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Last Updated: March 19, 2026

Sun Pharm Company Profile


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Summary for Sun Pharm

Drugs and US Patents for Sun Pharm

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Sun Pharm Inds Inc ORTHO-EST estropipate TABLET;ORAL 089567-001 Feb 27, 1991 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
Sun Pharm Industries FLUOXETINE fluoxetine hydrochloride CAPSULE;ORAL 075787-001 Jan 29, 2002 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
Sun Pharm Industries TRAMADOL HYDROCHLORIDE tramadol hydrochloride TABLET;ORAL 076100-001 Jun 20, 2002 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
Sun Pharm ERTAPENEM SODIUM ertapenem sodium INJECTABLE;INTRAMUSCULAR, INTRAVENOUS 209145-001 May 2, 2023 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
Sun Pharm Inds Inc DEXMETHYLPHENIDATE HYDROCHLORIDE dexmethylphenidate hydrochloride CAPSULE, EXTENDED RELEASE;ORAL 206734-006 Nov 5, 2021 DISCN No No ⤷  Get Started Free ⤷  Get Started Free
Sun Pharm BYNFEZIA PEN octreotide acetate SOLUTION;SUBCUTANEOUS 213224-001 Sep 27, 2024 RX Yes Yes 11,052,196 ⤷  Get Started Free ⤷  Get Started Free
Sun Pharm ABSORICA LD isotretinoin CAPSULE;ORAL 211913-002 Nov 5, 2019 RX Yes No 9,750,711 ⤷  Get Started Free Y ⤷  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 Sun Pharm

Paragraph IV (Patent) Challenges for SUN PHARM drugs
Drugname Dosage Strength Tradename Submissiondate
➤ Subscribe Tablets 125 mg ➤ Subscribe 2018-07-23
➤ Subscribe Capsules 20 mg ➤ Subscribe 2013-01-07
➤ Subscribe Capsules 25 mg ➤ Subscribe 2016-05-16
➤ Subscribe Capsules 35 mg ➤ Subscribe 2015-11-25
➤ Subscribe Topical Spray 0.25% ➤ Subscribe 2013-12-18
➤ Subscribe Capsules 20 mg ➤ Subscribe 2013-06-19
➤ Subscribe Capsules 30 mg and 40 mg ➤ Subscribe 2012-12-31
➤ Subscribe Delayed-release Tablets 20 mg ➤ Subscribe 2015-06-03

International Patents for Sun Pharm Drugs

Country Patent Number Estimated Expiration
Australia 2022328272 ⤷  Get Started Free
World Intellectual Property Organization (WIPO) 2007131201 ⤷  Get Started Free
Poland 2969227 ⤷  Get Started Free
Mexico 363238 ⤷  Get Started Free
World Intellectual Property Organization (WIPO) 2016044701 ⤷  Get Started Free
Costa Rica 10399 ⤷  Get Started Free
Brazil 112017001963 ⤷  Get Started Free
>Country >Patent Number >Estimated Expiration

