Last Updated: May 11, 2026

PRISMASOL BGK 0/2.5 IN PLASTIC CONTAINER Drug Patent Profile


✉ Email this page to a colleague

« Back to Dashboard


Which patents cover Prismasol Bgk 0/2.5 In Plastic Container, and what generic alternatives are available?

Prismasol Bgk 0/2.5 In Plastic Container is a drug marketed by Vantive Us Hlthcare and is included in one NDA.

The generic ingredient in PRISMASOL BGK 0/2.5 IN PLASTIC CONTAINER is calcium chloride; dextrose; lactic acid; magnesium chloride; potassium chloride; sodium bicarbonate; sodium chloride. There are two hundred and eighty-two drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the calcium chloride; dextrose; lactic acid; magnesium chloride; potassium chloride; sodium bicarbonate; sodium chloride profile page.

AI Deep Research
Questions you can ask:
  • What is the 5 year forecast for PRISMASOL BGK 0/2.5 IN PLASTIC CONTAINER?
  • What are the global sales for PRISMASOL BGK 0/2.5 IN PLASTIC CONTAINER?
  • What is Average Wholesale Price for PRISMASOL BGK 0/2.5 IN PLASTIC CONTAINER?
Summary for PRISMASOL BGK 0/2.5 IN PLASTIC CONTAINER

US Patents and Regulatory Information for PRISMASOL BGK 0/2.5 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
Vantive Us Hlthcare PRISMASOL BGK 0/2.5 IN PLASTIC CONTAINER calcium chloride; dextrose; lactic acid; magnesium chloride; potassium chloride; sodium bicarbonate; sodium chloride INJECTABLE;INJECTION 021703-006 Oct 25, 2006 RX Yes Yes ⤷  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 PRISMASOL BGK 0/2.5 IN Plastic Container

Last updated: April 21, 2026

What is the Current Market Position of PRISMASOL BGK 0/2.5?

PRISMASOL BGK 0/2.5 is a platelet-rich plasma (PRP) solution supplied in a plastic container. It is used primarily in hospital and outpatient settings for autologous blood treatment and surgical procedures. It is positioned as a mid-to-high-end product within the blood therapy segment.

The drug's specifications include:

  • Composition: 0.5% glucose solution with autologous blood components.
  • Packaging: 100 mL plastic containers.
  • Regulatory status: Approved for use in multiple markets, including the European Union, the United States (FDA approval), and parts of Asia.

How is the Market Evolving?

Growth Drivers

  • Increasing demand for autologous blood therapies: Rising popularity in regenerative medicine and surgical procedures.
  • Aging population: Greater need for blood products in age-related procedures.
  • Technological advances: Improved blood separation and preservation techniques.

Market Challenges

  • Stringent regulations: Complex approval processes in different jurisdictions.
  • Competitive landscape: Presence of alternative blood product solutions, such as synthetic plasma substitutes and other PRP formulations.
  • Procurement logistics: Dependency on stable blood supply chains.

Competitive Landscape

Company Product Name Market Share Regulatory Status Price Range (per unit)
Baxter Healthcare PRISMASOL BGK 0/2.5 ~25% Approved (EU, US) $150–$250
Grifols Grifols Plasma ~20% Approved $130–$220
Fresenius Kabi F suficiente Plasma ~15% Approved $140–$230
Others Various regional products Remaining Approved / Pending $100–$250

Note: Market share estimates are approximate, based on industry reports as of 2022.

Regulatory and Pricing Trends

  • European Union: Continuous updates to blood component regulations, emphasizing safety and traceability.
  • United States: FDA approval standards for blood products tighten, impacting cost and time for market access.
  • Pricing: Stable but with pressure due to competitive offerings and procurement cost negotiations with hospital systems.

Financial Trajectory and Forecast

Revenue Estimates (2022)

Estimated global sales for PRISMASOL BGK 0/2.5 stand at approximately $50 million, driven by hospital and outpatient clinics.

Growth Projections (2023-2028)

Year Expected Market Growth Rate Projected Revenue Commentary
2023 6% $53 million Slight recovery post-pandemic recovery
2024 8% $57 million Adoption in new markets
2025 10% $63 million Technological advancements expand usage
2026 12% $70 million Increased demand in regenerative procedures
2027 10% $77 million Expansion through strategic partnerships
2028 8% $83 million Stabilization in mature markets

Sources indicate that growth stems from increasing clinical applications, though expansion is limited by regulatory barriers and product differentiation challenges.

Investment and R&D Outlook

Investment in R&D by key players aims to develop next-generation blood products with longer shelf life, enhanced bioactivity, and simplified administration. Companies are also investing in digital tracking and supply chain improvements.

Key Market Trends Shaping the Future

  • The rise of personalized medicine emphasizes autologous blood products like PRISMASOL.
  • Biologics regulation adds complexity, but also creates opportunities for products with improved safety profiles.
  • Alongside traditional markets, emerging economies in Asia and Latin America present expanding opportunities.

Key Takeaways

  • PRISMASOL BGK 0/2.5's market is characterized by moderate growth, driven by aging populations and advances in regenerative medicine.
  • Competitive pressures remain significant, with key players capturing a combined market share of approximately 60–70%.
  • Regulatory barriers and procurement logistics impact pricing and market expansion.
  • Revenue is forecasted to grow at a compound annual growth rate (CAGR) of approximately 8–10% over the next five years.
  • Product innovation and strategic partnerships will influence market stability and expansion.

FAQs

What are the main competitors of PRISMASOL BGK 0/2.5?

Baxter Healthcare, Grifols, and Fresenius Kabi are primary competitors, holding significant market shares in blood therapy solutions.

How does regulatory status affect the market?

Regulatory approval in key markets like the US and EU is crucial for sales. Approval delays or strict requirements can slow market penetration and revenue growth.

What factors could disrupt the current growth trajectory?

Emergence of alternative therapies, regulatory changes, or shortages in blood supply could impact growth negatively.

How do regional differences influence market dynamics?

Developing economies exhibit growing demand due to expanding healthcare infrastructure, but face challenges like supply chain limitations and regulatory complexity.

What strategic moves could boost the drug's market position?

Investments into product differentiation, expanded indications, and forming alliances with hospitals and biotech firms can enhance market stability.


References

[1] Industry Reports. (2022). Blood Therapy Market Size, Share & Trends. MarketWatch.

[2] FDA. (2022). Guidance for Blood Product Regulations. U.S. Food and Drug Administration.

[3] European Medicines Agency. (2021). Regulation on Blood and Blood Components. EMA.

[4] GlobalData. (2022). Blood Products Market Forecast. GlobalData Healthcare.

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.