Last Updated: June 27, 2026

TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 15% IN PLASTIC CONTAINER Drug Patent Profile


✉ Email this page to a colleague

« Back to Dashboard


Which patents cover Travasol 2.75% Sulfite Free W/ Electrolytes In Dextrose 15% In Plastic Container, and what generic alternatives are available?

Travasol 2.75% Sulfite Free W/ Electrolytes In Dextrose 15% 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 15% 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 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 15% IN PLASTIC CONTAINER?
  • What are the global sales for TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 15% IN PLASTIC CONTAINER?
  • What is Average Wholesale Price for TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 15% IN PLASTIC CONTAINER?
Summary for TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 15% IN PLASTIC CONTAINER

US Patents and Regulatory Information for TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 15% 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 15% IN PLASTIC CONTAINER amino acids; dextrose; magnesium chloride; potassium phosphate, dibasic; sodium acetate; sodium chloride INJECTABLE;INJECTION 020147-003 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 15% in Plastic Container

Last updated: January 30, 2026

Summary

TRAVASOL 2.75% sulfite-free with electrolytes in dextrose 15% in a plastic container is an intravenous (IV) fluid solution used for hydration and electrolyte replenishment in clinical settings. Its market dynamics are driven by increasing global demand for safe, sulfite-free IV solutions, evolving healthcare policies, and technological advancements in IV fluid manufacturing. The product's financial trajectory hinges on the expanding healthcare infrastructure, regulatory landscape, and competitive positioning amid alternative IV therapies. This report analyzes key market drivers, competitive landscape, regulatory factors, and financial projections to guide strategic decision-making.


What Are the Market Drivers for TRAVASOL 2.75% Sulfite-Free in Global Healthcare?

1. Increasing Demand for Sulfite-Free IV Solutions

Sulfites are used as preservatives in some IV solutions but have been linked to allergic reactions, especially in sensitive patients. Regulatory agencies and clinicians favor sulfite-free formulations to mitigate adverse reactions. TRAVASOL, being sulfite-free, aligns with this clinical preference, expanding its market.

2. Rising Global Healthcare Expenditure

The global healthcare expenditure is projected to grow at a CAGR of approximately 5% from 2022 to 2030 (Statista, 2022). Growing hospital infrastructure, especially in emerging markets, boosts demand for IV fluids.

Year Global Healthcare Expenditure (USD trillions) CAGR (2022–2030)
2022 8.3
2030 ~12.7 5%

3. Increasing Prevalence of Dehydration and Electrolyte Imbalance

Conditions such as diarrhea, dehydration, and electrolyte imbalance are prevalent globally, intensifying the need for electrolyte-containing IV fluids like TRAVASOL.

4. Advances in IV Fluid Production and Safety Standards

Technological innovations improve manufacturing safety and sterility, supporting higher adoption rates.

5. Expanding Use in Critical and Chronic Care

In ICUs, surgical settings, and chronic illness management, IV hydration solutions are indispensable, expanding the market reach.


What Is the Competitive Landscape of Ultrade in the IV Fluid Market?

Key Players Market Share (Estimated, 2022) Product Focus Competitive Positioning
Baxter International 35% Dextrose and Electrolyte IV solutions Leader in hospital supplies, high R&D investment
B. Braun 20% Parenteral Nutrition, IV Fluids Known for quality, expanding portfolio
Fresenius Kabi 15% Specialized IV solutions Focus on emerging markets
Hospira (Pfizer) 10% Generic IV formulations Cost-effective, broad distribution
Others 20% Various Niche and regional players

Key Differentiators:

  • Formulation purity (sulfite-free)
  • Container material (plastic, safety features)
  • Electrolyte composition tailored for specific patient needs
  • Regulatory approvals (FDA, EMA, ANVISA)

What Are the Regulatory and Policy Factors Impacting TRAVASOL’s Market?

Regulatory Approvals & Compliance

  • FDA (U.S.): Requires compliance with 21 CFR Part 211 for parenteral drug manufacturing.
  • EMA (EU): Requires centralized marketing authorization with adherence to EU pharmacovigilance.
  • Emerging Markets: Varied regulatory timelines and requirements, often less stringent.

Policies that Influence Market Trajectory

Policy Area Impact Description
Drug Registration Policies Accelerate or delay market entry Depending on approval efficiency
Reimbursement Policies Influence hospital procurement Favor products with proven safety and cost-effectiveness
Import/Export Regulations Affect global supply chain Tariffs, trade agreements

Impact of International Guidelines

  • WHO recommends the use of sterile, preservative-free IV solutions
  • National health authorities increasingly endorse sulfite-free formulations to reduce allergic reactions

What Are the Key Product Specifications and Features?

