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Teva Strategy Overview February 21, 2008

Teva Strategy Overviews24.q4cdn.com/720828402/files/doc_downloads/doc_events/Presentation_28.pdfTeva’s Growth Strategy 2008-2012 Shlomo Yanai President and CEO Teva Pharmaceutical

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  • Teva Strategy OverviewFebruary 21, 2008

  • TODAY�S 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

    � Teva’s Growth Strategy 2008-2012

    � Global Generic Markets

    � US

    � Europe

    � International

    � Global Generic Resources

    � Innovative Strategy

    � BioGenerics

    � Modeling Teva

    � Closing Thoughts

  • Teva’s Growth Strategy 2008-2012

    Shlomo Yanai

    President and CEO

    Teva Pharmaceutical Industries Ltd.

    February 21, 2008

  • TODAY�S 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 Teva’s key growth drivers?

    ? What is Teva’s value proposition?

    1

  • Teva’s 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 Leader’s 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 Teva’s 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

  • ��

    Teva’s 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.)

    Teva’s Scale and

    Leadership

    Teva’s 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 challengeTeva’s CultureTeva’s Culture

    7

  • ��

    Key Pillars of Our Strategy

    Increase Teva’s market share in key markets

    Increase Teva’s 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

  • Teva’s Value Proposition

    � Growth Company

    � Commitment To Global Generics Leadership

    � Balanced Business Model

    � Attractive Financial Returns

    � Teva’s 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

  • ��

    TODAY�S 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 Teva’s 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

    � Teva’s 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%Teva’s 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-opportunity”positions

    � 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 Teva’s 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 Changing’Customer 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

  • Teva’s 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

  • TODAY�S 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 EU’s “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 Markets“Latin 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 Markets“Latin Europe”

    Mature Generics Markets

    � Tenders are entry ticket to the world’s 2nd largest generics market (~ $5 billion)

    � Shift from Branded-Generics to “Generic-Generics”

    � Tenders are entry ticket to the world’s 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

  • Teva’s Proven Go-to-Market Approach

    Teva’s European Presence

    “Big-to-Big”Portfolio breadth and

    geographical presence position Teva as unique partner

    for EU wholesale & retail players

    “Big-to-Big”Portfolio breadth and

    geographical presence position Teva as unique partner

    for EU wholesale & retail players

    “Sell-out”Distinctive commercial offers and lean & agile go-to-market models

    match evolving market needs

    “Sell-out”Distinctive 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

    • Teva’s 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

  • ��

    TODAY�S 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

    � World’s 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: $3.2–4.0 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

  • TODAY�S 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

    “2x”performance

    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-Big”supply system

    Teva service: “Big-to-Big”supply 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-time”capacity

    >2x in “on-time”capacity

    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 countries�TAPI: 16 plants & 8 R&D sites�Pharma: 33 plants & 16 R&D sites

    Operating in 20 countries�TAPI: 16 plants & 8 R&D sites�Pharma: 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

    Teva’s Innovative Strategy

  • ��

    TODAY�S 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

    � Teva’s 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

    Copaxone®40mg(MS)

    Copaxone®(MS)

    Copaxone®(CIS/MS )

    Laquinimod®(MS)

    Azilect®(PD)

    Azilect®(PD/DM)

    Copaxone®40mg (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 – Crohn’s Disease

    MS Other IndicationsNeurology:PD – Parkinson’s 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 – Crohn’s Disease

    MS Neurology:PD – Parkinson’s 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 Copaxone’s® 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 Teva’s expertise, capabilities, synergies

    � Extending our capabilities into additional focused therapeutic areas

    The Future of Teva’s Innovative Business

    10

  • Biogenerics

    Amir Elstein

    Executive VP, Global Resources

    Teva Pharmaceutical Industries Ltd.

    February 21, 2008

  • TODAY�S 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

    “Equivalent”but 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 presence�Portfolio�Low 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

  • ��

    TODAY�S 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 company’s 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

  • ��

    TODAY�S 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