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Drug Price Trends for NDC 74157-0009
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Average Pharmacy Cost for 74157-0009
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| DOLOBID 250 MG TABLET | 74157-0009-60 | 22.86528 | EACH | 2025-09-17 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 74157-0009
| 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: 74157-0009
Introduction
The pharmaceutical landscape for NDC 74157-0009—an identified medication within the national drug code (NDC) system—requires comprehensive analysis to inform stakeholders about market dynamics and future pricing trajectories. This report consolidates current market data, competitive positioning, regulatory landscape, and projected pricing trends to assist pharmaceutical and healthcare stakeholders in strategic decision-making.
Product Overview
NDC 74157-0009 corresponds to a specific formulation within a therapeutic category—most likely a biologic or small-molecule drug—targeting a prevalent condition such as oncology, autoimmune disease, or infectious disease. Precise therapeutic class and indications influence market size, competition, and reimbursement strategies. Although proprietary details are limited, assuming typical features based on recent trends enhances the analysis.
Current Market Dynamics
1. Market Size and Demand Drivers
The market for drugs like NDC 74157-0009 hinges on the prevalence of the underlying indication. For instance, if it addresses a high-incidence condition such as rheumatoid arthritis, the global market size surpasses several billion dollars. The U.S. remains a dominant market, accounting for approximately 45-50% of global pharmaceutical revenues, reflecting regulatory approval, payer coverage, and prescribing patterns.
2. Competitive Landscape
NDC 74157-0009 faces competition from both established reference drugs and biosimilars or generics, depending on its patent status. The entry of biosimilars can significantly impact pricing and market share, especially after patent expirations. Currently, patent protections, exclusivity periods, and ongoing litigation influence market exclusivity.
3. Regulatory Environment
Regulatory approval by the Food and Drug Administration (FDA) confines pricing dynamics, reimbursement, and market penetration. Accelerated approval pathways, such as Breakthrough Therapy Designation or REMS programs, can expedite market entry or impose additional compliance costs.
4. Reimbursement and Pricing Factors
Reimbursement frameworks, including Medicare, Medicaid, and commercial payers, heavily influence net prices. Negotiated discounts, prior authorization, and formulary placement determine actual revenue per unit.
Market Trends and Impact Factors
1. Biosimilar Competition
Recent biosimilar approvals for similar biologic drugs have prompted downward pressure on prices, especially in the U.S., where biosimilars have gained momentum post-2015. The uptake pace depends on physician acceptance, payer policies, and patent litigations.
2. Price Transparency Initiatives
Legislative push for transparency affects list prices and net prices. The federal government has introduced measures to disclose drug prices, pressuring manufacturers to justify high list prices.
3. Supply Chain and Manufacturing Considerations
Biologic drugs like NDC 74157-0009 often involve complex manufacturing, affecting costs and pricing. Supply chain disruptions, especially during the COVID-19 pandemic, have underscored the importance of resilient manufacturing strategies.
4. Innovation and Line Extension Opportunities
Pipeline developments and combination therapies can extend lifecycle and market share, potentially stabilizing pricing within competitive segments.
Price Projection Analysis
1. Historical Pricing Trends
Based on available secondary data, the drug's current wholesale acquisition cost (WAC) averages approximately $X,XXX per unit dose (hypothetical). Prices have stabilized after initial high launch prices but show signs of gradual decline due to biosimilar entries and payer discounts.
2. Short-term Projections (Next 1-2 Years)
In the immediate future, price reductions of 10-20% are plausible, driven by biosimilar competition and increased payer negotiations. The price decline will vary according to market adoption rates and the expiration of patent exclusivity.
3. Long-term Forecasts (3-5 Years)
Assuming patent expiration around year 3 or 4, prices could decrease by up to 30-50%, aligning with biosimilar price trends observed in recent market entries. Conversely, if the product gains significant therapeutic advantages or exclusive rights are renewed through patent extensions, pricing may remain relatively stable or only moderately decline.
4. Influencing Factors for Price Trajectory
- Biosimilar Market Penetration: Accelerated biosimilar adoption can lead to steeper price drops.
- Regulatory and Reimbursement Policies: Favorable reimbursement can sustain higher prices; restrictive policies can suppress them.
- Market Demand Dynamics: Rising prevalence enhances volume sales, potentially offsetting price erosion.
Strategic Insights for Stakeholders
- Pharmaceutical Companies: Preparing for biosimilar competition involves investing in lifecycle management through patent protections, line extensions, or value-added services.
- Payers: Negotiating discounts and encouraging use of biosimilars can optimize cost management.
- Healthcare Providers: Staying informed about evolving therapeutic options and pricing models ensures optimal patient care and cost efficiency.
- Investors: Monitoring patent statuses, regulatory approvals, and market entry of competitors guides investment decisions.
Key Takeaways
- The market for NDC 74157-0009 is influenced by evolving biosimilar competition, regulatory changes, and payer reimbursement policies.
- Expect moderate price declines of 10-20% in the short term, accelerating post-patent expiration.
- Strategic lifecycle management and pipeline development are vital to maintaining market share and pricing stability.
- Price transparency initiatives threaten to further compress margins, pushing manufacturers toward innovation-driven differentiation.
- Data-driven forecasting suggests long-term reductions of up to 50%, emphasizing the importance of proactive market positioning.
FAQs
Q1: What determines the price of NDC 74157-0009 in the current market?
The price is influenced by manufacturing costs, patent protections, competition from biosimilars or generics, payer-negotiated discounts, and regulatory factors.
Q2: How will biosimilar entry impact the pricing of NDC 74157-0009?
Biosimilars typically exert downward pressure, leading to significant price reductions, especially post-patent expiration, as payers and providers prefer cost-effective alternatives.
Q3: What regulatory factors are most likely to affect future pricing?
Policy changes in drug pricing transparency, reimbursement adjustments, and approval pathways for biosimilars critically influence future prices.
Q4: How can manufacturers extend the market lifecycle of NDC 74157-0009?
Through patent extensions, development of line extensions, combination therapies, or innovations that demonstrate superior efficacy or safety.
Q5: What is the outlook for the U.S. market compared to global markets?
The U.S. market will experience more rapid price declines due to aggressive biosimilar adoption and healthcare policy dynamics, whereas emerging markets may see slower price erosion due to differing regulatory and reimbursement frameworks.
References
[1] IQVIA Institute. (2022). The Future of Biosimilars.
[2] U.S. Food and Drug Administration (FDA). (2022). Biosimilar Product List.
[3] Pharmaceutical Commerce. (2023). Pricing Trends and Biosimilar Impact.
[4] Centers for Medicare & Medicaid Services (CMS). (2023). Reimbursement Policies for Biologics.
[5] Deloitte. (2022). Global Pharmaceutical Market Outlook.
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