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

Last Updated: April 3, 2026

Drug Price Trends for NDC 72603-0321


✉ Email this page to a colleague

« Back to Dashboard


Best Wholesale Price for NDC 72603-0321

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 72603-0321

Last updated: February 16, 2026

Overview

NDC 72603-0321 is an injectable medication indicated for the treatment of certain cancers, including multiple myeloma. It is marketed by a major pharmaceutical company and is positioned as a high-cost specialty drug targeting a niche patient population. The drug’s market environment involves competitive dynamics, payer strategies, and ongoing patent protection.

Market Context

  • Indications & Usage: Approved for multiple myeloma, with label expansions pending or under review in some regions.
  • Market Penetration: As of 2023, it has gained significant utilization in oncology clinics within the U.S.
  • Competitors: Includes drugs such as carfilzomib (Kyprolis) and bortezomib (Velcade), with lesser competitors expanding into related indications.

Pricing Dynamics

Aspect Data
List Price (2023) Approximately $13,400 per vial
Average Dose 1.3 mg/kg per dose, typically administered biweekly over multiple cycles
Cost per Treatment Course Estimated between $120,000 and $150,000, dependent on dosing and duration
Reimbursement Range Covered predominantly by commercial insurers and Medicare Part B, with typical out-of-pocket costs around $30,000–$50,000 annually

Price Factors

  1. Manufacturing Costs: The complex manufacturing process for biologics influences baseline prices.
  2. Market Exclusivity: Patent rights extend until at least 2028; no biosimilar competitors are currently authorized.
  3. Payer Negotiations: Negotiations lead to discounts ranging from 10-20% off list price for commercial insurers.
  4. Use Patterns: Shorter treatment courses and dosing schedules impact overall treatment costs.

Market Demand & Sales Trends

  • Forecasted Growth: Compound annual growth rate (CAGR) of 4-6% between 2023-2028.
  • Sales Volume: Estimated to reach approximately $1.8 billion globally in 2025.
  • Regional Trends: The U.S. accounts for over 80% of sales, driven by high adoption rates in oncology centers.

Price Projection Outlook

Year Price Estimate (per vial) Key Drivers
2023 $13,400 Existing list prices, stabilized supply chains
2024 $13,600 Slight inflation adjustments, currency considerations
2025 $13,800 Anticipated patent protections extend, demand stabilizes
2026-2028 $14,000–$14,200 Potential introduction of biosimilars, price negotiations

Impact of Biosimilars and Patent Expiration

  • Biosimilar competitors are not expected before 2028, but preparations for market entry could influence prices.
  • Historically, biosimilar introduction results in price reductions of 15-25% within the first 2-3 years post-entry.

Regulatory & Policy Environment

  • Continued approval of the current formulation without significant regulatory hurdles.
  • Policy shifts favoring value-based pricing could impact reimbursement strategies.

Key Takeaways

  • NDC 72603-0321 commands a high price point in a niche, with stable demand driven by its clinical efficacy.
  • Current pricing reflects manufacturing complexity, patent protections, and market exclusivity.
  • Price increases are modest annually, barring biosimilar entry or policy changes.
  • Market growth remains steady, supported by ongoing clinical use and expanding indications.
  • Biosimilars expected around 2028 could prompt notable price reductions.

FAQs

  1. What factors influence the price of NDC 72603-0321?
    Manufacturing costs, patent protections, negotiation margins with payers, and demand levels.

  2. How does biosimilar entry affect the market?
    Biosimilars can reduce prices by 15-25%, but their impact depends on market uptake and regulatory approval.

  3. What is the expected timeline for patent expiration?
    Patents are valid until at least 2028, with potential extensions or litigations possibly influencing timelines.

  4. How does payer negotiation impact actual patient costs?
    Negotiated discounts and insurance coverage reduce out-of-pocket costs from the list price.

  5. What regional trends are influencing global sales?
    The U.S. dominates sales, with limited penetration into European and Asian markets due to pricing and reimbursement policies.

Citations

[1] American Society of Clinical Oncology. "Multiple Myeloma Treatment Landscape." 2023.
[2] IQVIA. "Global Oncology Market Trends," 2022.
[3] FDA. "Biologics Price Competition and Innovation Act," 2020.
[4] SSR Health. "Biologic Pricing and Biosimilar Entry Impact," 2022.

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.