Last Updated: June 18, 2026

TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 10% IN PLASTIC CONTAINER Drug Patent Profile


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Which patents cover Travasol 2.75% Sulfite Free W/ Electrolytes In Dextrose 10% In Plastic Container, and what generic alternatives are available?

Travasol 2.75% Sulfite Free W/ Electrolytes In Dextrose 10% 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 10% 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 10% IN PLASTIC CONTAINER
US Patents:0
Applicants:1
NDAs:1

US Patents and Regulatory Information for TRAVASOL 2.75% SULFITE FREE W/ ELECTROLYTES IN DEXTROSE 10% 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 10% IN PLASTIC CONTAINER amino acids; dextrose; magnesium chloride; potassium phosphate, dibasic; sodium acetate; sodium chloride INJECTABLE;INJECTION 020147-002 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

Investment Scenario and Fundamentals Analysis for TRAVASOL 2.75% Sulfite-Free with Electrolytes in Dextrose 10% (Plastic Container)

Last updated: March 10, 2026

Market Overview

TRAVASOL 2.75% is a sterile, sulfite-free solution containing electrolytes in dextrose 10%, used primarily for intravenous (IV) fluid therapy. It competes mainly in hospital and clinical settings, where IV hydration, electrolyte correction, and nutritional support are key. The global IV fluid market was valued at approximately $9.2 billion in 2021 and is projected to reach $13.4 billion by 2028, growing at a CAGR of 5.4% (Research and Markets, 2022). Growth drivers include increasing hospitalizations, expanding ICU capacity, aging populations, and rising prevalence of chronic diseases.

Product Profile and Positioning

Key features:

  • Sulfite-free formulation reduces allergy risk.
  • Electrolyte balance supports hydration and electrolyte replenishment.
  • Dextrose provides caloric energy.
  • Plastic container ensures safety and convenience.

Potential advantages:

  • Suitable for sensitive patients due to sulfite-free status.
  • Compatibility with standard IV administration protocols.
  • Longer shelf life with plastic containers.

Regulatory and Patent Landscape

  • The product must meet the standards of regulatory bodies like the FDA (U.S.), EMA (Europe), and equivalent agencies elsewhere.
  • Patent restrictions may exist on specific formulations, manufacturing methods, or container technologies, possibly affecting generic entry or licensing.
  • No recent patent litigations reported for TRAVASOL formulations, suggesting market stability.

Competitive Environment

Major competitors include products from Baxter (e.g., Dextrose 10%), B. Braun, Fresenius, and local generic manufacturers. Market share is fragmented; no dominant player controls more than 25%. Differentiation relies on formulation safety, compatibility, and branding.

Key Competitors Market Share (est.) Unique Features
Baxter (Dextrose 10%) ~35% Established, broad distribution
B. Braun ~20% Known for safety features
Fresenius ~15% Cost-competitiveness
Generics/Private Label Remaining ~30% Price-sensitive segments

Pricing and Cost Factors

  • Average wholesale price per 1000 mL vial: approximately $3–$5.
  • Production costs are estimated between $0.80–$1.50 per unit, including raw materials, manufacturing, and regulatory compliance.
  • Margins depend on scale and market penetration.

Revenue and Growth Potential

  • Revenue estimates are sensitive to market penetration, hospital adoption rates, and formulary approvals.
  • For a mid-sized manufacturer: capturing 5% of the IV fluid market in North America over 5 years warrants sales of roughly 650,000 units annually (assuming an $4 price point).

Regulatory Entry and Barriers

  • Product approval requires FDA clearance or European CE marking.
  • Manufacturing facilities must comply with Good Manufacturing Practices (GMP).
  • Existing relationships with healthcare providers facilitate formulary listing.

Investment Outlook

Pros:

  • Steady demand driven by hospital needs.
  • Product differentiation (sulfite-free) appeals to sensitive patient segments.
  • Growing global IV fluid market.

Cons:

  • High competition from established brands.
  • Regulatory and patent barriers could delay market entry.
  • Price sensitivity limits premium positioning.

Risks:

  • Market saturation by generics.
  • Supply chain disruptions affecting production.
  • Regulatory changes impacting approval processes.

Key Takeaways

  • The IV fluid market is expanding with stable demand.
  • TRAVASOL’s sulfite-free, electrolyte-balanced formulation positions it favorably among safety-conscious clinical providers.
  • Competition is intense, requiring strategic branding and cost management.
  • Regulatory hurdles and patent landscape influence time-to-market and potential exclusivity.
  • Growth potential hinges on penetration in hospitals and eventual geographic expansion.

FAQs

1. What is the primary competitive advantage of TRAVASOL?
Its sulfite-free formulation reduces allergy risks and offers a safety profile appealing to hospitals and clinicians.

2. How does the market size influence investment prospects?
A growing IV fluid market, projected to reach $13.4 billion by 2028, offers opportunities for market share expansion, especially if TRAVASOL captures niche segments.

3. What are the major barriers to entry?
Regulatory approval, patent constraints, and establishing supply chain and distribution networks.

4. How sensitive is pricing in this segment?
Hospitals and clinics are cost-conscious, emphasizing bulk purchasing and generic options, which limit premium pricing opportunities.

5. What key risks should investors monitor?
Market saturation, price erosion from generics, supply chain disruptions, and regulatory changes.


References

[1] Research and Markets. (2022). Global Intravenous (IV) Fluid Market Analysis.
[2] U.S. Food and Drug Administration. (2022). Drug approval and regulation guidelines.
[3] European Medicines Agency. (2022). IV fluid regulatory standards.

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