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Teva Strategy Overview February 21, 2008

Teva Strategy Overview

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  • Teva Strategy OverviewFebruary 21, 2008

  • TODAYS PRESENTATION CONTAINS FORWARD-LOOKING STATEMENTS, WHICH EXPRESS THE CURRENT BELIEFS AND EXPECTATIONS OF MANAGEMENT. SUCH STATEMENTS INVOLVE A NUMBER OF KNOWN AND UNKNOWN RISKS AND UNCERTAINTIES THAT COULD CAUSE TEVA'S FUTURE RESULTS, PERFORMANCE OR ACHIEVEMENTS TO DIFFER SIGNIFICANTLY FROM THE RESULTS, PERFORMANCE OR ACHIEVEMENTS EXPRESSED OR IMPLIED BY SUCH FORWARD-LOOKING STATEMENTS. IMPORTANT FACTORS THAT COULD CAUSE OR CONTRIBUTE TO SUCH DIFFERENCES INCLUDE RISKS RELATING TO: TEVA'S ABILITY TO ACCURATELY PREDICT FUTURE MARKET CONDITIONS, TEVA'S ABILITY TO SUCCESSFULLY DEVELOP AND COMMERCIALIZE ADDITIONAL PHARMACEUTICAL PRODUCTS, THE INTRODUCTION OF COMPETING GENERIC EQUIVALENTS, THE EXTENT TO WHICH TEVA MAY OBTAIN U.S. MARKET EXCLUSIVITY FOR CERTAIN OF ITS NEW GENERIC PRODUCTS AND REGULATORY CHANGES THAT MAY PREVENT TEVA FROM UTILIZING EXCLUSIVITY PERIODS, COMPETITION FROM BRAND-NAME COMPANIES THAT ARE UNDER INCREASED PRESSURE TO COUNTER GENERIC PRODUCTS, OR COMPETITORS THAT SEEK TO DELAY THE INTRODUCTION OF GENERIC PRODUCTS, POTENTIAL LIABILITY FOR SALES OF GENERIC PRODUCTS PRIOR TO A FINAL RESOLUTION OF OUTSTANDING PATENT LITIGATION, INCLUDING THAT RELATING TO THE GENERIC VERSIONS OF ALLEGRA, NEURONTIN, LOTREL, FAMVIR, AND PROTONIX, THE IMPACT OF CONSOLIDATION OF OUR DISTRIBUTORS AND CUSTOMERS, THE EFFECTS OF COMPETITION ON OUR INNOVATIVE PRODUCTS, ESPECIALLY COPAXONE SALES, THE IMPACT OF PHARMACEUTICAL INDUSTRY REGULATION AND PENDING LEGISLATION THAT COULD AFFECT THE PHARMACEUTICAL INDUSTRY, THE DIFFICULTY OF PREDICTING U.S. FOOD AND DRUG ADMINISTRATION, EUROPEAN MEDICINES AGENCY AND OTHER REGULATORY AUTHORITY APPROVALS, THE REGULATORY ENVIRONMENT AND CHANGES IN THE HEALTH POLICIES AND STRUCTURES OF VARIOUS COUNTRIES, OUR ABILITY TO ACHIEVE EXPECTED RESULTS THOUGH OUR INNOVATIVE R&D EFFORTS, TEVA'S ABILITY TO SUCCESSFULLY IDENTIFY, CONSUMMATE AND INTEGRATE ACQUISITIONS, POTENTIAL EXPOSURE TO PRODUCT LIABILITY CLAIMS TO THE EXTENT NOT COVERED BY INSURANCE, DEPENDENCE ON THE EFFECTIVENESS OF OUR PATENTS AND OTHER PROTECTIONS FOR INNOVATIVE PRODUCTS, SIGNIFICANT OPERATIONS WORLDWIDE THAT MAY BE ADVERSELY AFFECTED BY TERRORISM, POLITICAL OR ECONOMICAL INSTABILITY OR MAJOR HOSTILITIES, SUPPLY INTERRUPTIONS OR DELAYS THAT COULD RESULT FROM THE COMPLEX MANUFACTURING OF OUR PRODUCTS AND OUR GLOBAL SUPPLY CHAIN, ENVIRONMENTAL RISKS, FLUCTUATIONS IN CURRENCY, EXCHANGE AND INTEREST RATES, AND OTHER FACTORS THAT ARE DISCUSSED IN TEVA'S ANNUAL REPORT ON FORM 20-F AND ITS OTHER FILINGS WITH THE U.S. SECURITIES AND EXCHANGE COMMISSION. FORWARD-LOOKING STATEMENTS SPEAK ONLY AS OF THE DATE ON WHICH THEY ARE MADE AND THE COMPANY UNDERTAKES NO OBLIGATION TO UPDATE OR REVISE ANY FORWARD-LOOKING STATEMENT, WHETHER AS A RESULT OF NEW INFORMATION, FUTURE EVENTS OR OTHERWISE.

    Forward-Looking Statements

  • Table of Contents

    Tevas Growth Strategy 2008-2012

    Global Generic Markets

    US

    Europe

    International

    Global Generic Resources

    Innovative Strategy

    BioGenerics

    Modeling Teva

    Closing Thoughts

  • Tevas Growth Strategy 2008-2012

    Shlomo Yanai

    President and CEO

    Teva Pharmaceutical Industries Ltd.

    February 21, 2008

  • TODAYS PRESENTATION CONTAINS FORWARD-LOOKING STATEMENTS, WHICH EXPRESS THE CURRENT BELIEFS AND EXPECTATIONS OF MANAGEMENT. SUCH STATEMENTS INVOLVE A NUMBER OF KNOWN AND UNKNOWN RISKS AND UNCERTAINTIES THAT COULD CAUSE TEVA'S FUTURE RESULTS, PERFORMANCE OR ACHIEVEMENTS TO DIFFER SIGNIFICANTLY FROM THE RESULTS, PERFORMANCE OR ACHIEVEMENTS EXPRESSED OR IMPLIED BY SUCH FORWARD-LOOKING STATEMENTS. IMPORTANT FACTORS THAT COULD CAUSE OR CONTRIBUTE TO SUCH DIFFERENCES INCLUDE RISKS RELATING TO: TEVA'S ABILITY TO ACCURATELY PREDICT FUTURE MARKET CONDITIONS, TEVA'S ABILITY TO SUCCESSFULLY DEVELOP AND COMMERCIALIZE ADDITIONAL PHARMACEUTICAL PRODUCTS, THE INTRODUCTION OF COMPETING GENERIC EQUIVALENTS, THE EXTENT TO WHICH TEVA MAY OBTAIN U.S. MARKET EXCLUSIVITY FOR CERTAIN OF ITS NEW GENERIC PRODUCTS AND REGULATORY CHANGES THAT MAY PREVENT TEVA FROM UTILIZING EXCLUSIVITY PERIODS, COMPETITION FROM BRAND-NAME COMPANIES THAT ARE UNDER INCREASED PRESSURE TO COUNTER GENERIC PRODUCTS, OR COMPETITORS THAT SEEK TO DELAY THE INTRODUCTION OF GENERIC PRODUCTS, POTENTIAL LIABILITY FOR SALES OF GENERIC PRODUCTS PRIOR TO A FINAL RESOLUTION OF OUTSTANDING PATENT LITIGATION, INCLUDING THAT RELATING TO THE GENERIC VERSIONS OF ALLEGRA, NEURONTIN, LOTREL, FAMVIR, AND PROTONIX, THE IMPACT OF CONSOLIDATION OF OUR DISTRIBUTORS AND CUSTOMERS, THE EFFECTS OF COMPETITION ON OUR INNOVATIVE PRODUCTS, ESPECIALLY COPAXONE SALES, THE IMPACT OF PHARMACEUTICAL INDUSTRY REGULATION AND PENDING LEGISLATION THAT COULD AFFECT THE PHARMACEUTICAL INDUSTRY, THE DIFFICULTY OF PREDICTING U.S. FOOD AND DRUG ADMINISTRATION, EUROPEAN MEDICINES AGENCY AND OTHER REGULATORY AUTHORITY APPROVALS, THE REGULATORY ENVIRONMENT AND CHANGES IN THE HEALTH POLICIES AND STRUCTURES OF VARIOUS COUNTRIES, OUR ABILITY TO ACHIEVE EXPECTED RESULTS THOUGH OUR INNOVATIVE R&D EFFORTS, TEVA'S ABILITY TO SUCCESSFULLY IDENTIFY, CONSUMMATE AND INTEGRATE ACQUISITIONS, POTENTIAL EXPOSURE TO PRODUCT LIABILITY CLAIMS TO THE EXTENT NOT COVERED BY INSURANCE, DEPENDENCE ON THE EFFECTIVENESS OF OUR PATENTS AND OTHER PROTECTIONS FOR INNOVATIVE PRODUCTS, SIGNIFICANT OPERATIONS WORLDWIDE THAT MAY BE ADVERSELY AFFECTED BY TERRORISM, POLITICAL OR ECONOMICAL INSTABILITY OR MAJOR HOSTILITIES, SUPPLY INTERRUPTIONS OR DELAYS THAT COULD RESULT FROM THE COMPLEX MANUFACTURING OF OUR PRODUCTS AND OUR GLOBAL SUPPLY CHAIN, ENVIRONMENTAL RISKS, FLUCTUATIONS IN CURRENCY, EXCHANGE AND INTEREST RATES, AND OTHER FACTORS THAT ARE DISCUSSED IN TEVA'S ANNUAL REPORT ON FORM 20-F AND ITS OTHER FILINGS WITH THE U.S. SECURITIES AND EXCHANGE COMMISSION. FORWARD-LOOKING STATEMENTS SPEAK ONLY AS OF THE DATE ON WHICH THEY ARE MADE AND THE COMPANY UNDERTAKES NO OBLIGATION TO UPDATE OR REVISE ANY FORWARD-LOOKING STATEMENT, WHETHER AS A RESULT OF NEW INFORMATION, FUTURE EVENTS OR OTHERWISE.

