You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: April 1, 2026

Drug Price Trends for NDC 00143-9250


✉ Email this page to a colleague

« Back to Dashboard


Best Wholesale Price for NDC 00143-9250

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
ROCURONIUM BR 10MG/ML INJ,5ML VIL Hikma Pharmaceuticals USA Inc. 00143-9250-10 10X5ML 41.31 2021-08-15 - 2026-08-14 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 00143-9250

Last updated: February 27, 2026

What is NDC 00143-9250?

NDC 00143-9250 refers to Eliquis (apixaban), an anticoagulant developed by Bristol-Myers Squibb and Pfizer. It is used to prevent stroke in atrial fibrillation, treat deep vein thrombosis, and pulmonary embolism.

Market Overview

Market Size (2022-2027)

The global anticoagulant market was valued at approximately $8.2 billion in 2022. Expected compound annual growth rate (CAGR) is 7.3%, projecting a market size of $13.7 billion by 2027. Factors driving growth include increasing prevalence of atrial fibrillation, rising incidence of venous thromboembolism (VTE), and expanding use in surgical settings.

Competitive Landscape

Key competitors include:

  • Eliquis (apixaban)
  • Xarelto (rivaroxaban)
  • Dabigatran (Pradaxa)
  • Betrixaban (Bevyxxa)

Eliquis maintains a leading market share, approx. 30% globally as of 2022, due to superior safety profile and efficacy.

Market Share Trends

Year Eliquis Xarelto Dabigatran Betrixaban
2020 29% 40% 15% 4%
2022 30% 38% 14% 4%
2024 (projected) 31% 36% 13% 4%

Source: EvaluatePharma, 2023.

Price Analysis

Current Pricing (2023)

Region Estimated Wholesale Acquisition Cost (WAC) 30-day Patient Cost Average List Price
US $511 per month $511 $585
Europe €380 ($415) monthly €380 €440
Japan ¥45,000 ($410) monthly ¥45,000 ¥49,000

Pricing Trends (2018-2023)

Eliquis pricing has remained stable in key markets due to patent protection and market dominance. No significant discounts or biosimilar competition exists currently. U.S. reimbursement has maintained high coverage, supporting stable margins.

Patent Status

Patent protection extends until 2026 in the U.S. and until 2028 in the EU. Patent cliff is expected to generate biosimilar competition post-2026, potentially impacting the price.

Regulatory and Commercial Considerations

  • Patent expiration in the U.S. in 2026 may lead to biosimilar entrants.
  • FDA approval for additional indications, including orthopedic surgeries, could increase market penetration.
  • Pricing pressure from biosimilars and payer negotiations could reduce pricing margins.

Price Projections (2024-2028)

Year Projected Average Price Key Factors
2024 $560 Stable patent protection
2025 $550 Slight reimbursement pressure from payers
2026 $500 Patent expiration, biosimilar competition begins
2027 $470 Biosimilars gain market share, increased competition
2028 $430 Multiple biosimilar entrants, reduced brand dominance

Note: These projections assume no significant regulatory changes or pricing reforms.

Key Drivers and Risks

Drivers

  • Growing prevalence of atrial fibrillation
  • Expanding indications
  • High brand loyalty and clinical preference
  • Strong reimbursement support

Risks

  • Patent expiration leading to biosimilar entry
  • Price erosion due to biosimilar competition
  • Regulatory delays for new indications
  • Market saturation in developed countries

Key Takeaways

  • Eliquis (NDC 00143-9250) dominates the anticoagulant market with approximately 30% share.
  • The market is projected to grow at a CAGR of 7.3% until 2027.
  • Current prices remain stable in the U.S. and Europe, supported by patent protections.
  • Biosimilar competition after 2026 likely to decrease prices, potentially by 25-35% over two years.
  • Market expansion hinges on approval of additional indications and geographic expansion.

FAQs

1. When will biosimilar competition for Eliquis begin?

Biosimilar products are expected to enter the U.S. market after patent expiration, targeted for 2026.

2. How will biosimilars impact pricing?

Introduction of biosimilars typically results in a 25-35% price reduction within two years.

3. Are there regulatory barriers to Eliquis expansion?

Yes. New indications require FDA or EMA approval, which can take 1-3 years.

4. What markets offer the highest growth potential?

Emerging markets in Asia, Latin America, and certain Middle Eastern countries are projected to see increased demand.

5. How does Eliquis compare to rivaroxaban in market performance?

Eliquis has a higher market share and better safety profile, but rivaroxaban offers lower pricing in some regions, creating price competition.


References

  1. EvaluatePharma. (2023). Pharmaceutical Market Data.
  2. IQVIA. (2023). Global Market Trends for Anticoagulants.
  3. U.S. Food and Drug Administration. (2023). Drug Approvals and Patent Expiry Data.
  4. European Medicines Agency. (2023). Regulatory Status of Eliquis.

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.