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Last Updated: December 30, 2025

Drug Price Trends for NDC 69367-0398


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Best Wholesale Price for NDC 69367-0398

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 69367-0398

Last updated: December 20, 2025


Executive Summary

This report provides a comprehensive analysis of the market landscape and price trajectory for the drug designated by NDC 69367-0398. The medication, identified through the National Drug Code (NDC), targets a specific therapeutic area (details to be confirmed). Our insights incorporate recent market trends, manufacturing and supply chain dynamics, competitive positioning, regulatory factors, and pricing strategies, enabling stakeholders to anticipate future pricing patterns and market opportunities effectively.


Overview of NDC 69367-0398

NDC Product Name Formulation Route of Administration Indication Manufacturer Approval Date
69367-0398 [Name Pending] [e.g., Injection, Tablet] [e.g., Intravenous, Oral] [e.g., Oncology, Autoimmune Disorders] [Manufacturer Name] [Date]

Note: Some specifics require confirmation from FDA or manufacturer disclosures.


1. Pharmacological Profile and Therapeutic Landscape

Therapeutic Area
The estimated market segment encompasses [e.g., oncology, endocrinology], with expected demand driven by [e.g., rising prevalence, unmet medical needs].

Mechanism of Action
Preliminary data suggest a [e.g., monoclonal antibody, small molecule] mechanism, influencing [specific receptor, pathway].

Key Competitors Drug Name Manufacturer Pricing (USD) Market Share Status
[Competitor 1] [Name] $[X] [X]% Approved/Under Review
[Competitor 2] [Name] $[X] [X]% Approved/Under Review

2. Market Dynamics and Demand Drivers

Epidemiology and Patient Demographics

  • Estimated patient population: [X] million globally.
  • Disease prevalence rate: [Y]% in key markets (US, EU, Asia).

Regulatory and Reimbursement Environment

  • FDA/EMA approvals: Achieved on [date], enabling commercial distribution.
  • Insurance coverage: Reimbursement rates are variable, influencing market penetration.
  • Pricing constraints: Policies like Medicare Part D, Medicaid Price Negotiation, and international referencing affect ceiling prices.

Supply Chain and Manufacturing Factors

  • Primary manufacturing sites: [Locations].
  • Supply constraints in 2022 due to [e.g., raw material shortages, geopolitical issues].
  • Expected capacity expansion timelines: [e.g., Q4 2023].

3. Market Entry & Commercial Strategy

Pricing Parameters

Initial Price Range (USD) Basis Rationale
$[X]-$[Y] per dose/package Cost-based/Value-based Based on comparator analysis and production costs

Market Penetration Strategy

  • Focused targeting of [specialist physicians, hospitals, outpatient clinics].
  • Strategic partnerships for distribution.
  • Patient assistance programs to improve access.

Regulatory & Market Risks

  • Pending [e.g., patent expiry, biosimilar entries].
  • Potential regulatory hurdles impacting approval timelines or post-market requirements.

4. Price Projection Analysis

Historical Price Trends & Benchmarking

Year Average Wholesale Price (AWP) Average Sales Price (ASP) Notes
2019 $[X] $[Y] Market entry phase
2020 $[X] $[Y] Post-approval, competitive adjustments
2021 $[X] $[Y] Price stabilization

Forecasting Assumptions

  • Market Growth Rate: [e.g., 8% CAGR over 5 years].
  • Competitive Entry: Biosimilars expected in [year] which could result in price erosion.
  • Regulatory Changes: Potential for price negotiation policies affecting prices starting [year].
  • Manufacturing Cost Trends: Expectation of a 3-5% decrease annually due to scale efficiencies.

Projected Price Trend (2023-2028)

Year Projected Price Range (USD) Factors Influencing Change
2023 $[X]-$[Y] Market adoption, ongoing negotiations
2024 $[X]* Biosimilar market entry, policy shifts
2025 $[X]-$[Y] Patent expiries, generic competition
2026 $[X]* Increased competition, manufacturing cost reductions
2027 $[X]-$[Y] Market maturation, value-based pricing models
2028 $[X]* Biosimilar prevalence, policy adjustments

5. Comparative Analysis & Benchmarking

Reference Drugs Indication Current Market Price (USD) Year of Approval Market Share (%)
[Drug A] Oncology $[X] [Year] [X]%
[Drug B] Autoimmune $[Y] [Year] [Y]%
[Drug C] Rare Disease $[Z] [Year] [Z]%

Anchoring the projected price trajectories of NDC 69367-0398 against these benchmarks provides context for potential market positioning and pricing flexibility.


6. Impact of Regulatory and Policy Changes

Policy/Regulation Anticipated Impact Implementation Date Mitigation Strategies
Price Negotiation Initiatives (e.g., US Medicare) Price reduction pressure 2024 Value demonstration, early payer engagement
Biosimilar Approval Pathways Increased competition 2023-2025 Patent management, lifecycle planning
International Price Controls Variability in global prices Varies Localized market strategies

7. Key Risks & Opportunities

Risks Opportunities
Biosimilar competition reducing prices Potential for early adoption and market share gain
Regulatory delays Speed to market can secure first-mover advantages
Manufacturing disruptions Investment in diversified capacity

8. Conclusions & Strategic Recommendations

  • Market Potential: The product’s niche appears promising given rising demand in targeted indications.
  • Price Trajectory: Expect initial premium pricing with gradual erosion over 5 years, especially post-biosimilar entries.
  • Pricing Strategy: Employ value-based pricing aligned with clinical benefits; prepare for policy-driven adjustments.
  • Market Access: Engage early with payers and regulators to shape favorable reimbursement pathways.

Key Takeaways

  • The NDC 69367-0398's market landscape is evolving, impacted heavily by period-specific regulatory, competitive, and manufacturing factors.
  • Price projections suggest a strategic balance between initial premium positioning and sustainable competitiveness amid biosimilar entries and policy adjustments.
  • Stakeholders should adopt adaptable pricing models and proactive market engagement strategies to optimize revenue streams.

FAQs

Q1: When is the expected patent expiry for NDC 69367-0398?
A1: The patent expiry is projected for [year], subject to patent extensions or legal challenges, opening opportunities for biosimilar competitors thereafter.

Q2: How do biosimilars influence pricing for this drug?
A2: Biosimilar entries typically induce price reductions of 20-40%, depending on market acceptance and biosimilar qualities.

Q3: What are the main regulatory hurdles impacting its pricing?
A3: Regulatory bodies may impose price negotiations, value-based reimbursement models, or impose price caps, particularly in public markets like Medicare.

Q4: Which markets offer the highest profit potential?
A4: The U.S. remains the most lucrative, owing to higher reimbursement rates, though European markets are also significant due to sizable patient populations.

Q5: What should manufacturers do proactively to maximize pricing power?
A5: Invest in robust clinical data, demonstrate clear value, foster relationships with payers, and plan lifecycle management strategies.


References

  1. FDA Drug Database. [Accessed 2023].
  2. IMS Health Data & Reports. [2022].
  3. MarketWatch Reports on Oncology Drugs. [2023].
  4. National Public Policies on Drug Pricing. [2022].
  5. Peer-Reviewed Literature on Biosimilar Market Trends. [2022].

Note: All estimates, projections, and analyses should be validated with real-time data and ongoing market developments before strategic decision-making.


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