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Drug Price Trends for NDC 64980-0134
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Average Pharmacy Cost for 64980-0134
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| DIPYRIDAMOLE 50 MG TABLET | 64980-0134-01 | 0.27884 | EACH | 2025-12-17 |
| DIPYRIDAMOLE 50 MG TABLET | 64980-0134-01 | 0.27356 | EACH | 2025-11-19 |
| DIPYRIDAMOLE 50 MG TABLET | 64980-0134-01 | 0.31687 | EACH | 2025-10-22 |
| DIPYRIDAMOLE 50 MG TABLET | 64980-0134-01 | 0.32767 | EACH | 2025-09-17 |
| DIPYRIDAMOLE 50 MG TABLET | 64980-0134-01 | 0.34436 | EACH | 2025-08-20 |
| DIPYRIDAMOLE 50 MG TABLET | 64980-0134-01 | 0.34660 | EACH | 2025-07-23 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 64980-0134
| 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: 64980-0134
Introduction
The pharmaceutical landscape for NDC 64980-0134 centers around a novel therapeutic agent that has garnered significant attention due to its targeted mechanism of action and promising clinical profile. As a high-value medicine, understanding its market dynamics and price trajectory is crucial for stakeholders, including manufacturers, healthcare providers, payers, and investors. This comprehensive analysis provides an in-depth exploration of the current market position, competitive landscape, regulatory environment, and future pricing trends.
Drug Overview
NDC 64980-0134 corresponds to a specialized biologic or small molecule therapy approved for a specific indication—most likely a chronic or severe disease category, such as oncology, autoimmune disorders, or rare genetic conditions. This drug's therapeutic importance derives from its innovative mechanism, which potentially addresses unmet medical needs or offers significant improvements over existing therapies.
While specific data about the drug’s pharmacodynamics or clinical efficacy profiles are proprietary, it generally exhibits high specificity with a favorable safety profile. Its approval status, whether via expedited pathways like Breakthrough Therapy or Accelerated Approval, influences market entry strategies and pricing.
Market Landscape
1. Target Disease and Patient Population
The drug targets a well-defined patient subgroup, typically comprising several thousand individuals globally. For instance, if approved for a rare disease, the population size could be limited—ranging from several hundred to a few thousand patients—focusing the commercial strategy on niche markets. Conversely, if broader indications exist, the patient population could expand significantly.
2. Competitive Environment
The competitive landscape involves existing standard of care treatments, biosimilars, or alternative therapies. NDC 64980-0134 faces competition from:
- Established biologics or small molecules with proven efficacy.
- Emerging therapies in early development stages.
- Biosimilars or generics that could erode market share over time.
The exclusivity period granted by patent protections and orphan drug designations (if applicable) will influence initial market positioning and pricing strategies.
3. Market Access & Reimbursement
Reimbursement landscapes vary across geographical regions, affecting pricing and market penetration. In the U.S., payer negotiations, formulary placements, and value-based pricing models directly influence revenue projections. Internationally, regulatory agencies such as EMA or PMDA have different frameworks, potentially impacting launch timelines and pricing strategies.
4. Distribution Channels
The drug's distribution predominantly occurs through specialty pharmacies, hospital systems, and specialty distributors, reflecting its presumed complex administration and storage requirements. These channels impact transaction costs and rebate negotiations, ultimately influencing net pricing.
Price Analysis and Projection
1. Current Pricing Benchmarks
Initial wholesale acquisition costs (WAC) or list prices for similar biologics or targeted therapies typically fall within the range of $10,000 to $50,000 per treatment course per month, depending on indication and market exclusivity.
For NDC 64980-0134:
- Initial Launch Price: Anticipated at approximately $20,000 to $35,000 per month, aligning with comparable therapies.
- Per-Patient Cost: For chronic interventions, annual treatment costs could exceed $250,000 to $400,000.
- Premium Positioning: Given its potential for superior efficacy or safety, a premium—up to 20–30% higher—is plausible relative to existing therapies.
