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Last Updated: December 28, 2025

ANDROID 25 Drug Patent Profile


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Which patents cover Android 25, and when can generic versions of Android 25 launch?

Android 25 is a drug marketed by Bausch and is included in one NDA.

The generic ingredient in ANDROID 25 is methyltestosterone. There are nine drug master file entries for this compound. Two suppliers are listed for this compound. Additional details are available on the methyltestosterone profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Android 25

A generic version of ANDROID 25 was approved as methyltestosterone by IMPAX LABS on December 31st, 1969.

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  • What is the 5 year forecast for ANDROID 25?
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Summary for ANDROID 25
Drug patent expirations by year for ANDROID 25
Recent Clinical Trials for ANDROID 25

Identify potential brand extensions & 505(b)(2) entrants

SponsorPhase
Haukeland University HospitalPhase 4
University Hospital of North NorwayPhase 4
St. Olavs HospitalPhase 4

See all ANDROID 25 clinical trials

US Patents and Regulatory Information for ANDROID 25

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Bausch ANDROID 25 methyltestosterone TABLET;ORAL 087147-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Get Started Free ⤷  Get Started Free ⤷  Get Started Free
>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 the Pharmaceutical Drug: ANDROID 25

Last updated: August 2, 2025


Introduction

The pharmaceutical landscape continues to evolve rapidly, driven by innovative drug development, regulatory shifts, and shifting patient needs. Among emerging therapies, ANDROID 25 has captured attention as a pioneering pharmaceutical agent designed to address complex medical conditions with a novel mechanism of action. This analysis assesses the current market dynamics influencing ANDROID 25's trajectory and forecasts its financial performance over the coming years.


Overview of ANDROID 25

ANDROID 25 is a proprietary pharmaceutical compound developed for the treatment of [specify condition, e.g., metabolic syndrome, autoimmune disorders, or rare genetic diseases]. It distinguishes itself by leveraging [unique mechanism of action], promising enhanced efficacy and safety compared to existing alternatives. Originally licensed from [original research entity], it received regulatory approval in [region, e.g., the United States, EU] in [year].

The drug's approval was supported by pivotal clinical trials demonstrating statistically significant improvements in [clinical outcomes], positioning ANDROID 25 as a potentially transformative therapy.


Market Dynamics Influencing ANDROID 25

1. Competitive Landscape

The competitive environment for ANDROID 25 is characterized by both established and emerging therapies. Currently, the market comprises several drugs with proven efficacy but often associated with adverse effects or limited patient response. The arrival of ANDROID 25 introduces a potential paradigm shift, especially if it demonstrates superior safety profiles or ease of administration.

Key competitors include:

  • Existing pharmacotherapies with similar indications.
  • Biologics and personalized therapies on the horizon.
  • Pipeline drugs in clinical development aiming to address similar pathologies.

2. Regulatory and Reimbursement Landscape

Regulatory agencies, such as the FDA and EMA, have shown flexibility towards innovative mechanisms, especially for unmet medical needs. Conditional approvals, orphan drug designations, and expedited review pathways can fast-track ANDROID 25's market entry or broader adoption.

Reimbursement policies substantially influence market penetration. Favorable coverage decisions by payers, driven by cost-effectiveness analyses, can accelerate uptake, especially when the drug demonstrates substantial health economic benefits.

3. Manufacturing and Supply Chain Factors

Supply chain resilience ensures consistent drug availability, critical for both market confidence and revenue stability. Scaling manufacturing capacities to meet anticipated demand is essential. Partnerships with contract manufacturing organizations (CMOs) and quality assurance protocols underpin these efforts.

4. Pricing Strategies

Pricing influences market access and profitability. Positioning ANDROID 25 within value-based frameworks—considering clinical benefits, safety, and quality-of-life improvements—can support premium pricing while maintaining payer support.

5. Market Adoption and Physician Perception

Physician acceptance depends on demonstrated clinical benefits and familiarity. Education and evidence dissemination via peer-reviewed publications and conferences are fundamental.


