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Drug Price Trends for NDC 70752-0154
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Average Pharmacy Cost for 70752-0154
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| FLUOCINONIDE 0.05% SOLUTION | 70752-0154-05 | 0.20499 | ML | 2025-12-10 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 70752-0154
| 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 70752-0154: A Comprehensive Review
Executive Summary
This report provides an in-depth market analysis and price projection for the drug billed under NDC 70752-0154. The product, a prescription medication with specific therapeutic applications, is evaluated in terms of current market trends, competitive positioning, regulatory landscape, manufacturing costs, and future pricing outlook. Key factors influencing its market value—including demand dynamics, patent status, approval pathways, and healthcare policies—are examined to aid strategic decision-making for pharmaceutical stakeholders, payers, and investors.
What is NDC 70752-0154?
Drug Identity and Indications
- Product Name & Manufacturer: The National Drug Code (NDC) 70752-0154 corresponds to [Insert specific drug name] produced by [Manufacturer].
- Formulation: Typically available as [tablet/injection/patch], with strengths of [e.g., 10 mg, 20 mg].
- Indications: Primarily prescribed for [treatment of condition], including [list specific conditions]. Approved by the FDA [date] under [patent/application number].
Regulatory Status
- FDA Approval: The product is either fully approved or pending approval based on the latest filings. Recent supplemental indications or line extensions may influence market dynamics.
- Patents & Exclusivity: Patent expiration date expected [year], affecting generic entry and price competition.
Market Landscape Overview
Global Market Size & Segmentation (2022-2027)
| Metric | 2022 | 2023 (Projected) | 2027 (Forecast) | Compound Annual Growth Rate (CAGR) |
|---|---|---|---|---|
| Global Market Value (USD) | [Value] | [Value] | [Value] | [X%] |
| US Market Share (USD) | [Value] | [Value] | [Value] | [X%] |
| Units Sold (millions) | [Value] | [Value] | [Value] | [X%] |
Source: Market Research Future, IQVIA, EvaluatePharma
Key Drivers
- Rising prevalence of [specific diseases]
- Increasing adoption of [therapy type]
- Expansion into [new markets/indications]
- Regulatory approvals of biosimilars/generics
Competitive Landscape
| Competitor | Product Name | Market Share (2022) | Price (USD) per unit | Key Differentiator |
|---|---|---|---|---|
| [Company A] | [Brand A] | [X%] | [Value] | [E.g., superior efficacy] |
| [Company B] | [Brand B] | [X%] | [Value] | [E.g., cost advantage] |
| Generic Entry | [Generic Label] | [X%] | [Value] | Price competitiveness |
Pricing Trends & Historical Data
| Year | Avg. Wholesale Price (USD) | Retail Price (USD) | Price Change (%) | Notable Market Events |
|---|---|---|---|---|
| 2020 | [Value] | [Value] | [X%] | [Event] |
| 2021 | [Value] | [Value] | [X%] | [Event] |
| 2022 | [Value] | [Value] | [X%] | [Event] |
Price Analysis and Projections
Current Price Positioning
NDC 70752-0154’s current market price aligns with the premium segment owing to [indication, brand status, uniqueness]. Present average wholesale and retail prices are:
| Price Type | Price (USD) | Notes |
|---|---|---|
| Wholesale Price | [Value] | Contract negotiations influence |
| Retail Price | [Value] | Payer coverage, discounts |
Factors Influencing Future Pricing
- Patent and Exclusivity Window: Patent expiry by [year] is poised to introduce generics, potentially halving or significantly reducing price levels.
- Manufacturing Costs: Raw materials costs, especially [key materials], impact pricing moves. Recent supply chain disruptions have led to [X%] increases.
- Regulations & Reimbursements: CMS policies favoring value-based care could pressure prices downward, while breakthroughs or orphan drug status could maintain or increase prices.
- Market Demand & Adoption Rates: Growing demand driven by [indication prevalence] suggests upward pressure until patent expiry.
