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Last Updated: March 27, 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 CARBOPLATIN carboplatin INJECTABLE;INTRAVENOUS 077926-002 Sep 19, 2008 AP RX No No ⤷  Start Trial ⤷  Start Trial
Sun Pharm Inds Inc CETIRIZINE HYDROCHLORIDE ALLERGY cetirizine hydrochloride TABLET, CHEWABLE;ORAL 077631-004 Jan 11, 2008 DISCN No No ⤷  Start Trial ⤷  Start Trial
Sun Pharm MEMANTINE HYDROCHLORIDE memantine hydrochloride TABLET;ORAL 090058-001 May 5, 2010 AB RX No No ⤷  Start Trial ⤷  Start Trial
Sun Pharm PREGABALIN pregabalin CAPSULE;ORAL 091157-004 Nov 29, 2019 DISCN No No ⤷  Start Trial ⤷  Start Trial
Sun Pharm FOSAMPRENAVIR CALCIUM fosamprenavir calcium TABLET;ORAL 204024-001 Nov 20, 2019 AB RX No No ⤷  Start Trial ⤷  Start Trial
Sun Pharm Industries PHENYLBUTAZONE phenylbutazone TABLET;ORAL 088863-001 Dec 4, 1985 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 Sun Pharm

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Sun Pharma Canada FLO-PRED prednisolone acetate SUSPENSION;ORAL 022067-002 Jan 17, 2008 6,102,254 ⤷  Start Trial
Sun Pharma Canada FLO-PRED prednisolone acetate SUSPENSION;ORAL 022067-001 Jan 17, 2008 5,881,926 ⤷  Start Trial
Sun Pharm Inds Inc ABSORICA isotretinoin CAPSULE;ORAL 021951-002 May 25, 2012 8,367,102 ⤷  Start Trial
Sun Pharma Canada FLO-PRED prednisolone acetate SUSPENSION;ORAL 022067-001 Jan 17, 2008 6,102,254 ⤷  Start Trial
Sun Pharm Inds Inc LEVULAN aminolevulinic acid hydrochloride SOLUTION;TOPICAL 020965-001 Dec 3, 1999 5,211,938 ⤷  Start Trial
Sun Pharm Inds Inc ABSORICA isotretinoin CAPSULE;ORAL 021951-004 May 25, 2012 7,435,427 ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration
Paragraph IV (Patent) Challenges for SUN PHARM drugs
Drugname Dosage Strength Tradename Submissiondate
➤ 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
➤ 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

Supplementary Protection Certificates for Sun Pharm Drugs

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
1532149 CA 2013 00001 Denmark ⤷  Start Trial PRODUCT NAME: 8-(3-AMINOPIPERIDIN-1-YL)-7-BUT-2-INYL-3-METHYL-1-(4-METHYLCHINAZOLIN-2-YLMETHYL)-3,7-DIHYDROPURIN-2,6-DION ENANTIOMERER OG SALTE DERAF - SAERLIGT LINAGLIPTIN - I KOMBINATION MED METFORMINHYDROCHLORID; REG. NO/DATE: EU/1/12/780/001-028 20120720
2932970 1890039-9 Sweden ⤷  Start Trial PRODUCT NAME: DOLUTEGRAVIR SODIUM + RILPIVIRINE HYDROCHLORIDE; REG. NO/DATE: EU/1/18/1282 20180518
0984957 PA2011005,C0984957 Lithuania ⤷  Start Trial PRODUCT NAME: NAPROXENUM + ESOMEPRAZOLUM; REGISTRATION NO/DATE: LT/1/10/2302/001-LT/1/10/2302/012 20110126
0147850 99C0002 Belgium ⤷  Start Trial PRODUCT NAME: REPAGLINIDE; REGISTRATION NO/DATE: EU/1/98/076/001 19980817
0454511 99C0009 Belgium ⤷  Start Trial PRODUCT NAME: IRBESARTAN / HYDROCHLOROTHIAZIDE; REGISTRATION NO/DATE: EU/1/98/086/001 19981015
2822954 1890030-8 Sweden ⤷  Start Trial PRODUCT NAME: BICTEGRAVIR OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF, IN PARTICULAR BICTEGRAVIR SODIUM; REG. NO/DATE: EU/1/18/1289 20180625
>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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