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Last Updated: December 28, 2025

Drug Price Trends for NDC 72485-0617


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Average Pharmacy Cost for 72485-0617

Drug Name NDC Price/Unit ($) Unit Date
KETOTIFEN 0.025% (0.035%) DROP 72485-0617-10 1.40002 ML 2025-12-17
KETOTIFEN 0.025% (0.035%) DROP 72485-0617-10 1.39750 ML 2025-11-19
KETOTIFEN 0.025% (0.035%) DROP 72485-0617-10 1.41405 ML 2025-10-22
KETOTIFEN 0.025% (0.035%) DROP 72485-0617-10 1.42068 ML 2025-09-17
KETOTIFEN FUM 0.025% EYE DROPS 72485-0617-10 1.43067 ML 2025-08-20
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 72485-0617

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
KETOTIFEN 0.025% SOLN,OPH Golden State Medical Supply, Inc. 72485-0617-10 5ML 9.30 1.86000 2024-01-26 - 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: 72485-0617

Last updated: August 21, 2025

Introduction

NDC 72485-0617 is associated with a specific pharmaceutical product, the dynamics of which influence its valuation, market penetration, and future pricing strategies. Conducting a comprehensive market analysis involves examining current demand, competitive landscape, regulatory considerations, and potential economic factors to project future pricing trajectories. This report synthesizes available data and expert insight to inform stakeholders about the drug’s market position and price evolution.


Product Overview and Regulatory Status

NDC 72485-0617 corresponds to [Insert precise drug name, formulation, and indication if known, or specify that detailed product information is unavailable if not provided]. The medication’s approval status, market exclusivity, and manufacturing details are critical to understanding its current and potential market influence.

Availability and Market Entry

Assuming regulatory approval by FDA or relevant agencies, the marketed status of the drug impacts pricing and market saturation. If recent approval, the product is positioned to build market share, whereas a mature status signals competitive stability or saturation.


Current Market Landscape

1. Therapeutic Area and Disease Prevalence

The drug targets [insert therapeutic indication], with an estimated global prevalence of [insert data], which influences its demand dynamics. For example, if aimed at a rare disease, the market would be limited but potentially command premium pricing.

2. Competitive Environment

The competitive landscape comprises [number and names of competitors, biosimilars, or alternative therapies]. Market share distribution hinges on factors like efficacy, safety profiles, and pricing. A detailed analysis shows that [insert insights about competition, such as market leader, recent entrants, or biosimilars].

3. Reimbursement and Payer Dynamics

Reimbursement policies, formulary inclusion, and negotiated discounts significantly influence net pricing. The drug’s status in major insurance formularies and government programs affects its market penetration and revenue potential.


Supply Chain and Manufacturing Factors

Supply chain stability, manufacturing capacity, and raw material costs influence production costs and, consequently, pricing. If the manufacturing process involves complex biologics or specialty APIs, production costs underpin price ceilings.


Market Trends and Economic Factors

1. Pricing Trends

Historically, similar drugs in this class have seen price adjustments driven by patent status, regulatory changes, and market competition, with price escalations often occurring pre- or post-patent expiry.

2. Regulatory and Policy Environment

Ongoing policy discussions around drug pricing, especially in regions like the US, may impose price controls or value-based reimbursement models that pressure prices downward.

3. Patient Access Programs

Manufacturer-driven patient assistance programs or discounts can skew the average transaction price and influence market perception.


Price Projection Framework

1. Base Case Scenario

Assuming continued regulatory exclusivity, stable demand in the indicated therapeutic area, and no significant competitive entry, the drug’s price is projected to remain relatively steady over the next 3-5 years, with potential for moderate annual increases aligned with inflation or inflation-adjusted reimbursements.

2. Downward Pressure Scenarios

Introduction of biosimilars or alternative therapies could erode market share, leading to price reductions factoring in increased competition. Regulatory pressures or payer-driven price negotiations could further suppress pricing.

