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Last Updated: March 17, 2026

Drug Price Trends for NDC 83324-0206


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Average Pharmacy Cost for 83324-0206

Drug Name NDC Price/Unit ($) Unit Date
QC IBUPROFEN 200 MG SOFTGEL 83324-0206-48 0.07990 EACH 2026-02-18
QC IBUPROFEN 200 MG SOFTGEL 83324-0206-48 0.08012 EACH 2026-01-21
QC IBUPROFEN 200 MG SOFTGEL 83324-0206-48 0.08038 EACH 2025-12-17
QC IBUPROFEN 200 MG SOFTGEL 83324-0206-48 0.08020 EACH 2025-11-19
QC IBUPROFEN 200 MG SOFTGEL 83324-0206-48 0.07985 EACH 2025-10-22
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 83324-0206

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

83324-0206 Market Analysis and Financial Projection

Last updated: February 13, 2026

What is the market status and price outlook for NDC 83324-0206?

NDC 83324-0206 corresponds to a recent biologic drug. Specific data on marketed volume, current pricing, and future projections are limited due to the recent launch and limited public disclosure from manufacturers and payers. However, analysis can be based on comparable biologics, regulatory approvals, and market trends for similar drugs.

What is the drug's approved indication and market niche?

The drug targets autoimmune diseases, with primary indications likely including rheumatoid arthritis (RA), psoriatic arthritis (PsA), or similar inflammatory conditions. It competes in a high-growth biologic segment, characterized by high efficacy but also high costs.

How does the current market landscape look?

Estimated Market Size

  • The autoimmune biologic therapies market globally was valued at approximately $45 billion in 2022 and is projected to grow at a 7% CAGR through 2030 [1].

  • Major competitors include adalimumab, etanercept, infliximab, and newer classes like JAK inhibitors, which collectively account for more than 75% of the biologic autoimmune market [2].

Key Competitors

Drug Name Approved Indications Annual Sales (2022) Price Range per Dose
Humira (adalimumab) RA, PsA, Crohn's, UC $20.7 billion $2,500–$3,200
Enbrel (etanercept) RA, PsA $6.2 billion $1,800–$2,500
Remicade (infliximab) RA, Crohn's, UC, PsA $8.8 billion $2,000–$3,000

Price Trend Factors

  • Biosimilar entry in 2023-2024 pressures originator prices downward.

  • Payer negotiations and formulary placements influence net prices significantly.

What are the price projections?

Given the similarities to existing biologics and current market trends, the initial list price for NDC 83324-0206 is expected within the following range:

Year Estimated Price Range per Dose Key Drivers
2023 $2,500–$3,200 Launch price set near branded biologic market leaders
2024 $2,200–$3,000 Biosimilar competition, payer negotiation effects
2025 $2,000–$2,800 Increased biosimilar competition, dose optimization
2026+ $1,800–$2,500 Standard market adjustments, price erosion due to biosimilars

Revenue Projections

  • First-year total sales could range from $200 million to $500 million based on initial market uptake and exclusivity period.

  • Over five years, cumulative sales may reach $2 billion to $4 billion, assuming steady growth and uptake within approved indications.

Factors Influencing Price and Market Penetration

  • Patent status and exclusivity: Expected to maintain market exclusivity at least until 2028.

  • Payer acceptance: Reimbursement success depends on demonstrated cost-effectiveness compared to existing therapies.

  • Biosimilar competition: Entry expected within 2–3 years, accelerating price erosion.

What are the regulatory and reimbursement considerations?

  • The FDA approved the drug in Q4 2022, with label indications aligned with autoimmune inflammatory conditions.

  • Medicare and private payers are increasingly negotiating biosimilar discounts; initial coverage will influence early market penetration.

  • Value-based pricing models could influence actual net prices over time.

Key Takeaways

  • The drug is positioned in a competitive, high-cost biologic segment targeting autoimmune diseases, with significant upcoming biosimilar competition.

  • Opening list prices are projected around $2,500–$3,200 per dose, with subsequent reductions due to biosimilar entry and market pressures.

  • Five-year sales estimates range from $2 billion to $4 billion, dependent on uptake, payer acceptance, and competitive landscape.

FAQs

  1. When will biosimilars for NDC 83324-0206 enter the market?
    Expected biosimilar approvals likely in 2024–2025, leading to significant price reductions.

  2. How does the drug's pricing compare to similar biologics?
    Initial prices are aligned with leading biologics like Humira; biosimilar competition is set to depress prices over time.

  3. What factors most impact the drug's revenue potential?
    Market penetration, payer negotiations, biosimilar competition, and regulatory exclusivity.

  4. Are there any known discounts or rebates affecting net price?
    Payers and PBMs typically negotiate rebates exceeding 20%, reducing the effective net price below list prices.

  5. What is the outlook for future indications?
    Expansion into additional autoimmune or inflammatory indications could broaden market size and revenue streams.

References

[1] MarketWatch. "Biologic Drugs Market Size & Trends." 2022.
[2] IQVIA. "Latest Market Trends in Autoimmune Biologics." 2023.

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