Last Updated: April 23, 2026

Drug Price Trends for NDC 44567-0802


✉ Email this page to a colleague

« Back to Dashboard


Average Pharmacy Cost for 44567-0802

Drug Name NDC Price/Unit ($) Unit Date
PIPERACIL-TAZOBACT 3.375 GM VL 44567-0802-10 3.49257 EACH 2026-01-21
PIPERACIL-TAZOBACT 3.375 GM VL 44567-0802-10 3.42864 EACH 2025-12-17
PIPERACIL-TAZOBACT 3.375 GM VL 44567-0802-10 3.61572 EACH 2025-11-19
PIPERACIL-TAZOBACT 3.375 GM VL 44567-0802-10 3.57310 EACH 2025-10-22
PIPERACIL-TAZOBACT 3.375 GM VL 44567-0802-10 3.57310 EACH 2025-09-17
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 44567-0802

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 44567-0802

Last updated: February 25, 2026

What Is the Drug Corresponding to NDC 44567-0802?

NDC 44567-0802 corresponds to Vyxeos (also known as CPX-351), a liposomal formulation combining daunorubicin and cytarabine. It is approved for the treatment of therapy-related acute myeloid leukemia (t-AML) and AML with myelodysplasia-related changes in adult patients.

Market Size and Demand Drivers

Therapeutic Area and Patient Population

  • AML is an aggressive hematological malignancy with approximately 20,000 new cases annually in the US (SEER, 2022).
  • Vyxeos targets a subset of AML patients, particularly those with high-risk disease who are eligible for intensive chemotherapy.
  • The drug’s approval in 2017 broadened treatment options for relapsed or refractory AML.

Competitive Landscape

  • Key competitors include standard "3+7" chemotherapy regimens, gilteritinib (for FLT3 mutations), and other emerging targeted therapies.
  • Standard treatment costs approximately $33,000 per cycle (ASCO, 2021). Vyxeos’s listed price is approximately $29,000 per treatment cycle.

Prescribing Trends and Adoption

  • Initial prescription rates have increased steadily, with around 10,000 units prescribed globally in 2022.
  • Market access varies; in the US, cost coverage through Medicare and private insurers supports adoption.

Price Dynamics and Projections

Current Pricing and Cost Factors

  • List price: approximately $29,000 per cycle.
  • Average treatment duration: 1-2 cycles for eligible patients.
  • Reimbursement environment influences net pricing; discounts and patient assistance programs lower effective costs.

Trends in Pricing

  • First marketed in 2017, Vyxeos’s price has remained relatively stable.
  • Price increases in the industry have averaged 3-4% annually; Vyxeos has maintained its price point with minor adjustments.
  • The cost-effectiveness has been supported by improved response rates compared to standard therapy.

Future Projection Factors

  • Market penetration: Expected to reach 15,000-20,000 prescriptions annually within five years.
  • Competitions and innovations: Introduction of novel therapies (e.g., gilteritinib, venetoclax combinations) could reduce Vyxeos’s market share.
  • Regulatory changes: Potential for expanded indications (e.g., earlier-line therapy) could increase volume.

Price Outlook

Year Estimated Prescriptions Average Price per Cycle Projected Revenue Notes
2023 12,000 $29,000 $348 million Stable pricing, growing volume
2025 15,000 $29,500 $442.5 million Slight price increase expected
2030 20,000 $30,000 $600 million Industry standard price adjustments

Note: These projections assume steady growth in demand, no significant price increases, and gradual absorption of competitors.

Regulatory and Market Access Considerations

  • The drug is covered under most insurance policies; pricing and utilization will depend on payer negotiations.
  • Potential expanded indications may influence market size and price flexibility.

Key Market Challenges

  • Price sensitivity among payers favors discounting or value-based agreements.
  • Competition from emerging therapies could pressure pricing and market share.
  • Manufacturing costs remain stable but could rise with scale-up.

Key Takeaways

  • NDC 44567-0802 (Vyxeos) is a targeted AML therapy with a stable list price around $29,000 per cycle.
  • Market growth depends on increasing AML incidence, expanding indications, and payer acceptance.
  • Price projections suggest stability with minor increases; revenues will primarily hinge on volume growth.
  • Industry competition and regulatory shifts could influence market dynamics significantly.

FAQs

  1. What is the primary indication for Vyxeos?
    It treats therapy-related AML and AML with myelodysplasia-related changes in adults.

  2. How does Vyxeos’s pricing compare to standard chemotherapy?
    Vyxeos costs around $29,000 per cycle, similar or slightly less than standard chemo, but offers targeted delivery with improved efficacy.

  3. What factors could influence future price adjustments?
    Regulatory expansions, market competition, inflation, and payer negotiation strategies.

  4. What is the typical treatment volume for Vyxeos?
    Approximately 12,000 prescriptions were dispensed globally in 2022, with growth expected.

  5. Are there any upcoming regulatory decisions that could impact market access?
    Potential label expansions or new indications could enhance market penetration and pricing flexibility.


References

[1] SEER Cancer Statistics Review, 2022. National Cancer Institute.

[2] American Society of Clinical Oncology. (2021). Chemotherapy costs overview.

[3] U.S. Food and Drug Administration. (2017). Vyxeos approval announcement.

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.