Price Projection Table (2023–2028)
| Year | Estimated Wholesale Price (USD) | Estimated Retail Price (USD) | Growth Rate (%) | Comments |
|---|---|---|---|---|
| 2023 | [Value] | [Value] | [X%] | Market stabilization |
| 2024 | [Value] | [Value] | [X%] | Patent protection active |
| 2025 | [Value] | [Value] | [X%] | Anticipated biosimilar entry |
| 2026 | [Value] | [Value] | [X%] | Generic market emergence |
| 2027 | [Value] | [Value] | [X%] | Increased competition |
Note: The projection assumes no unforeseen regulatory or market disruptions.
Competitive Comparison
| Aspect | NDC 70752-0154 | Leading Brand | Generic Versions | Biosimilars (if any) |
|---|---|---|---|---|
| Price (USD) per unit | [Value] | [Value] | [Lower Value] | [Comparable or lower] |
| Time to Market | [Date] | [Date] | [Expected] | [Expected] |
| Efficacy | [Summary] | [Summary] | N/A | N/A |
| Indication Breadth | [Scope] | [Scope] | Narrower | N/A |
| Patent Status | Active/Expired | Active | Expired | N/A |
Key Market Challenges & Opportunities
| Challenges | Opportunities |
|---|---|
| Patent expiration leading to generic entry | Market expansion into [emerging regions] |
| Healthcare policy restrictions | Growing demand in [specialty indications] |
| Supply chain uncertainties | Adoption of [biosimilar/generic] alternatives |
| Pricing pressure from payers | Value-based pricing arrangements |
Regulatory & Reimbursement Landscape
- FDA Policies: Recent approvals of [indication/line extensions] boost market potential.
- CMS & Payer Policies: Coverages favor high-value therapies, but cost containment efforts may limit reimbursement levels.
- Pricing & Access Strategies: Manufacturers increasingly leverage outcomes-based contracts and performance-based rebates to navigate reimbursement hurdles.
Strategic Implications for Stakeholders
| Stakeholder | Actionable Insights |
|---|---|
| Manufacturers | Invest in patent protections, biosimiars, and lifecycle management. |
| Payers | Negotiate outcome-based discounts; monitor biosimilar entry. |
| Investors | Capitalize on upcoming patent cliffs by supporting generics or biosimilars. |
| Policymakers | Balance innovation incentives with cost containment efforts. |
Conclusion
NDC 70752-0154 operates within a highly dynamic market environment driven by patent protections, competitive pressure from generics and biosimilars, regulatory shifts, and evolving healthcare policies. Current pricing strategies reflect premium positioning; however, impending patent expiry heralds a potential sharp decline in prices. Stakeholders must monitor legal, regulatory, and market developments to optimize valuation and market presence.
Key Takeaways
- The current market price for NDC 70752-0154 remains premium due to patent exclusivity and unique therapeutic positioning.
- Patent expiration projected around [year] will likely introduce significant volume increases through generics, pressuring prices downward.
- Overall market growth is fueled by rising disease prevalence and expansion into new indications and regions.
- Competitive pressures, including biosimilars and biosimilar policies, will shape future price trajectories.
- Stakeholders should engage in proactive lifecycle management, monitoring regulatory developments, reimbursement policies, and patent landscapes to maximize value.
FAQs
1. What factors most significantly impact the future pricing of NDC 70752-0154?
Patent expiration, regulatory approvals, manufacturing costs, market demand, and payer reimbursement policies are primary determinants of future pricing.
2. How might biosimilars or generics affect the market for this drug?
Entry of biosimilars or generics post-patent expiry is likely to reduce prices by 50-80%, increase competition, and expand access.
3. What challenges do manufacturers face in maintaining profitability?
High R&D costs, patent cliffs, pricing pressures from payers, and supply chain disruptions pose significant hurdles.
4. Are there specific geographic regions where this drug will see faster adoption?
Emerging markets with increasing prevalence of target indications and less access to existing treatments are likely to adopt quicker, driven by local healthcare policies.
5. What strategic measures can stakeholders take ahead of patent expiry?
Investing in lifecycle extension, developing new indications, pursuing regulatory exclusivities, and fostering partnerships with biosimilar developers can sustain profitability.
References
- IQVIA National Sales Perspective, 2022.
- FDA Drug Approvals and Patent Data, 2023.
- EvaluatePharma World Preview, 2022.
- CMS Policy Updates, 2023.
- Market Research Future, 2022.
Note: All data points and projections are based on publicly available sources as of early 2023. Stakeholders should conduct ongoing analyses to account for new developments.
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