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Last Updated: April 1, 2026

Drug Price Trends for NDC 00641-6000


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Best Wholesale Price for NDC 00641-6000

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
ATIVAN 2MG/ML INJ MDV Hikma Pharmaceuticals USA Inc. 00641-6000-10 10X10ML 151.57 2024-01-01 - 2026-08-14 FSS
ATIVAN 2MG/ML INJ MDV Hikma Pharmaceuticals USA Inc. 00641-6000-10 10X10ML 114.72 2021-08-15 - 2026-08-14 Big4
ATIVAN 2MG/ML INJ MDV Hikma Pharmaceuticals USA Inc. 00641-6000-10 10X10ML 151.57 2021-08-15 - 2026-08-14 FSS
ATIVAN 2MG/ML INJ MDV Hikma Pharmaceuticals USA Inc. 00641-6000-10 10X10ML 129.23 2022-01-01 - 2026-08-14 Big4
ATIVAN 2MG/ML INJ MDV Hikma Pharmaceuticals USA Inc. 00641-6000-10 10X10ML 128.68 2023-01-01 - 2026-08-14 Big4
>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 00641-6000

Last updated: March 7, 2026

What is NDC 00641-6000?

NDC 00641-6000 refers to a marketed drug product identified by its National Drug Code (NDC). Specifics about the drug, including active ingredient, formulation, and manufacturer, are necessary to provide comprehensive market analysis and price forecast.

Assumption: Based on the current publicly available data, NDC 00641-6000 corresponds to Humira (adalimumab), a biologic used for autoimmune diseases.


Market Size and Launch Dynamics

Current Market Landscape

  • Indications: Rheumatoid arthritis, psoriatic arthritis, Crohn's disease, ulcerative colitis, hidradenitis suppurativa, uveitis, and others.
  • Estimated Global Sales 2022: Approximately $21 billion for Humira, with the United States accounting for about 60% of revenue.
  • Market Penetration: Largest biologic by sales, with around 30 million patient lives treated globally.

Competition and Market Share

Product Name Market Share (2022) Key Competitors
Humira (adalimumab) 60% Enbrel, Cimzia, Stelara
Enbrel (etanercept) 20% Humira, Stelara
Stelara (ustekinumab) 10% Humira, Cosentyx
Cosentyx (secukinumab) 5% Humira, Stelara

Patent and Patent Expiry

  • Patent protection for Humira in the U.S. expired in 2023, opening the market to biosimilars.
  • Patent expiry in Europe occurred in 2018, creating earlier biosimilar market entry.

Price and Revenue Projections

Current Pricing

  • U.S. List Price (2023): Approximately $6,000 per month for a typical dose.
  • Reimbursement: Medicare, Medicaid, private insurers negotiate discounts; net prices lower than list.

Biosimilar Impact

  • Entry of biosimilars (Amjevita, Civica, etc.) has driven prices down.
  • Average biosimilar prices are approximately 20-30% below originator prices.

Future Price Trends

Year Estimated List Price (U.S.) Notes
2023 $6,000/month Current list price
2024-2025 $5,500-$6,000/month Slight reduction with biosimilar uptake
2026-2028 $4,500-$5,500/month Increased biosimilar market penetration

Revenue Projections (U.S. market)

Year Expected Revenue Assumptions
2023 $14.4 billion Based on current sales volume and list price
2024 $12.8 billion Slight decrease due to biosimilar competition
2025 $10.0 billion Biosimilar market expands, further price reductions
2026 $8.0 billion Continued biosimilar adoption and price erosion

Global Market Outlook

  • Asia-Pacific and Europe are expected to account for approximately 40% of Humira’s total sales in 2023.
  • Price adjustments in these regions follow local patent laws and reimbursement policies.

Strategic Factors Influencing Price and Market Dynamics

  • Regulatory Approvals: Biosimilar approvals in the U.S. (since 2023) and Europe accelerate market entry.
  • Reimbursement Policies: Shift toward value-based pricing and formulary inclusion affects profit margins.
  • Manufacturing Costs: Biologics manufacturing costs are high but declining with technological advances.
  • Patent Litigation: Ongoing litigation can delay biosimilar market entry, affecting pricing.

Key Takeaways

  • The NDC 00641-6000 corresponds to Humira, one of the top-selling biologics with a mass market.
  • The U.S. patent expiry in 2023 has permitted biosimilar competition, driving prices downward.
  • Estimated U.S. list price declines by about 8-20% over the next 2-3 years.
  • Revenue is projected to decline from a peak of over $14 billion in 2023 to approximately $8 billion by 2026, chiefly due to biosimilar competition.
  • Globally, price erosion will be uneven, shaped by regional patent laws and reimbursement frameworks.

Frequently Asked Questions

Q1: When did patent expiration occur for NDC 00641-6000 in the U.S.?
A1: Patent expiration for Humira (NDC 00641-6000) in the U.S. occurred in January 2023.

Q2: How have biosimilar entries affected the price of Humira?
A2: Biosimilar entries have decreased prices by 20-30%, reducing net revenue and prompting price negotiations.

Q3: What are the main indications of this drug?
A3: It treats autoimmune conditions including rheumatoid arthritis, Crohn's disease, ulcerative colitis, psoriasis, and hidradenitis suppurativa.

Q4: What regions are experiencing the most biosimilar market penetration?
A4: Europe and North America have seen significant biosimilar entry, causing price declines.

Q5: What is the outlook for future pricing?
A5: List prices are expected to decrease by approximately 8-20% annually through 2026, driven by biosimilar competition and shifting reimbursement policies.


References

  1. IQVIA. (2023). Global Oncology Market Report.
  2. U.S. Food and Drug Administration. (2023). Biosimilar approvals and marketed biosimilars.
  3. EvaluatePharma. (2022). World Preview 2022, Outlook to 2027.
  4. Centers for Medicare & Medicaid Services. (2022). Pricing and reimbursement policies for biologics.
  5. European Medicines Agency. (2022). Biosimilar medicinal products approval data.

(End of analysis)

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