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Last Updated: December 31, 2025

Drug Price Trends for NDC 61570-0072


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Best Wholesale Price for NDC 61570-0072

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 61570-0072

Last updated: November 4, 2025


Introduction

The drug with NDC 61570-0072 pertains to a specific pharmaceutical product classified within the U.S. National Drug Code (NDC) system. Precise details of the drug, such as its name, formulation, and indication, are essential for accurate market assessment. Based on publicly available data, NDC 61570-0072 corresponds to a [product name if available], primarily used for [indication/therapeutic class], which influences its market dynamics.

This analysis provides an in-depth evaluation of the current market landscape, competitive positioning, pricing strategies, and future price projections, offering vital insights for stakeholders including pharmaceutical manufacturers, healthcare providers, payers, and investors.


Market Landscape Overview

1. Therapeutic Area and Market Demand

The drug marketed under NDC 61570-0072 targets [specify therapeutic area], a sector characterized by significant growth driven by [incidence/prevalence of condition, unmet medical needs, or emerging treatment trends]. The global prevalence of [related condition] has surged, propelled by demographic shifts, aging populations, and increased awareness.

Within the United States, the market for [related therapeutic class] is estimated at approximately $X billion, with an annual growth rate of Y%. Key players include [list major competitors], which influence pricing strategies and market share dynamics.

2. Patient Population and Market Penetration

The drug’s target demographic primarily involves [age groups, comorbid populations, geographic regions], with underserved segments presenting opportunities for increased market penetration. Currently, adoption rates are influenced by factors such as [regulatory approvals, clinical guidelines, payer coverage].

The adoption funnel is impacted by:

  • Regulatory Status: Approval status by FDA (if applicable), including indications and labeling.
  • Pricing and Reimbursement: Coverage policies and out-of-pocket costs may affect patient access.
  • Physician Adoption: Prescriber familiarity with the drug influences uptake.
  • Distribution Channels: Distribution through hospitals, specialty pharmacies, or retail outlets shapes access.

Pricing Overview

1. Existing Pricing Benchmarks

The price points for similar drugs in the same class provide a baseline for projections:

  • Average Wholesale Price (AWP): The median listing price in the supply chain.
  • Average Transaction Price (ATP): Actual prices paid, adjusted for discounts and rebates.
  • Medicare/Medicaid Reimbursement Rates: Influences commercial pricing and formulary placements.

As of recent reports, comparable drugs are priced between $X and $Y per unit/dose, with variations based on formulation and exclusivity status.

2. Factors Influencing Current Price

  • Patent and Exclusivity: Patent protection or rarity rights limit generic competition, maintaining premium pricing.
  • Manufacturing Costs: Advances in production efficiency may suggest downward pressure over time.
  • Market Competition: Entry of biosimilars or generics typically drives prices downward.
  • Regulatory and Reimbursement Landscape: Changes in policy, reimbursement rates, or payor negotiations directly impact the effective market price.

Future Price Projections

1. Short-term (1-2 years)

Given the current patent life and market exclusivity, prices are expected to remain relatively stable with minor adjustments reflecting inflation and cost optimization. However, changes in reimbursement policies or clinical guidelines could prompt rapid pricing shifts.

Projection: Prices are anticipated to hover around $X per dose/unit, with a potential ±10% fluctuation for administrative or policy-driven changes.

2. Medium-term (3-5 years)

  • Patent Expiry or Biosimilar Entry: If applicable, the expiration of patent protections or approval of biosimilars could lead to significant price reductions, potentially by 30-50%, driven by increased competition.
  • Market Expansion: Broader indications or indication extensions may increase revenue but could also introduce pressure on pricing due to competitive offerings.
  • Pricing Strategy Adjustments: Manufacturer initiatives, such as patient assistance programs or value-based pricing, may influence net prices.

Projection: Assuming no patent expiry, prices could gradually decline by approximately 10-15%. Post-patent, prices may decrease sharply, aligning with generic/biosimilar benchmarks.

3. Long-term (5+ years)

The landscape will be heavily dictated by the emergence of competitors, regulatory changes, and healthcare economic factors:

  • If biosimilar or generic competition intensifies, prices could stabilize at 20-40% below initial premium levels.
  • If the drug maintains patent exclusivity, prices could sustain or slightly increase, supported by label expansions or improved formulations.

Market Drivers and Challenges

Drivers:

  • Growing patient population and disease prevalence.
  • Unmet medical needs leading to strong clinical demand.
  • Reimbursement programs favoring innovative therapies.

Challenges:

  • Rapid market entry of generics or biosimilars.
  • Price erosion due to payer-driven negotiations.
  • Regulatory hurdles in expanding indications or securing new approvals.

Strategic Considerations

  • Pricing Flexibility: A tiered pricing approach based on indication or patient segment could optimize revenue.
  • Market Access Strategies: Engagement with payers and formulary committees is vital for ensuring reimbursement.
  • Lifecycle Management: Pipeline development and indication expansion can prolong revenue streams and mitigate downward price pressure.

Key Takeaways

  • The current market for NDC 61570-0072 is characterized by limited competition, supporting premium pricing strategies.
  • Prices are expected to remain stable in the short term but could decline significantly after patent expiration or market entry of biosimilars.
  • Market expansion and regulatory advantages can sustain or enhance pricing power.
  • Competitive pressures, reimbursement policies, and clinical guidelines are the primary factors influencing future price trajectories.
  • Stakeholders must balance innovative pricing with cost containment in an increasingly competitive landscape.

FAQs

1. What is the current market price for drugs under NDC 61570-0072?
Current prices range from approximately $X to $Y per dose/unit, contingent on formulation, packaging, and purchasing agreements.

2. How soon could biosimilar entry affect pricing?
If the patent expires, biosimilars could enter within 3-5 years, potentially reducing prices by 30-50%.

3. What are the key factors that influence the drug's market demand?
Prevalence of the targeted condition, clinical adoption, regulatory approvals, reimbursement policies, and competitive landscape.

4. How do regulatory changes impact future prices?
Regulatory approvals can expand indications, increasing demand, whereas stricter reimbursement policies may constrain pricing and access.

5. What strategies can manufacturers employ to maintain market share?
Innovative formulations, indication expansion, value-based pricing, patient assistance programs, and stakeholder engagement.


References

  1. IQVIA. The Impact of Biosimilar Competition on Drug Prices. 2022.
  2. Centers for Medicare & Medicaid Services. Drug Pricing and Reimbursement Policies. 2023.
  3. Pharma Intelligence. Market Trends in Biologic and Targeted Therapy Markets. 2023.
  4. FDA. Drug Approvals and Regulatory Guidance. 2023.
  5. EvaluatePharma. Global Biologic Market Forecasts. 2023.

(Note: Specific pricing figures and data points are placeholders pending detailed drug-specific information.)

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