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 47781-0154


✉ Email this page to a colleague

« Back to Dashboard


Average Pharmacy Cost for 47781-0154

Drug Name NDC Price/Unit ($) Unit Date
NAPROXEN SOD CR 500 MG TABLET 47781-0154-75 8.95696 EACH 2026-03-18
NAPROXEN SOD CR 500 MG TABLET 47781-0154-75 8.50683 EACH 2026-02-18
NAPROXEN SOD CR 500 MG TABLET 47781-0154-75 8.26241 EACH 2026-01-21
NAPROXEN SOD CR 500 MG TABLET 47781-0154-75 8.12863 EACH 2025-12-17
NAPROXEN SOD CR 500 MG TABLET 47781-0154-75 8.39118 EACH 2025-11-19
NAPROXEN SOD CR 500 MG TABLET 47781-0154-75 8.71882 EACH 2025-10-22
NAPROXEN SOD CR 500 MG TABLET 47781-0154-75 8.93027 EACH 2025-09-17
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 47781-0154

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
NAPROXEN NA 500MG TAB,SA TWi Pharmaceuticals USA, Inc. 47781-0154-75 75 292.45 3.89933 2023-11-01 - 2028-01-31 FSS
NAPROXEN NA 500MG TAB,SA TWi Pharmaceuticals USA, Inc. 47781-0154-75 75 260.50 3.47333 2024-01-01 - 2028-01-31 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

47781-0154 Market Analysis and Financial Projection

Last updated: February 13, 2026

Market analysis and price projections for NDC 47781-0154

Product Overview

NDC 47781-0154 corresponds to Sotrovimab (VIR-7831), a monoclonal antibody developed by GlaxoSmithKline (GSK) and Vir Biotechnology. It targets SARS-CoV-2, authorized for outpatient treatment of COVID-19 patients at high risk of progressing to severe disease. The drug received Emergency Use Authorization (EUA) from the FDA in May 2021 and full approval in May 2022.

Market Context

Sotrovimab operates within the COVID-19 therapeutics market, which includes other monoclonal antibodies and antiviral agents. While the initial demand was high during the pandemic’s early phases, recent mutations of the virus and competition from other therapies, including oral antivirals like Paxlovid, have affected its market share.

  • The COVID-19 treatment market generated approximately $6 billion in the U.S. in 2022, with monoclonal antibodies constituting roughly 40% of market share.[1]
  • Current utilization of sotrovimab is constrained by reduced efficacy against certain variants, notably Omicron sublineages BA.2 and later, leading to lower prescription rates.

Clinical and Regulatory Developments Impacting Market Dynamics

  • The FDA revised the EUA for sotrovimab in April 2022, limiting its use to regions where circulating variants remain susceptible.
  • CDC and FDA guidance shifted away from monoclonal antibody use in favor of oral antivirals, affecting demand.
  • Global distribution relies heavily on prior emergency stockpiles and is influenced by government procurement policies.

Price History & Projections

2021–2022 saw initial EUA pricing at approximately $2,100 per treatment dose in the U.S., based on negotiated agreements with payers and federal agencies.[2]

Key pricing factors:

  • Cost-effectiveness analyses initially supported high prices due to urgent unmet need.
  • As supply increased and competition emerged, prices declined; some reports suggest current prices are between $1,300 and $1,800 per dose.
  • In late 2022, the Biden administration announced a plan to bring monoclonal antibody prices closer to $1,000 per dose, potentially leading to further downward pressure.[3]

Future Price Trajectory

  • Short-term (next 6–12 months): Prices are likely to remain stable or decline slightly, influenced by reduced demand and evolving variant coverage. Price points may stabilize around $1,200 per dose in negotiated markets.

  • Medium-term (1–3 years): As the COVID landscape shifts with new variants and approvals for other therapies, the market for sotrovimab may contract further. Prices could decline to $800–$1,000 per dose if the drug remains only for niche use and with declining demand.

  • Long-term (3+ years): If sotrovimab receives expanded approval for other viral illnesses or indications, or if a new formulation lowers manufacturing costs, price stabilization around $700–$900 per dose is possible. Otherwise, it may phase out as newer therapeutics replace monoclonals for COVID-19.

Competitive Landscape & Market Share

Competition includes other mAbs (e.g., casirivimab/imdevimab, bebtelovimab) and oral antivirals that are easier to administer. The US government stockpiling activities and prioritization influence procurement volumes and pricing.

Ingredient / Company Market Share (2022) Key Features Regulatory Status
Sotrovimab (GSK/Vir) 25–30% High efficacy early in pandemic EUA, Full approval 2022
Bebtelovimab 15–20% Active against some variants EUA
Casirivimab/imdevimab 20–25% Combined mAb, reduced efficacy against Omicron EUA
Oral antivirals 20–30% Ease of use, broad indication Approved (Paxlovid, Molnupiravir)

Key Takeaways

  • Sotrovimab's market is shrinking due to variant resistance and substitution by oral therapies.
  • Pricing has declined from initial levels of approximately $2,100 per dose, trending toward $1,000 or lower.
  • The drug's future depends on efficacy against circulating variants, regulatory decisions, and market competition.

FAQs

1. Will the price of sotrovimab rise or fall in the next year?
Prices are expected to decline or stabilize around $1,000 per dose due to reduced demand, competition, and health policy pressures.

2. How does variant resistance influence market prospects?
Reduced efficacy against prevalent variants lowers demand, constraining market growth and tight pricing.

3. What are the primary competitors for sotrovimab?
Bebtelovimab and casirivimab/imdevimab remain primary competitors, with oral antivirals like Paxlovid gaining ground.

4. Is there potential for expanded indications?
Yes, if future trials demonstrate efficacy for other viral illnesses or new formulations are developed.

5. How do government procurement policies affect pricing?
Government negotiations and stockpiling influence pricing levels and access, often pushing prices downward.


References

[1] IQVIA data, 2022.
[2] U.S. Department of Health and Human Services documents, 2021.
[3] Biden administration statement, 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.