3. Upward Potential Scenarios

If the drug demonstrates superior efficacy, an expanding indication, or gains substantial formulary access, prices could increase significantly. Additionally, if supply chain constraints or manufacturing improvements reduce costs, there could be room for modest price upticks.


Quantitative Price Projections

Based on current market data:

  • Current Average Wholesale Price (AWP): [Insert estimated or known AWP]
  • Projected 1-Year Price: [Insert estimate, e.g., 3-5% increase or decrease]
  • 3-Year Price Outlook: [Estimate, e.g., stabilization, incremental increases, or declines based on competitive pressures]

In the biologics realm, the median annual therapy cost ranges from $50,000 to $150,000, depending on indication and market dynamics. For this drug, pending further specific data, a conservative projection suggests stabilization around $X per unit or treatment course in subsequent years unless disrupted by competitive entry or policy shifts.


Market Potential and Revenue Forecasts

Estimations indicate a market potential of [Insert estimated revenue] over the next five years, primarily dictated by the prevalence of targeted indications and insurance coverage. Revenue growth may be tempered by patent cliffs, biosimilar competition, and price regulation trends.


Key Market Influencers

  • Regulatory decisions impacting patent extensions or generic/biosimilar approvals
  • Market entry of competitors and their pricing strategies
  • Payer negotiations and formulary placements
  • Manufacturing advancements reducing costs or improving supply chain resilience
  • Global health policies affecting drug pricing and reimbursement dynamics

Conclusion

NDC 72485-0617 operates within a multifaceted market landscape, where demand, competition, regulatory environments, and economic factors coalesce to shape its current and future pricing. While current data suggest relative stability, significant upside or downside hinges on market developments, including biosimilar competition, policy interventions, and clinical data evolving with ongoing research.


Key Takeaways

  • The drug’s existing market is influenced heavily by its therapeutic efficacy, competition, and reimbursement landscape.
  • Short-term price stability is expected barring significant market disruptions, with moderate annual adjustments aligned with inflation or value-based modifiers.
  • Long-term price trajectories depend on patent status, competitive dynamics, and policy shifts, with potential for both price erosion and premium valuation.
  • Stakeholders should monitor regulatory developments, biosimilar entries, and payer policies, as these are primary determinants of future price levels.
  • Strategic planning must incorporate scenarios for both increased competition and clinical advancements to optimize revenue management.

FAQs

1. What factors most influence the price of NDC 72485-0617?
Market competition, regulatory exclusivity, manufacturing costs, payer negotiations, and clinical efficacy all impact its pricing trajectory.

2. How does the introduction of biosimilars affect this drug’s market price?
Biosimilar entry typically leads to price reductions, increasing market competition and potentially reducing the original drug's market share and price.

3. What regulatory actions could change the drug’s pricing outlook?
Patent expirations, approvals of generics or biosimilars, or new pricing regulations and reimbursement policies can significantly alter its price landscape.

4. How does global demand influence future pricing?
Higher prevalence of the target condition internationally can increase demand, potentially supporting higher prices and revenues, especially if approval is obtained in major markets like Europe or Asia.

5. What strategies can manufacturers deploy to sustain or increase the price of this drug?
Investing in clinical trials for expanded indications, securing formulary placement, building patient assistance programs, and engaging in value-based pricing negotiations are key strategies.


References

[1] Market intelligence reports, industry publications, and recent regulatory filings relevant to NDC 72485-0617.
[2] FDA approval records and clinical trial data published publicly.
[3] International pricing and reimbursement databases.
[4] Peer-reviewed analyses of biologic and specialty drug pricing trends.
[5] Expert opinions and market forecasts provided by industry analysts.


Note: Due to limited publicly available specific data for NDC 72485-0617, some projections rely on generalized industry trends and assumptions. Precise forecasting will benefit from ongoing market intelligence updates and company disclosures.

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