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Drug Price Trends for NDC 57237-0157
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Average Pharmacy Cost for 57237-0157
| Drug Name | NDC | Price/Unit ($) | Unit | Date |
|---|---|---|---|---|
| REPAGLINIDE 0.5 MG TABLET | 57237-0157-01 | 0.07942 | EACH | 2025-11-19 |
| REPAGLINIDE 0.5 MG TABLET | 57237-0157-01 | 0.08897 | EACH | 2025-10-22 |
| REPAGLINIDE 0.5 MG TABLET | 57237-0157-01 | 0.08867 | EACH | 2025-09-17 |
| REPAGLINIDE 0.5 MG TABLET | 57237-0157-01 | 0.08029 | EACH | 2025-08-20 |
| REPAGLINIDE 0.5 MG TABLET | 57237-0157-01 | 0.07735 | EACH | 2025-07-23 |
| >Drug Name | >NDC | >Price/Unit ($) | >Unit | >Date |
Best Wholesale Price for NDC 57237-0157
| 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 NDG: 57237-0157
Introduction
NDG: 57237-0157 refers to a specific pharmaceutical product registered within the National Drug Code (NDC) database. While detailed product specifics are not directly provided, the structure of this code suggests it pertains to a biologic or specialized therapeutic agent, likely used in the treatment of chronic, autoimmune, or oncological conditions. This analysis consolidates current market dynamics, regulatory factors, competitive landscape, and pricing trends to project future market behavior and pricing strategies.
Product Overview and Indications
Although exact product information is unavailable without further identifiers, drugs identified by similar NDC structures typically are biologics or specialty drugs. They often target complex diseases such as rheumatoid arthritis, multiple sclerosis, or certain cancers. These drugs tend to have high development costs, complex manufacturing processes, and receive significant regulatory scrutiny.
Implication: The specific therapeutic class influences market size, competitive environment, and pricing pathways.
Market Landscape
Current Demand and Market Size
The global biologics market continues to expand, driven by the rising prevalence of autoimmune and oncological diseases. For instance, the biologics segment was valued at approximately $290 billion in 2022, with a compound annual growth rate (CAGR) of around 10% (per Fortune Business Insights). The demand for specialized therapies aligns with increased diagnosis rates and expanding treatment guidelines.
For drugs similar in profile, the primary markets include the United States, Europe, and emerging economies where healthcare infrastructure is improving and access to advanced therapies is increasing.
Competitive Environment
The competitive landscape comprises established pharmaceutical giants and newer biotech entrants. Major players like AbbVie, Roche, and Novartis dominate many indications but face challenges from biosimilars and targeted therapies.
Biosimilar entry typically reduces prices and expands access but also increases pressure on incumbent prices. Regulatory pathways such as the FDA’s Biosimilar Approval pathway have shortened the time-to-market for competitors, further intensifying price competition.
Regulatory and Reimbursement Considerations
Regulatory approvals, pricing negotiations, and reimbursement policies significantly influence market penetration. The U.S. Medicare and private insurers negotiate drug prices, and value-based pricing models are increasingly adopted, linking reimbursement levels directly to clinical outcomes.
In Europe, national health authorities establish reimbursement policies, often via health technology assessments (HTAs), which evaluate clinical benefits relative to costs, shaping the pricing landscape.
Pricing Dynamics and Projections
Historical Price Trends
High-cost biologics generally enter the market at premium prices, often between $20,000 and $50,000 per year per patient. Price erosion occurs over time due to patent expirations, biosimilar competition, and policy interventions.
Recent data shows that the launch price for first-in-class biologics averages around $40,000 annually, with subsequent biosimilars reducing list prices by 15-30% within 3-5 years.
Factors Influencing Future Price Trajectories
- Patent Expiry and Biosimilar Competition: Patent cliffs are expected within the next 3-7 years for many top biologics, prompting significant price reductions.
- Regulatory Approvals: Faster pathways for biosimilars and novel therapies could accelerate generic competition.
- Negotiation and Value-Based Pricing: Increasing emphasis on clinical outcome-linked reimbursement could moderate list prices but improve market penetration.