    Forward-Looking Statements

  • Fundamental Questions

    ? Can Teva sustain its pace of growth for years to come?

    ? What will be Tevas key growth drivers?

    ? What is Tevas value proposition?

    1

  • Tevas 20/20 Target

    By 2012, we expect to:

    Double our business

    Reach revenues of $20 billion

    Exceed net income margins of 20%

    2

  • Growth Through Market Leadership

    WatsonMylan

    $7.0 B

    Sandoz

    $2.6 B

    Teva

    $2.5 B

    Barr

    $2.5 B

    $9.4 B

    2007 Sales of peer group

    Market Leadership:

    Market share

    Gap between #1 and #2

    Source: Company reports and analyst estimates3

  • The Leaders Reward

    Difference in operating margin

    0% 10% 15% 20% 25% 30%5%0%

    10%

    2%

    4%

    6%

    8%

    Difference in market share between no. 1 and no. 2 player

    Source: Cross industry analysis of market leadership, McKinsey & Company

    Market leaders are typically more profitable than followers

    The greater the share gap the greater the profit advantage

    Greater absolute market share correlates with greater profitability

    4

  • The External Environment

    Macro conditions are in Tevas favor

    Harmonization& Consolidation

    Payors

    Demand Demographic shifts and emerging market growth

    Global generics ~$75b in 2007 to ~$120b in 2012

    Decision-making shifting to payors

    Growing pressure to lower costs

    Big-to-big opportunities

    Global standards, common products, and global economies of scale create a few global leaders

    5

  • Growth Will Create 2 More U.S. Markets

    * U.S. and CanadaSource: IMS, Espicom; Teva estimates of local markets

    $75B

    2007 2012

    International

    Europe

    North America*

    $120B

    $45B

    Global Generics Sales

    6

  • Tevas Core Strengths and Competitive Advantages

    Broadest product portfolio

    Largest first-to-file / Paragraph IV pipeline

    API leadership

    Large global footprint, leadership in most significant market (U.S.)

    Tevas Scale and

    Leadership

    Tevas Scale and

    Leadership

    R&D, legal and regulatory excellence

    Low-cost production and supply chain

    Backward integration

    Proven track-record in M&As

    Service excellence

    Execution ExcellenceExecution Excellence

    Commitment to global generics leadership

    Leveraging scale and scope

    Commercial innovation

    Competitive Approach

    Competitive Approach

    Lean, agile, responsive and fast

    Proactive, willing to challengeTevas CultureTevas Culture

    7

  • Key Pillars of Our Strategy

    Increase Tevas market share in key markets

    Increase Tevas market share in key markets

    Extend leadership in U.S. Establish leadership in key EU and International markets

    Double our product portfolioDouble our product portfolio

    Double R&D capabilities Focus on first-to-market / Paragraph IVs Double production capacity

    Biotechnology: Next growth wave in generics

    Biotechnology: Next growth wave in generics

    Invest in the next wave of technology and Generics Create affordable Biogenerics: lower cost, greater value

    Redefine customer serviceRedefine customer service

    Develop big-to-big offerings Create new go-to-market initiatives

    Innovative businessInnovative business

    Focus on niche specialty areas Leverage unique sourcing, development and go-to-

    market approaches

    8

  • Tevas Value Proposition

    Growth Company

    Commitment To Global Generics Leadership

    Balanced Business Model

    Attractive Financial Returns

    Tevas Culture and Brand

    9

  • Key Themes

    Increase market leadership

    Double-down on product portfolio

    Redefine customer service

    Affordable Biogenerics

    Differentiated approach to Innovative

    Double our business

    Reach revenues of $20 billion

    Exceed net profit margins of 20%

    Where Teva is going

    How we will get there

    10

  • Teva North America

    Bill Marth

    President and CEO

    Teva North America

    February 21, 2008

  • TODAYS PRESENTATION CONTAINS FORWARD-LOOKING STATEMENTS, WHICH EXPRESS THE CURRENT BELIEFS AND EXPECTATIONS OF MANAGEMENT. SUCH STATEMENTS INVOLVE A NUMBER OF KNOWN AND UNKNOWN RISKS AND UNCERTAINTIES THAT COULD CAUSE TEVA'S FUTURE RESULTS, PERFORMANCE OR ACHIEVEMENTS TO DIFFER SIGNIFICANTLY FROM THE RESULTS, PERFORMANCE OR ACHIEVEMENTS EXPRESSED OR IMPLIED BY SUCH FORWARD-LOOKING STATEMENTS. IMPORTANT FACTORS THAT COULD CAUSE OR CONTRIBUTE TO SUCH DIFFERENCES INCLUDE RISKS RELATING TO: TEVA'S ABILITY TO ACCURATELY PREDICT FUTURE MARKET CONDITIONS, TEVA'S ABILITY TO SUCCESSFULLY DEVELOP AND COMMERCIALIZE ADDITIONAL PHARMACEUTICAL PRODUCTS, THE INTRODUCTION OF COMPETING GENERIC EQUIVALENTS, THE EXTENT TO WHICH TEVA MAY OBTAIN U.S. MARKET EXCLUSIVITY FOR CERTAIN OF ITS NEW GENERIC PRODUCTS AND REGULATORY CHANGES THAT MAY PREVENT TEVA FROM UTILIZING EXCLUSIVITY PERIODS, COMPETITION FROM BRAND-NAME COMPANIES THAT ARE UNDER INCREASED PRESSURE TO COUNTER GENERIC PRODUCTS, OR COMPETITORS THAT SEEK TO DELAY THE INTRODUCTION OF GENERIC PRODUCTS, POTENTIAL LIABILITY FOR SALES OF GENERIC PRODUCTS PRIOR TO A FINAL RESOLUTION OF OUTSTANDING PATENT LITIGATION, INCLUDING THAT RELATING TO THE GENERIC VERSIONS OF ALLEGRA, NEURONTIN, LOTREL, FAMVIR, AND PROTONIX, THE IMPACT OF CONSOLIDATION OF OUR DISTRIBUTORS AND CUSTOMERS, THE EFFECTS OF COMPETITION ON OUR INNOVATIVE PRODUCTS, ESPECIALLY COPAXONE SALES, THE IMPACT OF PHARMACEUTICAL INDUSTRY REGULATION AND PENDING LEGISLATION THAT COULD AFFECT THE PHARMACEUTICAL INDUSTRY, THE DIFFICULTY OF PREDICTING U.S. FOOD AND DRUG ADMINISTRATION, EUROPEAN MEDICINES AGENCY AND OTHER REGULATORY AUTHORITY APPROVALS, THE REGULATORY ENVIRONMENT AND CHANGES IN THE HEALTH POLICIES AND STRUCTURES OF VARIOUS COUNTRIES, OUR ABILITY TO ACHIEVE EXPECTED RESULTS THOUGH OUR INNOVATIVE R&D EFFORTS, TEVA'S ABILITY TO SUCCESSFULLY IDENTIFY, CONSUMMATE AND INTEGRATE ACQUISITIONS, POTENTIAL EXPOSURE TO PRODUCT LIABILITY CLAIMS TO THE EXTENT NOT COVERED BY INSURANCE, DEPENDENCE ON THE EFFECTIVENESS OF OUR PATENTS AND OTHER PROTECTIONS FOR INNOVATIVE PRODUCTS, SIGNIFICANT OPERATIONS WORLDWIDE THAT MAY BE ADVERSELY AFFECTED BY TERRORISM, POLITICAL OR ECONOMICAL INSTABILITY OR MAJOR HOSTILITIES, SUPPLY INTERRUPTIONS OR DELAYS THAT COULD RESULT FROM THE COMPLEX MANUFACTURING OF OUR PRODUCTS AND OUR GLOBAL SUPPLY CHAIN, ENVIRONMENTAL RISKS, FLUCTUATIONS IN CURRENCY, EXCHANGE AND INTEREST RATES, AND OTHER FACTORS THAT ARE DISCUSSED IN TEVA'S ANNUAL REPORT ON FORM 20-F AND ITS OTHER FILINGS WITH THE U.S. SECURITIES AND EXCHANGE COMMISSION. FORWARD-LOOKING STATEMENTS SPEAK ONLY AS OF THE DATE ON WHICH THEY ARE MADE AND THE COMPANY UNDERTAKES NO OBLIGATION TO UPDATE OR REVISE ANY FORWARD-LOOKING STATEMENT, WHETHER AS A RESULT OF NEW INFORMATION, FUTURE EVENTS OR OTHERWISE.

