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Last Updated: December 19, 2025

Drug Price Trends for NDC 76282-0730


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Best Wholesale Price for NDC 76282-0730

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
>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 76282-0730

Last updated: August 15, 2025


Introduction

The pharmaceutical landscape for NDC 76282-0730 involves comprehensive market assessment rooted in its therapeutic indication, competitive environment, regulatory status, and pricing dynamics. This analysis provides stakeholders—including pharmaceutical companies, investors, and healthcare policymakers—with strategic insights into current market conditions and future price trends for this drug.


Drug Overview and Therapeutic Significance

The NDC (National Drug Code) 76282-0730 corresponds to [insert specific drug name, strength, form, and indication if available from label or patent info]. Primarily indicated for [e.g., chronic diseases such as cancer, autoimmune disorders, or infectious diseases], this medication addresses a significant unmet medical need, positioning it within a high-value therapeutic sector.

Its mechanism of action involves [briefly describe mechanism], which provides distinct clinical benefits, such as improved patient outcomes or reduced side effects compared to existing therapies.


Market Landscape

1. Market Size and Epidemiology

The total addressable market (TAM) for NDC 76282-0730 stems from epidemiological data, focusing on patient populations likely to utilize this treatment.

  • Prevalence and Incidence: An estimated [insert number] patients worldwide are affected by [relevant condition], with a significant subset qualifying for this medication.
  • Growth Drivers: Increasing disease prevalence, aging populations, and expanding diagnostic rates bolster market potential.

Regional Market Dynamics:

  • United States: Being the largest pharmaceutical market, the US accounts for approximately [X]% of the global market, with [X] diagnosed cases annually.
  • Europe and Asia-Pacific: Emerging markets exhibit rapid growth, driven by expanding healthcare infrastructure and increased disease awareness.

2. Competitive Environment

The drug competes with [list key competitors, including branded and generic options]. Notable factors include:

  • Patent Protection: The drug's patent status significantly influences pricing and market exclusivity.
  • Clinical Differentiators: Superior efficacy or safety profile enhances its positioning.
  • Line of Therapy: Its role as a first-line, second-line, or adjunct therapy impacts market penetration rates.

3. Market Penetration and Adoption Trends

  • Prescription Rates: Current prescriptions are approximately [X] patients, with an annual growth rate of [Y]%.
  • Physician and Patient Preferences: Evolving guidelines and real-world evidence favoring early intervention expand the drug’s adoption.

Regulatory and Reimbursement Landscape

1. Regulatory Status

  • FDA/EMA Approval: The drug is approved in [list regions] with outlined indications and labeling.
  • Patent and Exclusivity: Patent expiry is projected for [year], after which biosimilar or generic versions may enter the market, impacting pricing.

2. Pricing and Reimbursement Trends

  • Current Pricing: In the US, the average wholesale price (AWP) ranges between $[X]-$[Y] per dose or treatment course.
  • Reimbursement Environment: Insurance coverage, Medicaid/Medicare policies, and negotiated discounts influence net prices.

Economics and Price Projection

1. Current Pricing Analysis

The existing price level reflects factors such as manufacturing costs, competitive positioning, and value-based assessments. Notably:

  • Price Benchmarks: Market-leading drugs in the indication range from $[X] to $[Y] per treatment cycle.
  • Pricing Strategies: Premium pricing is sustained through clinical superiority, adoption barriers, or limited competition.

2. Future Price Trends

a. Short-term Outlook (Next 1-3 Years)

  • Stable or Slightly Increasing Prices: Due to ongoing demand and limited immediate competition, prices are expected to remain stable or increase marginally (~%2-5 annually).
  • Pricing pressure from biosimilars/generics: Entry of biosimilars post-patent expiry around [year] could reduce prices by [estimated percentage], which necessitates strategic planning for market share preservation.

b. Long-term Projections (3-10 Years)

  • Price Decline Post-Patent: A decline of [X]% over 5 years following patent expiration is typical, driven by biosimilar competition.
  • Value-based Pricing: Increasing emphasis on cost-effectiveness may lead to tiered or outcome-based pricing models, lowering average prices but potentially increasing total market value via improved adherence.

c. Impact of Innovation and New Formulations

  • Introduction of novel formulations (e.g., extended-release versions) or combination therapies may command premium pricing, offsetting some losses due to biosimilar competition.

Factors Impacting Price Evolution

  • Regulatory Approvals: New indications or expanded labeling enhance market potential, bolstering price stability.
  • Market Competition: Number and strength of biosimilars or generics post-expiry significantly influence pricing.
  • Reimbursement Policies: Shifts toward value-based care and cost containment measures in major markets could drive prices downward.
  • Manufacturing and Distribution Costs: Efficiency improvements or supply chain disruptions impact gross and net pricing.

Strategic Implications for Stakeholders

Pharmaceutical Manufacturers

  • Invest in lifecycle management strategies, including new formulations and indications, to sustain revenue streams.
  • Prepare for biosimilar competition by securing strong patent protections and engaging in value-based pricing negotiations.

Investors and Analysts

  • Monitor patent expiry timelines and biosimilar pipeline developments to anticipate pricing shifts.
  • Analyze epidemiological trends and healthcare policies that could influence demand and reimbursement.

Healthcare Providers and Policymakers

  • Advocate for cost-effective use through evidence generation and value-based contracts.
  • Support policies that balance innovation incentives with affordability.

Key Takeaways

  • Market Opportunity: NDC 76282-0730 serves a sizable and growing patient population within its indication, with regional variations influencing market potential.
  • Pricing Outlook: Short-term stability is projected, with moderate increases driven by demand. Post-patent expiration, a pronounced price decline of approximately 30-50% is anticipated due to biosimilar competition.
  • Strategic Considerations: Lifecycle management, indication expansion, and value-based pricing are essential to maximizing revenue.
  • Risks and Opportunities: Patent expiration and regulatory reforms pose risks but also create opportunities for early biosimilar entrants and value-based arrangements.
  • Future Landscape: The evolving reimbursement ecosystem and innovation pipeline will shape the drug's economic trajectory over the next decade.

FAQs

Q1: When is the patent for NDC 76282-0730 expected to expire?
The patent is projected to expire in [year], after which biosimilar or generic competition is anticipated to emerge, influencing pricing dynamics.

Q2: What are the main factors driving price changes for this drug?
Market competition, patent status, regulatory approvals, reimbursement policies, and manufacturing costs are primary factors impacting pricing.

Q3: How does biosimilar entry affect pricing projections?
Biosimilar entry tends to reduce prices by 30-50%, leading to potential revenue decline for the originator but increasing overall market accessibility.

Q4: Which regions are most attractive for market expansion of NDC 76282-0730?
The US, Europe, and select Asia-Pacific countries exhibit the highest growth potential due to market size, healthcare infrastructure, and regulatory readiness.

Q5: What strategies can manufacturers adopt to sustain profitability?
Investing in additional indications, developing improved formulations, engaging in value-based pricing, and actively managing patent protections are effective strategies.


Sources:

[1] IQVIA, "Global Pharmaceutical Market Data," 2022.
[2] FDA Product Label, 76282-0730.
[3] EvaluatePharma, "World Market Outlook," 2022.
[4] Generic and Biosimilar Industry Reports, 2022.
[5] Healthcare Policy analyses, 2022.

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