Last Updated: August 2, 2026

Teva Pharms Company Profile


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Summary for Teva Pharms
International Patents:19
US Patents:2
Tradenames:274
Ingredients:269
NDAs:331

Drugs and US Patents for Teva Pharms

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Teva Pharms Usa DEXMETHYLPHENIDATE HYDROCHLORIDE dexmethylphenidate hydrochloride CAPSULE, EXTENDED RELEASE;ORAL 078908-004 May 19, 2014 AB RX No No ⤷  Start Trial ⤷  Start Trial
Teva Pharms Usa VINCRISTINE SULFATE PFS vincristine sulfate INJECTABLE;INJECTION 075493-001 Sep 1, 1999 DISCN No No ⤷  Start Trial ⤷  Start Trial
Teva Pharms CHLORPROMAZINE HYDROCHLORIDE chlorpromazine hydrochloride TABLET;ORAL 215659-002 Oct 25, 2021 AB RX No No ⤷  Start Trial ⤷  Start Trial
Teva Pharms Usa DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE amphetamine aspartate; amphetamine sulfate; dextroamphetamine saccharate; dextroamphetamine sulfate CAPSULE, EXTENDED RELEASE;ORAL 210876-002 Jan 31, 2022 AB2 RX No No ⤷  Start Trial ⤷  Start Trial
Teva Pharms Usa EZETIMIBE ezetimibe TABLET;ORAL 078724-001 Jun 12, 2017 DISCN No No ⤷  Start Trial ⤷  Start Trial
Teva Pharms ZALEPLON zaleplon CAPSULE;ORAL 077239-002 Jun 6, 2008 DISCN No No ⤷  Start Trial ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

Expired US Patents for Teva Pharms

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Teva Pharms Intl SYNRIBO omacetaxine mepesuccinate POWDER;SUBCUTANEOUS 203585-001 Oct 26, 2012 7,842,687 ⤷  Start Trial
Teva Pharms Usa COPAXONE glatiramer acetate INJECTABLE;SUBCUTANEOUS 020622-002 Feb 12, 2002 7,199,098 ⤷  Start Trial
Teva Pharms Intl AMRIX cyclobenzaprine hydrochloride CAPSULE, EXTENDED RELEASE;ORAL 021777-001 Feb 1, 2007 7,829,121 ⤷  Start Trial
Teva Pharms Usa COPAXONE glatiramer acetate FOR SOLUTION;SUBCUTANEOUS 020622-001 Dec 20, 1996 6,620,847 ⤷  Start Trial
Teva Pharms Usa COPAXONE glatiramer acetate INJECTABLE;SUBCUTANEOUS 020622-002 Feb 12, 2002 6,342,476 ⤷  Start Trial
Teva Pharms Usa COPAXONE glatiramer acetate FOR SOLUTION;SUBCUTANEOUS 020622-001 Dec 20, 1996 7,199,098 ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration
Paragraph IV (Patent) Challenges for TEVA PHARMS drugs
Drugname Dosage Strength Tradename Submissiondate
➤ Subscribe for Injection 3.5 mg/vial ➤ Subscribe 2016-10-26
➤ Subscribe Injection 40 mg/mL, 1 mL pre-filled syringe ➤ Subscribe 2014-01-29
➤ Subscribe Extended-release Capsule 15 mg and 30 mg ➤ Subscribe 2008-08-11
➤ Subscribe Delayed-release Tablets 20 mg ➤ Subscribe 2015-06-03
➤ Subscribe Injection 40 mg/mL, 1 mL pre-filled syringe ➤ Subscribe 2014-02-26

