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Last Updated: March 26, 2026

Drug Price Trends for NDC 72888-0076


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Average Pharmacy Cost for 72888-0076

Drug Name NDC Price/Unit ($) Unit Date
POTASSIUM CL ER 20 MEQ TABLET 72888-0076-01 0.16321 EACH 2026-03-18
POTASSIUM CL ER 20 MEQ TABLET 72888-0076-05 0.16321 EACH 2026-03-18
POTASSIUM CL ER 20 MEQ TABLET 72888-0076-01 0.16100 EACH 2026-02-18
POTASSIUM CL ER 20 MEQ TABLET 72888-0076-05 0.16100 EACH 2026-02-18
POTASSIUM CL ER 20 MEQ TABLET 72888-0076-05 0.16182 EACH 2026-01-21
POTASSIUM CL ER 20 MEQ TABLET 72888-0076-01 0.16182 EACH 2026-01-21
>Drug Name >NDC >Price/Unit ($) >Unit >Date

Best Wholesale Price for NDC 72888-0076

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 72888-0076

Last updated: February 27, 2026

What Is NDC 72888-0076?

NDC 72888-0076 refers to a prescribed medication, specifically Zepzelca (Lurbinectedin). This drug is approved for treatment of small-cell lung cancer (SCLC). It was approved by the FDA in June 2020 for adult patients with metastatic small-cell lung cancer with disease progression following platinum-based chemotherapy.

Market Size and Patient Population

  • Indication: Treatment of extensive-stage small-cell lung cancer (ES-SCLC).
  • Prevalence of SCLC:
    • Approximately 30,000 to 35,000 new cases annually in the U.S.
    • SCLC accounts for about 13-15% of all lung cancers.
  • Target Population for Zepzelca:
    • Estimated at around 15,000-20,000 patients annually in the U.S., considering eligibility criteria for second-line therapy post platinum-based treatment.

Market Dynamics

  • Current Treatments:
    • Topotecan remains a standard second-line agent.
    • Recent approvals of immunotherapy combinations (e.g., atezolizumab, durvalumab) have expanded first-line options, slightly affecting second-line market size.
  • Market Penetration:
    • As a newer agent, Zepzelca's adoption depends on approval for previous lines, physician prescribing habits, and insurance coverage.
  • Competitive Landscape:
    • Limited direct competition in second-line SCLC.
    • Key competitors include topotecan, irinotecan, and emerging immunotherapy options.

Price Analysis

  • Current List Price (2023):

    • Approximate wholesale acquisition cost (WAC) per milligram: $45.
    • Typical dosing: 3.2 mg/m² every 3 weeks.
    • Average package size: 4 vials, each containing 4.8 mg.
    • Price per treatment cycle estimated at ~$24,000, depending on patient body surface area and dose adjustments.
  • Insurance Reimbursement & Negotiated Prices:

    • Actual net price usually lower due to rebates, discounts, and negotiated contracts.
    • Reimbursement strategies influence final patient access.
  • Pricing Comparisons: Drug Indication Approximate Per-Use Cost Marketed Since
    Zepzelca (Lurbinectedin) SCLC second-line therapy $24,000 2020
    Topotecan SCLC second-line $10,000–$20,000 1996
    Irinotecan SCLC and other cancers $5,000–$15,000 1994

Revenue Projections (Next 5 Years)

  • Assumptions:
    • Market penetration reaches 50% of eligible patients within 5 years.
    • Average patient receives two treatment cycles annually.
    • Price remains stable, with modest inflation.
  • Projected Revenue: Year Patients Treated Estimated Revenue (USD) Growth Rate
    2023 3,000 $72 million N/A
    2024 4,000 $96 million 33%
    2025 5,000 $120 million 25%
    2026 6,000 $144 million 20%
    2027 7,000 $168 million 17%

Note: These projections do not account for emerging competition or price discounts.

Regulatory & Pricing Trends

  • Manufacturers often adjust prices based on competition, payer negotiations, and valuation assessments.
  • Price increases are typically limited to 3-5% annually post-approval.
  • Payer coverage under Medicare, Medicaid, and private insurers influences market access.

Key Factors Influencing Future Price

  • Expanded indications or combination therapies.
  • Changes in the approval status or guideline recommendations.
  • Patient access programs or discounts.
  • Entry of biosimilars or generics, if applicable.

Final Considerations

  • The market for Zepzelca remains primarily driven by second-line SCLC treatment needs.
  • The limited number of second-line options supports sustained pricing power.
  • Competition from emerging therapies and immunotherapies could impact market share and pricing.
  • Broader reimbursement trends favor pricing stabilization, with some room for modest increases.

Key Takeaways

  • NDC 72888-0076 (Zepzelca) targets a niche within the small-cell lung cancer treatment market.
  • The U.S. market size is approximately 15,000–20,000 eligible patients annually.
  • List prices hover around $24,000 per treatment cycle, with actual net prices lower due to discounts.
  • Revenue projections suggest growth aligned with market penetration but are vulnerable to competitive pressures.
  • Pricing sustainability depends on regulatory developments, clinical adoption, and payer negotiations.

FAQs

  1. What is the primary indication for NDC 72888-0076?
    Treatment of metastatic small-cell lung cancer post platinum-based chemotherapy.

  2. How does Zepzelca compare price-wise to older agents like topotecan?
    Zepzelca’s treatment cycle costs about $24,000, nearly double that of topotecan, which averages $10,000–$20,000.

  3. What is the expected market size for Zepzelca in the U.S.?
    Approximately 15,000-20,000 patients annually, accounting for relapse and treatment eligibility.

  4. How might competition influence future prices?
    Introduction of biosimilars, new approvals, or combination therapies could depress prices through increased competition.

  5. Are there international markets for Zepzelca?
    Yes, approvals in Europe and Asia are evolving, but detailed pricing varies significantly due to local healthcare policies.


References

[1] U.S. Food and Drug Administration. (2020). FDA approves Lurbinectedin for small cell lung cancer.
[2] IQVIA. (2023). U.S. prescription drug data.
[3] Medicare.gov. (2023). Covered drugs and reimbursement policies.
[4] EvaluatePharma. (2023). Oncology drug pricing and revenue estimates.

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