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Last Updated: January 29, 2026

Jubilant Generics Company Profile


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What is the competitive landscape for JUBILANT GENERICS

JUBILANT GENERICS has forty-eight approved drugs.



Summary for Jubilant Generics
US Patents:0
Tradenames:43
Ingredients:42
NDAs:48

Drugs and US Patents for Jubilant Generics

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Jubilant Generics PERPHENAZINE perphenazine TABLET;ORAL 213694-002 Mar 18, 2025 AB RX No No ⤷  Get Started Free ⤷  Get Started Free
Jubilant Generics MEMANTINE HYDROCHLORIDE memantine hydrochloride TABLET;ORAL 091585-001 Oct 13, 2015 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
Jubilant Generics LURASIDONE HYDROCHLORIDE lurasidone hydrochloride TABLET;ORAL 210388-004 Dec 6, 2024 AB RX No No ⤷  Get Started Free ⤷  Get Started Free
Jubilant Generics OLANZAPINE olanzapine TABLET, ORALLY DISINTEGRATING;ORAL 200221-004 Sep 12, 2012 AB RX No No ⤷  Get Started Free ⤷  Get Started Free
Jubilant Generics PAROXETINE HYDROCHLORIDE paroxetine hydrochloride TABLET;ORAL 205528-002 Nov 27, 2015 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
Jubilant Generics BUPROPION HYDROCHLORIDE bupropion hydrochloride TABLET, EXTENDED RELEASE;ORAL 202774-002 Oct 11, 2013 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
Similar Applicant Names
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Pharmaceutical Competitive Landscape Analysis: Jubilant Generics – Market Position, Strengths & Strategic Insights

Last updated: January 10, 2026

Executive Summary

Jubilant Generics, a division of Jubilant Pharmova Limited, has established a significant footprint in the global pharmaceutical generics market. With a focus on affordable, high-quality medications, the company has expanded its operations across North America, Europe, Asia, and emerging markets. This analysis provides a detailed overview of Jubilant Generics' market position, core strengths, competitive advantages, and strategic initiatives. It synthesizes industry data, competitive benchmarking, and recent policy developments to aid stakeholders in making informed investment and partnership decisions.


Table of Contents

  1. Market Overview
  2. Jubilant Generics: Company Profile
  3. Market Position & Competitive Benchmarking
  4. Core Strengths & Differentiators
  5. Strategic Initiatives and Future Outlook
  6. Competitive Dynamics & Industry Trends
  7. Regulatory & Policy Environment
  8. SWOT Analysis
  9. Key Takeaways
  10. FAQs

1. Market Overview

Global Generics Market Dynamics

  • Market Size: Valued at approximately USD 370 billion in 2022, with projections reaching USD 460 billion by 2027 (CAGR: 4.6%) [1].
  • Growth Drivers: Patent expiries, cost-containment pressures, aging populations, and increasing access to healthcare in emerging markets.
  • Regional Breakdown:
Region % of Global Market (2022) Expected Growth (2023-2027) Major Trends
North America 45% 4.2% High patent cliff, shift to biosimilars
Europe 22% 3.8% Regulatory convergence, price pressures
Asia-Pacific 25% 5.5% Rising healthcare access, manufacturing hubs
Rest of World 8% 4.5% Market liberalization

Source: [1], industry reports

Key Market Challenges

  • Regulatory hurdles and quality standards
  • Price erosion in mature markets
  • Supply chain disruptions
  • Competition from biosimilars and innovative drugs

2. Jubilant Generics: Company Profile

Overview and Operations

  • Founded: 2000 in India
  • Headquarters: Noida, India
  • Revenue (FY 2022): Approx. USD 900 million [2]
  • Manufacturing Footprint: 15 manufacturing facilities globally, serving over 65 countries
  • Product Portfolio: Over 350 generic formulations, including tablets, injectables, topicals, and biosimilars

Strategic Focus Areas

  • Strengthening R&D capabilities for complex generics
  • Expanding US and European market presence
  • Enhancing manufacturing scale and quality

3. Market Position & Competitive Benchmarking

Key Competitors

Competitor Market Focus Revenue FY 2022 (USD millions) Market Share Estimates Notable Strengths
Teva Pharmaceuticals Global generics, biosimilars 14,000 4-5% Broad portfolio, global reach
Sandoz (Novartis) Biopharmaceuticals, Generics 13,300 3-4% Innovation-led generics, biosimilars
Mylan (now part of Viatris) US, Europe, Emerging 12,500 3-4% Cost leadership, extensive pipeline
Lupin Ltd India, US, Japan USD 3,000+ N/A Cost-efficient production, complex generics
Sun Pharma India, US, emerging markets USD 4,900+ N/A Research in complex generics, biosimilars

(Source: [3], industry reports)

Market Ranking & Share

  • Jubilant ranks within the top 10 global generics players by revenue, with an estimated market share of 0.8–1.2% [4].
  • Its strategic emphasis on specialized and complex generics positions it uniquely among mid-tier players.

Geographical Footprint

Region Share of Revenue Focus and Strategic Moves
North America 40% Robust expansion via FDA approvals
Europe 25% Entry via partnerships, acquisition strategies
India & Asia-Pacific 25% Strengthening manufacturing, local markets
ROW (Rest of World) 10% Penetration in emerging markets

4. Core Strengths & Differentiators

Robust R&D & Regulatory Capabilities

  • Over 350 ANDA (Abbreviated New Drug Application) filings in the US, with 200+ approvals as of 2022 [2].
  • Dedicated R&D centers in India and the US focusing on complex generics and biosimilars.
  • Strategic partnerships with contract research organizations (CROs).