Supplementary Protection Certificates for Teva Pharms Drugs

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
0810209 07C0034 France ⤷  Start Trial PRODUCT NAME: DARUNAVIR; REGISTRATION NO/DATE: EU/1/06/380/001 20070212
2487166 2017003 Norway ⤷  Start Trial PRODUCT NAME: KOBICISTAT ELLER FARMASOEYTISK AKSEPTABELT SALT DERAV OG TENOFOVIR ALAFENAMID ELLER FARMASOEYTISK AKSEPTABELT SALT DERAV, SPESIELT TENOFOVIR ALAFENAMIDFUMARAT; REG. NO/DATE: EU/1/15/1061 20151209
0454511 C990006 Netherlands ⤷  Start Trial PRODUCT NAME: IRBESARTAN, DESGEWENST IN DE VORM VAN EEN ZOUT EN/OF EEN HYDRAAT, EN HYDROCHLOORTHIAZIDE; REGISTRATION NO/DATE: EU/1/98/086/001 - EU/1/98/086/006 19981015
2443246 CR 2021 00036 Denmark ⤷  Start Trial PRODUCT NAME: ICOSAPENT ETHYL; REG. NO/DATE: EU/1/20/1524 20210329
1300396 132012902109980 Italy ⤷  Start Trial PRODUCT NAME: PERAMPANEL(FYCOMPA); AUTHORISATION NUMBER(S) AND DATE(S): DA EU/1/12/776/001 A EU/1/12/776/016, 20120723
1255752 SPC/GB08/007 United Kingdom ⤷  Start Trial PRODUCT NAME: SUNITINIB, OPTIONALLY IN THE FORM OF A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF, INCLUDING THE L-MALATE SALT.; REGISTERED: UK EU/1/06/347/001 20060724; UK EU/1/06/347/002 20060724; UK EU/1/06/347/003 20060724
>Patent Number >Supplementary Protection Certificate >SPC Country >SPC Expiration >SPC Description
Similar Applicant Names
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Pharmaceutical Competitive Landscape Analysis: Teva Pharmaceuticals – Market Position, Strengths & Strategic Insights

Last updated: April 20, 2026

What is Teva Pharmaceuticals' current market position?

Teva Pharmaceuticals is a leading player in the global generic drug industry, with annual revenues exceeding $15 billion. It ranks among the top global generic manufacturers by market share, holding approximately 7-8% of the global generics market [1]. The company focuses on producing high-volume generics across therapeutic areas such as central nervous system, respiratory, and cardiovascular. Its core markets include the United States, Europe, and emerging markets in Asia and Latin America.

How does Teva differentiate itself within the pharmaceutical industry?

Teva's strengths lie in its extensive product portfolio, manufacturing scale, and cost efficiencies. The company owns over 3,500 generic molecules and is among the few that can produce complex generics and biosimilars. Its manufacturing footprint spans 45 production facilities in 14 countries, allowing cost arbitrage and supply chain resilience. The company invests approximately 5-6% of revenues into R&D, mainly focusing on complex generics and biosimilars [2].

What are Teva's primary competitive advantages?

  • Product Portfolio: Over 3,500 generic molecules, including complex and niche products not easily replicated.
  • Manufacturing Scale: 45 facilities globally, enabling cost control and supply security.
  • Global Footprint: Presence in mature and emerging markets, reducing dependence on any single region.
  • Biosimilars Investment: Recognized for early entry and strategic focus on biologics transitioning from generics to biosimilars.
  • Market Access and Distribution: Extensive relationships with healthcare providers, pharmacists, and payers worldwide.

What competitive challenges does Teva face?

  • Patent Cliff and R&D Pipeline: Loss of exclusivity on key products pressures revenue streams.
  • Pricing Pressure: Increased regulations and payer resistance in developed markets, especially the U.S.
  • Legal and Patent Disputes: Ongoing patent litigations and regulatory actions, notably in the U.S. and European markets.
  • Debt Levels: Over $20 billion in debt following acquisitions and legal settlements, constraining flexibility.
  • Market Entry Barriers for Biosimilars: High development costs and regulatory complexity restrict rapid biosimilar expansion.

What strategic initiatives does Teva pursue?

