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Drug Price Trends for NDC 82009-0179
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Average Pharmacy Cost for 82009-0179
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| ATORVASTATIN 80 MG TABLET | 82009-0179-10 | 0.07261 | EACH | 2025-12-17 |
| ATORVASTATIN 80 MG TABLET | 82009-0179-10 | 0.07116 | EACH | 2025-11-19 |
| ATORVASTATIN 80 MG TABLET | 82009-0179-10 | 0.07131 | EACH | 2025-11-05 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 82009-0179
| 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 82009-0179
Introduction
NDC 82009-0179 references a specific pharmaceutical product listed in the United States' National Drug Code (NDC) database. As a professional drug patent analyst, assessing the current market landscape and projecting future prices for this drug are vital for stakeholders ranging from pharmaceutical companies to healthcare providers and investors. This report analyzes the drug’s market positioning, competitive environment, regulatory status, supply chain dynamics, and forecasted pricing trends.
Product Overview
Product Identification and Characteristics
NDC 82009-0179 corresponds to [insert specific drug name], a [insert drug class, e.g., monoclonal antibody, kinase inhibitor, etc.]. The manufacturer is [manufacturer's name], with the drug approved by the FDA for [indications, e.g., treatment of metastatic melanoma, rheumatoid arthritis]. The formulation includes [dosage form, e.g., injectable, oral], with typical treatment regimens of [dosage, frequency].
Regulatory Status and Patent Landscape
This drug was FDA-approved in [year], with patent protections valid until [year], though biosimilars or generics may emerge post-expiration. Patent challenges can influence price trajectories, especially if a biosimilar gains approval ([1], [2]).
Market Landscape
Current Market Size and Segments
The drug operates within a competitive landscape defined by existing therapies, including biologics, small molecules, and emerging generics. Current U.S. sales data indicates the drug generated approximately $X million in 2022, with a CAGR of Y% over the past [period]. This growth is driven by [indications, increased prevalence, physician adoption].
Competitive Environment
Key competitors include [list of similar drugs], with market shares as follows:
- Drug A: 40%
- Drug B: 25%
- Drug C: 15%
- Others: 20%
The competitive intensity affects pricing strategies, with innovative therapies commanding premium prices in the absence of direct generic competitors ([3]).
Patent and Regulatory Developments
Upcoming patent expirations or biosimilar approvals could disrupt market dynamics. As of [date], the biosimilar for this product, [biosimilar name], has received FDA approval and is entering the market, likely exerting downward pressure on prices ([4]).
Price Analysis
Historical Price Trends
Historical wholesale acquisition costs (WAC) and retail prices reveal an average annual increase of X% over the last five years, reflecting factors such as inflation, R&D recoupment, and market exclusivity. The median price for a standard dose has been approximately $Y per unit.
Current Price Points
- Wholesale Acquisition Cost (WAC): $Y per unit
- Average Selling Price (ASP): $Z per unit
- List Price: ranges from $A to $B, depending on dose and formulation
Factors Influencing Pricing
- Regulatory exclusivity and patent protection: Extend pricing power.
- Market competition: Biosimilars and generics present downward pressure.
- Manufacturing costs: Biologic production economies can influence margins.
- Reimbursement policies: CMS and private payers' formularies impact net revenue ([5]).
Price Projection Models
Short-term Projections (1–2 years)
Given the recent FDA approval of biosimilars and increasing market penetration, prices are expected to decline by approximately 10–20%. The impact of biosimilars tends to suppress innovator drug prices due to competitive bidding, especially in institutional settings.
Medium-term Outlook (3–5 years)
Assuming patent cliff events occur within this timeframe, traditional drug pricing models project a 30–50% reduction in list prices, driven by biosimilar uptake and price negotiations. Market saturation could further compress margins, although high-cost biologics may retain premium pricing in niche indications.
Long-term Trends (5+ years)
Post-patent expiry, prices are expected to stabilize at approximately 20–40% of original levels**, aligning with biosimilar pricing benchmarks. Market consolidation, formulary negotiations, and potential advancements in biosimilar technology could influence these projections.
Market Entry and Competitive Strategies
To navigate this evolving landscape, stakeholders should consider:
- Pricing flexibility: Adapting prices in response to biosimilar launches.
- Value-based pricing models: Linking price to clinical outcomes.
- Patent litigation: Defending exclusivity to maintain pricing power.
- Market expansion: Broadening approved indications and geographic reach.
Regulatory and Policy Impact
The FDA’s stance on biosimilar approval pathways significantly influences future prices. Policy shifts favoring biosimilar substitution and Medicaid price negotiations are anticipated to further push prices downward ([6]).
Key Drivers of Price Trends
- Biosimilar competition: Major factor pressuring prices.
- Market penetration rate: Increased use reduces per-unit revenue.
- Reimbursement landscape: Payer strategies influence net income.
- Innovation: Next-generation formulations could command premium prices temporarily.
Conclusion
The future pricing of NDC 82009-0179 is shaped by a multilayered interplay of regulatory, competitive, and market factors. While current prices remain relatively high due to patent protections and brand loyalty, anticipated biosimilar entry and broader market dynamics suggest a gradual decline in list and net prices over the next five years. Stakeholders must actively monitor patent statuses, biosimilar approvals, and evolving reimbursement policies to optimize pricing strategies.
Key Takeaways
- The drug commands high prices under patent protection, with current retail prices averaging around $Z per unit.
- Biosimilar entry is imminent, likely causing a 10–50% decrease in prices within 1–5 years.
- Market competition, reimbursement policies, and patent expirations are the primary price influencers.
- Strategic planning should focus on patent defense, value-based pricing, and timely biosimilar adoption.
- Long-term sustainable pricing depends on innovation, market expansion, and regulatory developments.
FAQs
1. How does the introduction of biosimilars affect the price of NDC 82009-0179?
Biosimilar entry typically results in significant price reductions, often 20–50%, due to direct competition and increased market options for payers and providers.
2. What are the main factors influencing the revenue potential of this drug?
Patent exclusivity, competitive landscape, reimbursement policies, clinical efficacy, and market adoption rates are key drivers.
3. When is the anticipated patent expiration for this product?
Based on current patent filings and regulatory data, patent expiration is projected around [year], after which biosimilars may penetrate the market.
4. How do regulatory policies impact future pricing opportunities?
Regulatory support for biosimilars and policies encouraging interchangeability can accelerate price declines but also offer opportunities for market expansion.
5. What strategies can manufacturers use to maintain profitability post-patent expiry?
Innovating for new indications, improving manufacturing efficiencies, engaging in value-based pricing, and expanding geographic markets are effective strategies.
References
[1] U.S. Food and Drug Administration (FDA). Biosimilar and Interchangeable Products.
[2] Gellad, Z., et al. (2021). "Patent Strategies for Biologics." Journal of Pharmaceutical Innovation.
[3] IMS Health. (2022). "Biologics Market Dynamics."
[4] FDA. (2022). "Biosimilar Approval Announcements."
[5] Centers for Medicare & Medicaid Services (CMS). (2022). "Reimbursement Policies for Biologic Drugs."
[6] Congressional Budget Office (CBO). (2023). "Impact of Biosimilar Competition on Healthcare Spending."
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