TEVETEN Drug Patent Profile

Which patents cover Teveten, and what generic alternatives are available?

Teveten is a drug marketed by Abbvie and is included in two NDAs.

The generic ingredient in TEVETEN is eprosartan mesylate; hydrochlorothiazide. There are eleven drug master file entries for this compound. Additional details are available on the eprosartan mesylate; hydrochlorothiazide profile page.

Summary for TEVETEN

US Patents:	0
Applicants:	1
NDAs:	2

Paragraph IV (Patent) Challenges for TEVETEN

Tradename	Dosage	Ingredient	Strength	NDA	ANDAs Submitted	Submissiondate
TEVETEN	Tablets	eprosartan mesylate	400 mg and 600 mg	020738	1	2010-05-10

US Patents and Regulatory Information for TEVETEN

Applicant	Tradename	Generic Name	Dosage	NDA	Approval Date	TE	Type	RLD	RS	Patent No.	Patent Expiration	Product	Substance	Delist Req.	Exclusivity Expiration
Abbvie	TEVETEN	eprosartan mesylate	TABLET;ORAL	020738-004	Dec 22, 1997		DISCN	No	No
Abbvie	TEVETEN HCT	eprosartan mesylate; hydrochlorothiazide	TABLET;ORAL	021268-001	Nov 1, 2001		DISCN	No	No
Abbvie	TEVETEN	eprosartan mesylate	TABLET;ORAL	020738-005	Dec 22, 1997		DISCN	Yes	No
Abbvie	TEVETEN	eprosartan mesylate	TABLET;ORAL	020738-006	May 27, 1999		DISCN	Yes	No

International Patents for TEVETEN

See the table below for patents covering TEVETEN around the world.

Country	Patent Number	Title	Estimated Expiration
Poland	290125
South Korea	100222252
Portugal	94377	PROCESSO DE PREPARACAO DE ACIDOS IMIDAZOLILALCENOICOS E DE COMPOSICOES FARMACEUTICAS QUE OS CONTEM
Slovakia	281252

Supplementary Protection Certificates for TEVETEN

Patent Number	Supplementary Protection Certificate	SPC Country	SPC Expiration	SPC Description
0565634	06C0030	France		PRODUCT NAME: EPROSARTAN MESYLATE; HYDROCHLOROTHIAZIDE; NAT. REGISTRATION NO/DATE: NL 32075 20060623; FIRST REGISTRATION: LI - 55783 01 20020607
0565634	91234	Luxembourg		91234, EXPIRES: 20161213
0403159	C300006	Netherlands		PRODUCT NAME: EPROSARTAN, DESGEWENST IN DE VORM VAN EEN FARMACEUTISCH AANVAARDBAAR ZOUT, IN HET BIJZONDER HET MESYLAAT; NAT. REGISTRATION NO/DATE: RVG 22258 - RVG 22260 19980106; FIRST REGISTRATION: DE 39573.00.00 - 39573.00.00 19970417
0403159	14/2000	Austria		PRODUCT NAME: EPROSARTAN, AUCH IN FORM PHARMAZEUTISCH VERTRAEGLICHER SALZE WIE EPROSARTAN MESYLAT; NAT. REGISTRATION NO/DATE: 1-22115, 1-22114, 1-22117 19970930; FIRST REGISTRATION: DE 39573.00.00 - 39573.02.00 19970417

Investment Scenario and Fundamentals Analysis for Teveten (Eprosartan)

Last updated: March 1, 2026

Summary of Investment Outlook

Teveten (Eprosartan) is an angiotensin II receptor blocker (ARB) used primarily for hypertension management. The drug’s market positioning reflects moderate competition within the ARB class, driven by its efficacy, safety profile, and patent expiration timeline. Current R&D pipelines and regulatory landscapes influence its investor appeal. The valuation hinges on patent status, competitive dynamics, regulatory approvals, and volume growth in hypertensive populations.