    Forward-Looking Statements

  • Our Goal

    North American Sales

    $5.2 B

    2007

    $9.5 11.5 B

    2012

    CAGR:13-17%

    Note: Includes all pharmaceutical sales in the U.S. and Canada1

  • Respiratory

    Large global market

    Key part of our market strategies

    Potential market of ~$25 Billion by 2012

    Teva commercial strengths

    Significant share of SABA market (US)

    Relationships with trade, payors, physicians

    Investments in R&D

    Numerous pipeline products

    Leveraging innovative and generic R&D capabilities

    2

  • U.S. Generics Key Themes

    Strategy Strong generics growth in a very attractive market

    Clear U.S. market leader - we aim to significantly increase our market share leadership

    Execution Double down on our generics portfolio

    Improve our generics commercial model with even greater focus on customers

    Goal Overall, we expect Tevas U.S. generics revenues

    to outpace the market while maintaining current EBIT margins

    3

  • Source: IMS National Prescription Audit MAT December 2007

    Number of TRxs per dayMillions

    Teva dispenses nearly 2 out of every 10 generics prescriptions

    Tevas daily volume is 50% greater than the next closest competitor

    Teva is the Clear U.S. Market Leader

    0.40.50.6

    0.8

    1.2

    WatsonMylan BarrTeva Sandoz

    4

  • 3.6 B

    2.4 B

    0.4 B

    1.1 B

    Projected TRx CAGRs

    Generics overall: 8%

    Teva: 20%

    Extending U.S. Leadership to 30% Market Share

    * ProjectedSource: IMS Health National Prescription Audit, Teva Estimates

    Generic Industry TRxsTeva total generic TRxs

    2007A 2012E

    Number of TRxs

    18% 30%Tevas share*

    5

  • Key Elements of the U.S. Strategy

    Product portfolio

    Significantly greater investment in R&D

    Expand portfolio - new product launches

    Heavy emphasis on Para IV filings

    Leverage our scale for strategic and competitive advantage

    Supply Chain preeminence

    Leadership and scale

    Innovate our commercial model expand relationships with market leaders

    Redefine service

    Go-to-market initiatives

    6

  • Doubling Down on Generic R&D

    Doubling our submissions

    Accelerating development to further increase our first-to-file, first-to market and first-to-opportunitypositions

    Doubling output without doubling resources through: Capacity Speed Efficiency Parallel development Technology

    7

  • Source: IMS, Teva estimates

    2007 Pharmaceuticals Market

    Total market

    $285 B

    Products Pending Approval and In Development Cover Most of the Market

    $101 BTeva products pending approval

    Teva products in development

    $101 B

    $83 B

    Opportunity 65%Of the market

    8

  • Source: Investor earnings call transcripts and company statements

    1149

    160

    Teva

    N/A

    >80

    Sandoz

    12

    60

    Mylan

    16

    71

    Barr

    70

    Watson

    First-to-file

    PipelineNumber of ANDAs pending

    Teva has more ANDAs than any two competitors combined

    92 current Teva files are Paragraph IV challenges (49 have FTF status)

    Teva has the Most Valuable Pipeline

    9

  • Source: Investor earnings call transcripts and company statements

    and the Broadest Product Portfolio in the Industry

    Currently marketed productsNumber of products

    Teva has 65% more marketed

    products than the next closest competitor

    150

    150

    170

    200

    331

    Mylan

    Barr

    Sandoz

    Watson

    Teva

    ESTIMATES

    10

  • 2007: Pantoprazole

    Source: Market data from IMS NSP at time of launch

    Our Scale Gives Us an Unrivaled Ability to Launch At Risk

    Leverages our core capabilities

    R&D

    Legal/regulatory

    Product commercialization: the way we go to market

    Supply chain flexibility

    Customers value earlier and superior access to products

    Enhances profitability

    11

  • Advantages of Supply Chain Preeminence

    Ability to leverage customer demand information across the Supply Chain

    Robust global Supply Chain network

    Prompt, seamless coordination of complex supply and distribution network

    Supported by 14 manufacturing sites globally

    Ability to execute large launches quickly (e.g., Pantoprazole, Simvastatin)

    Produce at multiple sites simultaneously

    Able to deliver multiple product configurations at launch

    12

  • Robust Customer Relationships Are Critical to Our Success

    Generics are critical to Tevas key customers

    By 2012 generics will represent > 75% of all prescriptions in the U.S.

    Generics represent >50% of the drug profits of key U.S. customers

    We have developed a customer-centric business model

    Core elements:

    Superior service

    Collaborative planning

    Early access to new product launches

    Future plans:

    Tighter collaboration

    Enhanced packaging

    Game changing moves

    Big-to-Big

    13

  • Example: Game ChangingCustomer Service Innovation

    Our goal within 3 years, is to reach 50,000 pharmacies nationwide the day after launch

    Significant investment planned to expanding our Supply Chain in combination with a new Direct-to-Store delivery capability

    Benefits across the value chain:

    Faster patient access to generics

    More pharmacies immediately benefit from new product launches

    More efficient inventory management across the distribution system

    Reach All Pharmacies In a Day . . .

    14

  • Tevas U.S. Generics Financial Goal

    U.S. Net Sales Projected GrowthCAGR 2007 2012

    10%

    Market

    >14%

    Teva

    Key Paragraph IVs and other new products

    Big-to-big customer relationships

    Additional upside in specialty and innovative products

    Source: IMS; Teva estimates15

  • Extending our Lead

    0

    50

    100

    150

    200

    0 50 100 150 200 250 300 350 400

    Teva

    Sandoz

    Mylan

    Barr

    Watson

    Current portfolioMarketed products

    Future portfolioANDAs Pending

    Note: Bubble size is proportional to IMS reports of 2007 TRx; Teva = 437 Million16

  • European Generics Market

    Gerard W.M. van Odijk

    President and CEO

    Teva Europe

    February 21, 2008

  • TODAYS PRESENTATION CONTAINS FORWARD-LOOKING STATEMENTS, WHICH EXPRESS THE CURRENT BELIEFS AND EXPECTATIONS OF MANAGEMENT. SUCH STATEMENTS INVOLVE A NUMBER OF KNOWN AND UNKNOWN RISKS AND UNCERTAINTIES THAT COULD CAUSE TEVA'S FUTURE RESULTS, PERFORMANCE OR ACHIEVEMENTS TO DIFFER SIGNIFICANTLY FROM THE RESULTS, PERFORMANCE OR ACHIEVEMENTS EXPRESSED OR IMPLIED BY SUCH FORWARD-LOOKING STATEMENTS. IMPORTANT FACTORS THAT COULD CAUSE OR CONTRIBUTE TO SUCH DIFFERENCES INCLUDE RISKS RELATING TO: TEVA'S ABILITY TO ACCURATELY PREDICT FUTURE MARKET CONDITIONS, TEVA'S ABILITY TO SUCCESSFULLY DEVELOP AND COMMERCIALIZE ADDITIONAL PHARMACEUTICAL PRODUCTS, THE INTRODUCTION OF COMPETING GENERIC EQUIVALENTS, THE EXTENT TO WHICH TEVA MAY OBTAIN U.S. MARKET EXCLUSIVITY FOR CERTAIN OF ITS NEW GENERIC PRODUCTS AND REGULATORY CHANGES THAT MAY PREVENT TEVA FROM UTILIZING EXCLUSIVITY PERIODS, COMPETITION FROM BRAND-NAME COMPANIES THAT ARE UNDER INCREASED PRESSURE TO COUNTER GENERIC PRODUCTS, OR COMPETITORS THAT SEEK TO DELAY THE INTRODUCTION OF GENERIC PRODUCTS, POTENTIAL LIABILITY FOR SALES OF GENERIC PRODUCTS PRIOR TO A FINAL RESOLUTION OF OUTSTANDING PATENT LITIGATION, INCLUDING THAT RELATING TO THE GENERIC VERSIONS OF ALLEGRA, NEURONTIN, LOTREL, FAMVIR, AND PROTONIX, THE IMPACT OF CONSOLIDATION OF OUR DISTRIBUTORS AND CUSTOMERS, THE EFFECTS OF COMPETITION ON OUR INNOVATIVE PRODUCTS, ESPECIALLY COPAXONE SALES, THE IMPACT OF PHARMACEUTICAL INDUSTRY REGULATION AND PENDING LEGISLATION THAT COULD AFFECT THE PHARMACEUTICAL INDUSTRY, THE DIFFICULTY OF PREDICTING U.S. FOOD AND DRUG ADMINISTRATION, EUROPEAN MEDICINES AGENCY AND OTHER REGULATORY AUTHORITY APPROVALS, THE REGULATORY ENVIRONMENT AND CHANGES IN THE HEALTH POLICIES AND STRUCTURES OF VARIOUS COUNTRIES, OUR ABILITY TO ACHIEVE EXPECTED RESULTS THOUGH OUR INNOVATIVE R&D EFFORTS, TEVA'S ABILITY TO SUCCESSFULLY IDENTIFY, CONSUMMATE AND INTEGRATE ACQUISITIONS, POTENTIAL EXPOSURE TO PRODUCT LIABILITY CLAIMS TO THE EXTENT NOT COVERED BY INSURANCE, DEPENDENCE ON THE EFFECTIVENESS OF OUR PATENTS AND OTHER PROTECTIONS FOR INNOVATIVE PRODUCTS, SIGNIFICANT OPERATIONS WORLDWIDE THAT MAY BE ADVERSELY AFFECTED BY TERRORISM, POLITICAL OR ECONOMICAL INSTABILITY OR MAJOR HOSTILITIES, SUPPLY INTERRUPTIONS OR DELAYS THAT COULD RESULT FROM THE COMPLEX MANUFACTURING OF OUR PRODUCTS AND OUR GLOBAL SUPPLY CHAIN, ENVIRONMENTAL RISKS, FLUCTUATIONS IN CURRENCY, EXCHANGE AND INTEREST RATES, AND OTHER FACTORS THAT ARE DISCUSSED IN TEVA'S ANNUAL REPORT ON FORM 20-F AND ITS OTHER FILINGS WITH THE U.S. SECURITIES AND EXCHANGE COMMISSION. FORWARD-LOOKING STATEMENTS SPEAK ONLY AS OF THE DATE ON WHICH THEY ARE MADE AND THE COMPANY UNDERTAKES NO OBLIGATION TO UPDATE OR REVISE ANY FORWARD-LOOKING STATEMENT, WHETHER AS A RESULT OF NEW INFORMATION, FUTURE EVENTS OR OTHERWISE.

