About Us

Welcome to Nivedita Chemicals Pvt. Ltd.!

The company was established in 1972, by Late Dr. Vasant Palkar.

Nivedita Chemicals Pvt. Ltd. is presently an exporter of Active Pharmaceuticals Ingredients (API's) and Intermediates. We have been serving the pharmaceutical industry in India since 1972 and international market since 1987 with quality products.

We are committed to help preserve life, and provide innovative yet affordable health care drugs.

Anek Prayog Pvt. Ltd. is our sister concern, established by Late. Dr. Vasant Palkar in 1979. Anek Prayog Pvt Ltd. is the only manufacturing site of Nivedita Chemicals Pvt. Ltd. Nivedita Chemicals Pvt. Ltd. also takes care of the financial, marketing and R&D aspects of the business.

Our goal is to manufacture vital drugs as import substitutes.

Over the years, with steady progress, astounding research results and strong regulatory support, we have earned the respect and trust of our customers and associates. Our superior and consistent quality of products coupled with timely deliveries has put us on the global map. Apart from supplying API's to India's top pharmaceutical companies, we export to more than 25 countries across Asia, Australia, Europe, North and South America. Our export turnover currently stands at 90% of our total turnover.

We are the world's largest manufacturer of Trimetazidine Dihydrochloride and the first Asian company to receive the Certificate of Suitability (CEP) for Trimetazidine Dihydrochloride.

Dr. Vivekanand Palkar, son of Dr. Vasant Palkar is now the Chairman and Managing Director of both these companies. The Board of Directors are common for both these companies.

Anek Prayog Pvt. Ltd. has state of-the-art plant facilities with a robust Quality Management system (QMS). The facility is equipped with sophisticated equipment's/instruments. The facility is situated on about two acres of land at Village-Dhatav, City - Roha, MIDC area in Maharashtra State, India.

Anek Prayog Pvt. Ltd. has been audited and approved by several regulatory agencies over the past few years. The company strictly adheres to the standard Good Manufacturing Practices laid down by the international regulatory authorities.

We have registered Drug Master Files of our products to various authorities in Europe and also in South America, South Africa, Korea, Taiwan, Israel, Iran, and East Asia.

We support our customers in all technical as well as regulatory aspects.

We are proud to say that we are one of the key contributors in alleviating human suffering, on a global scale.