Last Updated: May 5, 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 Pharma Canada NYSTATIN nystatin CREAM;TOPICAL 064022-001 Jan 29, 1993 AT RX No Yes ⤷  Start Trial ⤷  Start Trial
Sun Pharm Industries THIORIDAZINE HYDROCHLORIDE thioridazine hydrochloride TABLET;ORAL 088737-001 Sep 26, 1984 DISCN No No ⤷  Start Trial ⤷  Start Trial
Sun Pharm ERLOTINIB HYDROCHLORIDE erlotinib hydrochloride TABLET;ORAL 210300-002 Nov 5, 2019 DISCN No No ⤷  Start Trial ⤷  Start Trial
Sun Pharm Inds Inc CLOZAPINE clozapine TABLET;ORAL 075713-002 Nov 15, 2002 DISCN No No ⤷  Start Trial ⤷  Start Trial
Sun Pharm ALPRAZOLAM alprazolam TABLET;ORAL 090082-001 Jun 17, 2010 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 Pharm Inds Inc ABSORICA isotretinoin CAPSULE;ORAL 021951-002 May 25, 2012 9,078,925 ⤷  Start Trial
Sun Pharm Inds Inc LEVULAN aminolevulinic acid hydrochloride SOLUTION;TOPICAL 020965-001 Dec 3, 1999 8,216,289 ⤷  Start Trial
Sun Pharm Inds Inc LEVULAN aminolevulinic acid hydrochloride SOLUTION;TOPICAL 020965-001 Dec 3, 1999 5,954,703 ⤷  Start Trial
Sun Pharm Inds Inc ABSORICA isotretinoin CAPSULE;ORAL 021951-003 May 25, 2012 9,089,534 ⤷  Start Trial
Sun Pharm Inds Inc BACTRIM sulfamethoxazole; trimethoprim INJECTABLE;INJECTION 018374-001 Approved Prior to Jan 1, 1982 3,551,564 ⤷  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 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
➤ Subscribe Topical Spray 0.25% ➤ Subscribe 2013-12-18
➤ Subscribe Capsules 20 mg ➤ Subscribe 2013-06-19

Supplementary Protection Certificates for Sun Pharm Drugs

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
0321122 97C0009 Belgium ⤷  Start Trial PRODUCT NAME: TOPOTECAN HYDROCHLORIDE; NAT. REGISTRATION NO/DATE: EU/1/96/027/001 19961112 ; FIRST REGISTRATION: CH 53857 19961016
3141251 301099 Netherlands ⤷  Start Trial PRODUCT NAME: A MEDICINAL PRODUCT CONSISTING OF A COMBINATION OF A FIRST DOSE PHARMACEUTICAL COMPOSITION AND A SECOND DOSE PHARMACEUTICAL COMPOSITION, THE FIRST DOSE PHARMACEUTICAL COMPOSITION CONSISTING OF THE ACTIVE INGREDIENTS POLYETHYLENE GLYCOL, SODIUM SULPHATE, SODIUM CHLORIDE AND POTASSIUM CHLORIDE AND THE SECOND DOSE PHARMACEUTICAL COMPOSITION CONSISTING OF THE ACTIVE INGREDIENTS POLYETHYLENE GLYCOL, ASCORBIC ACID, SODIUM ASCORBATE, SODIUM CHLORIDE AND POTASSIUM CHLORIDE; NATIONAL REGISTRATION NO/DATE: RVG 120195 20171114; FIRST REGISTRATION: IS IS/1/17/083/01 20171016
1586316 SPC/GB11/054 United Kingdom ⤷  Start Trial PRODUCT NAME: BROMFENAC 2-AMINO-3-(4-BROMOBENZOYL)PHENYLACETIC ACID OR A PHARMACOLOGICALLY ACCEPTABLE SALT THEREOF OR A HYDRATE THEREOF; REGISTERED: UK EU/1/11/692/001 20110523
2021328 2015/055 Ireland ⤷  Start Trial PRODUCT NAME: SONIDEGIB OR A PHARMACEUTICALLY ACCEPTABLE SALT, HYDRATE OR SOLVATE THEREOF.; REGISTRATION NO/DATE: EU/1/15/1030(C(2015)5890 20150818
1532149 PA2012022 Lithuania ⤷  Start Trial PRODUCT NAME: LINAGLIPTINUM + METFORMINI HYDROCHLORIDUM; REGISTRATION NO/DATE: EU/1/12/780/001 - EU/1/12/780/034 20120720
>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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