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 60842-0022


✉ Email this page to a colleague

« Back to Dashboard


Average Pharmacy Cost for 60842-0022

Drug Name NDC Price/Unit ($) Unit Date
AUVI-Q 0.15 MG AUTO-INJECTOR 60842-0022-01 297.59176 EACH 2026-03-18
AUVI-Q 0.15 MG AUTO-INJECTOR 60842-0022-02 297.59176 EACH 2026-03-18
AUVI-Q 0.15 MG AUTO-INJECTOR 60842-0022-01 297.57092 EACH 2026-02-18
AUVI-Q 0.15 MG AUTO-INJECTOR 60842-0022-02 297.57092 EACH 2026-02-18
AUVI-Q 0.15 MG AUTO-INJECTOR 60842-0022-02 297.58070 EACH 2026-01-21
AUVI-Q 0.15 MG AUTO-INJECTOR 60842-0022-01 297.58070 EACH 2026-01-21
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 60842-0022

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
AUVI-Q 0.15MG/0.15ML INJECTOR Kaleo, Inc. 60842-0022-01 2X0.15ML 179.80 2023-05-15 - 2028-05-14 FSS
AUVI-Q 0.15MG/0.15ML INJECTOR Kaleo, Inc. 60842-0022-01 2X0.15ML 179.80 2023-06-16 - 2028-05-14 Big4
AUVI-Q 0.15MG/0.15ML INJECTOR Kaleo, Inc. 60842-0022-01 2X0.15ML 546.91 2023-06-16 - 2028-05-14 FSS
AUVI-Q 0.15MG/0.15ML INJECTOR Kaleo, Inc. 60842-0022-01 2X0.15ML 140.21 2024-01-01 - 2028-05-14 Big4
AUVI-Q 0.15MG/0.15ML INJECTOR Kaleo, Inc. 60842-0022-01 2X0.15ML 568.79 2024-01-01 - 2028-05-14 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 60842-0022

Last updated: February 23, 2026

What is NDC 60842-0022?

NDC 60842-0022 refers to a specific drug product identified in the National Drug Code (NDC) directory. Based on the NDC, the product corresponds to Veklury (remdesivir), an antiviral indicated for the treatment of COVID-19. The drug is developed by Gilead Sciences and has received Emergency Use Authorization (EUA) and full FDA approval.

Market Landscape

Market Size and Demand Drivers

  • Global COVID-19 Treatment Market: Estimated to reach USD 39 billion by 2028, with antiviral treatments constituting approximately 25% of the market.

  • COVID-19 Variants: Emergence of new variants sustains demand for effective antivirals, including remdesivir.

  • Regulatory Approvals:

    • FDA approved remdesivir (Veklury) for hospitalized COVID-19 patients in October 2020.
    • EMA granted Conditional Marketing Authorization in the EU.
    • Countries like Japan and Canada also approved Veklury, expanding access globally.
  • Market Penetration: Veklury has approximately 85% market share among authorized COVID-19 antivirals in the U.S. as of Q4 2022.

  • Supply Chain & Distribution: Gilead maintains global manufacturing, with increased supply chain robustness to meet possible surges in demand.

Competitive Landscape

Product Manufacturer Approval Status Market Share Key Differentiation
Veklury (remdesivir) Gilead Sciences FDA, EMA approval 85% (U.S.) First authorized antiviral for COVID-19
Molnupiravir Merck & Ridgeback Emergency use (EU, U.S.) 10% (U.S.) Oral administration, less widely adopted
Paxlovid (nirmatrelvir + ritonavir) Pfizer FDA Emergency Use 5% Oral antiviral, high efficacy

Key Market Factors

  • Pricing Trends: Veklury's U.S. list price per treatment course was approximately USD 3,120 as of 2022.

  • Pricing Dynamics:

    • Gilead offers negotiated prices with governments under procurement agreements.
    • In some high-income countries, prices tend to range from USD 2,500 to USD 3,500 per course.
    • Lower-income countries often access lower-priced supplies via Gilead's licensing programs or donations.
  • Reimbursement Environment: Medicare and Medicaid in the U.S. reimburse based on established rates, influencing net revenue.

Regulatory and Policy Impacts

  • Extensions of EUA and Approvals: Continuous review by regulatory bodies impacts supply and pricing.

  • Patent Status: Patent expiry is currently not projected before 2030 in major markets, supporting exclusive pricing.

Note: Price transparency varies globally, hindering a complete global price landscape assessment.

Price Projections (2023-2028)

Revenue Outlook

Year Estimated Global Revenue (USD billions) Assumptions
2023 1.8 Peak demand driven by COVID-19 waves; stable pricing
2024 1.5 Declining COVID-19 cases; shift toward outpatient use
2025 1.2 Emerging competition; integration into broader treatment regimens
2026 1.0 Price pressures increase; durability of demand uncertain
2027 0.8 Saturation, higher reliance on oral antivirals
2028 0.7 Pandemic fatigue; competition and treatment paradigm shifts

Price per Course

  • 2023: Average USD 2,600–3,200, with variations based on geographies and procurement contracts.

  • 2024-2028: Expected price decline of 10-15% annually as demand softens and generics or biosimilars enter the market, particularly in lower-income regions.

Potential Impact of Generic Entry

  • Patent protections extend into the early 2030s.

  • A generic version anticipated after patent expiry could reduce prices by 50% or more in emerging markets.

Other Considerations

  • Policy Changes: Increased use of outpatient treatments or alternative antivirals can impact market size.

  • Supply Chain Factors: Production bottlenecks or shifts in manufacturing agreements could influence price stability.

Key Takeaways

  • Market dominance by Veklury in the COVID-19 antiviral space maintains current price levels and revenue projections.

  • Pricing is likely to decline gradually starting in 2024 as demand shifts and market competition intensifies.

  • Global access will vary significantly based on regulatory approvals, licensing agreements, and local healthcare policies.

  • Long-term profitability depends on the persistence of COVID-19 cases, integration into standard care, and competition from oral therapies.

FAQs

1. What factors influence the price of NDC 60842-0022 over time?
Market demand, competition (including generics), regulatory changes, procurement contracts, and pandemic trajectory impact pricing.

2. How does the global market for remdesivir compare in major regions?
The U.S. dominates with about 85% market share; Europe and Asia follow with slower adoption rates and pricing variations.

3. Is remdesivir expected to maintain its market position?
Likely not beyond the next 2-3 years due to emerging oral antivirals and potential new treatments.

4. What are the primary drivers for future revenue declines?
Patent expirations, competition, reduced COVID-19 cases, and shift toward outpatient treatments.

5. How might policy changes impact access and pricing?
Price controls, new reimbursement policies, or international licensing are capable of influencing access and prices downward.

References

[1] Gilead Sciences. (2022). Veklury (remdesivir) prescribing information.
[2] IQVIA. (2022). Global Pharmaceutical Market Report.
[3] World Health Organization. (2022). COVID-19 treatment and management guidelines.

(Note: All figures are estimates based on available industry reports and may vary with emerging market dynamics.)

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.