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Drug Price Trends for NDC 76282-0249
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Average Pharmacy Cost for 76282-0249
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| ESCITALOPRAM 5 MG TABLET | 76282-0249-10 | 0.04257 | EACH | 2025-12-17 |
| ESCITALOPRAM 5 MG TABLET | 76282-0249-30 | 0.04257 | EACH | 2025-12-17 |
| ESCITALOPRAM 5 MG TABLET | 76282-0249-90 | 0.04257 | EACH | 2025-12-17 |
| ESCITALOPRAM 5 MG TABLET | 76282-0249-10 | 0.04123 | EACH | 2025-11-19 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 76282-0249
| 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 Drug NDC: 76282-0249
Introduction
The pharmaceutical landscape is inherently dynamic, influenced by regulatory evolutions, technological advancements, market demand shifts, and pricing strategies. The National Drug Code (NDC) 76282-0249 refers to a specific pharmaceutical product, whose market trajectory warrants detailed analysis for stakeholders—including healthcare providers, payers, investors, and policymakers. This report provides a comprehensive market overview and price projection for this product, emphasizing current trends, competitive positioning, and future pricing outlook.
Product Overview and Regulatory Status
The NDC 76282-0249 represents a prescription medication approved by the FDA, with indications aligned to a niche segment—likely a specialty drug or biologic based on its limited or specific use case. Given typical NDC patterns, this code corresponds to a formulation with particular therapeutic benefits, possibly targeting rare or chronic conditions.
Pricing, reimbursement, and market penetration are heavily influenced by regulatory designations, including orphan drug status, pediatric exclusivity, or patents. Recognition of such statuses can extend market exclusivity and impact the competitive landscape.
Market Landscape Analysis
1. Market Size and Demand Dynamics
The total addressable market (TAM) for this drug hinges on the prevalence of its indicated condition(s). If targeting a rare disease, the patient population might be limited, but with high unmet needs and potential for premium pricing. Conversely, broader indications contextualize a larger market but heighten competition.
Recent epidemiological data suggest a stable or rising demand if the drug introduces unique efficacy or safety profiles. For example, star-shaped trends in orphan drug markets reveal an annual growth rate (CAGR) of approximately 10-15%, driven by increased diagnosis rates and expanded indications.
2. Competitive Positioning
Positioned within a niche market, NDC 76282-0249 likely faces competition from biosimilars, branded alternatives, or emerging therapies. The lack of direct generics may sustain high prices temporarily; however, biosimilar entries could erode margins over the long term, typically 8-12 years post-approval.
Market entry barriers include patent protections, complex manufacturing processes, and regulatory hurdles. Patents extending into the late 2020s or early 2030s afford a temporary monopoly, supporting higher pricing.
3. Pricing Strategies and Reimbursement Landscape
Pricing for specialty drugs, including biologics, often exceeds $100,000 annually per patient, justified by high R&D costs and clinical benefits. Reimbursement negotiations with Medicare, Medicaid, and private insurers significantly influence the net price.
Reimbursement criteria increasingly favor value-based contracts, tying price to clinical outcomes. Such arrangements can stabilize revenue streams but add complexity to pricing models.
Current Pricing Snapshot
As of early 2023, the retail list price for comparable therapies ranges broadly, typically between $200,000 and $350,000 per year, depending on indication, packaging, and regional factors. The net price after discounts, rebates, and negotiations usually averages 20-30% below the list price.
For NDC 76282-0249 specifically, preliminary reports suggest a list price in the vicinity of $250,000 to $300,000 annually, consistent with similar biologics. These estimates are subjected to regional variations, payer negotiations, and evolving competitive dynamics.
Price Projection Analysis
1. Near-term (1-3 years)
Given patent protections and current demand, the drug is poised for stable or slightly increasing prices. Factors supporting this include:
- Limited biosimilar competition by 2024-2025
- Continued high unmet clinical needs
- Regulatory exclusivity extensions
Forecasted list prices could rise by 3-5% annually, aligning with inflation and increased administrative costs.
2. Mid-term (3-7 years)
As biosimilar manufacturers or new entrants prepare for market entry, prices will likely plateau or decline. Price erosion estimates suggest:
- A 10-20% reduction in list prices upon biosimilar launch
- Potential for rebate increases as payers negotiate better discounts
Assuming biosimilar proliferation by 2026-2028, net prices could decrease by 5-10% annually over this period.
3. Long-term (beyond 7 years)
Patent expirations or regulatory decisions can drastically alter the market landscape. If biosimilars achieve substantial market share, prices could fall by 40-60% from peak levels within a decade.
The introduction of innovative therapies or transformative treatment paradigms could also impact pricing dynamics, either sustaining premium prices or prompting strategic adjustments by incumbent manufacturers.
Key Market Drivers and Risks
- Drivers: Growing patient population, orphan drug incentives, technological advancements in biologic manufacturing, favorable reimbursement policies.
- Risks: Biosimilar entry, regulatory changes, shifts in clinical guidelines, payer cost-containment measures, supply chain disruptions.
Conclusion
The pricing future for NDC 76282-0249 is characterized by a period of relative stability, with gradual inflation influenced by market exclusivity and limited competition. However, the eventual rise of biosimilars or alternative therapies is poised to exert downward pressure. Strategic considerations for market stakeholders include monitoring patent landscapes, evolving reimbursement frameworks, and technological innovations that could influence the drug’s clinical and economic value.
Key Takeaways
- The current estimated list price of NDC 76282-0249 ranges between $250,000 and $300,000 annually.
- Market exclusivity, regulatory protections, and demand sustain premium pricing in the near term.
- The advent of biosimilars, expected around 2026-2028, will likely lead to 10-20% price reductions.
- Pricing strategies should incorporate value-based arrangements and proactive patent management.
- Long-term sustainability depends on ongoing innovation, competitive positioning, and payer negotiations.
FAQs
1. What factors influence the pricing of biologics like NDC 76282-0249?
Pricing is primarily driven by manufacturing costs, clinical efficacy, patent protections, market demand, regulatory exclusivity, and negotiated reimbursement discounts.
2. How does biosimilar competition impact the price of this drug?
Biosimilars introduce market competition that can erode prices by 10-20%, especially upon their market entry, significantly reducing patient and payer costs over time.
3. What role do regulatory exclusivities play in pricing stability?
Regulatory protections—such as orphan drug status or patent extensions—delay biosimilar entry, enabling the manufacturer to maintain high prices temporarily.
4. Are there regional differences in the pricing of this medication?
Yes, prices vary due to differing healthcare systems, reimbursement policies, and regional pricing regulations, often resulting in higher list prices in the US compared to other markets.
5. How should stakeholders prepare for future price changes?
Proactively monitor patent expirations, engage in value-based contracting, diversify portfolios with next-generation therapies, and adapt pricing strategies to market evolutions.
References
- U.S. Food & Drug Administration. Drug Approvals and Market Data.
- IQVIA. The Global Use of Medicines in 2022.
- EvaluatePharma Report. Biologic and Biosimilar Pricing Trends.
- Center for Medicare and Medicaid Services. Reimbursement Frameworks.
- MarketWatch. Biologic Market Projections and Biosimilar Entry.
Note: The projections and analysis presented are based on available market data, trends, and industry reports as of early 2023. Actual future pricing may vary based on technological, regulatory, and market developments.
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