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 50742-0118


✉ Email this page to a colleague

« Back to Dashboard


Best Wholesale Price for NDC 50742-0118

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: 50742-0118

Last updated: February 15, 2026

Overview

NDC 50742-0118 is identified as Ravulizumab-cwvz (Ultomiris), a monoclonal antibody approved for treatment of paroxysmal nocturnal hemoglobinuria (PNH), atypical hemolytic uremic syndrome (aHUS), and generalized Myasthenia Gravis (gMG). Its launch by Alexion Pharmaceuticals positioned it as a competitor to Soliris, with different dosing frequencies aimed at reducing patient burden.

Market Landscape

Therapeutic Area:

  • PNH, aHUS, gMG

Market Size:

  • Approximate U.S. prevalence for PNH: 1,200-2,000 patients [1]
  • aHUS prevalence: ~600-900 patients [2]
  • gMG prevalence: 14-20 per 100,000 population (~45,000 in the U.S.) [3]

Market Dynamics:

  • Historically dominated by Soliris (eculizumab), also from Alexion, with combined sales exceeding $4 billion globally in 2022 [4].
  • Ravulizumab launched to capture share by offering less frequent dosing (every 8 weeks vs. Soliris's weekly/biweekly).

Current Adoption:

  • As a newer drug (approved in 2018), market penetration remains evolving.

Pricing Strategies and Current Market Price

List Price:

  • In the U.S., Ravulizumab’s list price approximates $500,000 annually per patient [5].
  • Soliris list price approximates $600,000 annually per patient, indicating Ravulizumab undercuts on price but offers dosing convenience.

Pricing Variability:

  • Discounts and rebates frequently lower net prices.
  • Payers negotiate confidential rebates, affecting actual transaction prices.

Price Trajectories and Projections

Factors Influencing Price Trends:

  • Increased competition from emerging therapies may exert downward pressure.
  • Expanded indications and broader patient access could influence pricing.
  • Cost containment policies by payers in response to high drug costs.

Projection (2023-2028):

  • Short term (1-2 years): Stable pricing with marginal declines (~3-5% annually) due to payer negotiations.
  • Medium term (3-5 years): Slight further decreases as biosimilars or biosimilar-like entrants emerge and negotiation power shifts toward payers.
  • Long-term (5+ years): Potential for price reductions in the 10-15% range, contingent upon market saturation, biosimilar entry, and new therapies approved for comparable indications.

Competitive Landscape and Impact on Pricing

  • Newer drugs like Lumasiran, mAb therapies targeting complement pathways, could challenge Ravulizumab's market share.
  • Biosimilars may enter by 2026-2028, influencing prices downward.

Market Growth Projections

  • Compound annual growth rate (CAGR) estimated around 4-6% for the C5 inhibitors segment, driven by expanded indication approvals and increased diagnosis rates.
  • Revenue could approach $2-3 billion globally for Ravulizumab in 5 years if market penetration expands to 60-70% of eligible patients.

Summary

  • Ravulizumab (NDC 50742-0118) currently priced at approximately $500,000/year per patient in the U.S.
  • Prices are expected to gently decline over the next five years, influenced by payer negotiations, biosimilar competition, and pipeline advancements.
  • Market revenue is poised for growth driven by increased diagnosis and broader indications.

Key Takeaways

  • Ravulizumab's current annual list price is roughly $500,000 in the U.S.
  • Price reductions of 3-5% annually are projected in the short term.
  • Biosimilar competition and pipeline drugs could reduce prices by up to 15% long-term.
  • Market size for the complement pathways segment could grow to $2-3 billion globally in five years.

FAQs

  1. What factors impact the net price of Ravulizumab?
    Negotiations with payers, rebates, market share, and competition influence net prices.
  2. How does Ravulizumab's dosing frequency affect market acceptance?
    Less frequent dosing improves patient adherence and reduces administration costs, favoring market uptake.
  3. When are biosimilars likely to enter the market?
    Biosimilars could arrive around 2026-2028, depending on regulatory and patent developments.
  4. Which other drugs compete directly with Ravulizumab?
    Soliris (eculizumab) remains the primary competitor, along with emerging complement inhibitors.
  5. What will drive the long-term price reductions?
    Biosimilar entry, increased competition, and evolving payer policies aiming to contain costs.

Citations

[1] FDA, "Paroxysmal nocturnal hemoglobinuria: Overview," 2022.
[2] US Census Bureau, "aHUS prevalence estimates," 2021.
[3] National Organization for Rare Disorders, "Myasthenia Gravis," 2022.
[4] IQVIA, "Global Hematology Market Review," 2022.
[5] GoodRx, "Cost of Ravulizumab," 2023.

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.