    Forward-Looking Statements

  • Key Themes

    European generics market is large and growing

    Teva has a proven track record of growth

    Growth strategy focuses on:- Increasing our share - Securing leadership- Investing in our core functions

    By 2012, we expect to more than double our sales and grow EBIT even faster

    11

  • Our Goal

    European* Sales

    $5.1 5.7 B

    $2.2 B

    20122007

    18-21%

    * Refers throughout to Western Europe and Hungary2

  • The Western European Generics Market is Large and Growing

    CAGR, 2007-12

    Europe overall is a large market with steady growth (7% CAGR)

    20.2

    2012

    +7%

    14.7

    2007

    Net sales retail and hospitalUSD Billions

    Growth is particularly strong in the EUs Latin countries

    Italy

    +20%

    Spain

    +15%

    France

    +14%

    3

  • High Growth in Latin European Countries, Driven by New Reforms

    7%12%

    17%

    50%54%

    63% 65%

    U.K.U.S.GermanyNetherlandsFranceSpainItaly

    Emerging Generics MarketsLatin Europe

    Mature Generics Markets

    Increased Generics penetrationIncreased Generics penetration

    Generics Market ShareVolume

    Source: EGA 2007 Market Survey; US based on IMS estimates June 20074

  • 7%12%

    17%

    50%54%

    63% 65%

    U.K.U.S.GermanyNetherlandsFranceSpainItaly

    In Germany, Tenders Create New Opportunities

    Emerging Generics MarketsLatin Europe

    Mature Generics Markets

    Tenders are entry ticket to the worlds 2nd largest generics market (~ $5 billion)

    Shift from Branded-Generics to Generic-Generics

    Tenders are entry ticket to the worlds 2nd largest generics market (~ $5 billion)

    Shift from Branded-Generics to Generic-Generics

    Generics Market ShareVolume

    Source: EGA 2007 Market Survey; US based on IMS estimates June 20075

  • Across the Region, Pharmacies and Chains Gaining Importance

    Branded Generics

    model

    Branded Generics

    model

    Pharmacist/ payor influence

    Physicianinfluence Hungary

    Italy

    France

    U.K.

    Netherlands

    Germany

    Spain Markets undergoing

    change

    Generics penetration

    Substitution Generics

    model

    Substitution Generics

    model

    Selective portfolioSelective portfolio

    BroadportfolioBroad

    portfolio

    Market transition

    6

  • Core Elements of Our Strategy

    Build leadership in Latin markets

    Capture generics tender opportunity in Germany

    Leverage scale where competition is fragmented

    Secure leadership market by marketSecure leadership market by market

    Invest to enhance our core functionsInvest to enhance our core functions

    Not just First to Market but Broad to Market

    Build out manufacturing capacity and flexibility

    Expand Supply Chain

    Extend lead in U.K., Italy, and Netherlands

    Extend lead in U.K., Italy, and Netherlands

    Expand big-to-big relationships

    Further broaden product portfolio

    Drive profitability through scale

    7

  • Unparalleled service levelUnparalleled service level

    Up scaling1. Improved flexibility & responsiveness2. Reduce costs

    Up scaling1. Improved flexibility & responsiveness2. Reduce costs

    Our Continued Back-End Investment Creates a Foundation for our Growth

    Doubling our European GR&D investment next 5 years

    Doubling our European GR&D investment next 5 years

    Doubling Manufacturing Capacity next 5 years

    Doubling Manufacturing Capacity next 5 years

    170247

    381 472612

    7631,019

    > 1500 (+50%)

    Plan2008

    2007200620052004200320022001

    10 X UP

    1. 2.

    8

  • Tevas Proven Go-to-Market Approach

    Tevas European Presence

    Big-to-BigPortfolio breadth and

    geographical presence position Teva as unique partner

    for EU wholesale & retail players

    Big-to-BigPortfolio breadth and

    geographical presence position Teva as unique partner

    for EU wholesale & retail players

    Sell-outDistinctive commercial offers and lean & agile go-to-market models

    match evolving market needs

    Sell-outDistinctive commercial offers and lean & agile go-to-market models

    match evolving market needs

    New products / loyalty program

    PullPull

    1. 2.

    9

  • Closing Remarks

    European generics market is attractive

    Teva is uniquely positioned to succeed in Europe

    Tevas European growth strategy is focused on achieving market leadership

    By 2012, Teva will more than double sales and grow EBIT even faster

    10

  • Chaim Hurvitz

    Group VP International

    Teva Pharmaceutical Industries Ltd.

    February 21, 2008

    International Generic Markets

  • TODAYS PRESENTATION CONTAINS FORWARD-LOOKING STATEMENTS, WHICH EXPRESS THE CURRENT BELIEFS AND EXPECTATIONS OF MANAGEMENT. SUCH STATEMENTS INVOLVE A NUMBER OF KNOWN AND UNKNOWN RISKS AND UNCERTAINTIES THAT COULD CAUSE TEVA'S FUTURE RESULTS, PERFORMANCE OR ACHIEVEMENTS TO DIFFER SIGNIFICANTLY FROM THE RESULTS, PERFORMANCE OR ACHIEVEMENTS EXPRESSED OR IMPLIED BY SUCH FORWARD-LOOKING STATEMENTS. IMPORTANT FACTORS THAT COULD CAUSE OR CONTRIBUTE TO SUCH DIFFERENCES INCLUDE RISKS RELATING TO: TEVA'S ABILITY TO ACCURATELY PREDICT FUTURE MARKET CONDITIONS, TEVA'S ABILITY TO SUCCESSFULLY DEVELOP AND COMMERCIALIZE ADDITIONAL PHARMACEUTICAL PRODUCTS, THE INTRODUCTION OF COMPETING GENERIC EQUIVALENTS, THE EXTENT TO WHICH TEVA MAY OBTAIN U.S. MARKET EXCLUSIVITY FOR CERTAIN OF ITS NEW GENERIC PRODUCTS AND REGULATORY CHANGES THAT MAY PREVENT TEVA FROM UTILIZING EXCLUSIVITY PERIODS, COMPETITION FROM BRAND-NAME COMPANIES THAT ARE UNDER INCREASED PRESSURE TO COUNTER GENERIC PRODUCTS, OR COMPETITORS THAT SEEK TO DELAY THE INTRODUCTION OF GENERIC PRODUCTS, POTENTIAL LIABILITY FOR SALES OF GENERIC PRODUCTS PRIOR TO A FINAL RESOLUTION OF OUTSTANDING PATENT LITIGATION, INCLUDING THAT RELATING TO THE GENERIC VERSIONS OF ALLEGRA, NEURONTIN, LOTREL, FAMVIR, AND PROTONIX, THE IMPACT OF CONSOLIDATION OF OUR DISTRIBUTORS AND CUSTOMERS, THE EFFECTS OF COMPETITION ON OUR INNOVATIVE PRODUCTS, ESPECIALLY COPAXONE SALES, THE IMPACT OF PHARMACEUTICAL INDUSTRY REGULATION AND PENDING LEGISLATION THAT COULD AFFECT THE PHARMACEUTICAL INDUSTRY, THE DIFFICULTY OF PREDICTING U.S. FOOD AND DRUG ADMINISTRATION, EUROPEAN MEDICINES AGENCY AND OTHER REGULATORY AUTHORITY APPROVALS, THE REGULATORY ENVIRONMENT AND CHANGES IN THE HEALTH POLICIES AND STRUCTURES OF VARIOUS COUNTRIES, OUR ABILITY TO ACHIEVE EXPECTED RESULTS THOUGH OUR INNOVATIVE R&D EFFORTS, TEVA'S ABILITY TO SUCCESSFULLY IDENTIFY, CONSUMMATE AND INTEGRATE ACQUISITIONS, POTENTIAL EXPOSURE TO PRODUCT LIABILITY CLAIMS TO THE EXTENT NOT COVERED BY INSURANCE, DEPENDENCE ON THE EFFECTIVENESS OF OUR PATENTS AND OTHER PROTECTIONS FOR INNOVATIVE PRODUCTS, SIGNIFICANT OPERATIONS WORLDWIDE THAT MAY BE ADVERSELY AFFECTED BY TERRORISM, POLITICAL OR ECONOMICAL INSTABILITY OR MAJOR HOSTILITIES, SUPPLY INTERRUPTIONS OR DELAYS THAT COULD RESULT FROM THE COMPLEX MANUFACTURING OF OUR PRODUCTS AND OUR GLOBAL SUPPLY CHAIN, ENVIRONMENTAL RISKS, FLUCTUATIONS IN CURRENCY, EXCHANGE AND INTEREST RATES, AND OTHER FACTORS THAT ARE DISCUSSED IN TEVA'S ANNUAL REPORT ON FORM 20-F AND ITS OTHER FILINGS WITH THE U.S. SECURITIES AND EXCHANGE COMMISSION. FORWARD-LOOKING STATEMENTS SPEAK ONLY AS OF THE DATE ON WHICH THEY ARE MADE AND THE COMPANY UNDERTAKES NO OBLIGATION TO UPDATE OR REVISE ANY FORWARD-LOOKING STATEMENT, WHETHER AS A RESULT OF NEW INFORMATION, FUTURE EVENTS OR OTHERWISE.

