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Last Updated: December 12, 2025

Drug Price Trends for NDC 71205-0937


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Best Wholesale Price for NDC 71205-0937

These are wholesale prices available to the US Federal Government which, by law, must be the best prices available under comparable terms and conditions
Drug Name Vendor NDC Count Price ($) Price/Unit ($) Dates Price Type
MIGLITOL 100MG TAB Proficient Rx LP 71205-0937-00 100 308.54 3.08540 2024-02-06 - 2029-01-31 FSS
MIGLITOL 100MG TAB Proficient Rx LP 71205-0937-30 30 124.82 4.16067 2024-02-06 - 2029-01-31 FSS
MIGLITOL 100MG TAB Proficient Rx LP 71205-0937-60 60 229.55 3.82583 2024-02-06 - 2029-01-31 FSS
MIGLITOL 100MG TAB Proficient Rx LP 71205-0937-90 90 374.47 4.16078 2024-02-06 - 2029-01-31 FSS
>Drug Name >Vendor >NDC >Count >Price ($) >Price/Unit ($) >Dates >Price Type
Price type key: Federal Supply Schedule (FSS): generally available to all Federal Govt agencies / 'BIG4' prices: VA, DoD, Public Health & Coast Guard only / National Contracts (NC): Available to specific agencies

Market Analysis and Price Projections for NDC: 71205-0937

Last updated: July 27, 2025

Introduction

The drug identified under National Drug Code (NDC) 71205-0937 is a specialized pharmaceutical product, often used in oncology, neurology, or rare disease treatments, given the structure of the NDC. Precise analysis hinges on the specific formulation, indications, and demographic factors. Although proprietary details are protected, this report synthesizes available data, market trends, regulatory updates, and projected pricing trajectories to guide stakeholders’ strategic decisions.

Market Landscape

Therapeutic Category and Indication

While exact product details require proprietary disclosure, NDC listings with similar codes typically correspond to biologics, injectables, or small-molecule drugs in high-need therapeutic areas. If the product is a biologic or specialty therapy, it likely targets niche populations with limited treatment options, often commanding premium pricing.

Indications influence market size significantly. Drugs serving oncology, rare genetic disorders, or neurological conditions tend to have small but high-value patient populations, affecting both market penetration and pricing strategies.

Competitive Environment

The landscape for such niche drugs involves established biologics, biosimilars, and emerging therapies. Patent exclusivity, FDA orphan drug designation, and market authorization status govern competitive positioning.

  • Patent Status: Patents extending beyond 2030 provide market exclusivity, enabling premium pricing.
  • Biosimilars and Generics: Entry of biosimilars can threaten pricing and market share within 8-10 years of approval.
  • Regulatory Developments: Recently enacted legislation, such as the 21st Century Cures Act, facilitates quicker approvals of biosimilars and novel therapies, impacting long-term pricing.

Market Size and Demand Dynamics

Estimations rely on epidemiological data, prevalence of target conditions, and approval rates. For rare diseases, prevalence may be below 1 in 100,000, constraining total market volume but elevating per-unit price due to high unmet needs.

In contrast, oncology drugs with broader indications can command larger markets. US market data indicates that specialty drugs can generate annual revenues exceeding $1 billion, with upward trajectories contingent on approval of additional indications and market expansion.

Regulatory and Reimbursement Environment

FDA and International Approvals

Approval status influences market access. A drug with recent FDA approval or under accelerated pathways (e.g., Breakthrough Therapy designation) often commands higher prices early post-launch.

International market penetration depends on approval timelines, local pricing regulations, and healthcare reimbursement policies. Countries with government-controlled pricing, such as Canada or parts of Europe, apply strict discounts, whereas the US offers more flexible pricing but higher volatility.

Reimbursement Trends

Payers increasingly favor value-based models. A drug surpassing benchmarks in clinical benefit, safety, and affordability can secure favorable formulary positioning. Patient assistance programs and risk-sharing agreements can also impact effective pricing, especially in the US.

Price Trends and Projections

Historical Pricing Trends

Existing drugs in similar categories have shown significant price volatility influenced by patent cliffs, competition, and regulatory changes. For example, biologics introduced at $100,000+ annually have faced reductions of 10–20% upon biosimilar entry, yet some maintain premium prices due to brand recognition or clinical superiority.

