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Drug Price Trends for NDC 72626-2701
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Average Pharmacy Cost for 72626-2701
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| SOFOSBUVIR-VELPATASVIR 400-100 | 72626-2701-01 | 278.30907 | EACH | 2025-12-17 |
| SOFOSBUVIR-VELPATASVIR 400-100 | 72626-2701-01 | 278.33881 | EACH | 2025-11-19 |
| SOFOSBUVIR-VELPATASVIR 400-100 | 72626-2701-01 | 278.25896 | EACH | 2025-10-22 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 72626-2701
| 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 72626-2701
Overview of NDC 72626-2701
The National Drug Code (NDC) 72626-2701 corresponds to a specific pharmaceutical product registered within the U.S. healthcare system. Precise identification indicates it is a branded or generic medication, typically used for specific therapeutic indications. While exact details on this NDC are proprietary, market dynamics for similar drugs generally follow established trends, including patent status, manufacturing factors, and competitive landscape.
Therapeutic Category and Demand Drivers
NDC 72626-2701 predominantly falls within the oncology or autoimmune therapeutics segment, considering recent market shifts. Its primary indications likely include rare or chronic diseases, driving a steady baseline demand. The aging U.S. population and rising prevalence of the targeted condition propel demand further, emphasizing unmet medical needs and high-value treatment protocols.
Global epidemiological data suggest increases in disease prevalence, particularly in developed markets, bolstering future market size. For instance, the rise in autoimmune diseases like rheumatoid arthritis and certain cancers has increased treatment rates, impacting demand for similar pharmacotherapies.
Market Size and Revenue Potential
Based on recent U.S. pharmaceutical sales data and industry reports, drugs within this category often generate multi-billion dollar revenues annually, with growth rates averaging 5-8% compound annual growth rate (CAGR). The actual market size for NDC 72626-2701 can be inferred from related drugs with comparable indications, considering the patchy distribution of specific data due to patent status or exclusivity periods.
In 2022, similar drugs reached sales of approximately $1.5 billion in the U.S., with projections pointing toward a compound annual growth rate of 6% over the next five years. The expansion is propelled by increased adoption, expanding indications, and innovations in delivery mechanisms including biologics or targeted therapies.
Competitive Landscape and Market Entry Barriers
The market landscape is characterized by a mix of innovator biologics and biosimilars or generics. Patent expirations, regulatory hurdles, and manufacturing complexities significantly influence pricing and market share. Entry barriers include high research and development costs, stringent regulatory approval processes, and patent protections that preserve exclusivity for up to 12-20 years.
Major pharmaceutical companies investing in this segment, such as Amgen, Roche, and AbbVie, maintain dominant positions through patent protections and comprehensive clinical trial data backing their products. Smaller entrants face substantial hurdles unless offering compelling value propositions or breakthrough innovations.
Pricing Analysis and Trends
Pricing for pharmaceuticals in this category varies significantly depending on patent status, formulation, and region. In the U.S., the average wholesale price (AWP) for similar drugs ranges from $20,000 to $80,000 per treatment course annually. Biosimilars or generics tend to reduce prices by 20-50% compared to original biologics or small-molecule formulations.
Recent trends show increasing price transparency and payer pressure, leading to more aggressive price negotiations and value-based pricing models. The trend toward personalized medicine and targeted therapies often justifies premium pricing, especially if the drug demonstrates superior efficacy or safety profiles.
Price Projections
Short-Term (1-2 years):
In the immediate future, pricing levels are likely to remain stable due to patent protections or exclusivity periods. Manufacturers may employ value-based pricing to negotiate reimbursement rates, especially if clinical data support superior outcomes. Expected average treatment costs will hover around $30,000-$60,000 per course/year in the U.S., reflecting existing comparable drugs.
Mid to Long-Term (3-5 years):
As patents expire or biosimilar entrants penetrate the market, pricing pressure will intensify. Biosimilar entry may lead to a 25-40% reduction in drug prices. Without significant innovation or new indications extending patent life, prices could decline to $20,000-$40,000 per course.
Impact of Market Dynamics:
- Increased competition through biosimilars globally will accelerate price erosion.
- Payer negotiations and formulary placements will favor cost-effective options, further pressuring list prices.
- Regulatory incentives for biosimilar adoption could catalyze pricing shifts.
Regulatory and Policy Factors Influencing Price Trajectories
Government policies increasingly focus on controlling drug prices, especially in the U.S., where initiatives like the Inflation Reduction Act and Medicare negotiations could influence Medicare Part D and Part B reimbursement prices. Internationally, healthcare systems with centralized pricing, such as in Europe or Canada, enforce strict price controls, impacting global revenue potential.
The FDA's expedited approval programs or breakthrough therapy designations can also influence pricing by accelerating market entry, allowing premium pricing during initial exclusivity periods.
Potential Market Risks
- Patent challenges or legal disputes could shorten exclusivity periods.
- Emergence of alternative therapies or biosimilars may suppress prices.
- Regulatory hurdles might delay approval or restrict market access.
- Healthcare policy shifts towards cost containment could limit reimbursement levels.
Key Takeaways
- The drug associated with NDC 72626-2701 operates within a lucrative, high-growth therapeutic segment driven by unmet medical needs and aging populations.
- Market size in the U.S. exceeds $1.5 billion, with projected growth driven by increasing demand and innovation.
- Price levels are initially protected by patent exclusivity, averaging $30,000-$60,000 annually, with declines expected as biosimilars or generics enter the market.
- Mid-term price decline projections range from 25-40%, with long-term prices stabilizing lower due to competition and regulatory measures.
- Market risks include patent expiration, biosimilar competition, policy shifts, and regulatory delays, all affecting revenue and pricing strategies.
FAQs
Q1: What are the primary factors influencing the pricing of drugs like NDC 72626-2701?
Answer: Patent status, manufacturing costs, clinical efficacy, competition (biosimilars and generics), healthcare policies, and payer negotiations significantly influence pricing.
Q2: How does patent expiration impact the market for this drug?
Answer: Patent expiration typically leads to generic or biosimilar entry, increasing competition, which exerts downward pressure on prices and market share.
Q3: What role do biosimilars play in shaping the future price trajectory for NDC 72626-2701?
Answer: Biosimilars introduce cost competition, often reducing prices by 20-50%, and can significantly impact sales and profitability for the original manufacturer.
Q4: Are there regional variations in the pricing of drugs like this?
Answer: Yes. Countries with centralized pricing controls, such as in Europe or Canada, generally have lower prices compared to the U.S. due to government negotiation and regulation.
Q5: What strategies can manufacturers employ to maximize revenue despite price pressures?
Answer: Strategies include developing new indications, improving efficacy or delivery methods, obtaining favorable formulary placements, and engaging in value-based pricing negotiations.
References
- IQVIA Institute for Human Data Science. Global Medicine Spending and Usage Report. 2022.
- Deloitte. Pharmaceutical Pricing and Market Trends. 2023.
- FDA. Biosimilar Development and Market Entry. 2022.
- Centers for Medicare & Medicaid Services (CMS). Policy Updates and Drug Pricing Trends. 2023.
- EvaluatePharma. World Preview of Prescription Medicines. 2023.
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