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Gland Pharma Ltd

NSE: GLAND BSE: 543245

₹2502.90

(0.56%)

Fri, 07 Aug 2026, 11:23 am

Company History

1978

  • The company was incorporated as Gland Pharma Private Limited

1994

  • The name of the company was changed to Gland Pharma Limited pursuant to a special resolution passed by the shareholders

1995

  • A fresh certificate of incorporation was issued by the Registrar of Companies, Andhra Pradesh at Hyderabad consequent upon change of name and conversion into a public limited company

2000

  • The company set up the in-house R&D facility at Dundigal, Hyderabad

2003

  • The company received USFDA approval for the manufacturing facility at Dundigal

2005

  • The company launched Enoxaparin Sodium Injection (Cutenox) in India and Rest of the world markets

2007

  • The company received a capital infusion of approximately 1,000 million into the Company pursuant to private equity investment aggregating to approximately 1,200 million with EILSF Co-Invest I LLC

2010

  • The company launched Heparin Sodium Injection in the US

2012

  • The company received the Certificate of GMP Compliance of a Manufacturer from BGV Hamburg (Germany) for its manufacturing facility at Dundigal

2014

  • The company obtained USFDA approval for small volume parenteral manufacturing facility at Visakhapatnam
  • The company commissioned the Pashamylaram Unit-II manufacturing facility
  • The company received the Certificate of GMP Compliance of a Manufacturer from MHRA (UK) for manufacturing facility at Dundigal
  • The company received a capital infusion of US$ 100 million into the Company pursuant to private equity investment aggregating to approximately US$ 200 million with KKR Floorline Investment Pte Ltd

2016

  • The company obtained USFDA approval for its facilities at Jawaharlal Nehru Pharma City, Visakhapatnam
  • The company obtained USFDA approval for its manufacturing facility at Pashamylaram
  • The company obtained USFDA approval for its facility at the Visakhapatnam Special Economic Zone

2017

  • Fosun Singapore acquired 74% stake in the company

2018

  • The company received ANDA approval for Enoxaparin Sodium Injection USP for the US market
  • The company received ANDA approval for Olopatadine Hydrochloride Ophthalmic Solution USP, 0.1%, its first Ophthalmic product approval

2019

  • The company filed Dexrazoxane for Injection, its first filing with the National Medical Products Administration, China, and received clinical waiver

2020

  • Gland Pharma along with its partners MAIA Pharmaceuticals, Inc. and Athenex Pharmaceutical Division announce the launch of a Ready-to-Use Bivalirudin Injection in the United States of America

2021

  • Gland Pharma received approval for generic Foscarnet Sodium Injection, Single-Dose Bag for Infusion
  • Gland Pharma receives Tentative Approval for Sugammadex Injection
  • Gland Pharma receives tentative approval for Cangrelor injection

2022

  • Gland Pharma enters into put option agreement to acquire 100% of Cenexi Group
  • Gland Pharma announces launch of Bortezomib for Injection in US market

2024

  • The Company received approval from the United States Food and Drug Administration (US FDA) for Plerixafor Injection

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