About > About Us
Established in 1972, by Late Dr. Vasant Palkar
Nivedita Chemicals Pvt. Ltd. is a 53-year-old company, established in 1972 by Dr. Vasant Palkar. Since 1987, we have been serving the pharmaceutical industry both in India and internationally, delivering high-quality and affordable healthcare drugs across the globe.
Our sister concern, Anek Prayog Pvt. Ltd., serves as the exclusive manufacturing site for Nivedita Chemicals. The facility is located on approximately two acres of land in Village Dhatav, Roha MIDC, in the state of Maharashtra, India. Meanwhile, Nivedita Chemicals, headquartered in Mumbai, manages the financial, marketing, and R&D operations of the business.
Anek Prayog Pvt. Ltd. features state-of-the-art manufacturing facilities supported by a robust Quality Management System (QMS). The site is equipped with advanced instruments and equipment, ensuring precision and compliance with international standards. A dedicated manufacturing block for excipients is in place, with an annual production capacity of around 60 MT.
We are proud to be the world’s largest manufacturer of Trimetazidine Dihydrochloride and the first Asian company to receive the Certificate of Suitability (CEP) for this product.
Anek Prayog holds multiple prestigious regulatory accreditations. The facility is regularly audited by EU/EDQM and WHO, and has previously been inspected and approved by USFDA, Korean FDA, and Mexican FDA. Additionally, we maintain ANVISA cGMP certification for our products.
We have submitted Drug Master Files (DMFs) to regulatory authorities across Europe, South America, South Africa, Korea, Taiwan, Israel, Iran, and East Asia. We provide full technical and regulatory support to our customers worldwide.
We have built a strong reputation on the global stage. Along with supplying APIs and excipient to India’s top pharmaceutical companies, we export to more than 25 countries across Asia, Australia, Europe, North America, and South America. Currently, exports account for 90% of our total turnover.
Why Us?
- World-Class Manufacturing Facility: Our state-of-the-art manufacturing facility and infrastructure have received multiple national and international GMP approvals, ensuring the highest standards of quality, safety, and consistency in every product we deliver.
- Commitment to Quality and Innovation:We continuously strive to enhance our products in terms of quality, stability, and reproducibility, aligning with customer needs and regulatory expectations. Our goal is to provide affordable and reliable products without compromising on excellence.
- Strong Regulatory and Technical Support: Our experienced Regulatory Affairs Team provides comprehensive support to customers worldwide. The team is well-versed with the requirements of various global regulatory agencies, ensuring smooth documentation and compliance.
- Long-Term Business Relationships: We believe in nurturing long-term partnerships with our customers and associates. Our strong global network reflects this trust — exports account for nearly 90% of our total turnover.
- Sustainable and Safe Practices: We focus on developing reproducible, efficient, and hazard-free processes, ensuring a safe and sustainable work environment. We are equally committed to environmental protection and contributing positively to the community.
- Skilled and Dedicated Team: Our success is driven by our highly qualified and experienced team, who ensure quality and compliance at every stage of production.
- R&D Excellence: Our R&D department synthesizes and characterizes various impurity standards, which we supply to our customers worldwide. Continuous innovation and scientific expertise are at the core of our operations.
Milestones
Company’s significant milestones since inception.
| Year | Milestones |
| 2024 | Audited and approved by ANVISA authorities CBPF/GMP certificate received for Trimetazidine Dihydrochloride and Dexchlorpheniramine maleate |
| 2013 & 2017 | Audited and approved by EU authorities. EU-GMP Certificate received for Trimetazidine Dihydrochloride. |
| 2011 | US FDA has inspected and classified our manufacturing facility as acceptable as per USFDA regulatory requirements. |
| 2009 | Audited and approved by Korean FDA (MFDA). |
| 2008 | Maharashtra State Export Award |
| 2004 | Became a WHO-GMP certified company. |
| 1989-90 | Export Award and Certificate of Merit from Chemixcil. |
| 1987 | M.L. Dahanukar Enterpreneurship Award. |
| 1985 | Raigad District Award. |
| 1981 | R&D department is recognized by Department of Scientific and Industrial Research (DSIR), Government of India |
| 1979 | Republic Day National Award for Import Substitute -Vitamin B2-5 Phosphate Sodium |
| 1979 | Anek Prayog Pvt Ltd was founded |
| 1972 | Introduced Vitamin B2-5 Phosphate Sodium, for the first time in India. |
| 1972 | Nivedita Chemicals Pvt. Ltd founded. |
Mission
● To manufacture vital drugs as import substitutes, so that we can become a self-sufficient nation in the realm of medicine and healthcare.
●To ensure customer satisfaction on quality and timely delivery of our products, as per the regulatory and quality standards followed internationally.
● To provide a safe working environment through effective work practices, staff training, enhancement of infrastructure, and the use of state-of-the-art technology.
● To meet dynamically changing, diverse consumer needs through supply and marketing of quality products and services.
● To be engaged in continuous Research and Development activities in order to foster innovation in the pharmaceutical industry.
● To develop processes and policies that reflect our corporate social responsibility.
● We are committed to continual quality improvement that emphasizes the accountability of every employee for product quality, workplace excellence, and the overall growth of our business.
Vision
To be a preferred healthcare partner for pharmaceutical industries in India, and globally.