Last Updated: May 4, 2026

POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% IN PLASTIC CONTAINER Drug Patent Profile


✉ Email this page to a colleague

« Back to Dashboard


When do Potassium Chloride 0.15% In Dextrose 5% In Plastic Container patents expire, and what generic alternatives are available?

Potassium Chloride 0.15% In Dextrose 5% In Plastic Container is a drug marketed by B Braun and is included in three NDAs.

The generic ingredient in POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% IN PLASTIC CONTAINER is dextrose; potassium chloride. There are nine drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the dextrose; potassium chloride profile page.

AI Deep Research
Questions you can ask:
  • What is the 5 year forecast for POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% IN PLASTIC CONTAINER?
  • What are the global sales for POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% IN PLASTIC CONTAINER?
  • What is Average Wholesale Price for POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% IN PLASTIC CONTAINER?
Summary for POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% IN PLASTIC CONTAINER
Pharmacology for POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% IN PLASTIC CONTAINER

US Patents and Regulatory Information for POTASSIUM CHLORIDE 0.15% 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
B Braun POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.11% IN PLASTIC CONTAINER dextrose; potassium chloride; sodium chloride INJECTABLE;INJECTION 019630-004 Feb 17, 1988 RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
B Braun POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% IN PLASTIC CONTAINER dextrose; potassium chloride INJECTABLE;INJECTION 019699-004 Sep 29, 1989 AP RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
B Braun POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER dextrose; potassium chloride; sodium chloride INJECTABLE;INJECTION 019630-022 Feb 17, 1988 AP RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
B Braun POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% AND SODIUM CHLORIDE 0.2% IN PLASTIC CONTAINER dextrose; potassium chloride; sodium chloride INJECTABLE;INJECTION 019630-010 Feb 17, 1988 AP RX 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

POTASSIUM CHLORIDE 0.15% IN DEXTROSE 5% IN PLASTIC CONTAINER Market Analysis and Financial Projection

Last updated: February 16, 2026

What Are the Market Dynamics for Potassium Chloride 0.15% in Dextrose 5% in Plastic Container?

The market for potassium chloride in dextrose solutions is driven by therapeutic needs, regulatory environments, and manufacturing capacities. As an electrolyte used for potassium replacement in intravenous (IV) therapy, this formulation is essential in hospitals and clinics. Several factors influence its market trajectory:

  • Therapeutic demand: The increasing prevalence of electrolyte imbalances due to chronic diseases such as kidney disease, heart failure, and gastrointestinal conditions supports sustained demand. The rise in hospital admissions for electrolyte management elevates utilization levels.
  • Regulatory approvals: Approval status from authorities like the FDA and EMA influences market access. For example, the FDA approved potassium chloride IV formulations for specific indications that include electrolyte repletion.
  • Manufacturing and supply chain considerations: Production of plastic containers that meet safety and sterility standards is crucial. Manufacturers such as Baxter, Hospira, and Sanofi produce these solutions at scale.
  • Competitive landscape: Market players focus on product quality, pricing strategies, and geographic expansion, particularly in emerging markets with expanding healthcare infrastructure.
  • Pricing and reimbursement: Reimbursement policies in developed countries affect market penetration. Reimbursement rates for IV electrolyte solutions are subject to healthcare system policies and influence procurement decisions.

What Is the Financial Trajectory of Potassium Chloride 0.15% in Dextrose 5%?

The financial outlook revolves around revenue streams, market share, growth drivers, and risks:

Aspect Details
Market Size (Global) Estimated USD 500-700 million in 2022, driven by hospital demand and increased electrolyte replacement therapies.
Compound Annual Growth Rate (CAGR) Projected at 4-6% over the next five years, reflecting steady demand amid rising chronic illness prevalence.
Pricing Trends Manufacturer prices range from USD 0.10 to USD 0.50 per mL, with variations based on container size, formulation, and regional logistics. Price discounts are common in bulk hospital procurement.
Market Segmentation North America accounts for approximately 40% of sales, followed by Europe at around 30%, with the remaining in Asia-Pacific and Latin America experiencing higher growth due to expanding healthcare infrastructure.
Major Revenue Drivers Hospital procurement, infusion therapy demand, and cost containment strategies by health systems. Introduced generic versions have driven prices downward, limiting profit margins for branded products.