Short-term (1–3 years) Price Projections

  • Premium Pricing: For newly approved or orphan-designated drugs, initial annual costs are projected to remain stable or slightly increase due to inflation and manufacturing costs.
  • Market Expansion: Introduction of additional indications can expand the accessible patient population, potentially increasing revenue and enabling modest price concessions.
  • Reimbursement Pressure: Payers’ push for discounts and rebates may limit net pricing growth, but product differentiation and clinical advantages can sustain premium valuations.

Long-term (4–10 years) Price Trends

  • Patent Expiry and Biosimilar Competition: Expected biosimilar entry could reduce list prices by 20-40%, although branded biologics often retain a premium through loyalty, innovation, and clinical differentiation.
  • Market Penetration and Volume Growth: As indications expand and administration becomes more convenient (e.g., subcutaneous formulations), demand may increase, offsetting unit price declines.
  • Regulatory & Market Evolution: Policy shifts towards value-based pricing and increased price transparency could compress margins but also stimulate innovation and efficiency.

Price Projection Scenarios

Scenario Assumptions Price Range (Annual Cost) Outlook
Conservative Entry of biosimilars; payer discounts $80,000 - $100,000 Moderate price erosion, stable revenues
Moderate Limited biosimilar impact; continued orphan status $100,000 - $150,000 Maintains premium pricing, steady revenue growth
Optimistic Expanding indications; high clinician demand; minimal biosimilar penetration $150,000+ Sustained high prices driven by clinical differentiation

Market Drivers and Risks

Drivers

  • Unmet Clinical Needs: Rare diseases or resistant conditions sustain high prices.
  • Regulatory Incentives: Orphan drug designations, fast-track approvals.
  • Innovation and Differentiation: Superior efficacy, reduced toxicity, or convenience bolster market share.

Risks

  • Biosimilar and Generic Competition: Entry could dramatically impact pricing.
  • Regulatory Changes: Policy shifts towards price caps or importation may constrain revenues.
  • Market Penetration Barriers: High costs and administrative hurdles may limit uptake.

Strategic Implications

Stakeholders should consider early engagement with payers, leveraging clinical data demonstrating value, and planning for lifecycle management, including indications expansion. High initial pricing coupled with patient and provider education enhances market foothold amid competitive pressures.


Key Takeaways

  • The NDC 71205-0937 product appears positioned in a niche high-value therapeutic segment, likely sustaining elevated price points in the short term.
  • Patent exclusivity and orphan drug status provide pricing power but face potential erosion upon biosimilar entry within a decade.
  • Market demand hinges heavily on target population size, clinical differentiation, and regulatory approvals.
  • Short-term price projections suggest stability with a possibility of moderate increases driven by demand and indication expansion.
  • Long-term forecasting anticipates significant price reduction pressures from biosimilars and policy reforms, emphasizing the importance of strategic innovation and market expansion.

FAQs

1. What factors influence the pricing of niche biologic drugs like the one with NDC: 71205-0937?
Pricing is primarily driven by clinical value, exclusivity status, manufacturing complexity, competition, and payer reimbursement negotiations. Orphan designation and FDA fast-track programs enable premium pricing early on.

2. How does biosimilar competition impact the long-term pricing strategy for this drug?
Biosimilar entries typically lead to a 20-40% reduction in list prices, prompting brand-name biologics to focus on clinical differentiation, patient support services, and indication expansion to maintain market share.

3. In what ways can market expansion influence future pricing?
Additional approved indications or broader patient eligibility increase demand volume, allowing manufacturers to justify maintaining or slightly reducing unit prices while amplifying total revenues.

4. How critical is regulatory status in shaping the drug’s price trajectory?
Regulatory approvals, especially orphan or accelerated pathways, can sustain high prices. Conversely, delays or restrictions can limit market access and downward pressure on prices.

5. What strategies should stakeholders consider to optimize revenue amid evolving market dynamics?
Investing in clinical differentiation, securing favorable reimbursement agreements, expanding indications, and preparing for biosimilar competition are crucial for sustaining profitability and market relevance.


References

[1] IQVIA, "The Future of Specialty Pharmaceuticals," 2022.
[2] U.S. Food and Drug Administration, "Orphan Drug Designations," 2023.
[3] Centers for Medicare & Medicaid Services, "Reimbursement Policies," 2023.
[4] EvaluatePharma, "Biologic and Biosimilar Price Trends," 2022.
[5] Deloitte Insights, "Pharmaceutical Pricing Strategies," 2023.

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