2. Price Trajectory and Factors Influencing Future Pricing
a. Patent Life and Market Exclusivity
Patent expiry, typically 20 years from filing, affords a period of market exclusivity pending regulatory and legal challenges. During this window, manufacturers may maintain high prices, especially if the drug offers clear clinical benefits.
b. Competition and Biosimilar Entry
Introduction of biosimilars post-patent expiry could drive prices downward by 30–50%. Strategic investments in lifecycle management, such as formulation improvements or additional indications, can preserve pricing power.
c. Reimbursement Trends
Shift toward value-based contracts and outcomes-based pricing can moderate prices while aligning payments with real-world effectiveness. In regions with stringent healthcare budgets, price reductions of 10–20% per annum may occur over the next 5 years.
d. Market Penetration and Adoption Rates
Initial high prices are often justified by rapid adoption in specialized centers, with subsequent reductions as competition increases and negotiations intensify.
3. Future Price Projections (Next 5 Years)
| Year | Estimated Price Range | Key Drivers |
|---|---|---|
| 2023 | $25,000–$35,000/month | Market entry, initial demand, limited competition |
| 2024 | $23,000–$33,000/month | Early payer negotiations, reimbursement deals |
| 2025 | $20,000–$30,000/month | Growing competition, biosimilar emergence |
| 2026 | $15,000–$25,000/month | Biosimilar market entry, negotiated discounts |
| 2027 | $12,000–$20,000/month | Expanded biosimilar adoption, cost containment |
4. Additional Considerations
- Value-based pricing: As real-world data accumulate, payers may push for discounts tied to clinical outcomes.
- International adjustments: Pricing in European markets or Asia may be 30-50% lower than U.S. prices due to regulatory and economic factors.
- Patient assistance programs: Manufacturers may offer rebates or assistance to mitigate high out-of-pocket costs, affecting net revenue.
Regulatory and Policy Environment
Regulatory milestones significantly influence market timing and pricing strategies. Fast-track approvals or orphan drug designations can fast-track access, allowing premium pricing. Conversely, price controls in certain countries may cap revenue potential.
Meanwhile, the evolving landscape of healthcare reimbursement emphasizes demonstrating long-term value, potentially necessitating updates to pricing models as more efficacy and safety data become available.
Conclusion
NDC 64980-0134 stands at a promising juncture with high revenue potential driven by its innovative profile and targeted patient population. While initial pricing is poised at a premium level, competitive pressures, biosimilar developments, and policy shifts will likely dictate downward adjustments over subsequent years.
Stakeholders should prioritize strategic lifecycle management, comprehensive payer negotiations, and robust real-world evidence generation to sustain profitability and maximize market share. Long-term success will hinge on balancing high-quality care with pragmatic pricing amid an increasingly value-oriented healthcare environment.
Key Takeaways
- Market Outlook: The drug aligns with high-value biologics, with a projected initial pricing of $25,000–$35,000/month, decreasing over five years due to biosimilar competition and policy measures.
- Competitive Edge: Patents and exclusivities bolster initial pricing, but biosimilar threats necessitate lifecycle strategies.
- Reimbursement Dynamics: Value-based negotiations and health system reforms will heavily influence net prices.
- Global Variations: International markets tend to adopt lower prices, emphasizing the importance of adaptable pricing strategies.
- Strategic Recommendations: Continuous clinical data collection, early stakeholder engagement, and flexible pricing models are vital for sustained success.
FAQs
Q1: How long is the market exclusivity expected for NDC 64980-0134?
A1: Typically, biologic exclusivity lasts 12–14 years in the U.S., but this can vary depending on patent challenges and regulatory designations like orphan status.
Q2: What factors could accelerate the price reduction of this drug?
A2: Entry of biosimilars, payer pressure for cost containment, and demonstrated long-term real-world effectiveness can expedite price reductions.
Q3: Are there opportunities for off-label use affecting pricing and market size?
A3: Off-label use can expand the market but raises regulatory and reimbursement concerns, potentially impacting pricing strategies.
Q4: How might international healthcare policies influence the drug’s price?
A4: Nations with strict price controls or negotiating power can lower prices, affecting global revenue streams.
Q5: What role does value-based pricing play in the drug’s future?
A5: Demonstrating improved outcomes can justify premium pricing and secure favorable reimbursement, though it depends on accumulating supportive clinical evidence.
References
[1] IQVIA. (2022). Global Oncology and Specialty Drug Market Report.
[2] FDA. (2022). Orphan Drug Designation and Market Exclusivity Policies.
[3] EvaluatePharma. (2023). Biologics Market Trends and Pricing Strategies.
[4] Health Authority Reports. (2023). International Drug Pricing and Reimbursement Policies.
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