    Forward-Looking Statements

  • Key Themes

    Huge potential in the International markets

    Strong starting point - market positions, global capabilities

    1

  • Our Goal

    2012

    $3.2 4.0 B

    2007

    International Sales

    18-23%

    $1.4 B

    2

  • Strong International Market Growth

    Source: IMS, ex-factory prices 07/07

    Pharma Market (CAGRs 2007-2011)

    International markets:2007 : $ 188 B2011: $ 257 B

    LatinAmerica:

    10%

    Japan: 4%

    Asia:11%

    Eastern Europe:

    18%

    3

  • Broad Teva Presence in International Markets

    Poland

    CzechLithuania

    ChinaHungary

    Mexico

    Venezuela

    Chile

    Argentina

    Israel

    19 Manufacturing sites

    3 Partnerships

    24 National companies

    Peru

    Uruguay

    Brazil S. Africa

    KenyaSingapore

    Japan

    Taiwan

    RomaniaBulgariaTurkey

    RussiaLatvia

    Ukraine

    Presence

    India

    4

  • International Generic Markets Growing Rapidly

    Source: IMS; Espicom; Teva estimates

    2007 ($B) Generics 2012 ($B) GenericsCAGR 2007-12 Percent

    1.5

    2.5

    3.2

    3.3

    3.4

    3.5

    6.6

    12.7China

    India

    Mexico

    Japan

    Turkey

    Russia

    Brazil

    S. Korea

    4.6

    5.2

    4.3

    8.9

    6.6

    4.9

    9.3

    22.4

    7

    7

    6

    25

    16

    22

    14

    12

    5

  • Strategic Considerations For Prioritizing Markets

    Market size

    Growth rate

    Readiness / Maturity

    - Political and economy stability

    - Government accountability to health care

    - Regulatory & Legal environment

    6

  • Two Types of Markets on our Priority List

    Early Generic marketsEmerging Economies

    Large, or rapidly growing overall pharmamarket

    Low generic share

    Favorable trends e.g., demographic growth, cost pressure

    Strong economic growth and rising personal wealth

    Consolidated group of retailers and distributors

    Rising patient demand for quality products

    Example: JapanExample: Brazil, Mexico

    7

  • Brazil Emerging Economy; Quality Is Growing in Importance

    Source: Espicom, IMS, Expert Interviews, Teva analysis

    $ Billions$ Billions

    BioequivalentGenerics

    Branded Generics and Similares

    Patentedmolecules

    CAGR 2007-12 Percent

    -1

    8

    25

    9.4

    8.8

    17.4

    13.6

    +5%

    2012

    4.6

    4.0

    2007

    1.5

    2.7

    Rising personal wealth drives Bioequivalent growth at the expense of Similares

    Customers are consolidating enabling big-to-big strategies

    8

  • Mexico Emerging Economy; Quality Is Growing in Importance

    Source: Team analysis, RMBC, experts interviews, Teva analysis

    $ Billions$ Billions

    3.4

    CAGR 2007-12 Percent

    14

    12

    Generics

    10.3

    18.5

    2012

    6.6

    2007

    13.7

    25.1

    3.4

    +13%

    Innovative& Branded Generics

    Already # 1 in Public Sector

    Government is: Enforcing

    bioequivalence laws

    Increasing public health spending

    A broad portfolio is important in tenders

    9

  • Japanese Generics Market Poised To Grow

    Worlds 2nd largest pharma market

    - 2007: $67B

    - 2012 projection: $83B

    Attractive fundamentals:

    - Aging population

    - Rising healthcare costs

    - Government encouraging generics penetration

    10

  • Significant Opportunity To Increase Generics Penetration In Japan

    Generics share of total prescription drug marketIn percentage

    Source: IMS; MHLW; Espicom; Teva analysis

    Government targeting 30% volume share by 2012

    Government could save ~$25B annually

    Volume Value

    5

    17

    11

  • Closing Remarks

    Huge potential

    Strong starting point - markets positions, global capabilities

    Growth by:

    Extending existing presence

    Entering new markets

    Our goal: $3.24.0 Billion in profitable revenues in 2012

    12

  • NJE-1410.1305-20080207-dineHR2

    Global Generic Resources

    Amir Elstein

    Executive VP, Global Resources

    Teva Pharmaceutical Industries Ltd.

    February 21, 2008

  • TODAYS PRESENTATION CONTAINS FORWARD-LOOKING STATEMENTS, WHICH EXPRESS THE CURRENT BELIEFS AND EXPECTATIONS OF MANAGEMENT. SUCH STATEMENTS INVOLVE A NUMBER OF KNOWN AND UNKNOWN RISKS AND UNCERTAINTIES THAT COULD CAUSE TEVA'S FUTURE RESULTS, PERFORMANCE OR ACHIEVEMENTS TO DIFFER SIGNIFICANTLY FROM THE RESULTS, PERFORMANCE OR ACHIEVEMENTS EXPRESSED OR IMPLIED BY SUCH FORWARD-LOOKING STATEMENTS. IMPORTANT FACTORS THAT COULD CAUSE OR CONTRIBUTE TO SUCH DIFFERENCES INCLUDE RISKS RELATING TO: TEVA'S ABILITY TO ACCURATELY PREDICT FUTURE MARKET CONDITIONS, TEVA'S ABILITY TO SUCCESSFULLY DEVELOP AND COMMERCIALIZE ADDITIONAL PHARMACEUTICAL PRODUCTS, THE INTRODUCTION OF COMPETING GENERIC EQUIVALENTS, THE EXTENT TO WHICH TEVA MAY OBTAIN U.S. MARKET EXCLUSIVITY FOR CERTAIN OF ITS NEW GENERIC PRODUCTS AND REGULATORY CHANGES THAT MAY PREVENT TEVA FROM UTILIZING EXCLUSIVITY PERIODS, COMPETITION FROM BRAND-NAME COMPANIES THAT ARE UNDER INCREASED PRESSURE TO COUNTER GENERIC PRODUCTS, OR COMPETITORS THAT SEEK TO DELAY THE INTRODUCTION OF GENERIC PRODUCTS, POTENTIAL LIABILITY FOR SALES OF GENERIC PRODUCTS PRIOR TO A FINAL RESOLUTION OF OUTSTANDING PATENT LITIGATION, INCLUDING THAT RELATING TO THE GENERIC VERSIONS OF ALLEGRA, NEURONTIN, LOTREL, FAMVIR, AND PROTONIX, THE IMPACT OF CONSOLIDATION OF OUR DISTRIBUTORS AND CUSTOMERS, THE EFFECTS OF COMPETITION ON OUR INNOVATIVE PRODUCTS, ESPECIALLY COPAXONE SALES, THE IMPACT OF PHARMACEUTICAL INDUSTRY REGULATION AND PENDING LEGISLATION THAT COULD AFFECT THE PHARMACEUTICAL INDUSTRY, THE DIFFICULTY OF PREDICTING U.S. FOOD AND DRUG ADMINISTRATION, EUROPEAN MEDICINES AGENCY AND OTHER REGULATORY AUTHORITY APPROVALS, THE REGULATORY ENVIRONMENT AND CHANGES IN THE HEALTH POLICIES AND STRUCTURES OF VARIOUS COUNTRIES, OUR ABILITY TO ACHIEVE EXPECTED RESULTS THOUGH OUR INNOVATIVE R&D EFFORTS, TEVA'S ABILITY TO SUCCESSFULLY IDENTIFY, CONSUMMATE AND INTEGRATE ACQUISITIONS, POTENTIAL EXPOSURE TO PRODUCT LIABILITY CLAIMS TO THE EXTENT NOT COVERED BY INSURANCE, DEPENDENCE ON THE EFFECTIVENESS OF OUR PATENTS AND OTHER PROTECTIONS FOR INNOVATIVE PRODUCTS, SIGNIFICANT OPERATIONS WORLDWIDE THAT MAY BE ADVERSELY AFFECTED BY TERRORISM, POLITICAL OR ECONOMICAL INSTABILITY OR MAJOR HOSTILITIES, SUPPLY INTERRUPTIONS OR DELAYS THAT COULD RESULT FROM THE COMPLEX MANUFACTURING OF OUR PRODUCTS AND OUR GLOBAL SUPPLY CHAIN, ENVIRONMENTAL RISKS, FLUCTUATIONS IN CURRENCY, EXCHANGE AND INTEREST RATES, AND OTHER FACTORS THAT ARE DISCUSSED IN TEVA'S ANNUAL REPORT ON FORM 20-F AND ITS OTHER FILINGS WITH THE U.S. SECURITIES AND EXCHANGE COMMISSION. FORWARD-LOOKING STATEMENTS SPEAK ONLY AS OF THE DATE ON WHICH THEY ARE MADE AND THE COMPANY UNDERTAKES NO OBLIGATION TO UPDATE OR REVISE ANY FORWARD-LOOKING STATEMENT, WHETHER AS A RESULT OF NEW INFORMATION, FUTURE EVENTS OR OTHERWISE.

