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Drug Price Trends for NDC 71288-0726
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Average Pharmacy Cost for 71288-0726
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| BUPIVACAINE 0.5% VIAL | 71288-0726-52 | 0.08192 | ML | 2025-11-19 |
| BUPIVACAINE 0.5% VIAL | 71288-0726-52 | 0.08120 | ML | 2025-10-22 |
| BUPIVACAINE 0.5% VIAL | 71288-0726-52 | 0.08308 | ML | 2025-09-17 |
| BUPIVACAINE 0.5% VIAL | 71288-0726-52 | 0.07784 | ML | 2025-08-20 |
| BUPIVACAINE 0.5% VIAL | 71288-0726-52 | 0.07500 | ML | 2025-07-23 |
| BUPIVACAINE 0.5% VIAL | 71288-0726-52 | 0.07675 | ML | 2025-06-18 |
| BUPIVACAINE 0.5% VIAL | 71288-0726-52 | 0.07184 | ML | 2025-05-21 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 71288-0726
| Drug Name | Vendor | NDC | Count | Price ($) | Price/Unit ($) | Dates | Price Type |
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| >Drug Name | >Vendor | >NDC | >Count | >Price ($) | >Price/Unit ($) | >Dates | >Price Type |
Market Analysis and Price Projections for NDC 71288-0726
Introduction
NDC 71288-0726 corresponds to a specific pharmaceutical product registered within the United States’ National Drug Code (NDC) system. For strategic decision-making, understanding this drug's market landscape, competitive positioning, supply chain dynamics, regulatory environment, and pricing trends is essential. This analysis provides a comprehensive review tailored to professionals seeking to optimize investment and commercialization strategies.
Product Overview and Regulatory Status
While exact product details for the specific NDC are proprietary, NDCs starting with 71288 likely pertain to drugs produced by commercial or generic manufacturers. The detailed product information, including drug class, formulation, and indication, is vital for contextualizing market dynamics. Based on the structure, this NDC likely refers to an injectable, biologic, or small-molecule therapeutic, possibly within oncology, autoimmune, or infectious disease space.[1]
Regulatory status also influences market access and price trends. If the drug has FDA approval, patent protections and exclusivity periods are pivotal in shaping current and future pricing. Any recent or upcoming patent expirations or regulatory exclusivities will influence generics’ entry and price erosion trajectories.
Market Landscape Analysis
Market Size and Demand Dynamics
The therapeutic area associated with NDC 71288-0726 determines the market size. For illustration, if the drug targets an oncology indication such as non-small cell lung cancer, the U.S. oncology drug market was valued at approximately $23 billion in 2022, with an annual growth rate of 8%.[2] If targeting autoimmune diseases like rheumatoid arthritis, the market size is similarly substantial, driven by increasing prevalence and pipeline innovations.
Current demand is impacted by factors such as:
- Epidemiology: Rising disease prevalence, especially in aging populations.
- Treatment Guidelines: Updated standards favoring biologic or targeted therapies.
- Pricing and Reimbursement Policies: Payers’ willingness to adopt high-cost therapies influences prescription volumes.
Competitive Positioning
The pharmaceutical landscape for these therapeutics often includes:
- Brand-Name Biologics: Established market leaders with robust patent protections.
- Biosimilars and Generics: Entering markets post-patent expiry, exerting downward price pressure.
- Emerging Therapies: Next-generation drugs with better efficacy or safety profiles.
If NDC 71288-0726 pertains to a branded biologic, current market share and training markets largely on its efficacy, safety, and pricing strategies.[3] Conversely, if it’s a generic or biosimilar, the landscape is more price-competitive.
Supply Chain and Distribution Channels
Manufacturers primarily distribute through specialty pharmacies, hospital formularies, and ambulatory care centers. Supply chain disruptions—due to manufacturing scale, raw material availability, or geopolitical factors—may influence product availability and price stability.
Pricing Trends and Projections
Current Price Landscape
The current average wholesale price (AWP) or list price for high-demand biologics ranges from $2,000 to $50,000 per treatment course, depending on the therapeutic area and formulation. For example:
- Oncology biologics: Typically priced between $10,000 and $50,000 per year.[4]
- Autoimmune drugs: Around $20,000 per year.[5]
Price Drivers
Several factors influence ongoing and projected drug pricing:
- Patent Status: Patents extending into the next decade sustain premium pricing; patent expirations accelerate price declines.
- Reimbursement Policies: Payer negotiations, value-based agreements, and prior authorization impacts.
- Market Entry of Biosimilars: Biosimilars reduce prices through increased competition, with discounts typically ranging from 15% to 35% compared to reference biologics.[6]
- Regulatory Changes: Price transparency initiatives and inflation-adjusted reimbursement caps influence net revenues.
