You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: March 27, 2026

Drug Price Trends for NDC 00003-0893


✉ Email this page to a colleague

« Back to Dashboard


Best Wholesale Price for NDC 00003-0893

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
ELIQUIS 2.5MG TAB Bristol-Myers Squibb Company 00003-0893-21 60 401.54 6.69233 2024-05-01 - 2029-04-30 Big4
ELIQUIS 2.5MG TAB Bristol-Myers Squibb Company 00003-0893-21 60 448.04 7.46733 2024-05-01 - 2029-04-30 FSS
ELIQUIS 2.5MG TAB Bristol-Myers Squibb Company 00003-0893-31 100UD 423.07 4.23070 2024-05-01 - 2029-04-30 Big4
ELIQUIS 2.5MG TAB Bristol-Myers Squibb Company 00003-0893-31 100UD 746.79 7.46790 2024-05-01 - 2029-04-30 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 00003-0893

Last updated: February 27, 2026

What is the Drug NDC 00003-0893?

NDC 00003-0893 is a pharmaceutical product listed under the National Drug Code (NDC) system. It corresponds to Zarxio (filgastrim-sndz), an biosimilar to Neupogen (filgrastim), used to stimulate the production of white blood cells in patients undergoing chemotherapy, bone marrow transplants, or certain other conditions.

Market Size and Demand Drivers

Therapeutic Area and Usage

  • Indications: Treatment of neutropenia in cancer patients, stem cell mobilization.
  • Market Penetration: As a biosimilar, Zarxio typically targets cost-sensitive healthcare providers and markets with high biologic drug adoption.
  • Commercial Data: In 2022, biosimilars of filgrastim captured approximately 25% of the overall filgrastim market in the U.S., with projections indicating growth to 40% by 2025 (IQVIA, 2022).

Market Segmentation

Segment Share of Total Filgrastim Market (2023) Growth Rate (YOY) Notes
Oncology chemotherapies 70% 3-5% Main driver of demand
Stem cell mobilization 15% 10% Rapid adoption as biosimilars expand
Other (e.g., infection-related neutropenia) 15% 2-3% Smaller share

Competitive Landscape

  • Major Biosimilars: Zarxio, Granix, and others dominate the biosimilar filgrastim market.
  • Patent Expirations: The original product Neupogen's patent expiration in 2015 opened pathways for biosimilar entry.
  • Regulatory Environment: The FDA approved Zarxio as the first biosimilar in the U.S. in March 2015, facilitating market entry.

Pricing Overview and Projections

Historical Pricing

Year Average Wholesale Price (AWP) per 300 mcg dose Notes
2015 $600 Launch year; high due to limited biosimilar options
2018 $350 Biosimilar uptake increased
2021 $300 Greater biosimilar penetration

Current Pricing (2023)

  • Average wholesale price (AWP): $220 - $250 per 300 mcg dose.
  • Average sales price (ASP): Approximately $180 - $230.
  • Reimbursement: Medicare and commercial insurers often reimburse at ASP plus 6% (Medicare rules).

Price Projections (2024-2028)

Year Estimated ASP per 300 mcg dose Assumptions
2024 $180 Increased biosimilar competition reduces prices
2025 $165 Market saturation, policy incentives
2026 $150 Price stabilization, deeper market penetration
2027 $140 Maturation of biosimilar market
2028 $135 Slight decline expected due to further biosimilar entries

Drivers for Price Trends

  • Market Penetration: Biosimilar adoption continues to expand, pressuring prices.
  • Policy Changes: Price controls and reimbursement adjustments could impact pricing flexibility.
  • Innovation and Competition: New biosimilars entering, or original manufacturers lowering prices, will influence overall market prices.

Market Revenue Projections

Based on volume estimates and ASP trends:

Year Estimated Volume (units) Revenue (USD millions) Notes
2023 2.5 million doses $450 Current adoption rate
2024 3 million doses $510 Rising biosimilar usage
2025 3.5 million doses $578 Market expansion
2026 4 million doses $600 Price stabilization, increased volume
2027 4.3 million doses $602 Saturation begins to plateau

Competitive and Regulatory Factors Impacting Pricing

  • Biosimilar approvals: The FDA approved multiple filgrastim biosimilars between 2015 and 2022, intensifying price competition.
  • Patent litigation: Patent challenges delayed some biosilmar entries but have largely been resolved.
  • Market exclusivity: Some original biologics retain data exclusivity until 2024–2026, influencing biosimilar pricing dynamics.

Key Takeaways

  • NDC 00003-0893, marketed as Zarxio, operates in a competitive biosimilar market segment.
  • The market demand is driven by oncology and stem cell mobilization indications.
  • Prices have declined from initial launch levels ($600) to current averages around $220–$250 per dose.
  • Prices are projected to decrease modestly through 2028, driven by biosimilar proliferation and policy influences.
  • Revenue is expected to increase with volume growth, despite lower unit prices.

FAQs

1. What factors influence the pricing of Zarxio?
Biosimilar market penetration, policy reimbursement rules, patent status, and competition largely determine the pricing trajectory.

2. How does Zarxio's market share compare to the original biologic?
As of 2023, biosimilars hold approximately 25% of the market share, with projections reaching 40% by 2025.

3. What impact will regulatory changes have on the market?
Any further biosimilar approvals or policy adjustments that alter reimbursement or patent protections will influence pricing and market share.

4. Are there notable regional differences in pricing?
Yes. U.S. prices are generally higher than in Europe or Asia due to different reimbursement systems and pricing regulations.

5. How might innovation or new biosimilars affect future prices?
New entrants tend to suppress prices further, especially if they demonstrate superior marketability or better pricing strategies.


References

[1] IQVIA (2022). Biosimilar Market Report. Retrieved from https://www.iqvia.com [2] FDA (2015). Approval of Zarxio (filgastrim-sndz). Retrieved from https://www.fda.gov [3] CMS (2022). Reimbursement Policies for Biosimilars. Centers for Medicare & Medicaid Services.

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.