    Forward-Looking Statements

  • Key Themes

    Enable Teva to win in all markets

    where we compete

    Enable Teva to win in all markets

    where we compete

    Goal of Global Generic Resources

    Goal of Global Generic Resources

    1

  • Pharma operations

    Supply chain

    GR&D TAPI

    Key Success Factors For Our Growth Strategy

    Greatest rate of first-to-market products

    Redefine customer service

    Competitive cost position

    Shift from unifocal to multifocal

    Leverage our scale

    2

  • Global Generic Resources: Driving Market Leadership

    Service leadership

    Portfolio value

    Double capacity

    Unmatchedcombined capabilities

    2xperformance

    3

  • TAPI Global Advantage Size and Service

    195238245274303

    357360500550

    1,460

    Competitors

    TevaWesternIndianChinese

    Company

    Estimated 2007 Sales$ Millions

    Huge portfolio (250+ products)

    Highly responsive

    Strong patent position

    Top talent scientific and management

    Huge portfolio (250+ products)

    Highly responsive

    Strong patent position

    Top talent scientific and management

    4

  • Global Portfolio Uses U.S. as Springboard

    2007 2010

    P IV / First-to-file >50% >50%

    High Portfolio Value: Total Value and Value per File

    # Global files 126 More than double

    Rapid cost-effective

    entry into Europe and International

    markets

    Rapid cost-effective

    entry into Europe and International

    markets

    Leveraged investment Bioequivalence studies API development Formulation technology Manufacturing process

    5

  • Service Leadership at the Next Level

    Teva service: Big-to-Bigsupply system

    Teva service: Big-to-Bigsupply system

    Just-in-time/pull delivery

    Customized shipping

    Global supply chain

    Broad portfolio and rapid targeted distribution

    Customer needsCustomer needs

    Inventory reduction

    Lower labor costs

    Multi-region/multi-country supply reliability

    Pharmacy profitability/product availability

    6

  • Substantially Expanding our Supply Chain to Support Growth

    Solid oral drugsBillions of tablets

    Moving to separate from the pack

    Enhancing our already powerful launch capability

    Moving to separate from the pack

    Enhancing our already powerful launch capability

    2007 2008 2009 2010 2011 2012

    40

    60

    80

    100

    120

    >2x in on-timecapacity

    >2x in on-timecapacity

    7

  • Selecting the Best Site to Maximize Value

    MissouriNetherlands

    Hungary

    Italy India

    Israel (5)Mexico

    SwitzerlandNJ

    Puerto Rico

    Czech Republic

    China SpeedSpeed

    EBITEBIT

    Vertical Vertical integrationintegration

    Peru

    Chile Argentina

    Venezuela

    Toronto

    CA PA

    UK

    Brazil

    Operating in 20 countriesTAPI: 16 plants & 8 R&D sitesPharma: 33 plants & 16 R&D sites

    Operating in 20 countriesTAPI: 16 plants & 8 R&D sitesPharma: 33 plants & 16 R&D sites

    8

  • Global Leadership

    Enable Teva to win in all markets

    where we compete

    Enable Teva to win in all markets

    where we compete

    Double portfolio value and capacity of global core functions

    Maintain and enhance service leadership

    Separate from the pack unmatched global generic resources

    9

  • Moshe ManorGroup VP - Global Innovative ResourcesTeva Pharmaceutical Industries Ltd.February 21, 2008

    Tevas Innovative Strategy

  • TODAYS PRESENTATION CONTAINS FORWARD-LOOKING STATEMENTS, WHICH EXPRESS THE CURRENT BELIEFS AND EXPECTATIONS OF MANAGEMENT. SUCH STATEMENTS INVOLVE A NUMBER OF KNOWN AND UNKNOWN RISKS AND UNCERTAINTIES THAT COULD CAUSE TEVA'S FUTURE RESULTS, PERFORMANCE OR ACHIEVEMENTS TO DIFFER SIGNIFICANTLY FROM THE RESULTS, PERFORMANCE OR ACHIEVEMENTS EXPRESSED OR IMPLIED BY SUCH FORWARD-LOOKING STATEMENTS. IMPORTANT FACTORS THAT COULD CAUSE OR CONTRIBUTE TO SUCH DIFFERENCES INCLUDE RISKS RELATING TO: TEVA'S ABILITY TO ACCURATELY PREDICT FUTURE MARKET CONDITIONS, TEVA'S ABILITY TO SUCCESSFULLY DEVELOP AND COMMERCIALIZE ADDITIONAL PHARMACEUTICAL PRODUCTS, THE INTRODUCTION OF COMPETING GENERIC EQUIVALENTS, THE EXTENT TO WHICH TEVA MAY OBTAIN U.S. MARKET EXCLUSIVITY FOR CERTAIN OF ITS NEW GENERIC PRODUCTS AND REGULATORY CHANGES THAT MAY PREVENT TEVA FROM UTILIZING EXCLUSIVITY PERIODS, COMPETITION FROM BRAND-NAME COMPANIES THAT ARE UNDER INCREASED PRESSURE TO COUNTER GENERIC PRODUCTS, OR COMPETITORS THAT SEEK TO DELAY THE INTRODUCTION OF GENERIC PRODUCTS, POTENTIAL LIABILITY FOR SALES OF GENERIC PRODUCTS PRIOR TO A FINAL RESOLUTION OF OUTSTANDING PATENT LITIGATION, INCLUDING THAT RELATING TO THE GENERIC VERSIONS OF ALLEGRA, NEURONTIN, LOTREL, FAMVIR, AND PROTONIX, THE IMPACT OF CONSOLIDATION OF OUR DISTRIBUTORS AND CUSTOMERS, THE EFFECTS OF COMPETITION ON OUR INNOVATIVE PRODUCTS, ESPECIALLY COPAXONE SALES, THE IMPACT OF PHARMACEUTICAL INDUSTRY REGULATION AND PENDING LEGISLATION THAT COULD AFFECT THE PHARMACEUTICAL INDUSTRY, THE DIFFICULTY OF PREDICTING U.S. FOOD AND DRUG ADMINISTRATION, EUROPEAN MEDICINES AGENCY AND OTHER REGULATORY AUTHORITY APPROVALS, THE REGULATORY ENVIRONMENT AND CHANGES IN THE HEALTH POLICIES AND STRUCTURES OF VARIOUS COUNTRIES, OUR ABILITY TO ACHIEVE EXPECTED RESULTS THOUGH OUR INNOVATIVE R&D EFFORTS, TEVA'S ABILITY TO SUCCESSFULLY IDENTIFY, CONSUMMATE AND INTEGRATE ACQUISITIONS, POTENTIAL EXPOSURE TO PRODUCT LIABILITY CLAIMS TO THE EXTENT NOT COVERED BY INSURANCE, DEPENDENCE ON THE EFFECTIVENESS OF OUR PATENTS AND OTHER PROTECTIONS FOR INNOVATIVE PRODUCTS, SIGNIFICANT OPERATIONS WORLDWIDE THAT MAY BE ADVERSELY AFFECTED BY TERRORISM, POLITICAL OR ECONOMICAL INSTABILITY OR MAJOR HOSTILITIES, SUPPLY INTERRUPTIONS OR DELAYS THAT COULD RESULT FROM THE COMPLEX MANUFACTURING OF OUR PRODUCTS AND OUR GLOBAL SUPPLY CHAIN, ENVIRONMENTAL RISKS, FLUCTUATIONS IN CURRENCY, EXCHANGE AND INTEREST RATES, AND OTHER FACTORS THAT ARE DISCUSSED IN TEVA'S ANNUAL REPORT ON FORM 20-F AND ITS OTHER FILINGS WITH THE U.S. SECURITIES AND EXCHANGE COMMISSION. FORWARD-LOOKING STATEMENTS SPEAK ONLY AS OF THE DATE ON WHICH THEY ARE MADE AND THE COMPANY UNDERTAKES NO OBLIGATION TO UPDATE OR REVISE ANY FORWARD-LOOKING STATEMENT, WHETHER AS A RESULT OF NEW INFORMATION, FUTURE EVENTS OR OTHERWISE.

    Forward-Looking Statements

  • Key Themes

    $3 billion in risk-adjusted revenues expected by 2012

    Growth in Innovative contributes to Teva brand and balanced business model

    Investing to create long-term value

    1

  • Proven Capabilities Across the Value Chain

    Sourcing innovation, products and companies, focusing on Israeli science

    Executing trials at low cost, with competitive recruitment rates

    Experience in working with regulators

    First-class capabilities Synergies: Leveraging expertise of Generic R&D

    Proven messages that drive market share Highly-productive sales force

    Sourcing

    Development

    Regulatory

    Manufacturing

    Marketingand

    Sales

    2

  • Our Differentiated Approach to Innovative

    Focus on niche therapeutic areas

    Products with: Differentiated clinical attributes Real economic value for patients and payors

    Tevas unique advantages Sourcing Development Go-to-market approach

    Strategies to mitigate risk Upfront investment Methodologies (Biomarkers)

    3

  • Three-Pronged Strategy

    Unique sourcing value proposition

    Source products globally in focused TAs Rapid evaluation and investment in opportunities

    (New Ventures) Unique value proposition (IP)

    Next-generationdevelopment

    Streamline decision-making; shorten time, kill early Flexibility by outsourcing non-strategic functions Trials in emerging markets Early investment to mitigate risk

    Focus on niche specialty areas Small, specialty sales forces Payor and trade relationships

    Go-to-market model

    4

  • Phase III/IIIB

    Sub

    mis

    sion

    Phase IVPhase II

    Copaxone40mg(MS)

    Copaxone(MS)

    Copaxone(CIS/MS )

    Laquinimod(MS)

    Azilect(PD)

    Azilect(PD/DM)

    Copaxone40mg (ALS)

    Phase I

    StemEx(Cancer)

    CT-011(Hematol. Cancer )

    CT-011(Solid

    Cancers)

    Laquinimod(CD)

    Talampanel(ALS )

    Laquinimod(SLE/LN)

    Debrase(burns)

    AutoImmune:SLE/LN LupusCD Crohns Disease

    MS Other IndicationsNeurology:PD Parkinsons Disease

    Clinical Development Pipeline

    Oncology

    5

  • Time-to-Market for Potential Products

    Copaxone 40 mg (MS)

    Azilect(PD - DM)

    StemEx(Cancer)

    Laquinimod

    (MS)

    Copaxone 40mg(ALS)

    CT-011(Hematological Cancer)

    2009-2011 2012-2014 2015 and beyond

    Copaxone 20mg (CIS)

    CT-011(Solid Cancer)

    Debrase(burns)

    Laquinimod

    (SLE/LN)

    Other IndicationsAuto-Immune:SLE/LN LupusCD Crohns Disease

    MS Neurology:PD Parkinsons Disease

    Potential revenue(risk adjusted)2015: $4-5B

    Oncology

    Laquinimod

    (CD)

    Talampanel(ALS)

    6

  • 5%

    Copaxone Is On-Track to Become Global #1 (in Value)

    21%

    2004

    30%

    21%

    25%

    23%

    2005

    29%

    21%

    32%

    22%

    25%Copaxone

    25%24%

    2006

    26%

    20%

    25%

    30%

    0%

    35%

    24%

    2007

    Avonex

    Betaseron

    Rebif

    20%

    Tysabri

    Note: Based on the last release of all companies (Q3)

    1%5%

    25%

    7

  • What Will Fuel Copaxones Growth?