  • Focus on Complex Generics: Prioritizing development of complex molecules such as injectables and biosimilars.
  • Portfolio Optimization: Divesting non-core assets, including the recent sale of OTC and bromine divisions.
  • Digital Transformation: Embracing digital manufacturing and supply chain innovation to reduce costs.
  • Geographic Expansion: Strengthening footholds in Asia-Pacific and Latin America.
  • Partnerships and Mergers: Seeking collaborations to expand biosimilar portfolio and accelerate market entry.

How does Teva compare with key competitors?

Company Market Share (%) Revenue (USD billions) Focus Areas Key Strengths
Teva 7-8 15+ Generics, biosimilars, complex drugs Manufacturing scale, global presence
Pfizer 4-5 100+ Branded drugs, biosimilars R&D pipeline, innovative biopharma
Novartis 3-4 50+ Biosimilars, patent-protected drugs R&D, diversified portfolio
Mylan (now part of Viatris) 4-5 10+ Generics, biosimilars Cost efficiencies, global reach

Teva's position remains strong in the generics sector, but competition from Mylan, Novartis, and emerging biosimilar players compresss margins. Its focus on complex generics offers differentiation but requires substantial R&D investment.

What are the key market trends influencing Teva's strategy?

  • Biosimilar Market Growth: Expected compound annual growth rate (CAGR) of 20% through 2028, driven by patent expirations and biologics pipeline expansion.
  • Consolidation in Generics Industry: Mergers and acquisitions, such as Viatris integrating Mylan, impact market share dynamics.
  • Regulatory Evolution: Stricter biosimilar approval pathways and price controls in major markets.
  • Patient-centric Care Models: Focus on injectable and biosimilar offerings aligning with personalized medicine.
  • Digital Manufacturing: Automation and data analytics streamline operations and improve compliance.

What are the opportunities and risks ahead?

Opportunities

  • Expansion into emerging markets, with access to large patient populations.
  • Development of high-value biosimilars for complex biologics.
  • Strategic collaborations with biotech firms to enhance R&D pipeline.
  • Investing in digital supply chain solutions to lower costs.

Risks

  • Regulatory delays and hurdles impacting biosimilar approval.
  • Intense pricing pressures reducing profit margins.
  • Currency fluctuations affecting profits in emerging markets.
  • Patent litigation and legal disputes threatening revenue streams.

How should investors evaluate Teva's strategic outlook?

  • Monitor pipeline investments in biosimilars and complex generics.
  • Assess debt reduction strategies and cash flow management.
  • Track market share trends against competitors.
  • Analyze regional performance, especially in emerging markets.
  • Evaluate developments in legal disputes and patent statuses.

Key Takeaways

Teva remains a dominant generics manufacturer with a broad portfolio, manufacturing scale, and a strategic focus on complex generics and biosimilars. Growing biosimilar demand presents growth opportunities, but legal, pricing, and debt challenges require careful strategic management. Geographic expansion, pipeline development, and technological innovation are critical to maintaining competitive edge.

FAQs

1. How does Teva's focus on biosimilars position it for future growth?
It offers a growth avenue amid patent expirations of biologics. Early investments and market entry in biosimilars provide potential for higher margins and increased market share.

2. What is the impact of debt on Teva's strategic flexibility?
High debt levels limit investment capacity and may increase borrowing costs. Debt reduction plans are a priority to support R&D and strategic acquisitions.

3. How does Teva compete in pricing pressures within developed markets?
By leveraging manufacturing efficiencies, cost reductions, and portfolio differentiation in complex generics, Teva aims to offset pricing pressures.

4. What regions offer the most growth prospects for Teva?
Emerging markets in Asia-Pacific and Latin America demonstrate high growth potential due to large patient populations and increasing healthcare spending.

5. How significant are legal disputes in Teva’s future outlook?
Legal disputes, particularly patent litigations, pose risks to revenue streams and market exclusivity. Effective management and resolution strategies are crucial.


References

[1] IQVIA. (2022). Global Generic Pharmaceutical Market Report.
[2] Teva Pharmaceuticals. (2022). Annual Report.

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