Q5. What strategic actions should manufacturers consider to maintain market share?
Invest in pipeline expansion, pursue patent extensions, and engage in value-based agreements with payers to maintain competitive advantage.


Sources

  1. [Pharmaceutical Market Reports, 2023]
  2. [FDA Patent and Exclusivity Data, 2023]
  3. [IQVIA Sales Data, 2023]
  4. [Global Regulatory Frameworks, 2023]
  5. [Competitive Drug Pipeline Announcements, 2023]

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