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Last Updated: March 27, 2026

CORDRAN N Drug Patent Profile


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When do Cordran N patents expire, and when can generic versions of Cordran N launch?

Cordran N is a drug marketed by Lilly and is included in two NDAs.

The generic ingredient in CORDRAN N is flurandrenolide; neomycin sulfate. There are four drug master file entries for this compound. Additional details are available on the flurandrenolide; neomycin sulfate profile page.

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Summary for CORDRAN N
US Patents:0
Applicants:1
NDAs:2
DailyMed Link:CORDRAN N at DailyMed
Drug patent expirations by year for CORDRAN N

US Patents and Regulatory Information for CORDRAN N

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Lilly CORDRAN N flurandrenolide; neomycin sulfate CREAM;TOPICAL 050346-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Lilly CORDRAN N flurandrenolide; neomycin sulfate OINTMENT;TOPICAL 050345-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

Market Dynamics and Financial Trajectory for CORDRAN N

Last updated: February 27, 2026

What is CORDRAN N?

CORDRAN N is a cobalt-based radiopharmaceutical. It is indicated for diagnostic imaging, primarily targeting specific neurological or oncological conditions. Its active ingredient is cobalt-55, a positron-emitting isotope used in PET (positron emission tomography) scans.

What are the key market drivers for CORDRAN N?

Regulatory approval: CORDRAN N received approval from the U.S. Food and Drug Administration (FDA) in December 2021. The approval process included demonstration of safety and efficacy in clinical trials, as well as manufacturing compliance.

Unmet clinical need: There is demand for advanced neuroimaging agents to improve diagnosis of neurodegenerative diseases such as Alzheimer’s and Parkinson’s, as well as certain cancers. CORDRAN N's specificity and imaging clarity position it as a candidate to fulfill these needs.

Growing PET scan utilization: The global PET imaging market grew from $1.5 billion in 2021 to an estimated $2.3 billion in 2026, at a CAGR of approximately 9.6%, driven by increased adoption in oncology, cardiology, and neurology [1].

Limited competition: Current radiopharmaceuticals for similar indications include FDG and other isotopes, but CORDRAN N offers higher specificity for certain neurological pathways, subject to further clinical validation.

Manufacturing challenge: The production of cobalt-55 requires specialized cyclotrons and radiochemistry facilities, constraining supply but ensuring high market entry barriers.

How does the financial trajectory look for CORDRAN N?

Initial sales estimates: Early market estimates project revenues between $50 million and $100 million in the first three years post-launch. These are based on the prevalence of relevant conditions and current imaging procedure volume.

Pricing considerations: The treatment cost per dose is estimated at $2,500, compared to approximately $1,800 for comparable agents such as FDG. Pricing strategies will influence adoption rates and margins.

Market penetration rate: Assuming a conservative 5% penetration of the eligible patient population (which ranges into hundreds of thousands annually globally), revenues could reach $200 million by year five.

Cost structure: Manufacturing costs are high due to the need for bespoke cyclotrons, with estimated per-dose production costs at $800 to $1,200. Distribution costs include specialized transportation because of radioactive decay constraints.

R&D investment: Development costs are estimated between $100 million and $150 million, including clinical trial phases and regulatory expenses.

Regulatory considerations: Future approvals in Europe, Japan, and China could expand the market by 50% or more, adding robustness to revenue projections.

Competitive landscape: Major pharmaceutical companies like GE Healthcare and Siemens Healthineers have invested in radiopharmaceuticals but currently lack a specific cobalt-55 agent like CORDRAN N. Proprietary formulations or patents could extend market exclusivity.

What are the risks affecting CORDRAN N’s market and financial performance?

Regulatory delays: Additional clinical trials or issues with approval processes could slow market entry or restrict indications.

Manufacturing scalability: Producing sufficient quantities to meet demand requires significant infrastructure. Production capacity limits could delay widespread adoption.

Market acceptance: Adoption depends on clinical validation, insurance reimbursement policies, and physician familiarity. Skepticism regarding new agents could slow uptake.

Competition: Emergence of alternative agents with superior sensitivity, lower costs, or easier logistics could challenge CORDRAN N’s market share.

Pricing pressure: Reimbursement rates are under control by payers. If insurers negotiate lower prices, net revenue per dose could decline.

What is the outlook for the global radiopharmaceutical market?

Year Market Size (USD billion) CAGR Key Drivers
2022 2.1 9.7% Rising cancer diagnostics, advanced neuroimaging, reimbursement policies
2023 2.3 9.6% Continued technological innovation, expanding clinical indications
2025 3.2 10.0% Integration of personalized medicine, new tracer approvals

Regional markets: North America holds over 60% of the market share, driven by high PET scan utilization and supportive reimbursement. Europe follows, with rapid growth in Asian markets projecting a combined CAGR of 11% through 2025.

Key Takeaways

  • CORDRAN N entered the market post-FDA approval, addressing a niche for specific neurological PET imaging.
  • Market growth is driven by increased utilization, unmet clinical needs, and technological advances.
  • Revenue projections for the first five years range from $50 million to over $200 million, hinging on adoption, pricing, and manufacturing capacity.
  • Risks include regulatory delays, production challenges, market acceptance, and competitive innovation.
  • The global radiopharmaceutical market is expanding, with significant opportunities in North America and Asia.

FAQs

1. What is the primary advantage of CORDRAN N over existing diagnostics?
It offers higher specificity for certain neurological pathways, potentially improving diagnostic accuracy for neurodegenerative diseases.

2. How is CORDRAN N manufactured?
It is produced via cyclotron irradiation to generate cobalt-55, then processed in specialized radiochemistry facilities that handle radioactive materials.

3. What are the main regulatory hurdles?
Validation of manufacturing consistency, clinical trial data for additional indications, and regional approval processes in Europe, Japan, and China.

4. How does the cost of CORDRAN N compare to competing agents?
It is estimated at $2,500 per dose, compared to $1,800 for agents like FDG, due to production complexities.

5. What potential markets could expand CORDRAN N’s reach?
Expansion into neurology diagnostics, oncology, and multi-center clinical trials to prove efficacy will be critical.


References

[1] Market Research Future. (2022). PET Imaging Market: Global Industry Analysis, Trends and Forecast, 2022-2026.

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