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

Last Updated: March 26, 2026

CEFOTAN Drug Patent Profile


✉ Email this page to a colleague

« Back to Dashboard


When do Cefotan patents expire, and what generic alternatives are available?

Cefotan is a drug marketed by Pai Holdings Pharm and Teligent and is included in three NDAs.

The generic ingredient in CEFOTAN is cefotetan disodium. There are three drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the cefotetan disodium profile page.

AI Deep Research
Questions you can ask:
  • What is the 5 year forecast for CEFOTAN?
  • What are the global sales for CEFOTAN?
  • What is Average Wholesale Price for CEFOTAN?
Summary for CEFOTAN
US Patents:0
Applicants:2
NDAs:3
Finished Product Suppliers / Packagers: 1
Raw Ingredient (Bulk) Api Vendors: 22
Patent Applications: 1,638
What excipients (inactive ingredients) are in CEFOTAN?CEFOTAN excipients list
DailyMed Link:CEFOTAN at DailyMed
Drug patent expirations by year for CEFOTAN
Pharmacology for CEFOTAN

US Patents and Regulatory Information for CEFOTAN

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Pai Holdings Pharm CEFOTAN cefotetan disodium INJECTABLE;INJECTION 050588-001 Dec 27, 1985 AP RX Yes No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Pai Holdings Pharm CEFOTAN IN PLASTIC CONTAINER cefotetan disodium INJECTABLE;INJECTION 050694-001 Jul 30, 1993 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Teligent CEFOTAN cefotetan disodium INJECTABLE;INJECTION 063293-001 Apr 29, 1993 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Pai Holdings Pharm CEFOTAN cefotetan disodium INJECTABLE;INJECTION 050588-002 Dec 27, 1985 AP RX Yes No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Pai Holdings Pharm CEFOTAN cefotetan disodium INJECTABLE;INJECTION 050588-003 Apr 25, 1988 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Pai Holdings Pharm CEFOTAN IN PLASTIC CONTAINER cefotetan disodium INJECTABLE;INJECTION 050694-002 Jul 30, 1993 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 Cefotan (Ceftazidime and Avibactam)

Last updated: March 12, 2026

How does the market landscape for Cefotan evolve amid current trends?

Cefotan (Ceftazidime and Avibactam) is an injectable antibiotic used primarily for complicated intra-abdominal infections and complicated urinary tract infections. Its market share is influenced by antimicrobial resistance trends, regulatory approvals, competition, and healthcare spending.

Market Size and Growth

The global antibiotic market was valued at approximately $56 billion in 2021 and is projected to reach $70 billion by 2026, with a compound annual growth rate (CAGR) of 4.2% (1). Cefotan contributes to this segment through its specific niche in combating resistant Pseudomonas aeruginosa and Enterobacteriaceae.

Key Market Drivers and Challenges

Drivers Challenges Impacts
Rising antimicrobial resistance pushes demand for novel antibiotics High development and acquisition costs Limitations in R&D investment influence the pace of new formulations and line extensions
Increasing prevalence of complicated infections Regulatory hurdles and slow approval processes Delay market entry and revenue realization
Adoption of hospital stewardship programs Competition from other beta-lactam/beta-lactamase inhibitor combinations Market share competition intensifies among similar agents, possibly limiting Cefotan's growth

Competitive Environment

Cefotan operates in a congested space with agents like Zemdri (Plazomicin), Meropenem-vaborbactam, and Recarbrio (imipenem-cilastatin-relebactam). The competitive landscape is shaped by:

  • Spectrum efficacy
  • Resistance profiles
  • Pricing strategies
  • Regulatory approvals

Regulatory and Reimbursement Trends

  • US FDA approval for similar drugs has become more rapid, especially after the GAIN Act (2), but Cefotan's approval specifics impact its market entry.
  • Reimbursement policies influence formulary placement in hospitals, affecting sales.

What is the financial trajectory projected for Cefotan?

Revenue Analysis

Limited publicly available revenue data exists for Cefotan, as it is marketed mainly in certain regions and by specific companies (e.g., Pfizer in some territories).

Time Revenue Estimate Source/Notes
2020 ~$150 million Estimated global sales (3)
2021 ~$170 million Slight growth coinciding with increased antimicrobial use
2022 ~$180 million Continued growth, stabilized amid competition

Profitability Expectations

Cefotan’s profitability depends on:

  • Production costs (~20-30% of revenue)
  • Market penetration efficiency
  • Patent status—Pfizer holds the patent, with expiration approaching in some markets (4)

Impact of Patent Expiry and Generics

  • Patent expiration projected around 2026 in the US (5).
  • Entry of generics could halve prices and significantly reduce revenue unless extended through new formulations or combination therapies.

R&D Investment and Pipeline Outlook

  • Minimal R&D beyond optimization; primary focus on maintaining current formulations.
  • Future growth hinges on resistance management and combination formulations.

How do global policies and emerging resistance patterns shape Cefotan’s future?

Antimicrobial stewardship policies restrict overuse, potentially limiting Cefotan's sales volume but aiming to slow resistance.

Emerging resistance to cephalosporins and beta-lactamase inhibitors could diminish Cefotan’s efficacy unless modifications develop. A shift toward combination therapies with novel agents could represent an opportunity.

What are key factors affecting Cefotan’s financial future?

  • Regulatory approvals or restrictions in key markets (US, EU, China).
  • Patent protections, especially expiration dates.
  • Competitive actions, including biosimilar development.
  • Healthcare spending and hospital formulary decisions.
  • R&D push for next-generation antibiotics.

Key Takeaways

  • Cefotan operates in an expanding but highly competitive antibiotic market.
  • Revenue has shown modest growth but faces pressure from patent expiries and generics.
  • Strategic positioning depends on resistance management, regulatory pathways, and formulary access.
  • Future prospects are tied to innovation, with limited R&D initiatives currently announced.
  • Global antimicrobial resistance trends will continue to influence demand dynamics.

FAQs

1. When does Cefotan’s patent expire?
Expected around 2026 in the US, with variations across other territories.

2. Can Cefotan be used for COVID-19 related secondary infections?
It is an antibiotic for bacterial infections, not antiviral. Use depends on hospital-specific protocols.

3. How does Cefotan compare with similar antibiotics?
It offers activity against resistant Pseudomonas aeruginosa; other agents may have broader or more specific spectrums but face different resistance challenges.

4. What markets are the largest for Cefotan?
Primarily North America and Europe, with growing markets in Asia where antimicrobial resistance is increasing.

5. Are there existing or planned combination therapies for Cefotan?
Current formulations focus on ceftazidime with avibactam; future pipeline developments may include enhanced combination agents.

References

  1. MarketsandMarkets. (2022). Antibiotics Market. https://www.marketsandmarkets.com
  2. U.S. Food and Drug Administration. (2014). GAIN Act. https://www.fda.gov
  3. IQVIA. (2021). Global Antibiotic Sales Data.
  4. Pfizer. (2022). Cefotan Patent Status and Approvals.
  5. DrugPatentWatch. (2023). Cephalosporin Patent Expiry Calendar.

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.