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

Last Updated: April 1, 2026

Drug Price Trends for NDC 00904-7107


✉ Email this page to a colleague

« Back to Dashboard


Best Wholesale Price for NDC 00904-7107

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 00904-7107

Last updated: March 13, 2026

What is NDC 00904-7107?

NDC 00904-7107 identifies Remdesivir (Veklury), an antiviral medication approved by the FDA in October 2020 for treating COVID-19 in hospitalized patients. The drug is developed by Gilead Sciences.

Market Scope and Competitive Landscape

Market Size and Usage

  • Global COVID-19 treatment market reached approximately $30 billion in 2022. Expected growth is minor, due to increasing vaccination rates and treatment options.
  • Remdesivir's market share peaked during 2020-2021, accounting for an estimated 50% of antiviral treatments for COVID-19 in the US.
  • Expected market volume: approximately 10 million treatment courses globally in 2022, with a projected compound annual growth rate (CAGR) of 2-3% through 2025.

Key Competitors

  • Pfizer's Paxlovid: Oral antiviral, gained rapid adoption.
  • Merck's Lagevrio (molnupiravir): Oral antiviral, with emergency use authorization (EUA).
  • Other supportive therapies: Dexamethasone, monoclonal antibodies.

Treatment Dynamics

  • Remdesivir is administered intravenously over 5-10 days, typically in hospital settings.
  • Usage declined in late 2022 as oral antivirals gained popularity for early outpatient treatment.
  • Variability in adoption depends on regulatory approvals, hospital protocols, and insurance coverage.

Regulatory and Reimbursement Landscape

  • Approved or authorized in over 60 countries.
  • Reimbursed primarily through government programs like Medicare, Medicaid, and private insurers in the US.
  • Price negotiations and utilization caps impact revenue potential.

Price Trends and Projections

Historical Pricing Data

  • 2019-2020: The drug was in development; prices were not publicly disclosed.
  • 2020: Gilead initially set the list price at $520 per vial, totaling $3,120 for a typical 6-day treatment course (6 vials).
  • 2021: The price remained stable amid high demand.

Current Pricing and Market Factors

  • Actual prices paid by healthcare providers tend to be lower due to negotiations.
  • Average invoice price: estimated between $390 and $450 per vial.
  • Insurance Reimbursement: Medicare has approved a $520 per vial rate for outpatient use in 2022, but hospitals often pay less due to negotiations.

Projected Price Trends (2023-2025)

Year Expected Price per Vial Comments
2023 $350 - $400 Price pressure from generic / biosimilar options, increased competition with oral antivirals
2024 $330 - $380 Market saturation, decline in demand for hospitalized treatments
2025 $310 - $350 Continued market share decline, shift toward outpatient treatments

Market Drivers Affecting Prices

  • Generic/formulation competition: Available in some regions as off-label or unlicensed versions.
  • Supply chain dynamics: Manufacturing capacity has increased, stabilizing procurement costs.
  • Regulatory status: EUA transitions to full approval could influence pricing and procurement policies.
  • Policy shifts: US government stockpiling and stock release policies impact demand instability.

Revenue and Profitability Outlook

  • Projected global sales of remdesivir are expected to decline by 15-20% annually from 2023 onwards.
  • Gilead's revenue attributable to remdesivir may peak at approximately $3 billion in 2022 before gradually decreasing.
  • Margins are likely to compress from 60-70% in 2022 to 40-50% by 2025 as generic competition and price pressures intensify.

Key Takeaways

  • The COVID-19 antiviral market is mature, with remdesivir's peak demand likely behind.
  • Pricing is volatile, influenced by negotiations, competition, and regulatory transitions.
  • Expected decline in sales volume and prices from 2023 onward signals reduced profitability.
  • Gilead may need to diversify their antiviral portfolio to sustain growth.

FAQs

1. Will remdesivir's price decline further post-2023?

Yes. Market saturation, increased competition from oral antivirals, and regulatory shifts are expected to lower procurement prices progressively.

2. How does remdesivir compare with new oral COVID-19 treatments?

Oral treatments like Paxlovid and Lagevrio are more convenient, leading to decreased hospital use and diminished remdesivir demand.

3. Are biosimilars or generics expected to impact remdesivir’s pricing globally?

In some countries, biosimilars are entering the market, which will pressure prices downward, especially outside the US.

4. What are the main factors that could sustain remdesivir prices?

Regulatory barriers delaying biosimilar entry, supply chain constraints, or renewed indications could temporarily stabilize prices.

5. Are there new indications for remdesivir beyond COVID-19?

Currently, remdesivir’s primary indication remains COVID-19; ongoing research into other viral illnesses has not yet resulted in approval.


Sources

[1] Gilead Sciences. (2022). Veklury (Remdesivir) Prescribing Information.
[2] IQVIA. (2022). Global COVID-19 antiviral treatment market report.
[3] U.S. Food and Drug Administration. (2020). Remdesivir Emergency Use Authorization.

Note: All projections are estimates based on current market dynamics and are subject to change as new data emerge.

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.