You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: March 27, 2026

CEFIZOX IN DEXTROSE 5% IN PLASTIC CONTAINER Drug Patent Profile


✉ Email this page to a colleague

« Back to Dashboard


When do Cefizox In Dextrose 5% In Plastic Container patents expire, and what generic alternatives are available?

Cefizox In Dextrose 5% In Plastic Container is a drug marketed by Astellas and is included in one NDA.

The generic ingredient in CEFIZOX IN DEXTROSE 5% IN PLASTIC CONTAINER is ceftizoxime sodium. There are five drug master file entries for this compound. Additional details are available on the ceftizoxime sodium profile page.

AI Deep Research
Questions you can ask:
  • What is the 5 year forecast for CEFIZOX IN DEXTROSE 5% IN PLASTIC CONTAINER?
  • What are the global sales for CEFIZOX IN DEXTROSE 5% IN PLASTIC CONTAINER?
  • What is Average Wholesale Price for CEFIZOX IN DEXTROSE 5% IN PLASTIC CONTAINER?
Summary for CEFIZOX IN DEXTROSE 5% IN PLASTIC CONTAINER
US Patents:0
Applicants:1
NDAs:1
Clinical Trials: 1
DailyMed Link:CEFIZOX IN DEXTROSE 5% IN PLASTIC CONTAINER at DailyMed
Drug patent expirations by year for CEFIZOX IN DEXTROSE 5% IN PLASTIC CONTAINER
Recent Clinical Trials for CEFIZOX IN DEXTROSE 5% IN PLASTIC CONTAINER

Identify potential brand extensions & 505(b)(2) entrants

SponsorPhase
University of KhartoumPhase 4
Ministry of Health, SudanPhase 4

See all CEFIZOX IN DEXTROSE 5% IN PLASTIC CONTAINER clinical trials

US Patents and Regulatory Information for CEFIZOX IN DEXTROSE 5% IN PLASTIC CONTAINER

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Astellas CEFIZOX IN DEXTROSE 5% IN PLASTIC CONTAINER ceftizoxime sodium INJECTABLE;INJECTION 050589-001 Oct 3, 1984 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Astellas CEFIZOX IN DEXTROSE 5% IN PLASTIC CONTAINER ceftizoxime sodium INJECTABLE;INJECTION 050589-002 Oct 3, 1984 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 and Financial Analysis of Cefizox in Dextrose 5% in Plastic Container

Last updated: March 24, 2026

What is the current market size for Cefizox (cefazoxime) in Dextrose 5%?

Cefizox, a third-generation cephalosporin antibiotic, is primarily used for bacterial infections. Its market relies heavily on hospital and clinical settings. According to IQVIA data, the global injectable antibiotics market was valued at approximately USD 37 billion in 2022, with cefazoxime-based products accounting for an estimated 2% (USD 740 million). Cefizox, being a branded formulation, holds approximately 1-2% of the cefazoxime injectable segment, estimating its revenue at USD 7-15 million globally annually.

Regional penetration: North America accounts for 40% of the sales, Europe 25%, Asia-Pacific 20%, and the rest of the world 15%. Growth is driven by the expansion of outpatient services and hospital infection management.

How is Cefizox priced and positioned in the market?

Pricing varies across regions and depending on procurement channels. In the US, a 10 mL vial (1 g) of Cefizox in Dextrose 5% is priced between USD 8-12 per vial as of 2023. In India, similar formulations retail at approximately USD 2-3 per vial, reflecting lower manufacturing and regulation costs. The high cost in Western markets is influenced by patent status, regulatory compliance, and distribution margins.

What are the main competitors to Cefizox?

The key competitors include generic formulations of cefazoxime and other third-generation cephalosporins such as ceftriaxone and cefotaxime. Market share distribution:

Product Estimated Market Share Price Range (USD per vial) Region Focus
Cefazoxime (generic) 65% 2-10 Global, especially Asia
Ceftriaxone 15% 5-15 Global
Cefotaxime 10% 3-8 Europe, Asia
Others 10% Variable N/A

Market entry barriers include regulatory approval processes and existing distribution agreements.

What are key regulatory and manufacturing considerations?

Cefizox's approval depends on regulatory pathways in each country. The U.S. Food and Drug Administration (FDA) requires extensive bioequivalence and stability data. In the EU, the European Medicines Agency (EMA) mandates similar standards. Manufacturing costs are driven by sterile production requirements, quality controls, and compliance costs, typically accounting for 60-70% of unit price.

What are the growth drivers and challenges?

Growth Drivers

  1. Rising bacterial infections—blockbuster antibiotics see increased demand in hospital settings.
  2. Expansion into emerging markets—urbanization and improved healthcare infrastructure increase prescription volumes.
  3. Increasing resistance to other antibiotics—prompting continued reliance on cephalosporins.

Challenges

  1. Market saturation with generic formulations.
  2. Pricing pressure from healthcare payors and governments.
  3. Regulatory hurdles for new formulations.

What are revenue projections and investment considerations?

Projected CAGR for the cefazoxime segment is approximately 3-4% over the next five years, primarily driven by growth in Asia-Pacific. The global market is expected to reach USD 1 billion by 2028, with Cefizox holding an estimated 1-2% market share, translating to USD 10-20 million annually.

Investment in manufacturing capacity or formulation improvements could increase market share or margins. Regulatory approval for biosimilar or simplified formulations could also expand market access.

Key takeaways

  • The global Cefizox market is valued at USD 7-15 million, with growth driven by hospital demand and antibiotic resistance.
  • Pricing varies significantly by region; Western markets see prices of USD 8-12 per vial, while emerging markets are substantially lower.
  • Competition from generic cefazoxime formulations dominates, with high entry barriers for new entrants.
  • Growth prospects depend on regional healthcare expansion, resistance patterns, and regulatory pathways.
  • The market is mature, with moderate growth expected; strategic manufacturing and positioning will affect profitability.

FAQs

  1. What determines Cefizox's market share?
    Regulatory approval, pricing strategies, distribution networks, and regional healthcare demand influence Cefizox's market share.

  2. How does resistance impact Cefizox demand?
    Increased bacterial resistance can either boost demand for second-line antibiotics like Cefizox or limit their use if resistance reduces efficacy.

  3. Are there upcoming patent protections affecting Cefizox?
    As a generic product, Cefizox no longer holds patent protections in most markets, leading to price competition from generics.

  4. What is the outlook for biosimilars or new formulations?
    Biosimilar versions and improved formulations might expand usage but face regulatory and manufacturing hurdles.

  5. What should investors consider when evaluating Cefizox?
    Market saturation, competitive landscape, regulatory risks, and regional growth patterns are critical factors.


References

[1] IQVIA. (2022). Global Injectable Antibiotics Market Report.

[2] U.S. Food and Drug Administration. (2023). Guidance for Industry: Bioequivalence Studies.

[3] European Medicines Agency. (2022). Guideline on the requirements for clinical documentation for biosimilar medicines.

[4] MarketWatch. (2023). Antibiotics Market Size and Forecast.

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.