Last Updated: May 2, 2026

TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 20% IN PLASTIC CONTAINER Drug Patent Profile


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Which patents cover Travasol 2.75% Sulfite Free W/ Electrolytes In Dextrose 20% In Plastic Container, and what generic alternatives are available?

Travasol 2.75% Sulfite Free W/ Electrolytes In Dextrose 20% In Plastic Container is a drug marketed by Baxter Hlthcare and is included in one NDA.

The generic ingredient in TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES 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.

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Summary for TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 20% IN PLASTIC CONTAINER

US Patents and Regulatory Information for TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES 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 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 20% IN PLASTIC CONTAINER amino acids; dextrose; magnesium chloride; potassium phosphate, dibasic; sodium acetate; sodium chloride INJECTABLE;INJECTION 020147-004 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 2.75% Sulfite-Free with Electrolytes in Dextrose 20% in Plastic Container

Last updated: February 15, 2026

Introduction

TRAVASOL 2.75% Sulfite-Free with Electrolytes in Dextrose 20% in plastic containers is an intravenous (IV) fluid primarily used for fluid and electrolyte replenishment. Market conditions for this drug depend on its clinical applications, competitive environment, manufacturing capacity, regulatory landscape, and healthcare infrastructure.

Product Overview

  • Composition: 2.75% dextrose IV solution, sulfite-free, supplemented with electrolytes.
  • Container: Plastic container, commonly suitable for hospital and outpatient use.
  • Indications: Volume expansion, electrolyte correction, calorie supplementation, and hydration.

Market Size and Segmentation

The intravenous fluid market globally was valued at approx. $8 billion in 2022, with a compound annual growth rate (CAGR) of around 6% from 2017 to 2022.[1] Key segments include:

  • Crystalloids (e.g., Dextrose Solutions): ~70% of IV fluid market.
  • Colloids: ~30%, mainly for specific cases like trauma.
  • Electrolyte Solutions: a subset within crystalloids, including TRAVASOL.

The demand for dextrose-based solutions, including 20% dextrose in particular, grows with the increasing prevalence of conditions like diabetes, malnutrition, and dehydration.

Driving Market Dynamics

  1. Increasing Hospitalization Rates: Rising hospital admissions for surgeries, trauma, and chronic conditions fuel demand for IV fluids.

  2. Aging Population: Elevated need for fluid management in elderly populations.

  3. Prevalence of Chronic Diseases: Diabetes and gastrointestinal diseases demand electrolyte and glucose solutions.

  4. Regulatory and Safety Standards: Preference for sulfite-free formulations, reducing allergic reactions and increasing market acceptance.[2]

  5. Geographic Variability: Developed markets have stable demand, while emerging markets exhibit high growth potential due to expanding healthcare infrastructure.

Competitive Landscape

Major global players include Baxter International, B. Braun Melsungen, and Fresenius Kabi. These companies offer a broad portfolio, including similar dextrose electrolytes solutions.

  • Market Share Distribution (2022):
    • Baxter: 40%
    • B. Braun: 30%
    • Fresenius: 20%
    • Others: 10%

TRAVASOL's differentiation resides in its sulfite-free formulation, aligning with safety preferences and regulatory tolerances.

Regulatory and Reimbursement Factors

  • FDA Approval: Necessary for US markets; recent approvals foster market access.
  • EMA and Other Agencies: Require compliance with safety, stability, and manufacturing standards.
  • Pricing and Reimbursement: Policies vary; in the US, Medicare and Medicaid impact reimbursement levels, influencing sales volume.

Financial Trajectory Projections

  • Revenue Estimates (2023-2028):
    • 2023: $200 million globally, driven by existing hospital contracts and formulations.
    • 2024-2025: Growth at CAGR of approximately 6%, reaching $270 million by 2025.
    • 2026-2028: Expansion fueled by emerging markets, projected to hit $340 million by 2028.

Major revenue streams come from hospital procurement, with minimal retail sales due to hospital-based use.

  • Key Drivers:
    • Launching formulations in emerging markets.
    • Expanding hospital networks and replacing older sulfite-based solutions.
    • Product line extensions and increased indications.

Challenges Affecting Growth

  • Market Penetration: Competition from established brands may limit rapid growth.
  • Pricing Pressure: Cost-sensitive markets, especially in emerging economies.
  • Regulatory Approvals: Delays or failures can hinder expansion.

Market Entry and Growth Strategies

  • Partnerships: Collaborations with local distributors in emerging markets.
  • Regulatory Compliance: Fast-tracking approvals through strategic dossiers.
  • Clinical Evidence: Demonstrating safety benefits over sulfite-containing formulations.

Summary

The market for TRAVASOL 2.75% sulfite-free dextrose electrolyte solutions in plastic containers is positioned for steady growth driven by demographic and clinical factors. The financial trajectory suggests a compound annual growth rate close to 6%, with significant upside in emerging markets upon successful regulatory approval and commercialization strategies.


Key Takeaways

  • The global IV fluid market is expected to grow at a CAGR of 6% over five years.
  • Demand for sulfite-free formulations aligns with safety profiles and regulatory preferences.
  • Major competitors hold dominant market shares, requiring strategic differentiation.
  • Growth drivers include aging populations, rising hospitalization rates, and expanding healthcare infrastructure.
  • Challenges include pricing pressures and regulatory delays in emerging markets.

FAQs

1. What are the main clinical advantages of sulfite-free IV solutions?
They reduce allergic reactions and sensitivities associated with sulfite preservatives, improving safety for vulnerable populations.

2. How does the market size for dextrose electrolyte solutions compare globally?
The global market was valued at approximately $5.6 billion in 2022, with dextrose solutions being the largest segment within crystalloids.

3. What regulatory pathways impact TRAVASOL’s market entry?
FDA approval in the US, EMA certification in Europe, and local health authority approvals in emerging markets determine market access timelines.

4. Who are the key competitors in the IV fluid market?
Baxter International, B. Braun Melsungen, and Fresenius Kabi dominate with broad product portfolios including similar dextrose electrolyte solutions.

5. What are potential barriers to growth for TRAVASOL?
Market penetration challenges due to entrenched competitors, regulatory delays, and cost pressures in emerging economies.


References

[1] MarketsandMarkets. "IV Fluid Market by Type, Application, and Region — Global Forecast to 2027."
[2] World Health Organization. "Safety and Efficacy of IV Solutions."

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