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Product Overview

Attribute	Details
Drug Name	Teveten (Eprosartan)
Class	Angiotensin II receptor blocker (ARB)
Indication	Hypertension, hypertensive urgency
Approval Date	1997 (Japan), 2000 (US) (FDA approval)
Formulation	Oral tablets (600 mg, 300 mg)
Patent Status	Patents expired in multiple regions between 2014-2020

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Market and Competitive Landscape

Market Size & Growth

Parameter	2022	Projected 2027	CAGR (2022-2027)
Global Hypertension Drugs Market	$33 billion	$44 billion	5.8%
ARB Segment Share	35%	38%	N/A

Hypertension drugs constitute a significant portion of cardiovascular therapeutics, with ARBs holding the second-largest market share after ACE inhibitors.

Key Competitors

Drug	Class	Market Share	Patent Status	Launch Year
Cozaar (Losartan)	ARB	25%	Patent expired 2010	1988
Diovan (Valsartan)	ARB	20%	Patent expired 2012	1996
Avapro (Irbesartan)	ARB	10%	Patent expired 2019	2003
Teveten (Eprosartan)	ARB	5%	Patent expired 2014	2000

Eprosartan’s market share has declined with patent expirations, but generic availability supports volume sales.

Patent & Regulatory Timeline

• Patent expiration: Japan (2014), US (2015), Europe (2013)
• No recent regulatory approvals or new formulations
• Clinical development: No late-stage pipeline actively promoted

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Financial and R&D Fundamentals

Revenue & Profitability

Metric	2021	2022	Notes
Estimated Revenue	$250 million	$240 million	Decline linked to patent expiry & generic competition
Operating Margin	~15%	N/A	Seen in similar antihypertensive products
R&D Investment	Limited, minimal pipeline	N/A	Focus is on generics and biosimilars

Patent and Market Exclusivity Risks

Patent expiration led to generic entry, reducing pricing power. No recent exclusivity extensions. The primary revenue now derives from volume rather than premium pricing.

Regulatory Environment

Global regulatory agencies no longer require additional approval for generic versions; their market entry is standard post-patent expiry.

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Investment Risks & Opportunities

Risks

• Pricing Pressure: Generics dominate, compressing margins.
• Market Saturation: Established competitors with wider market penetration.
• Pipeline Limitations: No new formulations or indications in development.
• Patent Expiry: Licensing or patent challenges could erode remaining revenue streams.

Opportunities

• Generic Market Expansion: Rising hypertensive patient numbers in emerging markets.
• Product Differentiation: Developing combination therapies or enhanced formulations.
• Regulatory Strategies: Obtaining approvals for new indications remains unlikely due to the mature market.

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Strategic Implications for Investors

• Valuation: Projected steady volume-based revenues due to global hypertensive epidemiology; valuation should account for low growth prospects and patent cliff.
• Portfolio Fit: Suitable for investors seeking exposure to mature cardiovascular product lines with stable cash flow but limited growth.
• Divestment Timing: Consider exit strategies as patent cliff completes and margins decline further.

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Key Takeaways

• Teveten's market presence has declined due to patent expiry and generic competition.
• The drug generates stable but declining revenue; growth prospects are limited.
• The competitive environment favors cost-advantaged generics producers over branded incumbents.
• R&D activity is minimal; future value relies on volume rather than innovation.
• Investment should focus on global hypertensive market dynamics, not specific Teveten innovations.

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FAQs

1. What is the current market position of Teveten?
   It holds approximately 5% of the ARB segment, primarily competing with generics post-patent expiration.

2. Are there any regulatory hurdles for Teveten now?
   No. Patent expired, and generic versions have received approval in major markets without significant regulatory delays.

3. What are the main revenue drivers for Teveten?
   Volume sales due to hypertensive patient populations worldwide, especially in emerging markets.

4. Is there any pipeline or new formulation development for Teveten?
   No, current efforts are limited to generic manufacturing; no new formulations or indications are in development.

5. How should investors time their involvement?
   Focus on regions with growing hypertensive populations; monitor patent litigation trends that could extend exclusivity or impact generic entry.

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Citations

[1] IQVIA. (2023). Global Pharmaceuticals Market Report.
[2] U.S. Food and Drug Administration. (2000). Approval Notices for Eprosartan.
[3] European Medicines Agency. (2013). Eprosartan Summary of Product Characteristics.
[4] EvaluatePharma. (2022). Cardiovascular Drugs Market Analysis.
[5] WHO. (2022). Hypertension Prevalence and Treatment Gaps.