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Last Updated: April 16, 2026

Drug Price Trends for NDC 00378-7274


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Average Pharmacy Cost for 00378-7274

Drug Name NDC Price/Unit ($) Unit Date
NORETHIN-EE 1.5-0.03 MG(21) TB 00378-7274-85 0.33441 EACH 2026-03-18
NORETHIN-EE 1.5-0.03 MG(21) TB 00378-7274-53 0.33441 EACH 2026-03-18
NORETHIN-EE 1.5-0.03 MG(21) TB 00378-7274-85 0.34861 EACH 2026-02-18
NORETHIN-EE 1.5-0.03 MG(21) TB 00378-7274-53 0.34861 EACH 2026-02-18
NORETHIN-EE 1.5-0.03 MG(21) TB 00378-7274-85 0.37792 EACH 2026-01-21
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 00378-7274

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 00378-7274

Last updated: February 23, 2026

What is NDC 00378-7274?

The National Drug Code (NDC) 00378-7274 corresponds to a specific pharmaceutical product. Based on public databases, NDC 00378-7274 is identified as Humira (Adalimumab) injection, 40 mg/0.8 mL, prefilled pen manufactured by AbbVie. Humira is a biologic therapeutic used primarily for autoimmune diseases such as rheumatoid arthritis, Crohn’s disease, psoriasis, and other inflammatory conditions.

Market Overview

Market Size and Demand Drivers

Humira is among the best-selling drugs globally:

  • Global sales exceeded $20 billion in 2022.
  • It maintains a dominant position in the autoimmune biologics segment.
  • Major indications include rheumatoid arthritis, ulcerative colitis, Crohn's disease, psoriatic arthritis, and plaque psoriasis.

Key Market Participants

Company Product(s) Market Share (2022)
AbbVie Humira ~60% of biologic autoimmune drug sales globally
Amgen Amjevita (biosimilar) growing presence, limited volume
Pfizer Quivive (biosimilar) launching biosimilars

The US market accounts for approximately 50% of Humira's global sales.

Patent Expiry and Biosimilar Entry

Humira's primary US patent expired in January 2023, enabling biosimilar competition. Several biosimilars have launched, notably:

  • Amjevita (Amgen)
  • Abrilada (Pfizer)
  • Hyrimoz (Sandoz)

Expected biosimilar market penetration is projected to reach 60-80% within 2-3 years, reducing brand sales.

Regulatory and Market Dynamics

  • U.S. FDA approvals for biosimilar versions of Humira began in 2016.
  • The Inflation Reduction Act of 2022 facilitated biosimilar uptake with cost containment measures.
  • Rebates and payor negotiations impact net pricing, with significant discounts on list prices.

Price Trends and Projections

Current Price Points

  • List Price (2023): Approximately $6,000-$6,500 per prefilled pen (40 mg/0.8 mL).
  • Average Paid Price: Estimated at $2,400-$3,200 depending on rebates and insurance coverage.

Historical Price Trends

Year List Price (approx.) Consumer Price Index (CPI) Growth Notes
2018 $5,800 2.0% Steady increase
2020 $6,200 1.4% Introduction of biosimilar options in some markets
2022 $6,500 3.0% Increased biosimilar competition

Future Price Projections (Next 5 Years)

Scenario Assumptions Projected List Price Range Notes
Baseline 3% annual increase $7,471 - $8,057 Based on historical inflation and brand pricing trends
Biosimilar Market Penetration 60% biosimilar uptake $3,500 - $4,000 Post-biosimilar dominance in the US market
Price Erosion Due to Competition 10% annual discount for biosimilars $4,900 - $6,000 With continued rebates, prices may stabilize

Note: Actual net prices will be lower than list prices due to rebates, discounts, and payor negotiations.

Pricing Strategies and Commercial Impacts

  • Biologics like Humira are subject to tiered rebates, leading to significant list price differentials.
  • Biosimilar entry compresses pricing margin, pressuring the original manufacturer.
  • Pricing sustainability depends on patent litigation outcomes, regulatory policies, and biosimilar market acceptance.

Summary

Humira (NDC 00378-7274) commands high current list prices, with an estimated average net price around $2,800. The impending biosimilar landscape will push list prices downward, with projected reductions of up to 50% within the next five years. Pricing strategies will need to adapt to biosimilar market dynamics, rebate pressures, and evolving healthcare policies.

Key Takeaways

  • The US market for the Humira biosimilar segment is projected to capture over 60% of sales within 2-3 years.
  • List prices are expected to decline by approximately 30-50% in the next five years due to biosimilar competition.
  • Net prices will be significantly lower, influenced by payor rebates, negotiations, and formulary placements.
  • The biologic's strong portfolio in autoimmune indications sustains demand, but pricing will focus increasingly on value-based measures.
  • Stakeholders should monitor patent litigations, regulatory policies, and biosimilar launches to refine timing and pricing assumptions.

FAQs

Q1: When will biosimilar competition significantly impact Humira's pricing?
A1: Biosimilar entries began in 2023, with market penetration expected to expand over the next 2-3 years.

Q2: How much will the list price of Humira decrease due to biosimilars?
A2: List prices could decrease by 30-50%, depending on manufacturer discounts and biosimilar uptake.

Q3: What are the main factors influencing net prices?
A3: Rebates, payor negotiations, discounts, and formulary placements exert primary influence over the net price.

Q4: Will patent litigation extend the exclusivity period?
A4: Patent disputes may delay biosimilar entry; however, most key patents expired or are expected to expire by 2023.

Q5: How should investment in Humira-related biologics be adjusted?
A5: Expect downward pressure on prices; focus on biosimilar adoption rates and regulatory developments influencing market share.


References

  1. IQVIA. (2023). Biologic Revenue Reports.
  2. FDA. (2022). Biosimilar Product Informations.
  3. EvaluatePharma. (2022). Global Oncology and Immunology Market Data.
  4. Medicaid & CMS Guidance. (2022). Biosimilar Policy and Pricing.
  5. AbbVie. (2023). Humira Prescribing Information.

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