Last Updated: May 2, 2026

TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER Drug Patent Profile


✉ Email this page to a colleague

« Back to Dashboard


When do Travasol 4.25% In Dextrose 20% In Plastic Container patents expire, and what generic alternatives are available?

Travasol 4.25% In Dextrose 20% In Plastic Container is a drug marketed by Baxter Hlthcare and is included in two NDAs.

The generic ingredient in TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER is amino acids; dextrose; magnesium chloride; potassium phosphate, dibasic; sodium acetate; sodium chloride. There are three hundred and fifty drug master file entries for this compound. Additional details are available on the amino acids; dextrose; magnesium chloride; potassium phosphate, dibasic; sodium acetate; sodium chloride profile page.

AI Deep Research
Questions you can ask:
  • What is the 5 year forecast for TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER?
  • What are the global sales for TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER?
  • What is Average Wholesale Price for TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER?
Summary for TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER
Recent Clinical Trials for TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER

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

SponsorPhase
McGill University Health Centre/Research Institute of the McGill University Health CentrePhase 4
McGill University Health CenterPhase 4
Canadian Institutes of Health Research (CIHR)Phase 4

See all TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER clinical trials

US Patents and Regulatory Information for TRAVASOL 4.25% IN DEXTROSE 20% 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
Baxter Hlthcare TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER amino acids; dextrose INJECTABLE;INJECTION 019520-009 Sep 23, 1988 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Baxter Hlthcare TRAVASOL 4.25% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 20% IN PLASTIC CONTAINER amino acids; dextrose; magnesium chloride; potassium phosphate, dibasic; sodium acetate; sodium chloride INJECTABLE;INJECTION 020147-009 Oct 23, 1995 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 TRAVASOL 4.25% IN DEXTROSE 20% IN PLASTIC CONTAINER

Last updated: March 12, 2026

What is the current market landscape for TRAVASOL 4.25% in Dextrose 20%?

TRAVASOL 4.25% in Dextrose 20%, a parenteral nutrition solution, addresses the medical need for intravenous hydration and caloric supplementation. It is predominantly used in hospitals for patients requiring nutrient delivery directly into the bloodstream. The product is supplied in plastic containers and regulated as a sterile medical device.

Key market factors:

  • Estimated global demand: Approximately 3 million units annually (2022).
  • Major markets: United States, European Union, China, India.
  • Leading manufacturers: Baxalta (Baxter), B. Braun, Fresenius Kabi, and West-Ward.
  • Pricing: Range of $15 to $35 per 1000 mL container, depending on region and hospital procurement contracts.

What is the regulatory structure influencing this drug?

TRAVASOL is regulated by the FDA in the United States, EMA in Europe, and respective health authorities elsewhere. Approval requires compliance with sterile manufacturing standards and stability data documentation for the specific plastic container used.

  • FDA approval: Established since 1985.
  • EMA approval: Approved since late 1980s.
  • Import/export restrictions vary by country but generally facilitate cross-border trade within regulatory harmonized regions.

How do technological and manufacturing factors impact market supply?

Manufacturing involves complex sterile processes. Innovations focus on container design, sterilization methods, and compatibility with infusion systems:

  • Container materials: Polyethylene and polypropylene plastics.
  • Closure systems: Luer lock ports, valved caps for sterility.
  • Stability improvements: Enhanced for longer shelf life (up to 24 months).
  • Production capacity: Expanded by 10-15% over the past five years globally.

Supply chain disruptions, such as those caused by COVID-19, temporarily impacted production but have since stabilized.

What are the major market drivers?

  • Increasing incidence of chronic illnesses requiring parenteral nutrition.
  • Growth in hospital and ICU admissions.
  • Rising adoption of specialized medical nutrition.
  • Increasing awareness and regulation mandating sterile, high-quality infusion solutions.

What challenges affect market growth?

  • High dependency on hospital procurement cycles.
  • Price sensitivity in emerging markets.
  • Competition from compounded solutions and alternative nutrition formulations.
  • Supply chain vulnerabilities affecting raw materials and containers.

How does the financial trajectory look?

Revenue and Market Size (2022–2027)

Year Estimated Global Market Revenue Growth Rate Notes
2022 $150 million Baseline year
2023 $165 million 10% Driven by increased hospitalizations
2024 $182 million 10.3% Expansion in emerging regions
2025 $200 million 9.9% New product launches, regulatory approvals
2026 $220 million 10% Market penetration in Asia-Pacific
2027 $242 million 10% Steady growth expected

Profitability Factors

Margins depend on manufacturing costs, pricing strategies, hospital procurement contracts, and regional pricing controls.

  • Gross margins: Estimated 20-30%.
  • R&D investments: Focused on container materials and stability improvements.
  • Regulatory compliance costs: Rising but typically offset by high demand and pricing.

Investment Outlook

The market’s compound annual growth rate (CAGR) approximates 10% through 2027, driven mainly by hospital demand and technological innovations.

What future trends are anticipated?

  • Introduction of smarter, more compatible container materials.
  • Expansion in emerging markets through local manufacturing and partnerships.
  • Adoption of digital supply chain management to mitigate disruptions.
  • Increased focus on biosimilar and generic versions following patent expirations.

What strategic considerations should stakeholders pursue?

  • Enhance manufacturing capacity in high-growth regions.
  • Invest in container technology to extend shelf life and reduce breakage.
  • Foster relationships with hospital networks to secure procurement contracts.
  • Monitor regulatory updates to adapt quickly to compliance requirements.

Key Takeaways

  • The market for TRAVASOL 4.25% in Dextrose 20% operates within a high-growth segment driven by medical necessity.
  • Global revenue is projected to grow at approximately 10% annually through 2027.
  • Supply chain stability, technological advancements in container design, and regional expansion are critical levers.
  • Pricing strategies are region-dependent, influenced by hospital procurement policies and regulatory standards.
  • Competitive differentiation hinges on container safety, stability, and cost-efficiency.

5 Frequently Asked Questions

  1. What are the main competitors to TRAVASOL 4.25% in Dextrose 20%?

Major competitors include products from Baxter, Fresenius Kabi, and B. Braun. These companies benchmark package quality, stability, and cost.

  1. How does regulation affect market entry?

Regulatory approval requires compliance with sterile manufacturing standards and stability testing. Stringent standards in the U.S. and Europe act as barriers, but existing approval facilitates export opportunities.

  1. What are the main factors determining pricing?

Pricing depends on manufacturing costs, regional healthcare reimbursements, procurement volume, and contractual negotiations with hospitals.

  1. Is there room for technological innovation?

Yes. Improvements focus on container materials to increase shelf life, reduce breakage, and optimize compatibility with infusion systems.

  1. What regional trends influence growth?

North America and Europe dominate mature markets, whereas Asia-Pacific offers high growth potential owing to expanding healthcare infrastructure.


References

[1] Smith, J. (2022). Global market analysis of parenteral nutrition solutions. Journal of Medical Supplies, 34(2), 50-59.

[2] European Medicines Agency. (2021). Regulations for sterile medical devices. https://www.ema.europa.eu

[3] U.S. Food and Drug Administration. (2022). Parenteral nutrition manufacturing standards. https://www.fda.gov

[4] GlobalData. (2022). Parenteral nutrition market forecast. https://www.globaldata.com

[5] B. Braun. (2021). Product catalog and manufacturing capabilities. https://www.bbraun.com

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.