Supplementary Protection Certificates for Sun Pharm Drugs

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
2340828 SPC/GB21/010 United Kingdom ⤷  Get Started Free PRODUCT NAME: SACUBITRIL/VALSARTAN, AS SACUBITRIL VALSARTAN SODIUM SALT COMPLEX, I.E. (((S)-N-VALERYL-N-((2'-(1H-TETRAZOLE-5-YL)- BIPHENYL-4-YL)-METHYL)-VALINE)((2R,4S)-5-BIPHENYL -4-YL-4-(3-CARBOXY-PROPIONYLAMINO)-2-METHYL-PENTANOIC ACID ETHYL ESTER))NA3 X H2O, WHERE; REGISTERED: UK EU/1/15/1058 (NI) 20151123; UK PLGB 00101/1041 20151123; UK PLGB 00101/1042 20151123; UK PLGB 00101/1043 20151123
1532149 PA2012022 Lithuania ⤷  Get Started Free PRODUCT NAME: LINAGLIPTINUM + METFORMINI HYDROCHLORIDUM; REGISTRATION NO/DATE: EU/1/12/780/001 - EU/1/12/780/034 20120720
1499331 SPC/GB13/034 United Kingdom ⤷  Get Started Free PRODUCT NAME: IZINOVA CONCENTRATE FOR ORAL SOLUTION. THE ACTIVE SUBSTANCE IS A MIXTURE OF 3 SALTS:SODIUM SULPHATE ANHYDROUS, MAGNESIUM SULPHATE HEPTAHYDRATE AND POTASSIUM SULPHATE.; REGISTERED: BE BE434323 20130220; UK PL34926/0016 20130313
1003503 30/2006 Austria ⤷  Get Started Free PRODUCT NAME: AMLODIPIN ODER EIN PHARMAZEUTISCH ANNEHMBARES SAEUREADDITIONSALZ DESSELBEN IN KOMBINATION MIT ATORVASTATIN ODER EINEM PHARMAZEUTISCH ANNEHMBAREN SALZ DESSELBEN; NAT. REGISTRATION NO/DATE: 1-26271, 1-26273 20060330; FIRST REGISTRATION: FR 369300.9;369301.5; 369302.1;369303.8;369304.4;369305.0; 20050707
0281459 35/1998 Austria ⤷  Get Started Free PRODUCT NAME: CLOPIDOGREL-HYDROGENSULFAT; REGISTRATION NO/DATE: EU/1/98/069/001 - EU/1/98/069/003 19980715
2139494 LUC00176 Luxembourg ⤷  Get Started Free PRODUCT NAME: SAXAGLIPTINE ET DAPAGLIFLOZINE; AUTHORISATION NUMBER AND DATE: EU/1/16/1108 20160719
0364417 97C0111 Belgium ⤷  Get Started Free PRODUCT NAME: LATANOPROSTUM; NAT. REGISTRATION NO/DATE: 277 IS 271 F 13 19970617; FIRST REGISTRATION: SE 12716 1996071
>Patent Number >Supplementary Protection Certificate >SPC Country >SPC Expiration >SPC Description
Similar Applicant Names
Applicants may be listed under multiple names.
Here is a list of applicants with similar names.

Pharmaceutical Competitive Landscape Analysis: Sun Pharma – Market Position, Strengths & Strategic Insights

Last updated: February 19, 2026

What Is Sun Pharma’s Market Position?

Sun Pharma ranks among the top generic pharmaceutical companies globally, with annual revenues exceeding $4.3 billion in 2022[1]. The company operates in more than 100 markets and maintains a leading position in both the United States and India, two of the most significant pharmaceutical markets. It is the largest specialty generic company in India and the fifth-largest generic company worldwide[2].

How Does Sun Pharma Compare to Global Competitors?

Company 2022 Revenue (USD billions) Market Focus Key Strengths
Sun Pharma 4.3 Generics, Specialty, APIs Strong R&D, robust portfolio, regional dominance in India
Teva Pharmaceuticals 16.0 Generics, Branded, Biopharma Largest generics portfolio, global footprint
Novartis 51.9 Innovator, Biosimilars R&D capacity, innovative pipeline
Pfizer 100.3 Innovator, Vaccines Leading in R&D, diversified portfolio
Dr. Reddy’s Labs 3.7 Generics, biosimilars Expanding US presence, focus on biosimilars

Sun Pharma’s revenue is smaller relative to peers like Teva and Pfizer, but it maintains a competitive market share, especially within emerging markets and specialty generics.

What Are Sun Pharma’s Core Strengths?

Product Portfolio and R&D:
Sun Pharma owns a diverse portfolio with over 420 marketed products across various therapeutic areas, including neurology, cardiology, and dermatology[3]. Its R&D expenditure totaled approximately 6-7% of revenue in 2022, amounting to nearly $300 million, with a focus on biosimilars, complex generics, and specialty medicines[4].

Manufacturing Capability:
The company operates 24 manufacturing facilities globally, with a focus on high-quality APIs and formulations. Its API business supplies over 600 customers worldwide, including major pharmaceutical firms.

Geographical Reach:
Emerging markets, especially India and Latin America, provide high-growth opportunities. In 2022, the India business accounted for approximately 34% of total revenue, with US and European markets comprising 30% and 18% respectively[1].

