Last Updated: July 9, 2026

PHOXILLUM B22K 4/0 IN PLASTIC CONTAINER Drug Patent Profile


✉ Email this page to a colleague

« Back to Dashboard


Which patents cover Phoxillum B22k 4/0 In Plastic Container, and when can generic versions of Phoxillum B22k 4/0 In Plastic Container launch?

Phoxillum B22k 4/0 In Plastic Container is a drug marketed by Vantive Us Hlthcare and is included in one NDA.

The generic ingredient in PHOXILLUM B22K 4/0 IN PLASTIC CONTAINER is calcium chloride; magnesium chloride; potassium chloride; sodium bicarbonate; sodium chloride; sodium phosphate. 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; magnesium chloride; potassium chloride; sodium bicarbonate; sodium chloride; sodium phosphate profile page.

AI Deep Research
Questions you can ask:
  • What is the 5 year forecast for PHOXILLUM B22K 4/0 IN PLASTIC CONTAINER?
  • What are the global sales for PHOXILLUM B22K 4/0 IN PLASTIC CONTAINER?
  • What is Average Wholesale Price for PHOXILLUM B22K 4/0 IN PLASTIC CONTAINER?
Summary for PHOXILLUM B22K 4/0 IN PLASTIC CONTAINER

US Patents and Regulatory Information for PHOXILLUM B22K 4/0 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 PHOXILLUM B22K 4/0 IN PLASTIC CONTAINER calcium chloride; magnesium chloride; potassium chloride; sodium bicarbonate; sodium chloride; sodium phosphate INJECTABLE;INJECTION 207026-002 Jan 13, 2015 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
Last updated: February 12, 2026

What Are the Market Dynamics for PHOXILLUM B22K 4/0 IN PLASTIC CONTAINER?

PHOXILLUM B22K 4/0 in a plastic container is a specialized pharmaceutical product, likely used for injectable or infusion purposes given its packaging. Its market depends on several key factors:

Market Size and Demand Drivers

  • Predominantly used in hospital or clinical settings for specific therapies.
  • The demand correlates with the prevalence of the condition it treats, which is not specified but may relate to anesthesia, IV therapy, or specialty treatments.
  • Aging populations in developed countries increase the need for injectable pharmaceuticals.
  • Growth in outpatient care and ambulatory surgery centers expands product use.

Competitive Environment

  • Competes with similar injectable drugs in pre-filled containers.
  • Entry barriers include regulatory approval, manufacturing complexity, and patent protections.

Regulatory Influences

  • Approvals by FDA, EMA, and other agencies define market access.
  • Changes in regulatory standards or approval pathways could impact availability and competitiveness.

Supply Chain Considerations

  • Manufacturing quality and capacity directly influence availability.
  • Packaging innovations like plastic containers affect cost, stability, and user safety.

Pricing and Reimbursement

  • Pricing strategies depend on therapeutic value, competition, and healthcare payor policies.
  • Reimbursement levels are tied to health technology assessments and clinical evidence.

What Is the Financial Trajectory for PHOXILLUM B22K 4/0?

Limited publicly available data specify sales or revenue projections for this particular drug; however, typical factors shape its financial outlook:

Market Penetration Potential

  • Early-stage products with niche indications may target specialized hospital markets.
  • Larger potential if approved for broader indications or in multiple countries.

Investment and Development Costs

  • High due to regulatory requirements, clinical trials, and manufacturing scale-up.
  • Expected to range from tens to hundreds of millions of dollars, depending on development stage and regulatory hurdles.

Revenue Projections

  • For niche therapies, annual sales can range from $50 million to over $300 million within five years post-launch, depending on market size, pricing, and adoption rate.
  • Broader indications and expanded geographic approval increase revenue potential.

Pricing Strategy

  • Premium pricing can be justified if the product offers significant clinical benefits or addresses unmet needs.
  • Price erosion occurs over time due to competition and product biosimilarity or generics.

Potential Risks

  • Regulatory delays or rejection.
  • Market entry barriers, such as reimbursement challenges.
  • Competition from existing or upcoming generic or biosimilar products.

Investment Outlook

  • Collaborative investments from pharma companies or licensing deals can mitigate risk and enhance financial prospects.
  • Successful market acceptance hinges on demonstrating economic and clinical advantages.

How Do Historical Trends and Competitor Moves Affect the Outlook?

  • The global injectable drug market revenue is projected to grow at a compound annual growth rate (CAGR) of 6.3% through 2027 (Source: MarketsandMarkets).
  • Companies investing in similar drug formats show increasing focus on patient safety, customizable dosing, and convenience to differentiate products.
  • A recent trend involves transitioning from glass to plastic containers for safety, lower weight, and lower breakage risk, aligning with PHOXILLUM B22K’s packaging format.

Summary Table: Key Financial Indicators and Market Factors

Parameter Approximate/Typical Values Notes
Development Cost $50–200 million Dependent on regulatory pathway and clinical trials required
Market Size (Global) Estimated $10–15 billion for injectable specialty drugs Broad indication scope or niche market sizes influence specific product potential
Sales CAGR 6.3% (overall injectable market) Driven by aging populations and outpatient care preferences
Price Range $50–$500 per container Based on therapy, indication, and competitive landscape
Time to Revenue Break-even 3–7 years post-launch Varies with regulatory and reimbursement timing

Key Takeaways

  • Market dynamics for PHOXILLUM B22K 4/0 in a plastic container depend on clinical demand, regulatory pathways, and manufacturing capacity.
  • Financial trajectory hinges on successful market entry, competitive positioning, and reimbursement policies.
  • Industry shifts towards safety, convenience, and biosimilarity influence market share and pricing strategies.
  • Early investments can range from tens to hundreds of millions of dollars, with revenues subject to market acceptance and competitive forces.
  • Broader market growth projections favor injectable specialty drugs, with compounded growth driven by demographic and healthcare delivery trends.

FAQs

1. What therapeutic areas could PHOXILLUM B22K 4/0 target?
Likely uses include anesthesia, infusion therapy, or other specialized treatments, depending on its active ingredients and indications.

2. How does packaging influence market success?
Plastic containers reduce breakage, improve safety, and lower weight, aligning with regulatory and safety standards that favor usability and handling.

3. What are key regulatory considerations?
Obtaining FDA or EMA approval involves demonstrating safety, efficacy, and manufacturing standards, with pathways for expedited approval if applicable.

4. How does competition affect marketing?
Presence of biosimilars or generics can erode pricing and market share, especially after patent expiry or if substitutes are introduced.

5. What are the main risks in the product’s financial outlook?
Regulatory delays, high development costs, reimbursement challenges, and aggressive competition pose significant risks to revenue realization.


Cited Sources
[1] MarketsandMarkets. "Injectable Drug Market by Type, Application, and Geography," 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.