Manufacturing Excellence & Quality

  • Strict adherence to USFDA, EUGMP, and WHO standards.
  • ISO-certified facilities with capabilities in sterile injectables and complex molecules.
  • Cost efficiencies driven by Indian manufacturing base and global scale.

Product Portfolio & Market Diversification

  • Strong foothold in sterile injectables, a high-margin segment.
  • Growing biosimilars pipeline targeting autoimmune and oncology indications.
  • Diversification reduces dependence on any single therapeutic area or geography.

Strategic Market Access & Distribution

  • Local manufacturing in emerging markets supports compliance and cost containment.
  • Key partnerships with global pharma companies for co-marketing and licensing.
  • Digital marketing and supply chain innovations to improve reach and operational resilience.

5. Strategic Initiatives & Future Outlook

Recent Initiatives

  • US Market Expansion: Approved 25+ ANDAs in FY 2022, with pipeline exceeding 50 filings.
  • Biosimilars Development: Collaborations with global biotech firms, focus on Insulin and monoclonal antibodies.
  • Manufacturing Upgrades: Capital expenditure of USD 150 million over 3 years to modernize facilities.
  • Acquisition & Partnerships: Explore acquisitions to accelerate entry into European markets; licensing agreements with innovative biotech firms.

Future Market Strategies

Focus Area Strategic Initiatives Timeline
Portfolio Expansion Launch of complex generics and biosimilars in US/EU 2023-2025
Geographic Penetration Strengthen presence in China and Latin America 2023-2024
R&D Innovation Enhance biosimilar research, AI-driven drug development 2022-2026
Supply Chain & Manufacturing Enhance capacity, adopt Industry 4.0 standards 2023-2025

6. Competitive Dynamics & Industry Trends

Emerging Opportunities and Challenges

Trends Implications for Jubilant Generics
Biosimilar Growth Investing in biosimilars offers higher margins, competitive advantage
Patent Expiration Wave Continuous pipeline development necessary for sustained growth
Regulatory Modernization Need to comply with evolving standards; leverage early approvals
Market Consolidation Potential M&A to accelerate scale and product portfolio

Competitive Strategies

  • Differentiation via quality and complex generic offerings.
  • Strategic collaborations and licensing to expedite pipeline.
  • Digital transformation for supply chain and R&D efficiency.

7. Regulatory & Policy Environment

Key Regulations Impacting Generics

Region Regulations/Policies Recent Changes & Impact
US (FDA) ANDA approval process, Hatch-Waxman Act incentives Streamlined approval pathways, REMS considerations
Europe (EMA) Centralized & decentralized procedures, patent expiry harmonization Increased focus on quality standards, biosimilar regulations
India (DCGI) New GMP guidelines, patent law reforms Strengthened quality requirements, faster approvals
China Drug registration reforms, patent policies Greater regulatory transparency, incentives for biotech innovation

Impact on Jubilant Generics

  • Opportunities from device-friendly policies and accelerated approvals.
  • Challenges from increasing compliance costs and evolving standards.

8. SWOT Analysis

Strengths Weaknesses
Extensive R&D for complex generics and biosimilars Moderate global market share
Strong manufacturing base in India Heavy dependence on regulated markets in US and Europe
Diversified product portfolio Limited presence in some mature markets
Opportunities Threats
Growing biosimilar demand globally Heightened regulatory scrutiny
Entry into emerging markets Intense price competition in mature markets
Collaborations with biotech firms Patent litigation risks

9. Key Takeaways

  • Market Position: Jubilant Generics ranks among the top 10 global generics firms, with a focus on high-margin complex generics and biosimilars.
  • Strengths: R&D excellence, manufacturing quality, diversified portfolio, and strategic global partnerships.
  • Strategic Advantage: Early mover in biosimilars with a robust pipeline and manufacturing infrastructure.
  • Growth Drivers: Expanding US approvals, biosimilar development, emerging markets penetration.
  • Risks: Price erosion, regulatory hurdles, market consolidation pressures.
  • Recommendations: Leverage innovation in biosimilars, pursue strategic M&A, diversify geographical footprint, and invest in digital transformation.

10. FAQs

Q1: How does Jubilant Generics compare with global leaders like Teva and Sandoz?

A: While Teva and Sandoz dominate with larger portfolios and global footprints, Jubilant excels in complex generics and biosimilars, with significant R&D investments and manufacturing capabilities. Its niche focus allows competitive differentiation, especially in emerging markets and specialized segments.

Q2: What are Jubilant Generics' key growth avenues for the next 3-5 years?

A: Priority areas include biosimilars development, expanding ANDA filings in the US, entering new markets like China and Latin America, and forming strategic collaborations to accelerate pipeline growth.

Q3: How is regulatory policy impacting Jubilant Generics' operations?

A: Evolving global regulations necessitate rigorous compliance and continuous quality upgrades. Increased regulatory scrutiny heightens compliance costs but also presents opportunities for early approvals and market differentiation through quality.

Q4: What risks does Jubilant face in expanding its biosimilar portfolio?

A: Biosimilars face complex regulatory pathways, high developmental costs, and intense competition from established innovator biologics, which demand significant investment and strategic partnerships for success.

Q5: How important are emerging markets for Jubilant's future growth?

A: Critical. Emerging markets offer high growth potential due to increasing healthcare access and lower costs. Jubilant’s local manufacturing presence and regulatory familiarity position it well to capitalize on this trend.


References

[1] MarketsandMarkets, Generics Market Growth & Forecast, 2022.

[2] Jubilant Pharmova Limited Annual Report, FY 2022.

[3] IQVIA, Global Pharmaceuticals Market Data, 2022.

[4] EvaluatePharma, Top 10 Generics Companies by Revenue, 2022.

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