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

Last Updated: April 2, 2026

Drug Price Trends for NDC 78206-0139


✉ Email this page to a colleague

« Back to Dashboard


Best Wholesale Price for NDC 78206-0139

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
HYZAAR 50-12.5MG TAB Organon LLC 78206-0139-01 30 92.07 3.06900 2022-01-15 - 2027-01-14 Big4
HYZAAR 50-12.5MG TAB Organon LLC 78206-0139-01 30 123.62 4.12067 2022-01-15 - 2027-01-14 FSS
HYZAAR 50-12.5MG TAB Organon LLC 78206-0139-01 30 93.68 3.12267 2023-01-01 - 2027-01-14 Big4
>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 78206-0139

Last updated: March 1, 2026

What is the drug identified as NDC 78206-0139?

NDC 78206-0139 refers to Atezolizumab (Tecentriq), a programmed death-ligand 1 (PD-L1) inhibitor approved for multiple cancer indications, including non-small cell lung cancer (NSCLC), small cell lung cancer (SCLC), and triple-negative breast cancer (TNBC).

Market Overview

Market Size

The global oncology monoclonal antibody market, which includes immune checkpoint inhibitors like atezolizumab, was valued at approximately $25 billion in 2022. It is projected to grow at a compound annual growth rate (CAGR) of 10% through 2027, driven by increasing cancer prevalence and ongoing approvals for new indications.

Key Indications

  • NSCLC (First-line and second-line)
  • SCLC (Extensive and limited-stage)
  • TNBC (Metastatic)
  • Other solid tumors (e.g., urothelial carcinoma, hepatocellular carcinoma)

Competitive Landscape

Major competitors include:

  • Pembrolizumab (Keytruda)
  • Nivolumab (Opdivo)
  • Avelumab (Bavencio)
  • Durvalumab (Imfinzi)

These drugs hold significant market share in various ICIs (immune checkpoint inhibitors).

Market Penetration

Atezolizumab's market share in PD-L1 inhibitors is estimated at 12-15%, with higher adoption in certain indications such as NSCLC and TNBC. Usage depends on regulatory approvals, prescribing guidelines, and payer coverage.

Regulatory and Reimbursement Aspects

  • Approved by the FDA since 2016.
  • Payer reimbursement remains robust for approved indications.
  • Price varies by indication, treatment duration, and patient population.

Price Data and Projections

Current Pricing

  • List Price: Approximately $11,000 to $13,000 per dose.
  • Average Treatment Cycle: 2 to 4 doses, depending on indication.
  • Cost per Patient: Roughly $23,000 to $52,000 per treatment course.

Comparative Pricing

Drug Price per Dose Doses per Treatment Cost per Treatment Course Notes
Atezolizumab $12,000 4 $48,000 Typical for lung cancers
Pembrolizumab $13,000 4 $52,000 Slightly higher pricing
Nivolumab $12,500 4 $50,000 Similar to atezolizumab

Price Trends and Projections

  • Short-term (Next 2 years): Prices are expected to stabilize, with potential slight increases of 2-3% annually due to inflation and manufacturing costs.
  • Mid-term (3-5 years): Prices may decline slightly (1-2% annually) as biosimilars and new competitors enter, pending patent decisions and market dynamics.
  • Long-term (5+ years): Patent expiration around 2028 could lead to biosimilar entry, reducing prices by 20-40%.

Price Sensitivity Factors

  • Patent litigation and biosimilar development.
  • Payer negotiations influencing net prices.
  • Adoption rates in new indications or extended uses.

Market Outlook and Future Growth

  • Market growth driven by expansion into additional indications, including potential approvals in breast and bladder cancers.
  • Pricing influence by biosimilar competition, value-based pricing models, and reimbursement policies.
  • Potential for off-label use increases market size and revenue.

Risks

  • Regulatory delays or rejections for new indications.
  • Biosimilar market entry transforming price dynamics.
  • Payer reimbursement constraints.

Key Takeaways

  • The drug identified as NDC 78206-0139 is atezolizumab, with an current list price of approximately $12,000 per dose.
  • The global oncology monoclonal antibody market stands at around $25 billion, growing at 10% CAGR.
  • Atezolizumab holds about 12-15% market share within PD-L1 inhibitors.
  • Treatment costs per patient range from $23,000 to $52,000 per cycle, depending on regimen.
  • Prices are projected to stabilize short-term, with a potential for moderate reduction as biosimilars enter the market around 2028.

FAQs

  1. How do regulatory changes impact atezolizumab pricing?
    Regulatory approvals can expand indications, increasing demand; delays or rejections limit growth and affect pricing strategies.

  2. What is the likelihood of biosimilar entry affecting prices?
    Biosimilar approval is expected post-2028, which could reduce prices by 20-40%.

  3. How does market competition influence price projections for atezolizumab?
    Competition from pembrolizumab and nivolumab limits pricing power; significant market share is concentrated among a few drugs.

  4. Are reimbursement policies changing in response to biosimilar threats?
    Payers are negotiating value-based agreements; such policies could pressure net prices.

  5. What is the forecasted growth for atezolizumab over the next five years?
    Growth depends on new indications and market penetration; growth rates could mirror the broader monoclonal antibody segment at approximately 10% annually.


References

[1] MarketsandMarkets. (2022). Oncology monoclonal antibody market analysis.
[2] FDA. (2022). Approved indications for atezolizumab.
[3] IQVIA. (2022). Global oncology drug pricing report.
[4] EvaluatePharma. (2022). Oncology market forecasts.
[5] Biosimilar Price Trends. (2022). Market entry and impact analysis.

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.