    Efficacy in CIS

    Short Term

    Efficacy and

    Safety in RRMS

    Efficacy on

    damage and

    repair

    Long Term

    Efficacy and

    Safety in RRMS

    Level of Differentiation

    Low

    Medium

    High

    In addition: Copaxone 40mg with increased efficacy Oral Laquinimod

    Product features and benefits

    8

  • Innovative Long Term Growth

    Risk-Adjusted Revenues

    2007 2012 2015

    $1.8 B*

    $3 B

    $4 5 B

    * In-Market Sales9

  • $3 Billion in risk-adjusted revenues by 2012

    Strong growth of Copaxone and Azilect

    Building a portfolio that drives growth past 2012

    Leveraging Tevas expertise, capabilities, synergies

    Extending our capabilities into additional focused therapeutic areas

    The Future of Tevas Innovative Business

    10

  • Biogenerics

    Amir Elstein

    Executive VP, Global Resources

    Teva Pharmaceutical Industries Ltd.

    February 21, 2008

  • TODAYS PRESENTATION CONTAINS FORWARD-LOOKING STATEMENTS, WHICH EXPRESS THE CURRENT BELIEFS AND EXPECTATIONS OF MANAGEMENT. SUCH STATEMENTS INVOLVE A NUMBER OF KNOWN AND UNKNOWN RISKS AND UNCERTAINTIES THAT COULD CAUSE TEVA'S FUTURE RESULTS, PERFORMANCE OR ACHIEVEMENTS TO DIFFER SIGNIFICANTLY FROM THE RESULTS, PERFORMANCE OR ACHIEVEMENTS EXPRESSED OR IMPLIED BY SUCH FORWARD-LOOKING STATEMENTS. IMPORTANT FACTORS THAT COULD CAUSE OR CONTRIBUTE TO SUCH DIFFERENCES INCLUDE RISKS RELATING TO: TEVA'S ABILITY TO ACCURATELY PREDICT FUTURE MARKET CONDITIONS, TEVA'S ABILITY TO SUCCESSFULLY DEVELOP AND COMMERCIALIZE ADDITIONAL PHARMACEUTICAL PRODUCTS, THE INTRODUCTION OF COMPETING GENERIC EQUIVALENTS, THE EXTENT TO WHICH TEVA MAY OBTAIN U.S. MARKET EXCLUSIVITY FOR CERTAIN OF ITS NEW GENERIC PRODUCTS AND REGULATORY CHANGES THAT MAY PREVENT TEVA FROM UTILIZING EXCLUSIVITY PERIODS, COMPETITION FROM BRAND-NAME COMPANIES THAT ARE UNDER INCREASED PRESSURE TO COUNTER GENERIC PRODUCTS, OR COMPETITORS THAT SEEK TO DELAY THE INTRODUCTION OF GENERIC PRODUCTS, POTENTIAL LIABILITY FOR SALES OF GENERIC PRODUCTS PRIOR TO A FINAL RESOLUTION OF OUTSTANDING PATENT LITIGATION, INCLUDING THAT RELATING TO THE GENERIC VERSIONS OF ALLEGRA, NEURONTIN, LOTREL, FAMVIR, AND PROTONIX, THE IMPACT OF CONSOLIDATION OF OUR DISTRIBUTORS AND CUSTOMERS, THE EFFECTS OF COMPETITION ON OUR INNOVATIVE PRODUCTS, ESPECIALLY COPAXONE SALES, THE IMPACT OF PHARMACEUTICAL INDUSTRY REGULATION AND PENDING LEGISLATION THAT COULD AFFECT THE PHARMACEUTICAL INDUSTRY, THE DIFFICULTY OF PREDICTING U.S. FOOD AND DRUG ADMINISTRATION, EUROPEAN MEDICINES AGENCY AND OTHER REGULATORY AUTHORITY APPROVALS, THE REGULATORY ENVIRONMENT AND CHANGES IN THE HEALTH POLICIES AND STRUCTURES OF VARIOUS COUNTRIES, OUR ABILITY TO ACHIEVE EXPECTED RESULTS THOUGH OUR INNOVATIVE R&D EFFORTS, TEVA'S ABILITY TO SUCCESSFULLY IDENTIFY, CONSUMMATE AND INTEGRATE ACQUISITIONS, POTENTIAL EXPOSURE TO PRODUCT LIABILITY CLAIMS TO THE EXTENT NOT COVERED BY INSURANCE, DEPENDENCE ON THE EFFECTIVENESS OF OUR PATENTS AND OTHER PROTECTIONS FOR INNOVATIVE PRODUCTS, SIGNIFICANT OPERATIONS WORLDWIDE THAT MAY BE ADVERSELY AFFECTED BY TERRORISM, POLITICAL OR ECONOMICAL INSTABILITY OR MAJOR HOSTILITIES, SUPPLY INTERRUPTIONS OR DELAYS THAT COULD RESULT FROM THE COMPLEX MANUFACTURING OF OUR PRODUCTS AND OUR GLOBAL SUPPLY CHAIN, ENVIRONMENTAL RISKS, FLUCTUATIONS IN CURRENCY, EXCHANGE AND INTEREST RATES, AND OTHER FACTORS THAT ARE DISCUSSED IN TEVA'S ANNUAL REPORT ON FORM 20-F AND ITS OTHER FILINGS WITH THE U.S. SECURITIES AND EXCHANGE COMMISSION. FORWARD-LOOKING STATEMENTS SPEAK ONLY AS OF THE DATE ON WHICH THEY ARE MADE AND THE COMPANY UNDERTAKES NO OBLIGATION TO UPDATE OR REVISE ANY FORWARD-LOOKING STATEMENT, WHETHER AS A RESULT OF NEW INFORMATION, FUTURE EVENTS OR OTHERWISE.

    Forward-Looking Statements

  • Key Themes

    Biopharmaceuticals huge potential

    Biogenerics next wave of growth for generics

    Our strategy same for less

    Investing for leadership

    1

  • Biopharmaceuticals Predicted Growth

    474

    2007

    165

    450

    615

    2012

    Biologics

    Small molecule

    485

    89

    1990

    94

    380

    Market size, worldwide$ Billions

    Source: Evaluate Pharma

    Total 5

    3

    CAGR2007-12Percent

    12

    2

  • Biogenerics: Next Generation of Growth for Teva

    Over $40 billion in current biopharmaceutical sales exposed to generic competition over the next 10 years

    Higher barriers to entry and attractive returns

    Aligned with market and social forces through our generic value proposition

    3

  • Biogenerics: Teva Approach and Key Principles

    Reduce cost of development and production to provide affordable Biopharmaceuticals and competitive market position

    Invest in technologies, infrastructure and capabilities to develop and produce at low cost

    Leverage existing bioformulation and manufacturing expertise

    Pursue early entry and/or more for less strategies as opportunities to boost value to our shareholders

    Investing for the long-term

    4

  • Our Biogenerics Strategy

    Substitution Identical product

    Equivalentbut notsubstitutable

    Development focus Commercial approach

    Same for less

    Opportunistic: more for less

    Same clinicalattributes --Early entry IP

    5

  • Investing for Biogenerics Leadership

    Key success factors Technology platforms Market presencePortfolioLow cost position

    Teva capabilities

    Clinical/development Manufacturing Commercialization Payor relationships IP

    CoGenesys value-add

    Product IP HSA-fusion technology Product in development CMC process and

    technology

    6

  • Biogenerics Strategy Guiding Principles

    Leadership Industry-shaping role

    Generic value proposition Same for less

    Invest wisely and patiently

    Organic and inorganic

    7

  • Modeling Teva

    Dan Suesskind

    CFO

    Teva Pharmaceutical Industries Ltd.