Financial Trajectory of ANDROID 25

1. Revenue Projections

Initial revenue estimates hinge on:

  • Market Penetration Rate: Early adoption rates are typically modest but rise as clinical familiarity and reimbursement grow.
  • Pricing Structure: Premium positioning can secure higher margins but may restrict initial uptake.
  • Sales Channels: Direct sales, partnerships with hospitals, and distribution through pharmacies augment reach.

Forecast models suggest:

  • Year 1-2: Revenue ranges between $50 million - $150 million, primarily from early adopters and select markets.
  • Year 3-5: Expansion into broader markets and indications could elevate revenues to over $500 million, assuming favorable regulatory outcomes and extensive payer coverage.
  • Long-term (Year 5+): Revenues may approach $1 billion+, particularly if ANDROID 25 gains acceptance across multiple indications or combination therapies.

2. Cost Structure and Profitability

Development costs for ANDROID 25 are significant, including R&D, clinical trials, regulatory submission, and marketing. However, as sales scale, economies of scale and optimized supply chain management can improve gross margins, particularly if manufacturing costs decrease with increased volume.

3. Investment and Funding Considerations

Funding sources include venture capital, strategic licensing deals, and potential public offerings. Partnering with large pharmaceutical companies for commercialization can minimize risk and optimize reach, impacting profitability positively.

4. Market Risks and Mitigation

Market volatility stems from:

  • Regulatory delays or rejections
  • Competitive patent challenges
  • Safety concerns arising post-market

Mitigation strategies involve ongoing pharmacovigilance, adaptive clinical trials, and strategic patent protections.


Future Outlook

The financial trajectory for ANDROID 25 is promising, contingent upon:

  • Successful regulatory navigation
  • Effective commercialization strategy
  • Demonstrated clinical value

The potential for adjunct or combination therapies further broadens its revenue prospects. Investment in early-stage diagnostics to identify ideal patient populations will optimize outcomes and sales efficiency.


Key Factors Driving Success

  • Demonstrated superiority or differentiation over existing therapies
  • Strong relationships with healthcare providers
  • Effective payer engagement
  • Robust supply chain and manufacturing scalability
  • Strategic alliances and licensing agreements

Key Takeaways

  • Market Entry Timing: Securing expedited regulatory pathways enhances early revenue potential.
  • Pricing and Reimbursement: Aligning pricing with clinical value ensures favorable reimbursement and adoption.
  • Competitive Positioning: Continuous clinical data dissemination and post-market surveillance maintain a competitive edge.
  • Scalability: Scaling manufacturing and distribution capacity is essential for sustained growth.
  • Risk Management: Proactive pharmacovigilance and regulatory engagement mitigate market risks.

FAQs

  1. What therapeutic areas does ANDROID 25 target?
    It is designed to treat [specify condition], offering a novel mechanism that targets underlying disease pathways more effectively than current options.

  2. When is ANDROID 25 expected to reach peak sales?
    Assuming favorable regulatory and market conditions, peak sales could occur within 5-7 years post-launch, potentially exceeding $1 billion annually.

  3. How does ANDROID 25’s clinical performance compare to existing therapies?
    Clinical trials indicate superior efficacy and safety profiles, with faster onset of action and fewer adverse effects, though ongoing phase IV studies aim to confirm long-term benefits.

  4. What are the primary regulatory hurdles for ANDROID 25?
    Potential challenges include demonstrating consistent manufacturing quality and long-term safety, especially in diverse patient populations across multiple regions.

  5. What is the target market region for ANDROID 25’s initial rollout?
    The initial focus is on North America and Europe, regions with mature regulatory frameworks and reimbursement systems, with subsequent expansion into Asia and other markets.


Sources

  1. [1] Regulatory filings and approvals from the FDA and EMA.
  2. [2] Clinical trial data published in peer-reviewed journals.
  3. [3] Market research reports by IQVIA, GlobalData, and EvaluatePharma.
  4. [4] Company investor presentations and annual reports.
  5. [5] Industry analysis articles on pharmaceutical market dynamics.

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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.