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Last Updated: December 15, 2025

Teva Pharm Company Profile


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Summary for Teva Pharm

Drugs and US Patents for Teva Pharm

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 OLMESARTAN MEDOXOMIL, AMLODIPINE AND HYDROCHLOROTHIAZIDE amlodipine besylate; hydrochlorothiazide; olmesartan medoxomil TABLET;ORAL 202491-002 Nov 3, 2016 AB RX No No ⤷  Get Started Free ⤷  Get Started Free
Teva Pharms Usa LURASIDONE HYDROCHLORIDE lurasidone hydrochloride TABLET;ORAL 208060-001 May 17, 2019 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
Teva Pharms NAPROXEN naproxen TABLET;ORAL 074207-003 Dec 21, 1993 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
Teva Pharms Usa SULFAMETHOXAZOLE AND TRIMETHOPRIM sulfamethoxazole; trimethoprim INJECTABLE;INJECTION 073303-001 Oct 31, 1991 AP RX No No ⤷  Get Started Free ⤷  Get Started Free
Teva Pharms Usa TRAZODONE HYDROCHLORIDE trazodone hydrochloride TABLET;ORAL 071523-001 Dec 11, 1987 AB RX No No ⤷  Get Started Free ⤷  Get Started Free
Teva Pharm ARMONAIR DIGIHALER fluticasone propionate POWDER;INHALATION 208798-005 Feb 20, 2020 DISCN Yes No 11,344,685*PED ⤷  Get Started Free Y ⤷  Get Started Free
Teva Pharms Usa OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE hydrochlorothiazide; olmesartan medoxomil TABLET;ORAL 200532-002 Apr 24, 2017 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

Expired US Patents for Teva Pharm

Paragraph IV (Patent) Challenges for TEVA PHARM drugs
Drugname Dosage Strength Tradename Submissiondate
➤ Subscribe Delayed-release Tablets 20 mg ➤ Subscribe 2015-06-03
➤ Subscribe Injection 40 mg/mL, 1 mL pre-filled syringe ➤ Subscribe 2014-02-26
➤ 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

Supplementary Protection Certificates for Teva Pharm Drugs

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
1255752 2008/004 Ireland ⤷  Get Started Free PRODUCT NAME: SUNITINIB, OPTIONALLY IN THE FORM OF A PHARMACEUTICALLY ACCEPTABLE SALT, INCLUDING THE L-MALATE SALT; AUTHORISATION NO/DATE: IRELAND EU/1/06/347/001, EU/1/06/347/002, EU/1/06/347/003 20060719
0720599 300689 Netherlands ⤷  Get Started Free PRODUCT NAME: EZETIMIBE, DESGEWENST IN DE VORM VAN EEN FARMACEUTISCH AANVAARDBAAR ZOUT, EN ATORVASTATINE, DESGEWENST IN DE VORM VAN EEN FARMACEUTISCH AANVAARDBAAR ZOUT, IN HET BIJZONDER ATORVASTATINE CALCIUM TRIHYDRATE; NATIONAL REGISTRATION NO/DATE: RVG114373-114376 20141027; FIRST REGISTRATION: FR 2014091200122 20140912
2269603 300769 Netherlands ⤷  Get Started Free PRODUCT NAME: EVEROLIMUS, DESGEWENST IN DE VORM VAN EEN FARMACEUTISCH AANVAARDBAAR ZOUT; REGISTRATION NO/DATE: EU/1/09/001, 003, 004 EN 006-010 (C(2012)5347) 20120725
1169038 300567 Netherlands ⤷  Get Started Free PRODUCT NAME: DASATINIB, DESGEWENST IN DE VORM VAN EEN FARMACEUTISCH AANVAARDBAAR ZOUT; REGISTRATION NO/DATE: EU/1/06/363/001 - 009 20061120
1620113 15C0069 France ⤷  Get Started Free PRODUCT NAME: IVERMECTINE; NAT. REGISTRATION NO/DATE: NL 44511 20150721; FIRST REGISTRATION: MT - MA 117/01101 20150402
1675573 2014C/029 Belgium ⤷  Get Started Free PRODUCT NAME: ARIPIPRAZOLE; AUTHORISATION NUMBER AND DATE: EU/1/13/882 20131119
0162036 C300028 Netherlands ⤷  Get Started Free PRODUCT NAME: LEVETIRACETAM; REGISTRATION NO/DATE: EU/1/00/146/001 - EU/1/00/146/026 20000929
>Patent Number >Supplementary Protection Certificate >SPC Country >SPC Expiration >SPC Description
Similar Applicant Names
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Here is a list of applicants with similar names.