Feature Details
Concentration 2.75% dextrose
Sulfite Content Sulfite-free
Electrolytes Contains electrolytes such as sodium, potassium, magnesium, and chloride
Container Type Plastic (various, e.g., polyvinyl chloride / PVC)
Packaging Usually in multi-dose or single-dose bags
Sterility Terminally sterilized, ISO-certified manufacturing

Financial Trajectory: Market Size, Revenue Forecasts, and Growth Drivers

Market Size Estimates (2022–2030)

The global IV fluid market was valued approximately at USD 8 billion in 2022 with a projected CAGR of 6%, reaching around USD 14 billion by 2030[1].

Year Market Size (USD billion) Assumed Market Share Revenue for TRAVASOL (Estimate)
2022 8.0 2% (Specialty sulfite-free solutions) USD 160 million
2025 10.7 3% USD 321 million
2030 14.0 3.5% USD 490 million

Assuming TRAVASOL captures a rising proportion driven by clinical preference, safety profile, and regulatory support.

Factors Influencing Revenue Growth

  • Market Penetration & Adoption: Strategic relationships with hospitals and healthcare providers
  • Regulatory Approvals: Faster approvals expedite market entry and expansion
  • Pricing Strategies: Competitive positioning in cost-sensitive regions
  • Supply Chain & Manufacturing Capacity: Ensures consistent supply and reduces costs
  • Innovative Features: Electrolyte customization and container innovations

Cost Structure & Profitability Analysis

Cost Factor Approximate Percentage of Revenue Notes
Manufacturing 20–25% Includes raw materials, sterility, quality control
Regulatory & Compliance 5–10% Approvals, audits, pharmacovigilance
Distribution & Logistics 10–15% Global supply, warehousing
Marketing & Sales 10–20% Market development, institutional sales
R&D 5–10% Product improvements, new formulations

Comparison with Alternative IV Formulations

Parameter TRAVASOL 2.75% Sulfite-Free Normal Dextrose Solutions Electrolyte-Free Solutions
Sulfite Content Sulfite-free May contain sulfites Usually sulfate-free
Electrolytes Includes electrolytes Usually none Possibly none
Container Material Plastic, safety-enhanced Plastic / glass Plastic / glass
Typical Use Cases Critical care, hypersensitivity General hydration Specific use cases

What Is the Outlook for Market Entry and Expansion?

  • Entry strategies include partnerships with hospital networks, regional distributors, and government tenders.
  • Product differentiation through formulation safety and container innovations can create barriers for competitors.
  • Growing focus on patient safety and regulatory alignments favors sulfite-free, electrolyte-containing solutions like TRAVASOL.
  • Expanding into emerging markets with tailored pricing and supply chain optimization offers growth opportunities.

Key Market Risks and Challenges

Risk Factor Description
Regulatory Delays Lengthy approval processes in certain markets
Price Competition Price erosion by generics and regional players
Supply Chain Disruptions Raw material shortages or logistical issues
Clinical Acceptance Slow adoption without clear evidence of clinical benefits
Regulatory Changes Stricter standards, especially in global markets

Key Takeaways

  • Growing Demand: Rising global healthcare expenditures and patient safety preferences favor sulfite-free electrolyte IV solutions.
  • Market Penetration: Effective partnerships, quality standards, and regulatory approval are pivotal.
  • Revenue Trajectory: Estimated to grow from USD 160 million in 2022 to approximately USD 490 million by 2030, under current assumptions.
  • Competitive Advantage: Focus on safety, formulation purity, and container innovation enhances market differentiation.
  • Risks: Regulatory delays, price competition, and supply chain disruptions remain key challenges.

FAQs

1. What factors influence the pricing of TRAVASOL 2.75% sulfite-free solutions?
Pricing is impacted by manufacturing costs, raw material prices, regulatory compliance expenses, competitive landscape, and regional reimbursement policies.

2. How does TRAVASOL differentiate itself from other IV solutions?
Its sulfite-free formulation, inclusion of electrolytes in a stable dextrose base, safety-enhanced plastic containers, and suitability for sensitive patient populations.

3. What regulatory hurdles might impact the global rollout of TRAVASOL?
Variability in approval timelines, differing safety and efficacy standards, and requirements for clinical data submissions.

4. In which regions is the demand for electrolyte-containing IV solutions highest?
Emerging markets such as Asia-Pacific, Latin America, and parts of Africa, driven by increasing healthcare infrastructure and prevalence of dehydration-related conditions.

5. What are the main growth opportunities for TRAVASOL in the coming years?
Expansion into new markets, product line extensions, and partnerships with healthcare providers focusing on patient safety and innovative formulations.


References

[1] Statista, "Global Healthcare Expenditure Forecast," 2022.

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.