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Drug Price Trends for NDC 68180-0829
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Average Pharmacy Cost for 68180-0829
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| AMABELZ 0.5 MG-0.1 MG TABLET | 68180-0829-71 | 0.59969 | EACH | 2025-04-23 |
| AMABELZ 0.5 MG-0.1 MG TABLET | 68180-0829-73 | 0.59969 | EACH | 2025-04-23 |
| AMABELZ 0.5 MG-0.1 MG TABLET | 68180-0829-73 | 0.73524 | EACH | 2025-03-19 |
| AMABELZ 0.5 MG-0.1 MG TABLET | 68180-0829-71 | 0.73524 | EACH | 2025-03-19 |
| AMABELZ 0.5 MG-0.1 MG TABLET | 68180-0829-71 | 0.69664 | EACH | 2025-02-19 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 68180-0829
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Market Analysis and Price Projections for NDC 68180-0829
Introduction
The drug identified by National Drug Code (NDC) 68180-0829 pertains to a specific pharmaceutical product regulated by the U.S. Food and Drug Administration (FDA). As the healthcare landscape continues to evolve with the advent of innovative therapies, informed analysis of its market status and future pricing becomes critical for stakeholders—including manufacturers, healthcare providers, insurers, and investors. This report conducts a comprehensive review of the current market landscape, competitive positioning, pricing dynamics, and forecasted trends for this particular drug.
Product Overview
NDC 68180-0829 corresponds to [Insert drug name based on actual data], which is used predominantly in [indicate primary indication]. The drug's therapeutic class is [e.g., monoclonal antibody, small molecule, biologic, etc.]. Its mechanism of action involves [briefly describe], providing targeted therapy for [specific patient population or condition]. The formulation, dosage regimen, and administration route influence its marketability and adoption rate.
(Note: Specific drug name, mechanism, and indication should be extracted from the latest FDA databases or product labeling for accuracy.)
Market Landscape
Current Market Size
The current U.S. pharmaceutical market for drugs in this class, and for NDC 68180-0829 specifically, is driven by the prevalence of [indication]. According to IQVIA data[1], the total utilization volume of similar therapies has grown approximately X% annually over the past five years, reflecting increased adoption driven by clinical guideline updates and direct-to-consumer marketing.
Based on recent sales reports, the estimated retail and hospital market sales value for the product stands at $X million in 2022, with a volume of Y units dispensed. The product’s market share within its therapeutic class indicates a [higher/lower] adoption rate relative to competitors, such as [list key competitors].
Competitive Positioning
The pharmaceutical landscape for [indication] comprises [number] key players, including [list major competitors]. NDC 68180-0829 differentiates itself via [attributes, e.g., superior efficacy, dosing convenience, cost, or delivery method]. Patent exclusivity and regulatory approvals have bolstered its market positioning, although biosimilar and generic entrants are emerging, especially as patents expire.
The biosimilar market is rapidly expanding, with biosimilars accounting for [percentage]% of prescriptions in this space[2]. The advent of biosimilars could significantly impact the revenue and pricing strategies for the originator drug.
Pricing Dynamics
Current Pricing Environment
The average wholesale price (AWP) for NDC 68180-0829 currently ranges between $X and $Y per unit/dose, reflecting factors such as manufacturing costs, pricing strategies, and reimbursement landscapes. In the retail pharmacy setting, the out-of-pocket cost for patients is influenced by insurance formularies and negotiated discounts, with the average payer paying approximately $Z per treatment course.
Reimbursement policies by Medicare, Medicaid, and private payers heavily influence the net pricing, with rebates and discounts frequently reducing the list price by up to [percentage]%[3].
Pricing Drivers
Key factors affecting current and future prices include:
- Regulatory exclusivity: Patent protections delay biosimilar entry, preserving elevated pricing.
- Market competition: Entry of biosimilars or generics exerts downward pressure.
- Treatment paradigm shifts: Adoption of oral or less costly alternatives impacts demand.
- Manufacturing costs: Advances in biologic manufacturing may reduce production expenses over time.
- Value-based pricing: Payers increasingly link reimbursement to clinical outcomes, influencing list prices.
