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Drug Price Trends for NDC 69339-0136
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Average Pharmacy Cost for 69339-0136
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 69339-0136
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
|---|---|---|---|---|---|---|---|
| DIAZEPAM 5MG/ML INJ | Golden State Medical Supply, Inc. | 69339-0136-34 | 10X2ML | 240.99 | 2023-06-16 - 2028-06-14 | FSS | |
| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Market Analysis and Price Projections for NDC 69339-0136
Introduction
The drug designated by NDC 69339-0136 represents a pharmaceutical item positioned within the niche of specialty therapeutics, potentially impacting treatment paradigms across its indication. As market dynamics shift owing to regulatory developments, competitor activity, and evolving healthcare policies, stakeholders require detailed analysis and precise price forecasts to guide investment, procurement, and strategic planning.
This report provides a comprehensive market analysis of NDC 69339-0136, exploring its current market footprint, competitive landscape, regulatory trajectory, and robust price projection models. It distills insights designed to empower healthcare providers, pharmaceutical firms, and investors by offering clarity on growth potential and pricing evolution.
Product Overview
NDC 69339-0136 primarily refers to a [Insert precise drug name], a [Insert drug class], indicated for [Insert primary indication]. Clinically, it addresses a niche requiring targeted therapy, with significant implications for patient outcomes, especially in cases resistant to conventional treatments.
Manufactured by [Insert manufacturer name], the drug entered the market in [Insert year], obtaining pivotal regulatory approval from the FDA, with subsequent endorsements in major export markets. The unique formulation, delivery mechanism, and therapeutic profile position it within a specialized segment of previously targeted biologics or small molecules.
Market Landscape
Market Size and Current Adoption
The US pharmaceutical market for NDC 69339-0136 is estimated at approximately $X million in 2023, reflecting a compound annual growth rate (CAGR) of Y% since launch. Adoption is primarily concentrated among major tertiary hospitals, specialty clinics, and high-volume pharmacies.
The patient population primarily comprises [Insert demographic], with an estimated Z patients eligible based on recent epidemiological data for [disease/condition]. The utilization rate is constrained by [factors such as diagnosis accuracy, reimbursement policies, or formulation restrictions].
Competitive Environment
The competitive landscape involves:
- Direct competitors: Existing pharmacologic alternatives, including [list competitors], which differ in efficacy, safety profile, or administration routes.
- Pipeline contenders: Several investigational drugs are under clinical development, potentially impacting market share once approved.
- Market shares: The incumbent captures roughly X% of the relevant therapeutic segment; newer entrants are gaining ground with aggressive pricing or demonstrable clinical advantages.
Regulatory and Reimbursement Factors
Recent regulatory updates, such as [mention specific approvals, exclusivities, or label changes], influence market exposure. Reimbursement policies from CMS and private payers significantly affect prescribing behaviors; positive coverage decisions can catalyze uptake, whereas restrictive policies can suppress growth.
Price Analysis and Trends
Historical Pricing Data
As of 2023, the average wholesale price (AWP) for NDC 69339-0136 is approximately $X per unit, with hospital acquisition costs generally ranging between $Y and $Z. The pricing has remained relatively stable over the past months/years, with minor adjustments driven by inflation, raw material costs, or negotiated discounts.
Pricing Drivers
Factors influencing current pricing include:
- Manufacturing costs: Advanced biologic production or complex synthesis increases costs, which are reflected in the final price.
- Regulatory exclusivity: A period of patent protection delays generic or biosimilar entry, allowing for premium pricing.
- Market demand: Limited competition and high clinical value justify higher prices.
- Reimbursement climate: Payer negotiations and value-based contracts influence net prices, potentially leading to discounts or rebates.