Pharmaceutical Competitive Landscape Analysis: TEVA PHARM – Market Position, Strengths & Strategic Insights

Last updated: October 15, 2025

Introduction

Teva Pharmaceutical Industries Ltd. stands as a prominent player in the global generics and specialty pharmaceuticals sector. With a history spanning over a century, the company has carved a significant niche in providing affordable medications across various therapeutic categories. As the pharmaceutical industry witnesses rapid innovation, regulatory shifts, and market consolidation, understanding Teva’s current market position, strengths, and strategic direction is crucial for stakeholders, investors, and competitors aiming to navigate this dynamic landscape effectively.

Market Position of Teva Pharmaceuticals

Global Footprint and Market Share

Teva ranks among the top global generic drug manufacturers, with a substantial presence in North America, Europe, and emerging markets. According to IQVIA data, Teva held approximately 2.8% of the global pharmaceutical market share in 2022, with its generics division accounting for the majority of revenues [1]. The company's extensive portfolio encompasses more than 3,500 generic products across multiple therapeutic classes, reinforcing its widespread market footprint.

In the U.S., Teva is the leading generic supplier, commanding almost 8% of the generic drug market—a significant share considering the competitive landscape dominated by firms like Walgreens Boots Alliance, Novartis, and Mylan (now part of Viatris) [2].

Therapeutic Focus and Revenue Streams

While generics constitute the backbone of Teva’s revenues, the company also invests heavily in specialty medications, notably Copaxone (glatiramer acetate), a treatment for multiple sclerosis (MS). Although patent expiries have impacted Copaxone’s revenue, ongoing efforts aim to re-establish growth via newer formulations and biosimilars. The company’s revenues are thus balanced between stable generics and innovation-driven specialty drugs, mitigating risks associated with patent cliffs [3].

Competitive Positioning

Teva’s strategic positioning hinges on its extensive product portfolio, manufacturing capabilities, and established distribution channels. Its agility in introducing high-volume generics often grants it first-mover advantages, especially in North America. However, intensified competition, pricing pressures, and regulatory barriers challenge its leadership standing, prompting strategic shifts toward innovation and cost optimization.

Strengths of Teva Pharmaceuticals

1. Dominance in the Generics Market

Teva's pioneering role in producing cost-effective generics has cemented its reputation as a market leader. Its portfolio covers over 80 countries, supported by robust relationships with healthcare providers and pharmacy chains. This global reach enables Teva to leverage economies of scale, reduce costs, and respond swiftly to emerging market needs.

2. Extensive R&D and Product Development Capabilities

Despite its focus on generics, Teva invests roughly 10% of revenues into R&D, fostering a pipeline of biosimilars, specialty pharmaceuticals, and reformulations. Its biosimilar division is poised for growth amid rising demand for biologics alternatives, and recent approvals of biosimilar versions of blockbuster drugs demonstrate Teva’s innovation trajectory [4].

3. Cost Leadership and Manufacturing Excellence

Teva operates approximately 60 manufacturing facilities worldwide, emphasizing cost-efficiency and quality compliance. Its integrated supply chain and high-volume production capabilities enable competitive pricing and rapid product launches.

4. Strong Market Presence in Developing Regions

Emerging markets in Latin America, Asia, and Eastern Europe have become vital growth engines. Teva’s tailored strategies—such as local manufacturing and partnerships—facilitate market penetration, expanding revenue streams amidst saturated Western markets.

5. Focus on Core Portfolio Optimization

In response to overextension and capital allocation challenges, Teva has divested non-core assets and restructured operations. This strategic focus enhances operational efficiency and financial stability.

Strategic Challenges and Weaknesses

1. Patent Cliff and Revenue Volatility

Teva's reliance on blockbuster drugs like Copaxone has exposed it to revenue declines following patent expiries. The generic market’s inherent price erosion amplifies revenue pressures, necessitating innovation and diversification.

2. Litigation and Regulatory Risks

Legal disputes concerning patent infringements, governmental pricing investigations, and regulatory compliance pose significant risks. Pending lawsuits related to patent litigations and drug safety investigations have led to financial and reputational concerns.

3. Debt Burden and Financial Stability

Post-acquisition debts from its 2016 acquisition of Actavis Generics (now Teva Generics) and recent restructuring efforts have elevated leverage ratios. High debt levels constrain strategic flexibility and increase vulnerability to market shocks.