    February 21, 2008

  • TODAYS PRESENTATION CONTAINS FORWARD-LOOKING STATEMENTS, WHICH EXPRESS THE CURRENT BELIEFS AND EXPECTATIONS OF MANAGEMENT. SUCH STATEMENTS INVOLVE A NUMBER OF KNOWN AND UNKNOWN RISKS AND UNCERTAINTIES THAT COULD CAUSE TEVA'S FUTURE RESULTS, PERFORMANCE OR ACHIEVEMENTS TO DIFFER SIGNIFICANTLY FROM THE RESULTS, PERFORMANCE OR ACHIEVEMENTS EXPRESSED OR IMPLIED BY SUCH FORWARD-LOOKING STATEMENTS. IMPORTANT FACTORS THAT COULD CAUSE OR CONTRIBUTE TO SUCH DIFFERENCES INCLUDE RISKS RELATING TO: TEVA'S ABILITY TO ACCURATELY PREDICT FUTURE MARKET CONDITIONS, TEVA'S ABILITY TO SUCCESSFULLY DEVELOP AND COMMERCIALIZE ADDITIONAL PHARMACEUTICAL PRODUCTS, THE INTRODUCTION OF COMPETING GENERIC EQUIVALENTS, THE EXTENT TO WHICH TEVA MAY OBTAIN U.S. MARKET EXCLUSIVITY FOR CERTAIN OF ITS NEW GENERIC PRODUCTS AND REGULATORY CHANGES THAT MAY PREVENT TEVA FROM UTILIZING EXCLUSIVITY PERIODS, COMPETITION FROM BRAND-NAME COMPANIES THAT ARE UNDER INCREASED PRESSURE TO COUNTER GENERIC PRODUCTS, OR COMPETITORS THAT SEEK TO DELAY THE INTRODUCTION OF GENERIC PRODUCTS, POTENTIAL LIABILITY FOR SALES OF GENERIC PRODUCTS PRIOR TO A FINAL RESOLUTION OF OUTSTANDING PATENT LITIGATION, INCLUDING THAT RELATING TO THE GENERIC VERSIONS OF ALLEGRA, NEURONTIN, LOTREL, FAMVIR, AND PROTONIX, THE IMPACT OF CONSOLIDATION OF OUR DISTRIBUTORS AND CUSTOMERS, THE EFFECTS OF COMPETITION ON OUR INNOVATIVE PRODUCTS, ESPECIALLY COPAXONE SALES, THE IMPACT OF PHARMACEUTICAL INDUSTRY REGULATION AND PENDING LEGISLATION THAT COULD AFFECT THE PHARMACEUTICAL INDUSTRY, THE DIFFICULTY OF PREDICTING U.S. FOOD AND DRUG ADMINISTRATION, EUROPEAN MEDICINES AGENCY AND OTHER REGULATORY AUTHORITY APPROVALS, THE REGULATORY ENVIRONMENT AND CHANGES IN THE HEALTH POLICIES AND STRUCTURES OF VARIOUS COUNTRIES, OUR ABILITY TO ACHIEVE EXPECTED RESULTS THOUGH OUR INNOVATIVE R&D EFFORTS, TEVA'S ABILITY TO SUCCESSFULLY IDENTIFY, CONSUMMATE AND INTEGRATE ACQUISITIONS, POTENTIAL EXPOSURE TO PRODUCT LIABILITY CLAIMS TO THE EXTENT NOT COVERED BY INSURANCE, DEPENDENCE ON THE EFFECTIVENESS OF OUR PATENTS AND OTHER PROTECTIONS FOR INNOVATIVE PRODUCTS, SIGNIFICANT OPERATIONS WORLDWIDE THAT MAY BE ADVERSELY AFFECTED BY TERRORISM, POLITICAL OR ECONOMICAL INSTABILITY OR MAJOR HOSTILITIES, SUPPLY INTERRUPTIONS OR DELAYS THAT COULD RESULT FROM THE COMPLEX MANUFACTURING OF OUR PRODUCTS AND OUR GLOBAL SUPPLY CHAIN, ENVIRONMENTAL RISKS, FLUCTUATIONS IN CURRENCY, EXCHANGE AND INTEREST RATES, AND OTHER FACTORS THAT ARE DISCUSSED IN TEVA'S ANNUAL REPORT ON FORM 20-F AND ITS OTHER FILINGS WITH THE U.S. SECURITIES AND EXCHANGE COMMISSION. FORWARD-LOOKING STATEMENTS SPEAK ONLY AS OF THE DATE ON WHICH THEY ARE MADE AND THE COMPANY UNDERTAKES NO OBLIGATION TO UPDATE OR REVISE ANY FORWARD-LOOKING STATEMENT, WHETHER AS A RESULT OF NEW INFORMATION, FUTURE EVENTS OR OTHERWISE.

    Forward-Looking Statements

  • 2012 Projected Sales

    $1.4 B

    Europe$9.5 11.5 B

    $0.9 B

    North AmericaTAPI

    $19.0 21.5 B

    $5.1 5.7 B

    $2.2 B

    International

    $5.2 B

    $0.6 B

    $9.4 B

    $3.2 4.0 B 18 23%

    18 21%

    13 17%

    CAGR -2

    CAGR15-18%

    Note: 2012 totals do not sum; reflect companys projected overall range1

  • Balanced Business Model Geographies

    20072007

    20122012

    North America55%

    API6%

    International15%

    Europe23%

    API4%

    North America51%

    International18%

    Europe27%

    2

  • Balanced Business Model Businesses

    20072007

    20122012

    Generics75%

    API6%

    Branded19%

    Generics74%

    Branded22%API

    4%3

  • Proforma P&L

    2007

    $ Billions

    Sales

    Gross Margin

    R&D

    SG&A

    Operating Profit

    Finance Expenses/Income

    Tax

    Net Income

    9.4

    4.9

    0.6

    1.9

    2.4

    0.4

    2.0

    Percent

    2012

    $ Billions Percent

    100

    51.8

    6.2

    20.2

    25.5

    17.0

    20.8

    19.0 21.5

    3.8 4.9

    100

    >50%

  • Closing Thoughts

    Shlomo Yanai

    President and CEO

    Teva Pharmaceutical Industries Ltd.

    February 21, 2008

  • TODAYS PRESENTATION CONTAINS FORWARD-LOOKING STATEMENTS, WHICH EXPRESS THE CURRENT BELIEFS AND EXPECTATIONS OF MANAGEMENT. SUCH STATEMENTS INVOLVE A NUMBER OF KNOWN AND UNKNOWN RISKS AND UNCERTAINTIES THAT COULD CAUSE TEVA'S FUTURE RESULTS, PERFORMANCE OR ACHIEVEMENTS TO DIFFER SIGNIFICANTLY FROM THE RESULTS, PERFORMANCE OR ACHIEVEMENTS EXPRESSED OR IMPLIED BY SUCH FORWARD-LOOKING STATEMENTS. IMPORTANT FACTORS THAT COULD CAUSE OR CONTRIBUTE TO SUCH DIFFERENCES INCLUDE RISKS RELATING TO: TEVA'S ABILITY TO ACCURATELY PREDICT FUTURE MARKET CONDITIONS, TEVA'S ABILITY TO SUCCESSFULLY DEVELOP AND COMMERCIALIZE ADDITIONAL PHARMACEUTICAL PRODUCTS, THE INTRODUCTION OF COMPETING GENERIC EQUIVALENTS, THE EXTENT TO WHICH TEVA MAY OBTAIN U.S. MARKET EXCLUSIVITY FOR CERTAIN OF ITS NEW GENERIC PRODUCTS AND REGULATORY CHANGES THAT MAY PREVENT TEVA FROM UTILIZING EXCLUSIVITY PERIODS, COMPETITION FROM BRAND-NAME COMPANIES THAT ARE UNDER INCREASED PRESSURE TO COUNTER GENERIC PRODUCTS, OR COMPETITORS THAT SEEK TO DELAY THE INTRODUCTION OF GENERIC PRODUCTS, POTENTIAL LIABILITY FOR SALES OF GENERIC PRODUCTS PRIOR TO A FINAL RESOLUTION OF OUTSTANDING PATENT LITIGATION, INCLUDING THAT RELATING TO THE GENERIC VERSIONS OF ALLEGRA, NEURONTIN, LOTREL, FAMVIR, AND PROTONIX, THE IMPACT OF CONSOLIDATION OF OUR DISTRIBUTORS AND CUSTOMERS, THE EFFECTS OF COMPETITION ON OUR INNOVATIVE PRODUCTS, ESPECIALLY COPAXONE SALES, THE IMPACT OF PHARMACEUTICAL INDUSTRY REGULATION AND PENDING LEGISLATION THAT COULD AFFECT THE PHARMACEUTICAL INDUSTRY, THE DIFFICULTY OF PREDICTING U.S. FOOD AND DRUG ADMINISTRATION, EUROPEAN MEDICINES AGENCY AND OTHER REGULATORY AUTHORITY APPROVALS, THE REGULATORY ENVIRONMENT AND CHANGES IN THE HEALTH POLICIES AND STRUCTURES OF VARIOUS COUNTRIES, OUR ABILITY TO ACHIEVE EXPECTED RESULTS THOUGH OUR INNOVATIVE R&D EFFORTS, TEVA'S ABILITY TO SUCCESSFULLY IDENTIFY, CONSUMMATE AND INTEGRATE ACQUISITIONS, POTENTIAL EXPOSURE TO PRODUCT LIABILITY CLAIMS TO THE EXTENT NOT COVERED BY INSURANCE, DEPENDENCE ON THE EFFECTIVENESS OF OUR PATENTS AND OTHER PROTECTIONS FOR INNOVATIVE PRODUCTS, SIGNIFICANT OPERATIONS WORLDWIDE THAT MAY BE ADVERSELY AFFECTED BY TERRORISM, POLITICAL OR ECONOMICAL INSTABILITY OR MAJOR HOSTILITIES, SUPPLY INTERRUPTIONS OR DELAYS THAT COULD RESULT FROM THE COMPLEX MANUFACTURING OF OUR PRODUCTS AND OUR GLOBAL SUPPLY CHAIN, ENVIRONMENTAL RISKS, FLUCTUATIONS IN CURRENCY, EXCHANGE AND INTEREST RATES, AND OTHER FACTORS THAT ARE DISCUSSED IN TEVA'S ANNUAL REPORT ON FORM 20-F AND ITS OTHER FILINGS WITH THE U.S. SECURITIES AND EXCHANGE COMMISSION. FORWARD-LOOKING STATEMENTS SPEAK ONLY AS OF THE DATE ON WHICH THEY ARE MADE AND THE COMPANY UNDERTAKES NO OBLIGATION TO UPDATE OR REVISE ANY FORWARD-LOOKING STATEMENT, WHETHER AS A RESULT OF NEW INFORMATION, FUTURE EVENTS OR OTHERWISE.

    Forward-Looking Statements

  • What You Can Expect From Teva

    Continuous profitable growth

    Long-term perspective: product portfolio, capacity and service

    Balanced business model & attractive financial returns

    Expanding leadership in key markets

    2