Onyx Biotec Limited was incorporated on May 13, 2005 as a private limited company as ‘Onyx Biotec Private Limited’, under the Companies Act, 1956, pursuant to a certificate of incorporation dated May 13, 2005 issued by the Registrar of Companies, Punjab, H.P. & Chandigarh. Further, the company was converted into a public limited company pursuant to a resolution passed by its Board of Directors in its meeting held on May 1, 2024, and by the Shareholders in an Extraordinary General Meeting held on May 27, 2024 and consequently the name of the company was changed to ‘Onyx Biotec Limited’ and a fresh certificate of incorporation dated July 23, 2024 was issued by the Registrar of Companies, Central Processing Centre.

The company started its operation in pharmaceutical industry with sterile water for injections in the year 2010. Since then, the company has been associated with the healthcare segment and offering Sterile Pharmaceutical products and has become a prominent supplier of sterile products to major corporations, which includes the top pharma companies at pan India level. It is committed to provide high-quality products at affordable price. Also, the company manufactures Sterile Water for Injections, and acts as a pharmaceutical contract manufacturer offering a comprehensive range of Dry Powder Injections and Dry Syrup for India and overseas. 

Its products are being processed and manufactured in accordance with best Food and Drug Administration (FDA) practices available globally. Its system and product are tested constantly at each level to ensure international standards of quality in-house and FDA Certified Laboratories. Its core business is focused on providing end-to-end product development and manufacturing solutions to its clients. Its service also include preparation and filing of regulatory dossiers in the Indian and global markets. Its manufacturing units are equipped with Modern Equipment, ensures Quality Control and follows Sustainable Practices. Its manufacturing units have been accredited by global regulatory agency i.e. World Health Organization Good Manufacturing Practice (WHO-GMP). 

Business area of the company

The company is engaged in the business of Manufacturing of Pharmaceutical Products such as sterile water ampoule, dry injection, dry syrup etc.

Products of the company 

• Sterile water for injections
• Dry powder injections
• Dry powder syrups

History and milestones

• 2010: The company commenced commercial production at its Unit I with two line of Form Fill and Seal setup with capacity of 2 lakh units per day.
• 2017: Capacity expansion at its Unit I from 130 million unit per annum to 230 million units per annum. 
• 2017: The company received a certificate for Good Manufacturing Practice from Deputy Drugs Controller cum Licensing Authority, Health & Family.
• 2023: The company commenced commercial production at its Unit II.