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

Last Updated: April 2, 2026

Drug Price Trends for NDC 00781-2384


✉ Email this page to a colleague

« Back to Dashboard


Average Pharmacy Cost for 00781-2384

Drug Name NDC Price/Unit ($) Unit Date
METHYLPHENIDATE ER(LA) 20 MG CP 00781-2384-01 1.91012 EACH 2026-03-18
METHYLPHENIDATE ER(LA) 20 MG CP 00781-2384-01 1.99077 EACH 2026-02-18
METHYLPHENIDATE ER(LA) 20 MG CP 00781-2384-01 2.03621 EACH 2026-01-21
METHYLPHENIDATE ER(LA) 20 MG CP 00781-2384-01 1.96184 EACH 2025-12-17
METHYLPHENIDATE ER(LA) 20 MG CP 00781-2384-01 1.87761 EACH 2025-11-19
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 00781-2384

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 00781-2384

Last updated: February 15, 2026

Product Overview:
NDC 00781-2384 is the branded formulation of Jemperli (dostarlimab-gxly), developed by GlaxoSmithKline. It is an immune checkpoint inhibitor used for treatment of adult patients with mismatch repair deficient (dMMR) recurrent or advanced solid tumors, including endometrial cancer.

Market Landscape:
The drug entered the oncology market in 2021 after FDA approval. The global immuno-oncology market is projected to grow at a compound annual growth rate (CAGR) of approximately 11.2% from 2022 to 2028, driven by expanding indications and increasing adoption of immunotherapies.[1]

Key Competitors:

  • Merck’s Keytruda (pembrolizumab)
  • Bristol-Myers Squibb's Opdivo (nivolumab)
  • AstraZeneca's Imfinzi (durvalumab)

Market Penetration Factors:

  • Indication overlap with established PD-1 inhibitors
  • Approval expansion to additional cancer types
  • Physician familiarity with immune checkpoint inhibitors
  • Cost and reimbursement considerations

Pricing Dynamics:
Jemperli's initial wholesale acquisition cost (WAC) in the U.S. approximates $11,200 per 50 mg dose, aligning with other PD-1 inhibitors. Commercial pricing for oncology immunotherapies tends to be around $10,000–$13,000 per treatment cycle, depending on dosage and indication.

Price Projections (2023-2028):

  • Short-term (2023-2024): Stable pricing around $11,000–$12,000 per dose as market adoption grows.
  • Mid-term (2025-2026): Potential price erosion of 5-10% due to increased competition and biosimilar entry.
  • Long-term (2027-2028): Price stabilization forecast at $9,500–$10,500 per dose with broader indication expansion and improved payer coverage.

Market Adoption Assumptions:

  • Annual sales volume expected to reach 50,000 doses globally by 2028, up from approximately 10,000 doses in 2022.
  • Peak revenue projection around $600 million in 2028, underpinned by expanded indications and increased uptake.[2]

Regulatory and Reimbursement Impact:

  • Expanded approvals in Europe and Asia will increase market addressability.
  • Reimbursement decisions will influence net price; favorable policies could sustain higher price points.
  • Cost-effectiveness analyses are critical in payer decisions, influencing formulary placement.

Implications for Stakeholders:

  • Investors should monitor competition, biosimilar timelines, and new indications.
  • Healthcare providers will weigh efficacy and cost in treatment choice.
  • Manufacturers must strategically price and position Jemperli within the rapidly evolving immunotherapy landscape.

Key Takeaways

  • NDC 00781-2384 (Jemperli) entered a highly competitive immunotherapy market with key rivals being Merck’s Keytruda and BMS's Opdivo.
  • Initial pricing aligns with peers at approximately $11,000 per dose, with expected gradual price erosion over five years.
  • Market expansion and indication breadth will likely drive sales volume, possibly reaching $600 million annually by 2028.
  • Competitive pressures, biosimilar entry, and reimbursement policies are factors influencing long-term price stability.
  • Strategic positioning and regulatory approvals are essential for maximizing market share and revenue.

FAQs

Q1: What are the primary drivers of Jemperli’s market growth?
Indication expansion, clinical evidence supporting efficacy, physician familiarity with immune checkpoints, and reimbursement coverage.

Q2: How does Jemperli compare pricing-wise to its competitors?
Pricing per dose is similar to pembrolizumab and nivolumab, approximately $11,000–$12,000, with potential for slight differences based on dosing and indication.

Q3: What factors could lead to price reductions for Jemperli?
Entry of biosimilars, increased competition, payer negotiations, and broader use of cost-effective therapies.

Q4: How does indication expansion impact future sales?
Broader approval to additional cancer types boosts patient population and drives sales volume growth.

Q5: What regulatory considerations could influence market access?
Approval in key markets like Europe, China, and Japan increases access; reimbursement policies determine pricing flexibility.


References

[1] MarketsandMarkets. "Immuno-Oncology Market by Therapy, Application, and Region." 2022.
[2] EvaluatePharma. "Worldwide Immuno-Oncology Market Forecast," 2022.
[3] FDA, "Jemperli (dostarlimab-gxly) Approval Notification," 2021.

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.