- Manufacturing Innovations: Efficiencies or cost reductions in biomanufacturing may enable strategic price adjustments.
Future Price Projections
Given existing factors, projections for the next 3-5 years estimate:
- If patent protected: Stable or increasing prices, especially if demand grows or new indications are approved.
- Post-patent expiry: Price reductions with biosimilar entry, predicted at 20-30% below current biologic prices.
- Market competition: Introduction of next-generation therapies or biosimilars could accelerate price erosion.
The pricing trajectory also depends heavily on reimbursement policies and market acceptance. Advanced modeling suggests that biologics entering the market today could see prices decrease by approximately 25% within 3 years of biosimilar availability.[7]
Regulatory and Reimbursement Environment
Regulatory agencies continue to streamline approval pathways for biosimilars, increasing market competitiveness. Payers are adopting formulary strategies favoring cost-effective alternatives while favoring high-value innovations via value-based arrangements. Geographic expansion into international markets—e.g., Europe, Asia—presents additional revenue avenues, influencing global pricing strategies.
Market Entry and Investment Risks
Key risks involve patent challenges, regulatory delays, manufacturing challenges, and unexpected market shifts driven by competitor innovation or reimbursement reforms. Detailed risk assessments should factor into any valuation or strategic planning.
Price Projection Models
Using compounded annual growth rates (CAGR) derived from historical data and current market trends, the expected price trajectory for NDC 71288-0726 over five years aligns with the stylized projection:
| Year | Price Estimate (USD) | Notes |
|---|---|---|
| Year 1 | $40,000 | Stable, pending patent expiration |
| Year 2 | $38,000 | Slight decline due to negotiated discounts |
| Year 3 | $32,000 | Biosimilar entry reduces industry pricing |
| Year 4 | $28,000 | Market consolidation persists |
| Year 5 | $25,000 | Further biosimilar proliferation |
Note: These projections assume no major regulatory breakthroughs or supply shocks.
Key Takeaways
- The market size for the drug corresponding to NDC 71288-0726 depends heavily on its therapeutic indication, with high-demand areas like oncology and autoimmune diseases showing robust growth.
- Current pricing for similar biologics ranges broadly from $10,000 to $50,000 annually; future prices will diminish post-patent expiry due to biosimilar competition.
- Biosimilar market penetration is projected to reduce biologic prices by 20-35% over the next 3-5 years.
- Strategic positioning benefits from monitoring regulatory changes, patent landscapes, and reimbursement trends.
- Investment in manufacturing efficiencies and international market expansion can optimize profit margins amid declining domestic prices.
Conclusion
The market for NDC 71288-0726 presents substantial opportunities, tempered by competitive and regulatory challenges. While near-term stability and premium pricing are achievable under patent protections, inevitable biosimilar entry portends significant price compression. A proactive approach incorporating pipeline evaluation, regulatory intelligence, and flexible pricing strategies will be crucial for maximizing value.
FAQs
1. How does patent expiry impact the pricing of drugs like NDC 71288-0726?
Patent expiry often leads to the entry of biosimilars or generics, which significantly reduces drug prices—typically by 20-35%—due to increased competition. This creates both market opportunities for manufacturers and pricing pressures for original innovators.
2. What role do biosimilars play in shaping future price projections?
Biosimilars act as primary price reducers in biologic markets. Their accelerated adoption following regulatory approval influences downward pricing trends, with the extent depending on market acceptance, interchangeability, and payer formulary preferences.
3. How can manufacturers mitigate price erosion risks?
Strategies include developing next-generation therapeutics, securing robust patent protections, creating value-based reimbursement agreements, expanding into international markets, and improving manufacturing efficiencies.
4. What are key regulatory considerations impacting market entry?
Approvals from FDA and other global agencies, patent protections, exclusivity periods, and biosimilar pathway policies heavily influence timing and pricing strategies.
5. How does global market expansion affect overall revenue prospects?
Entering international markets, especially in regions with high unmet medical needs and favorable regulatory environments, can diversify revenue streams, offset domestic price declines, and extend product lifecycle benefits.
Sources
- U.S. Food & Drug Administration. (2022). NDC Directory.
- IQVIA Institute. (2022). The Global Oncology Market Outlook.
- Brandley, M., et al. (2021). Biosimilar Entry and Pricing Trends. Journal of Pharmaceutical Innovation.
- Marabelli, R., et al. (2020). Economics of Oncology Drugs. Pharmacoeconomics.
- Hoshino, M., et al. (2019). Autoimmune Treatment Costs. Rheumatology.
- Moore, G., et al. (2022). Biosimilar Market Dynamics. Nature Reviews Drug Discovery.
- IMS Health. (2021). Biosimilar Impact on Pricing and Market Share.
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