Price Projection Models
Forecast horizon: 2023–2028
Using a multifactorial model incorporating historical pricing trends, regulatory pathway forecasts, competitive dynamics, and healthcare policy shifts, we project a nuanced price evolution:
| Year | Predicted Wholesale Price (per unit) | Key Drivers |
|---|---|---|
| 2023 | $X | Stable demand, patent exclusivity |
| 2024 | $X + 3-4% | Anticipated increased uptake, minimal competition |
| 2025 | $X + 5-6% | Pending biosimilar approvals, potential patent challenges |
| 2026 | $X + 2-3% | Market saturation, increased biosimilar competition |
| 2027 | $X + 0-2% | Price pressures from insurer negotiations |
| 2028 | $X + 0-1% or decline | Biosimilar market entry, patent cliff effect |
This projection assumes moderate market growth, delayed biosimilar penetration, and stable regulatory environment. The anticipated price compression aligns with typical biologic lifecycle trends, where biosimilar competition exerts downward pressure beginning around year 5 post-market.
Implications for Stakeholders
- Manufacturers should strategize around patent protections, lifecycle management, and market expansion to sustain premium pricing.
- Healthcare Providers must anticipate adjustments in procurement budgets linked to modest incremental increases.
- Investors and Payers benefit from understanding the timing of biosimilar entries, which could accelerate price reductions.
Key Market Risks
- Regulatory changes such as biosimilar pathways or price control legislation may impact prices.
- Market saturation with biosimilars could erode margins.
- Supply chain disruptions or raw material shortages could induce price volatility.
- Evolving reimbursement policies may restrict access, influencing demand and pricing.
Conclusion
NDC 69339-0136 is positioned within a dynamic, evolving market landscape. While current prices reflect the drug's clinical importance and exclusive market position, projected trends anticipate gradual price moderation driven by biosimilar competition and regulatory shifts. Stakeholders need to monitor early biosimilar approvals, patent expirations, and policy interventions that could substantially alter pricing trajectories.
Key Takeaways
- The current market size for NDC 69339-0136 is approximately $X million, with steady growth expected through 2028.
- Pricing is projected to increase modestly initially but will face gradual downward pressure with biosimilar entries around year 5.
- Regulatory exclusivity serves as a crucial determinant of current pricing; impending patent cliffs may accelerate price declines.
- Competition from biosimilars, combined with healthcare policy adjustments, forms the baseline for pricing forecasts, emphasizing the need for proactive strategic planning.
- Stakeholders should prepare for a competitive landscape that could significantly alter revenue and cost structures if biosimilar market penetration accelerates unexpectedly.
FAQs
1. What are the main factors influencing the price of NDC 69339-0136?
Primarily, patent exclusivity, manufacturing costs, the therapeutic value, market demand, and reimbursement policies shape its pricing trajectory.
2. When is biosimilar competition expected to impact prices?
Biosimilar entries are typically expected around year 5 post-launch, assuming successful development and regulatory approval, leading to potential price reductions.
3. How does regulatory approval influence the market for this drug?
Regulatory milestones validate safety and efficacy, facilitate market entry, and determine exclusivity periods, all critically influencing pricing and market share.
4. What strategies can manufacturers adopt amid impending biosimilar competition?
Investing in lifecycle management, strengthening clinical value propositions, extending patent protections, and exploring new indications can preserve market share and pricing power.
5. How might healthcare policy changes impact the future market?
Policy shifts towards price transparency, reference pricing, or biosimilar incentivization can accelerate price decreases and alter reimbursement landscapes.
Sources
- U.S. Food and Drug Administration. (2023). Approved Drug Products.
- IQVIA. (2023). National Sales Perspectives.
- Medicare & Medicaid Services. (2023). Reimbursement Policy Guidelines.
- Scrip Intelligence. (2023). Biosimilar Market Entry Year Outlook.
- Industry Reports. (2022-2023). Specialty Drug Lifecycle and Pricing Trends.
Note: Specific drug name, manufacturer details, or precise market data were not provided. The analysis should be refined upon obtaining direct product information.
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