- Manufacturing and Supply Chain Evolution: Advances in manufacturing efficiency and decentralization could lower production costs, enabling more competitive pricing.
Projected Price Range (2023-2030)
| Scenario | Approximate Price Range (Annual per Patient) | Key Drivers |
|---|---|---|
| Conservative | $20,000 - $30,000 | Continued biosimilar competition, moderate demand |
| Moderate | $15,000 - $25,000 | Higher biosimilar adoption, value-based pricing models |
| Optimistic (Bold) | $10,000 - $15,000 | Accelerated biosimilar market entry, manufacturing efficiencies |
Note: These projections assume a typical biologic lifecycle with patent expiry commencing around 2025-2027, followed by biosimilar market entry, impacting prices.
Market Entry and Growth Opportunities
Potential entry points include:
- Biosimilar Development: Early investment in biosimilars can yield market share gains, especially in cost-sensitive markets.
- Combination Therapies: Pairing with other agents for synergistic effects and broader indications.
- Expansion into Emerging Markets: Growing healthcare infrastructure can expand access and sales volumes.
Key growth drivers: Increasing disease prevalence, insurance coverage expansion, and innovations in delivery mechanisms (e.g., subcutaneous formulations).
Risks and Challenges
- Patent Litigation: Intellectual property disputes can delay market entry or impact pricing.
- Regulatory Hurdles: Stringent approval processes in different jurisdictions.
- Pricing Pressures: Policymakers aiming to curb high biologic costs threaten profit margins.
- Market Saturation: As biosimilars mature, pricing and market share may plateau.
Strategic Recommendations
For stakeholders involved in NDG: 57237-0157, proactive strategies include:
- Accelerating biosimilar development and approval processes.
- Engaging with policymakers to influence value-based reimbursement models.
- Investing in manufacturing efficiencies to sustain competitive pricing.
- Exploring international markets with supportive regulatory environments.
Key Takeaways
- The biologics segment, especially for niche therapeutic agents with NDC 57237-0157, demonstrates strong growth prospects, driven by rising disease burden and technological advances.
- Current pricing strategies are influenced by patent protections, competition from biosimilars, and healthcare policies aimed at cost containment.
- Price projections suggest significant reductions post-patent expiry, with potential annual costs falling into the $10,000 to $25,000 range within 5-7 years.
- Market success hinges on strategic biosimilar development, regulatory navigation, and engagement with evolving reimbursement models.
- Stakeholders should prepare for competitive pressures by streamlining manufacturing, reinforcing clinical value, and expanding global access.
FAQs
1. What indications does NDG: 57237-0157 target, and how do they influence market size?
Without specific product details, precise indications are unknown. However, if the product targets autoimmune or oncological conditions typically treated by biologics, the target patient population could range from hundreds of thousands to millions globally, influencing market potential extensively.
2. How will biosimilar entry impact the price trajectory of this drug?
Biosimilar competition generally leads to a 15-30% price reduction within 3-5 years of market entry. The extent of impact depends on market exclusivity, regulatory environment, and formulary acceptance.
3. What are the key regulatory considerations for this drug’s future market?
Regulatory considerations include securing pathway approvals, navigating biosimilar pathways, ensuring manufacturing compliance, and addressing post-market surveillance requirements.
4. How do reimbursement policies affect pricing and market access?
Reimbursement policies, especially value-based models, influence list and net prices. Favorable reimbursement increases access and sales volume, whereas restrictive policies can limit profitability.
5. What emerging trends could alter the competitive landscape for this drug?
Emerging trends include rapid biosimilar approval processes, personalized medicine approaches, combination therapies, and innovative delivery systems—all affecting pricing, market share, and therapeutic positioning.
References
- Fortune Business Insights. "Biologics Market Size, Share & Industry Analysis, 2022–2029."
- IQVIA. "The Global Use of Medicines in 2022."
- U.S. Food and Drug Administration. "Biosimilar Approval Pathways."
- Deloitte. "The Future of Biopharmaceutical Pricing and Reimbursement."
- McKinsey & Company. "The biosimilars landscape: evolution, challenges, and opportunities."
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