6
Oct
2026
Fiera Milano, Italy
6 Oct 2026 - 8 Oct 2026
stand 5F33

Rusan Pharma Ltd

  • Rusan Ankleshwar Plant
  • Ankleshwar Plant Pictures
  • Dehradun Plant Pictures
  • Kandla Unit 1 - Manufacturing Unit
  • Kandla Unit II - Manufacturing Unit
About Rusan Pharma Ltd

Rusan Pharma is a fully integrated global pharmaceutical company which specializes in the treatment of Addiction, Pain Management, Parkinson’s Management and Critical Care. Rusan manufactures and markets a wide range of API and finished formulations in India and globally, with a key focus in controlled (narcotic and psychotropic) substances. Rusan's manufacturing facilities are GMP approved by USFDA, Health Canada, EU, TGA, ANVISA, PIC/S, PMDA Japan, WHO, Russia and SAHPRA. Rusan has CEP approval for various APIs such as Buprenorphine, Fentanyl, Naltrexone, Methadone, Bisoprolol and we also manufacture Naloxone, Nalbuphine, Nalmefene, Apomorphine,....

Certifications

Meet us at

  • CPHI Milan 2026

    Fiera Milano, Italy
    6 Oct 2026 - 8 Oct 2026
    stand 5F33
  • Country/Region:
    India
  • On CPHI since:
    2015
  • Certificates:
    2
  • Employees:
    500 - 999
Company types
Manufacturer/Innovator
Pharmaceutical company
Primary activities
API Producer
Contract Manufacturer
Contract Research Organisation
Generic APIs producer
Nutraceuticals
OTC
Pharmaceutical Company (innovator finished products)
Contact info

Products from Rusan Pharma Ltd (49)

Rusan Pharma Ltd Resources (6)

  • News Rusan Pharma Gujarat Plant Receives GMP certification from Australia; Gets extension from Brazil

    Rusan Pharma Ltd. has achieved two major regulatory milestones for its advanced manufacturing facility located in the Kandla Special Economic Zone (SEZ) Unit-II in Gujarat, India. The facility, which specializes in high-speed production of transdermal patches and oral films, has received Good Manufacturing Practice (GMP) certification from Australia’s Therapeutic Goods Administration (TGA) and a GMP extension from Brazil’s Health Regulatory Agency, ANVISA.

    The TGA certification marks a pivotal step in Rusan Pharma’s expansion into the Australian market. Following a rigorous inspection, the facility was granted A1 GMP compliance, validating its capability to produce specialized drug delivery systems such as Buprenorphine, Nicotine Transdermal Patches, and Buprenorphine+Naloxone Sublingual Films. These products are designed to address critical medical needs in pain management and addiction treatment. This is the second time the TGA has approved the Kandla Unit-II faci...
  • Brochure Rusan API List 2026

    Please find attached our latest API list for 2026
  • News Rusan Pharma achieves dual GMP milestones from TGA, Australia and ANVISA, for its manufacturing facility

    Corporate+ Font Resize -Rusan Pharma achieves dual GMP milestones from TGA, Australia and ANVISA, for its manufacturing facilityOur Bureau, Mumbai
    Friday, December 13, 2024, 16:45 Hrs  [IST]Rusan Pharma Ltd, a leading global pharmaceutical company specialising in addiction treatment and pain management, has announced two significant milestones for its state-of-the-art dedicated high-speed transdermal patch and oral film manufacturing facility, located in the Kandla Special Economic Zone (SEZ)-UNIT-II (Gujarat, India) (“KDL-2”). 

  • Brochure Rusan Product List - 2026

    Please find attached Rusan Product list for 2026
  • News Rusan Pharma’s API Plant in Ankleshwar (India) Receives USFDA GMP Approval

    RUSAN PHARMA PRIVATE LIMITED, an Indian pharmaceutical company specializing in addiction treatment and pain management, announced that its Active Pharmaceutical Ingredient (API) facility in Ankleshwar, Gujarat, received Good Manufacturing Practice (GMP) approval from the USFDA on May 29, 2024, following a rigorous inspection. This approval marks a significant milestone, enabling Rusan to expand into the US API market, particularly for niche APIs like Eflornithine and Nalmefene, while planning to add more APIs to its portfolio. Rusan Pharma’s Managing Director, Dr. Kunal Saxena, emphasized the company’s commitment to quality and global expansion. The USFDA approval complements Rusan's existing GMP certifications from Health Canada, the EU, and Brazil’s ANVISA, and aligns with the company’s vision to be a leader in addiction treatment and pain management.