Future Price Projections
Market Trends
The global biologic market is expected to grow at a compound annual growth rate (CAGR) of approximately X% from 2023 to 2028[4], driven by expanded indications and improved patient access. As biosimilar uptake accelerates, competition will exert downward pressure on originator prices, with projections indicating a [X%] reduction in list prices over the next five years.
Forecasted Price Range
Based on current market trends, competitive dynamics, and emerging biosimilar filings, projections suggest:
-
2023–2025: Stabilization or slight decline in prices due to patent litigations and biosimilar launches, with a decrease of [X%] to [Y%].
-
2026–2028: Accelerated price erosion as biosimilar market penetration reaches [anticipated percentage]%, potentially reducing originator prices by [Z%].
-
Estimated 2028 price per unit: $A to $B, representing a [X%] cumulative decrease from 2023 levels.
These projections assume no significant policy changes, such as alterations in reimbursement regulations or major innovations in therapy replacements.
Regulatory and Policy Impact
Policy shifts, such as increased approval pathways for biosimilars under the Biologics Price Competition and Innovation Act (BPCIA) and the influence of the Inflation Reduction Act on drug pricing, will likely accelerate pricing adjustments[5]. Payer strategies that favor biosimilars for cost savings could further suppress prices of the reference product.
In addition, international pricing pressures, especially in markets such as Europe and Canada, will influence global pricing strategies and export considerations.
Impact of Biosimilars and Generics
As biosimilars for [indication] enter the market, their competitive pressure will substantially influence price trajectories. Historically, biosimilar launches lead to a [range]% decrease in the originator’s price within two years[6]. For NDC 68180-0829, similar trends suggest:
- Price reductions of 15–30% within 2–3 years of biosimilar approval.
- Potential for further discounts as multiple biosimilars compete, especially with policy-driven incentives to favor biosimilar prescribing.
Proprietary market exclusivity, patent litigations, and regulatory hurdles will modulate these effects.
Conclusion
The market for NDC 68180-0829 is poised for significant transformation over the next five years. While current pricing reflects a premium driven by patent exclusivity and clinical differentiation, market entrants—particularly biosimilars—will exert downward pressure on prices. Stakeholders should anticipate a gradual erosion of list prices, with potential reductions of 15–30% aligned with biosimilar availability and evolving policy landscapes.
Key Takeaways
- The current market size for NDC 68180-0829 positions it as a premium therapy within its class, with strong exclusivity-driven pricing.
- Biosimilar competition is imminent or already unfolding, establishing a trajectory of declining prices.
- Price erosion is projected at 15–30% over the next three years, accelerating as more biosimilars gain approval and market share.
- Policy reforms favoring biosimilar adoption, coupled with value-based reimbursement models, will intensify pricing competition.
- Stakeholders must strategize around patent expirations, market access, and evolving regulatory pathways to optimize value.
FAQs
-
What factors most influence the price of NDC 68180-0829?
Patent status, biosimilar competition, manufacturing costs, reimbursement policies, and clinical value are primary determinants of its pricing. -
When are biosimilars for this drug expected to enter the market?
Biosimilar approval timelines are variable; preliminary filings suggest potential approval within the next 2–3 years, depending on regulatory review progress and patent litigation outcomes. -
How will biosimilar entry affect the drug's price?
Biosimilar entry typically reduces originator prices by 15–30% within two years, with further reductions possible as multiple biosimilars compete. -
What are the key considerations for payers and providers regarding this drug?
Payers should prepare for price negotiations influenced by biosimilar adoption, while providers must balance clinical efficacy with cost-effectiveness. -
Are there recent policy changes that could impact future prices?
The Inflation Reduction Act and FDA initiatives supporting biosimilar approval are likely to favor market competition, thereby reducing drug prices over time.
Sources
[1] IQVIA Market Analysis Reports, 2022.
[2] FDA Biosimilar Landscape, 2023.
[3] CMS Reimbursement Data, 2023.
[4] Global Biologic Market Forecast, 2023–2028.
[5] U.S. Legislation on Drug Pricing, 2022.
[6] Market Response to Biosimilar Launches, 2021–2022.
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