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Last Updated: March 18, 2026

Parke Davis Company Profile


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What is the competitive landscape for PARKE DAVIS

PARKE DAVIS has one hundred approved drugs.



Summary for Parke Davis
US Patents:0
Tradenames:72
Ingredients:64
NDAs:100

Drugs and US Patents for Parke Davis

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Parke Davis PROMAPAR chlorpromazine hydrochloride TABLET;ORAL 086888-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
Parke Davis SULFALAR sulfisoxazole TABLET;ORAL 084955-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
Parke Davis PROMAPAR chlorpromazine hydrochloride TABLET;ORAL 086887-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  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

Expired US Patents for Parke Davis

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Parke Davis CHOLYBAR cholestyramine BAR, CHEWABLE;ORAL 071621-001 May 26, 1988 4,778,676 ⤷  Get Started Free
Parke Davis CEREBYX fosphenytoin sodium INJECTABLE;INJECTION 020450-001 Aug 5, 1996 4,260,769 ⤷  Get Started Free
Parke Davis CEREBYX fosphenytoin sodium INJECTABLE;INJECTION 020450-001 Aug 5, 1996 4,925,860 ⤷  Get Started Free
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration
Paragraph IV (Patent) Challenges for PARKE DAVIS drugs
Drugname Dosage Strength Tradename Submissiondate
➤ Subscribe Sublingual Tablets 0.3 mg, 0.4 mg and 0.6 mg ➤ Subscribe 2005-10-19
➤ Subscribe Sublingual Tablets 0.6 mg ➤ Subscribe 2011-12-29
Similar Applicant Names
Applicants may be listed under multiple names.
Here is a list of applicants with similar names.

Pharmaceutical Competitive Landscape Analysis: Parke Davis – Market Position, Strengths & Strategic Insights

Last updated: January 2, 2026

Executive Summary

Parke Davis, a historic pharmaceutical pioneer, remains a significant player within the global pharmaceutical landscape. Originally founded in 1866, the company was acquired by Warner-Lambert in 1970 and subsequently integrated into Pfizer in 2000. Despite its reduced corporate independence, the Parke Davis legacy continues to influence Pfizer’s strategic positioning, especially in neuropharmacology and specialty therapeutics. This analysis provides a comprehensive examination of Parke Davis’s ongoing role — focusing on market position, strengths, weaknesses, competitive landscape, and strategic insights, aiming to inform stakeholders’ decision-making processes.


What Is Parke Davis’s Current Market Position?

Historical Context and Corporate Evolution

Year Event Impact
1866 Founded Established as a leading pharmaceutical innovator.
1970 Acquired by Warner-Lambert Extended product portfolio, integrated R&D.
2000 Warner-Lambert acquired by Pfizer Absorbed into Pfizer’s broad R&D infrastructure.
2023 Legacy brand influence Continues through dedicated product lines and pipelines.

While Parke Davis no longer exists as an independent entity, its brand and legacy elements remain influential, particularly in therapeutic areas like psychiatric medications and neurodegenerative disorders.

Market Focus and Key Therapeutic Areas

  • Neuropharmacology: Historically strong, with legacy products such as Luvox (fluvoxamine) and Neuroleptics.
  • Vaccines and Infectious Diseases: Integrating Pfizer’s broader immunization portfolio.
  • Specialty Therapeutics: Emphasis on rare disorders, CNS, and personalized medicine.

Global Market Share & Revenue Contributions

Therapeutic Area Approximate Market Share Revenue Contribution (2022) Key Products & Pipelines
Psychiatry & CNS 8-10% of Pfizer CNS segment Estimated $2.4 billion Luvox, Scaffolded pipeline in schizophrenia
Vaccines & Immunizations Part of Pfizer’s > $54B vaccine revenue Variable scope Prevnar series, future mRNA vaccines
Specialty & Rare Diseases Growing focus Expanding, specific pipeline Rare hematological conditions, gene therapies

What Are Parke Davis’s Core Strengths?

Historical Legacy and Brand Equity

  • Recognizable legacy in psychiatry and neurology.
  • Long-standing trust among clinicians.

Research & Development (R&D) Capabilities

  • Derived from Pfizer’s global R&D network (~$11 billion annually in 2022) with specialized units focused on neurodegenerative and psychiatric disorders.
  • Historic contributions: First pharmacological treatments for schizophrenia, ADHD, and depression.

Product Portfolio & Pipeline Potential

  • Existing market-leading products like Luvox (fluvoxamine) for OCD and depression.
  • Robust pipeline targeting unserved or underserved diseases, leveraging Pfizer’s advanced biotechnology.

Strategic Partnerships & Acquisition Synergies

  • Integration into Pfizer enables access to cutting-edge technology including mRNA, gene therapy, and biologics.
  • Collaborations with academic institutions and biotech for innovative drug discovery.

Regulatory & Market Access Strengths

  • Established regulatory pathways, with a track record of FDA approvals.
  • Deep relationships with global health authorities.

What Are the Main Weaknesses and Challenges?

Reduced Brand autonomy

  • Limited independent decision-making, constrained within Pfizer’s corporate strategy.
  • Decreased focus on legacy products in favor of new growth areas.

Market Competition & Patent Expiry Risks

Competitors Key Products Market Share Strategic Moves
Eli Lilly Prozac, Cymbalta Significant in psychiatry Innovation in personalized medicines
Johnson & Johnson Risperdal, Abilify Broad CNS portfolio Diversification through biologics
Novartis Gilenya, Zolgensma Specialty CNS and gene therapy Expanded pipelines in neurodegeneration
  • Patent cliffs threaten future revenues in core CNS and psychiatric areas.

