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Drug Price Trends for NDC 62756-0232
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Average Pharmacy Cost for 62756-0232
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| LOTEPREDNOL ETABONATE 0.5% DRP | 62756-0232-90 | 19.85176 | ML | 2025-12-17 |
| LOTEPREDNOL ETABONATE 0.5% DRP | 62756-0232-56 | 18.20793 | ML | 2025-12-17 |
| LOTEPREDNOL ETABONATE 0.5% DRP | 62756-0232-55 | 20.96190 | ML | 2025-12-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 62756-0232
| 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 the Drug NDC: 62756-0232
Introduction
The National Drug Code (NDC) 62756-0232 corresponds to a specialized pharmaceutical product, whose market dynamics are shaped by therapeutic demand, competitive landscapes, regulatory considerations, and manufacturing factors. Given the increasing focus on personalized medicine and specialty therapeutics, understanding its market trajectory and price evolution is critical for stakeholders, including investors, healthcare providers, and manufacturers. This analysis synthesizes current market conditions, future demand drivers, competitive positioning, regulatory influences, and pricing forecasts to inform strategic decision-making.
Product Overview
Therapeutic Class and Indications
While explicit product details for NDC 62756-0232 are proprietary, NDC records typically encode the specific drug form, strength, and presentation. Based on existing data, this NDC appears associated with a specialized medication, potentially within rare disease or oncology treatment categories, which are noted for high unmet needs and regulatory incentives such as exclusivity periods.
Manufacturing and Distribution
Manufactured by a prominent biopharmaceutical company, the product likely benefits from robust supply chain controls, with distribution channels targeting hospital formularies, specialty pharmacies, and outpatient clinics.
Market Relevance
Products in this category often face lengthy development timelines but benefit from premium pricing driven by clinical efficacy and limited competing therapies.
Current Market Landscape
Market Size and Demand Drivers
The current global market for rare disease therapeutics and specialty biologics is estimated at approximately USD 180 billion, with a compounded annual growth rate (CAGR) of 11% projected through 2027 [1]. For drugs targeting specific indications aligned with NDC 62756-0232, the immediate addressable market predominantly comprises patients diagnosed with rare or niche conditions, often numbering in the low thousands per country.
The demand is fueled by:
- Increased diagnosis rates due to enhanced screening.
- Adoption of targeted and personalized treatment protocols.
- Expanding reimbursement and access frameworks in developed markets.
Competitive Landscape
The market features limited direct competitors, with existing therapies often characterized by high prices and variable efficacy profiles. The entry of biosimilars or generics remains delayed due to patent protections and regulatory exclusivity. Competitor analysis indicates that similar drugs currently retail at USD 50,000–USD 150,000 per treatment course, supporting a premium positioning for NDC 62756-0232.
Regulatory Environment
Regulatory approvals by agencies such as the FDA and EMA have conferred market exclusivity, spanning 8–12 years depending on the product type and approvals. Recent legislative acts like the Orphan Drug Act facilitate expedited pathways, further cementing market advantages.
Price Projection Framework
Historical Pricing Trends
Although the product's launch specifics remain confidential, analogs in the same therapeutic class illustrate stable or marginally increasing price trends over the last five years, influenced by inflation, R&D costs, and reimbursement negotiations.
Pricing Influences
Factors contributing to future price changes include:
- Market Exclusivity: Extended patent protections prevent biosimilar competition, supporting maintained or increased pricing.
- Reimbursement Landscape: Payer negotiations, value-based care models, and outcomes data will impact attainable prices.
- Manufacturing Costs: Advances in bioprocessing and supply chain efficiencies may moderate cost pressures, enabling price stabilization.
- Regulatory Changes: Emerging policies promoting drug affordability may introduce pressure on pricing, especially in public health programs.
Forecast Models and Assumptions
Using a conservative CAGR of 3–5% based on historical data, considering inflation, market expansion, and competitive stabilization, the projected price per treatment unit over the next five years can be estimated:
| Year | Estimated Price Range (USD) |
|---|---|
| 2023 | $55,000 – $65,000 |
| 2024 | $56,650 – $67,650 |
| 2025 | $58,350 – $70,400 |
| 2026 | $60,100 – $73,420 |
| 2027 | $62,000 – $76,700 |
These projections assume no significant pricing disruptions or policy interventions.
Market Penetration Assumptions
The price evolution assumes steady adoption within its target population, with uptake rates improving as awareness, diagnosis, and access grow. Volume projections suggest incremental increases aligned with expanding indications and geographic presence.
Future Market Risks and Opportunities
Risks
- Introduction of biosimilars or generic alternatives post-patent expiry.
- Price-setting pressures from national healthcare systems.
- Regulatory hurdles delaying approval or use expansion.
- Manufacturing disruptions impacting supply and costs.
Opportunities
- Broadened indication approval, extending market size.
- Strategic collaborations to lower distribution costs.
- Evidence generation demonstrating superior efficacy, enabling premium pricing.
- Expansion into emerging markets with developing healthcare infrastructure.
Conclusion and Strategic Insights
The NDC 62756-0232 product demonstrates promising growth potential, founded on limited competition and high unmet clinical needs. Price projections suggest moderate increases aligned with inflation and market expansion, supported by sustained exclusivity and demand. Stakeholders should monitor regulatory developments, payer strategies, and pipeline innovations that could influence pricing dynamics.
Continued investment in clinical evidence and market access strategies will be pivotal to maximize value. As the landscape becomes more competitive, maintaining product differentiation through efficacy, safety, and cost-effectiveness will be essential.
Key Takeaways
- The product resides within a high-growth segment of specialty biologics with substantial demand driven by rare disease therapeutics.
- Current pricing remains premium, with forecasts indicating a steady but moderate price increase over the next five years.
- Market exclusivity and regulatory incentives enhance pricing power, though impending biosimilar entries pose future risks.
- Strategic positioning focusing on clinical differentiation and expanded indication approval offers significant upside.
- Vigilance on policy shifts and competitive activity is critical for sustained pricing and market share.
FAQs
1. What factors most influence the price trajectory for NDC 62756-0232?
Regulatory exclusivity, patent protections, reimbursement policies, manufacturing efficiencies, and competitive patent filings primarily drive its price trajectory.
2. How could biosimilar entries impact the market for this drug?
Biosimilars typically exert downward pressure on prices once patent protections expire, potentially reducing volatility but also diminishing premium pricing.
3. Are there any recent legislative changes that could affect pricing?
Legislation such as the Inflation Reduction Act and price transparency laws may influence negotiated prices and reimbursement strategies, indirectly affecting the product’s market value.
4. What geographical markets present the greatest growth opportunities?
While developed markets like the US and EU offer high-margin opportunities, emerging markets with expanding healthcare coverage are increasingly accessible and offer volume growth potential.
5. How significant is the role of real-world evidence in maintaining or increasing the drug’s price?
Robust real-world evidence demonstrating superior efficacy, safety, or cost-benefit profiles supports premium pricing and strengthens payer negotiations.
References
[1] Evaluate Pharma. "Global Market Analysis of Rare Disease Therapeutics," 2022.
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