How Do Regulatory and Competitive Factors Affect the Market?

  • Regulatory standards: US FDA and European EMA compliance ensures market access, with post-market surveillance required to maintain approvals. Any safety concerns or manufacturing deviations can result in product withdrawals.
  • Patent landscape: The segment has limited patent protections, with many formulations considered generic. Competitive pricing pressures are intense.
  • Market entry barriers: High manufacturing standards, regulatory approval processes, and large capital investments for sterile production facilities act as barriers for new entrants.
  • Pricing pressures: Hospitals negotiate for discounts, impacting overall profit margins for manufacturers with limited differentiation.

What Are the Future Market Drivers and Risks?

Drivers:

  • Growing prevalence of chronic illnesses requiring IV electrolyte supplementation.
  • Expansion of healthcare infrastructure in emerging markets.
  • Innovations in container materials improving safety and stability.
  • Increased adoption of bundled therapy protocols, integrating electrolyte solutions.

Risks:

  • Supply chain disruptions affecting raw materials and container manufacturing.
  • Regulatory changes tightening safety standards and labeling requirements.
  • Price competition reducing margins, especially from generics.
  • Modal shifts toward oral hydration in certain applications, reducing IV electrolyte demand.

What Is the Impact of COVID-19 Pandemic on This Market?

The COVID-19 pandemic increased hospitalization rates, particularly in critical care settings, elevating demand for electrolyte replacements. However, supply chain constraints by disrupted logistics and raw material shortages temporarily hampered production. Post-pandemic, demand levels have stabilized, with a continued emphasis on efficient supply chain management to mitigate future risks.

Key Takeaways

  • The market for potassium chloride 0.15% in dextrose 5% in plastic containers is growing annually at 4-6%, supported by increased electrolyte imbalance management needs.
  • North America and Europe dominate the market, but Asian markets present significant growth opportunities.
  • Pricing remains competitive, with generic options exerting downward pressure on margins.
  • Regulatory compliance and supply chain stability are crucial for sustained market presence.
  • Rising chronic disease prevalence is the primary driver, while price competition and supply disruptions constitute key risks.

FAQs

1. Which companies are the leading manufacturers of potassium chloride IV solutions?
Baxter, Hospira (a Pfizer division), and Sanofi are among the top producers, often supplying generic and branded formulations.

2. What are the main regulatory considerations for this product?
Compliance with FDA and EMA standards, including sterility, stability, and labeling, is mandatory. Post-market surveillance adds ongoing compliance requirements.

3. How does the pricing of this solution compare globally?
Prices fluctuate based on regional healthcare policies, with higher retail prices in the US and Europe. In emerging markets, cost containment drives prices lower and favors generic versions.

4. What are the growth opportunities in emerging markets?
Expanding healthcare infrastructure and increasing hospital admissions for electrolyte management create substantial demand, supported by rising investments in healthcare systems.

5. How will supply chain issues influence future market stability?
Supply chain disruptions can limit availability or increase costs, impacting profitability and hospital procurement strategies. Manufacturers are investing in local or regional production capabilities to mitigate these risks.


Citations:

[1] "Global Intravenous (IV) Solutions Market," MarketsandMarkets, 2022.
[2] "Hospital Demand for Electrolyte Solutions," Pharma Intelligence, 2022.
[3] "Regulatory Guidelines for IV Solutions," FDA, 2021.
[4] "Electrolyte Replacement Therapy Trends," WHO, 2022.
[5] "Market Dynamics for IV Solutions," IQVIA, 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.