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Last Updated: April 2, 2026

Drug Price Trends for NDC 78206-0158


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Best Wholesale Price for NDC 78206-0158

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
REMERON SOLTAB 30MG Organon LLC 78206-0158-01 30 98.36 3.27867 2022-01-15 - 2027-01-14 Big4
REMERON SOLTAB 30MG Organon LLC 78206-0158-01 30 132.01 4.40033 2022-01-15 - 2027-01-14 FSS
REMERON SOLTAB 30MG Organon LLC 78206-0158-01 30 101.46 3.38200 2023-01-01 - 2027-01-14 Big4
REMERON SOLTAB 30MG Organon LLC 78206-0158-01 30 138.48 4.61600 2023-01-01 - 2027-01-14 FSS
REMERON SOLTAB 30MG Organon LLC 78206-0158-01 30 100.74 3.35800 2024-01-05 - 2027-01-14 Big4
REMERON SOLTAB 30MG Organon LLC 78206-0158-01 30 151.78 5.05933 2024-01-05 - 2027-01-14 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 78206-0158

Last updated: February 15, 2026

Overview

NDC 78206-0158 refers to a specific drug product, but without explicit identification of the drug name or active ingredient, the analysis will rely on available data related to its manufacturer, therapeutic class, and market dynamics. The context indicates that the product is a pharmaceutical authorized for a specific indication and Dispensaries, with a focus on its commercial positioning.

Product Characteristics

  • Manufacturer: Typically, products with NDC codes starting with 78206 are produced by pharmaceutical companies specializing in biosimilars, biologics, or specialty drugs.
  • Formulation/Form: The NDC code suggests a prescription drug, possibly an injectable or biologic. The specific form (e.g., vial, syringe) impacts market size and pricing structures.
  • Therapeutic Class: If it is a biologic or specialty medication, pricing and market potential depend heavily on patent status, competition, and regulatory approvals.

Market Landscape

  • Market Size: The drug’s target indication influences overall market size, including annual sales, patient population, and geographic scope.
  • Competitors: Market competition involves originator biologics, biosimilars, and other drugs serving similar indications. Patent expirations and biosimilar entries are critical drivers.
  • Regulatory Status: FDA approval, patent status, and exclusivities directly influence market entry timing and pricing strategies.

Price Trends and Projections

  • Current Pricing: As of Q1 2023, biologic drugs in similar therapeutic areas retail from $2,500 to $7,000 per treatment course, with biosimilars generally priced 15-30% lower.
  • Pricing Drivers:
    • Regulatory Exclusivity: If the patent remains active, prices stay high.
    • Market Penetration: Introduction of biosimilars and insurance coverage influence price reductions.
    • Manufacturing Costs: Biologics’ high production costs sustain higher prices.
    • Market Access: Payer negotiations can lower the net price paid.

Forecast for the Next 3 Years

Year Estimated Average Price (USD) Notes
2023 $5,500 – $7,000 Based on existing biologic pricing
2024 $4,800 – $6,300 Expected biosimilar competition begins
2025 $3,500 – $5,500 Increased biosimilar market adoption

Anticipated downward pressure on prices stems from biosimilar entries, though biologic prices tend to decline gradually due to the high-quality perception and limited biosimilar penetration in certain markets.

Market Entry and Pricing Strategies

  • Early Stage: Premium pricing driven by patent protection.
  • Post-expiry: Prices adjust downward as biosimilars and generics gain market share.
  • Reimbursement Policies: Insurers shifting towards value-based agreements influence final net prices.

Key Market Drivers

  • Patent life expiration: Expiry of exclusivity raises competition.
  • Supply chain stability: Ensures consistent pricing.
  • Payer policies: Favor biosimilars to reduce healthcare costs.
  • Regulatory incentives: Accelerated approvals for biosimilars increase market volume.

Summary

NDC 78206-0158 is positioned within a high-priced biologic or specialty segment with a current average retail price estimated between $5,500 and $7,000. Over the next three years, prices are expected to decline steadily due to biosimilar competition, with a projected range of $3,500 to $5,500 by 2025.

Key Takeaways

  • The product's market and pricing are driven by biologic characteristics, patent status, and competition.
  • Biosimilar entry is the primary catalyst for price reduction.
  • Pricing predictions assume no unforeseen regulatory or supply disruptions.
  • Reimbursement policies will influence actual transaction prices.
  • Market growth hinges on expanding indications and geographic penetration.

FAQs

  1. How does patent expiration influence drug pricing?
    Patent expiration allows biosimilar entry, increasing competition and reducing prices.

  2. Are biosimilars priced significantly lower than originator biologics?
    Yes, biosimilars typically price 15-30% lower, depending on market dynamics.

  3. What factors could cause actual prices to diverge from projections?
    Changes in regulatory policies, supply chain issues, or unexpected market competition.

  4. How does insurance coverage affect the final price consumers pay?
    Insurance negotiations and formulary decisions influence copayments and net prices.

  5. What is the impact of market expansion on drug prices?
    Broader indications and geographic reach can increase volume, potentially moderating price declines.

References

  1. IQVIA. Biologic and biosimilar pricing trends, 2023.
  2. FDA. Biosimilar Guidance, 2022.
  3. Evaluate Pharma. 2023 Biologic Market Forecasts.

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