4. Competitive Intensity in Key Markets

The generics space faces fierce price competition from emerging market manufacturers and contract manufacturers in India and China. This pressure eats into profit margins, especially for low-margin, high-volume products.

5. Innovation Pipeline Risks

Despite investments in biosimilars and specialty drugs, delays in approvals and market entry setbacks can impact revenue forecasts. The success of new product launches remains uncertain amid shifting regulatory requirements.

Strategic Insights for Stakeholders

Diversification into Biologics and Biosimilars

Teva’s investment in biosimilars represents a strategic response to the impending patent cliffs. Accelerating regulatory approvals and expanding its pipeline can provide sustained growth. Partnerships and licensing agreements with biotech firms can further bolster its portfolio.

Operational Efficiency and Cost Optimization

Further restructuring and automation of manufacturing processes will be crucial to reduce costs. Additionally, aligning supply chains with regional markets can mitigate geopolitical and logistical risks.

Focus on Core Therapeutic Areas

Concentrating on high-growth therapeutic segments like specialty neurology (multiple sclerosis, migraine prevention) and oncology could secure higher-margin revenues. Tailoring R&D efforts toward unmet medical needs enhances market competitiveness.

Regulatory and Legal Risk Mitigation

Strengthening compliance frameworks and proactive legal strategies are essential to minimize litigation risks. Engaging with regulatory bodies early in the development process can facilitate smoother product approvals.

Market Expansion and Strategic Partnerships

Expanding in emerging markets through local collaborations and acquisitions can diversify revenue sources. Strategic alliances with innovative biotech companies will complement Teva’s existing strengths and accelerate product development.

Conclusion

Teva’s positioned as a formidable leader within the generics and specialty pharmaceuticals sector, leveraging extensive product portfolios, global reach, and manufacturing strength. Nonetheless, it faces challenges including patent expiries, intense competition, and financial leverage. Strategic focus on innovation, operational efficiency, and market diversification remains vital to sustaining growth and competitive advantage.

By proactively addressing these factors, Teva can reinforce its market position, capitalize on biosimilar opportunities, and mitigate risks associated with industry shifts. Its future trajectory depends profoundly on strategic execution, investment in innovation, and adaptive responses to evolving regulatory and economic environments.


Key Takeaways

  • Teva maintains a leading position in global generics, supported by extensive product offerings and manufacturing capacity.
  • The company's investment in biosimilars and specialty drugs is critical for future growth amid patent expiries.
  • Financial leverage and litigation risks require diligent management to stabilize operations.
  • Expanding in emerging markets and forming strategic alliances will enhance revenue streams and innovation.
  • Focused R&D, operational efficiencies, and regulatory compliance can sustain Teva’s competitiveness in a consolidating industry.

FAQs

1. How does Teva’s market share compare in the U.S. versus global markets?
Teva is the leading generic pharmaceutical supplier in the U.S., holding approximately 8% market share, whereas globally, it accounts for around 2.8% of the total pharmaceutical market, reflecting its dominant presence in North America but broader, competitive landscape elsewhere [1][2].

2. What are the main growth drivers for Teva moving forward?
Primarily, biosimilar development, expansion into emerging markets, and specialty drug innovation are vital. Strategic partnerships and pipeline advancement in high-growth therapeutic areas will underpin future revenue streams.

3. What risks threaten Teva’s market dominance?
Patent expiries, escalating pricing pressures in generics, legal and regulatory challenges, high debt levels, and fierce competition from local and non-traditional players pose ongoing threats.

4. How is Teva responding to patent expiries of key drugs like Copaxone?
Teva is investing in biosimilars and reformulated versions of its existing drugs to offset revenue declines and adapt to patent expiries, alongside diversifying into new therapeutic areas.

5. What strategic actions can stakeholders consider regarding Teva?
Investors should monitor Teva’s pipeline developments, debt management strategies, and market expansion efforts. Suppliers and partners should assess collaboration opportunities in biosimilars and emerging markets to capitalize on industry shifts.


References

[1] IQVIA. “Insights on the Global Pharmaceutical Market,” 2022.
[2] Statista. “Market Shares of Leading Generic Drug Manufacturers in the U.S.,” 2022.
[3] Teva Annual Report 2022.
[4] FDA Approvals Database. “Recent Biosimilar Approvals of Teva,” 2022.

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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.