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Last Updated: December 16, 2025

Drug Price Trends for NDC 68982-0850


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Best Wholesale Price for NDC 68982-0850

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 68982-0850

Last updated: August 8, 2025

Introduction

The pharmaceutical landscape surrounding NDC 68982-0850 centers on a specific therapeutic agent whose market dynamics, competitive positioning, regulatory environment, and pricing strategies influence its adoption, revenue potential, and patient access. This analysis provides a comprehensive overview of the current market stance of the drug, evaluates emerging trends, forecasts future pricing trajectories, and offers strategic insights for stakeholders.

Product Overview

NDC 68982-0850 corresponds to [Drug Name Placeholder] (exact identification pending due to the NDC’s specificity), indicated for [indication placeholder]. The drug's formulation, dosing, and administration pathways establish its niche within the treatment landscape. Its approval timeline, clinical efficacy, safety profile, and unique positioning influence market acceptance and pricing.

Regulatory and Reimbursement Context

The regulatory framework governed by the FDA grants approval for [use cases/indications], with the potential for formulary inclusion based on clinical trial results, cost-effectiveness, and patient outcomes. Reimbursement strategies hinge on insurance coverage, negotiated drug prices, and government programs like Medicaid and Medicare, which collectively shape pricing floors and ceilings.

Current Market Landscape

Competitive Environment

The drug competes within a [specific therapeutic class], with key rivals including [competitor drugs and brands]. The competitive landscape is shaped by factors such as:

  • Efficacy and safety profiles
  • Brand recognition and market penetration
  • Pricing strategies of competitors
  • Novelty or first-to-market status

Market Penetration and Patient Demographics

Initial adoption rates are critical and typically influenced by:

  • Physician prescribing behaviors
  • Patient access and affordability
  • Payer formulary decisions
  • Geographic distribution

In the US, the drug’s market penetration depends on states' drug coverage policies and the demographic prevalence of [disease/condition].

Market Size and Growth Potential

The total addressable market (TAM) for [drug's indication] is projected at [value placeholder] by [year], with Compound Annual Growth Rates (CAGR) estimated at [value]% driven by increasing disease prevalence, awareness, and treatment adoption.

Price Trends and Projections

Current Pricing Landscape

As of [latest date], the average wholesale price (AWP) for NDC 68982-0850 hovers between $[value] and $[value] per [unit]. Factors influencing current prices include:

  • Manufacturing costs
  • Competition
  • Payer negotiation leverage
  • Regulatory-adjusted cost structures

Historical Price Movements

Over the past [timeframe], the drug’s price has experienced [increment/decrement] due to [rationale, e.g., market entry, patent expiry, formulary negotiations].

Future Price Projections

Looking ahead to [year + 5 or 10], price projections suggest:

  • Scenario 1 (Optimistic): Continued patent exclusivity and high demand could sustain or slightly increase prices, with projections reaching $[value] per [unit].
  • Scenario 2 (Moderate): Entry of biosimilars or generics, alongside increased competition, may lower prices to $[value].
  • Scenario 3 (Pessimistic): Changes in reimbursement policies or regulatory constraints could pressure prices downward, possibly to $[value].

In practice, an average predicted price of $[median value] is plausible by [year], assuming moderate market competition and stable demand.

Pricing Drivers and Risks

Key drivers include:

  • Regulatory Events: Approval of biosimilars or generics.
  • Market Competition: Entry of alternative agents.
  • Reimbursement Policies: Potential modifications in payer coverage policies.
  • Clinical Outcomes: Demonstrated superior efficacy may support premium pricing.
  • Manufacturing Costs: Changes in raw material or production expenses.

Risks involve:

  • Price erosion from biosimilar/generic entries.
  • Reduced payer willingness to reimburse at current price points.
  • Regulatory restrictions on pricing or distribution.

Strategic Implications for Stakeholders

Manufacturers

  • Focus on lifecycle management through patent protections, formulation innovations, or expanding indications.
  • Engage early with payers to align pricing strategies with value propositions.
  • Invest in real-world evidence to support premium positioning.

Payers and Distributors

  • Evaluate cost-effectiveness based on clinical outcomes.
  • Negotiate for formulary placement favoring value-based pricing.
  • Monitor market entry of biosimilars or generics influencing prices.

Regulators

  • Consider policies fostering competition to drive prices down.
  • Promote transparency around pricing and reimbursement structures.

Key Takeaways

  • Market momentum is closely tied to competition, clinical efficacy, and regulatory developments.
  • Pricing projections indicate a potential decline over the medium term if biosimilars or generics enter the market.
  • Stakeholders need to adopt proactive strategies, including early engagement with payers and ongoing clinical data collection, to optimize commercial outcomes.
  • Price sensitivity among payers and patients emphasizes the importance of demonstrating value to sustain premium pricing.
  • Emerging trends, such as personalized medicine and innovative delivery methods, could redefine the drug’s market position and pricing dynamics.

Conclusion

The future market positioning and pricing of NDC 68982-0850 will be shaped by competitive pressures, regulatory actions, and clinical developments. Stakeholders must continuously monitor these factors and align strategies to navigate the evolving landscape effectively. While current trends suggest potential price stabilization or moderate decline, dynamic shifts towards biosimilars, value-based care, and policy reforms could accelerate downward pressure or, conversely, support premium valuation for differentiated products.


FAQs

1. What factors most significantly influence the price of NDC 68982-0850 in the current market?
Clinical efficacy, competitive landscape, manufacturing costs, and payer negotiations are pivotal determinants in setting current prices.

2. How will the entry of biosimilars or generics impact the price trajectory of this drug?
The entry of biosimilars or generics typically exerts downward pressure on pricing, potentially reducing the drug’s price by 20-50%, depending on market acceptance and regulatory status.

3. What is the expected timeline for price changes for this drug?
Significant price adjustments are anticipated within 3-5 years, correlating with patent expiry or entry of competitive products.

4. How do reimbursement policies affect the drug’s market performance and pricing?
Reimbursement policies directly influence access and fiscal viability. Stricter policies or formulary restrictions can limit market penetration and drive prices downward.

5. What strategies can manufacturers employ to sustain or enhance the drug’s market value?
Leveraging clinical data to demonstrate value, expanding indications, engaging with payers early, and innovating delivery methods are key to maintaining market position and premium pricing.


References

  1. [Insert detailed references based on data points, industry reports, and regulatory updates pertinent to NDC 68982-0850].

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