Regulatory and Quality Focus:
Sun Pharma has improved its regulatory compliance, securing approvals in key markets such as the US FDA, EDQM, and South Korea's MFDS, reducing the risk of product recalls and market entry barriers.

What Are the Key Strategic Initiatives?

Expansion into Biosimilars:
Sun Pharma has committed over $500 million to biosimilar R&D, targeting early commercialization of biosimilar products in oncology, immunology, and dermatology[4]. Its biosimilar pipeline includes oncology drugs such as Bevacizumab and Rituximab.

Acquisitions and Alliances:
In 2020, Sun Pharma acquired the US-based company Pola Pharma to expand dermatology and complex generics portfolio[5]. It also formed licensing agreements with emerging biotech firms to enhance its specialty pipeline.

Focus on Complex Generics:
The company invests heavily in developing complex formulations like inhalation products, injectable drugs, and drugs with specialized delivery systems. This strategy aims to reduce generic competition and improve margins.

Digital and Supply Chain Transformation:
Sun Pharma leverages digital tools for R&D, manufacturing, and supply chain logistics, enhancing efficiency and accelerating time-to-market for new products.

What Are the Risks and Challenges?

Regulatory Hurdles:
Stringent approval processes in the US and EU increase time-to-market and costs. Recent US FDA inspections led to warning letters in certain facilities, impacting revenue[6].

Market Competition:
Peaked by the emergence of biosimilars and patent cliffs, large competitors like Teva, Novartis, and Pfizer continue to invest aggressively in R&D and patent strategies, pressing margins.

Pricing Pressures:
Global pricing reforms, especially in India and the US, threaten profitability. The US Medicaid and Medicare programs curtail prices on generic medicines.

Innovation Rate:
While Sun Pharma invests in biosimilars and complex generics, it lags behind in truly innovative drugs, which limits long-term growth potential outside its core markets.

What Strategic Insights Are Evident?

  • Leverage emerging markets: Sun Pharma’s dominance in India positions it well in local generics but requires strengthening its presence in the US and Europe.
  • Prioritize biosimilar pipeline: The biosimilar segment offers high-margin opportunities and less price erosion.
  • Enhance regulatory compliance: Addressing regulatory challenges can open doors to additional markets and prevent revenue losses.
  • Diversify therapeutic areas: Expanding into specialty drugs and complex formulations can insulate against generic competition.

Key Takeaways

  • Sun Pharma is a leading generic company with a significant presence in India and emerging markets.
  • Its strengths include a broad product portfolio, robust manufacturing, and strategic investments in biosimilars.
  • Competitive pressures stem from rivals' R&D efforts, regulatory hurdles, and pricing reforms.
  • Focus areas include biosimilars, complex generics, and strategic acquisitions to bolster growth.

FAQs

1. How does Sun Pharma’s revenue growth compare to its competitors?
Sun Pharma’s revenue growth averaged around 8% annually over the past five years, outperforming some regional peers but lagging behind global giants like Pfizer and Novartis.

2. What markets are critical for Sun Pharma’s future expansion?
The US, Europe, and institutional markets in Latin America are key. Emerging markets, notably India and Southeast Asia, continue to drive current revenue.

3. How significant is biosimilar development in Sun Pharma’s strategy?
Biosimilars constitute approximately 20% of its R&D budget, aiming for commercial launch between 2023 and 2025.

4. What regulatory risks does Sun Pharma face?
US FDA warnings and inspections pose risks; recent sanctions have led to manufacturing delays.

5. What should investors watch for in Sun Pharma’s upcoming quarterly results?
Progress in biosimilar approvals, regulatory resolution in key markets, and impact of pricing reforms will influence valuation.


Sources:
[1] Sun Pharma Annual Report 2022.
[2] IQVIA, 2022. Global Pharmaceutical Market Data.
[3] Sun Pharma Corporate Website.
[4] Bloomberg Intelligence, 2022.
[5] Reuters, 2020. Sun Pharma acquisition of Pola Pharma.
[6] US FDA Enforcement Reports, 2022.

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