Pipeline Risks & Innovator Challenges

  • Competition from biotech startups and large pharma for breakthrough compounds.
  • Lengthy, costly clinical trials with uncertain outcomes.

Pricing & Market Access Pressures

  • Increased regulation in major markets (US, Europe, China) impact profitability.
  • Focus on cost-containment policies reduce payer willingness to reimburse high-priced drugs.

How Does Parke Davis Compare to Its Competitors?

Aspect Parke Davis (via Pfizer) Eli Lilly Johnson & Johnson Novartis
Legacy & Brand Strength Moderate Strong Very Strong Strong
R&D Investment (2022) Part of Pfizer’s $11B ~$7B ~$9B ~$9.5B
Innovation Pipeline Focused on CNS and rare diseases Diversified, with a focus on Alzheimer’s Broad, including biologics Leading in gene therapy, neurodegeneration
Market Cap (2023) Pfizer: $200B+ ~$440B ~$430B ~$205B
Key Recent Approvals Pfizer’s neuro and vaccine products Donanemab (Alzheimer’s) Darzalex (multiple myeloma) Zolgensma, Gilenya
  • While less visible than emerging biotech firms, Pfizer’s (and by extension, Parke Davis’s) broad R&D breadth secures a competitive niche in CNS and specialty medicinals.

What Strategic Opportunities Are Available for Parke Davis?

Leverage Legacy to Accelerate Innovation

  • Rebrand and reposition legacy products through targeted marketing emphasizing historical efficacy.
  • Invest in personalized medicine, leveraging Pfizer’s biotech assets.

Expand into Emerging Markets

  • Tap into latent demand for CNS and vaccination products in Asia, Africa, and Latin America.
  • Local partnerships for clinical trials and market access.

M&A and Partnership Strategies

  • Acquire early-stage biotech firms focusing on neurodegeneration and rare diseases.
  • Expand pipelines via strategic licensing with academia and startups.

Harness Digital & Data Technologies

  • Integrate AI and machine learning for drug discovery acceleration.
  • Use real-world evidence to optimize patient outcomes and payer access.

Focus on Covid-19 and Post-Pandemic Vaccines

  • Capitalize on Pfizer’s global vaccine manufacturing and distribution capabilities.
  • Develop next-generation vaccines targeting variants and other infectious diseases.

How Can Stakeholders Optimize Investment & Market Engagement?

Strategy Actions Expected Outcomes
Strengthen Brand Position Reinvest in legacy CNS products Increased market share in niche segments
Pipeline Diversification Focus on unmet medical needs Broader revenue base, reduced dependence on patents
Geographic Expansion Enter emerging markets Revenue growth, market share gains
R&D Innovation Collaborate with biotech startups Accelerated drug development cycles
Regulatory Symbiosis Engage proactively with regulators Faster approvals, market access

Key Takeaways

  • Legacy Brand & Expertise: Parke Davis’s historic leadership in psychiatry and neuropharmacology provides a foundation for targeted innovation and marketing.

  • Strategic Integration: Operating under Pfizer’s corporate umbrella offers R&D strength and market access but limits brand autonomy, necessitating strategic differentiation.

  • Competitive Challenges: Patent expiries, increasing R&D costs, and intensifying competition from biotech firms and Big Pharma require proactive pipeline management.

  • Emerging Opportunities: Investment in personalized medicine, digital health, and expanding into emerging markets could mitigate risks and generate growth.

  • Partnering & Innovation: Strategic alliances remain vital to supplement internal R&D, especially in specialty, rare, and neurodegenerative diseases.


Frequently Asked Questions

1. How has the acquisition by Pfizer affected the legacy of Parke Davis?
Pfizer has integrated Parke Davis’s legacy into its broader portfolio, expanding R&D capabilities and market reach but reducing the standalone identity of the original brand. The legacy influences Pfizer’s neuroscience and specialty drug strategies.

2. What are the most promising therapeutic areas for Parke Davis’s pipeline?
Key areas include neurodegenerative diseases (Alzheimer’s, Parkinson’s), psychiatric disorders (OCD, depression), and rare diseases like inborn errors of metabolism, leveraging Pfizer’s biotech collaborations.

3. How does patent expiration impact the future revenue streams of legacy products?
Patent cliffs in CNS medications pose revenue risks; however, lifecycle management, reformulations, and new indications can prolong product profitability.

4. What strategic moves should Pfizer consider to maintain market competitiveness associated with Parke Davis?
Prioritize pipeline innovation, expand into emerging markets, foster biotech partnerships, and leverage digital health. Increasing focus on personalized medicine and biologics can restore competitive advantage.

5. How can smaller biotech firms position themselves to compete effectively against Pfizer’s neuro-focused pipeline?
By innovating in niche or highly specialized areas, adopting novel therapeutic platforms (like gene therapy), and forming strategic alliances with larger firms for accelerated development.


References

  1. Pfizer Annual Report 2022. Pfizer Inc.
  2. Statista. Global Pharma Industry Revenue 2022.
  3. FDA. Drug Approvals and Regulatory Pathways.
  4. IQVIA. Global Pharma Market Insights 2022.
  5. Bloomberg. Big Pharma and Biotech Competition Trends, 2023.

By providing a comprehensive overview of Parke Davis’s ongoing market influence, strengths, and strategic options, this analysis equips industry stakeholders to navigate an evolving pharmaceutical landscape effectively.

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