Supporting Global Healthcare
with WHO GMP-Compliant API
Manufacturing

A reliable manufacturer of APIs and pharmaceutical
intermediates serving domestic and global markets.

Suleshvari Pharma Ltd

20+ Years of Industry Experience

Led by industry experts with 20–40 years of pharmaceutical manufacturing experience.

Diverse API Portfolio

Manufacturing APIs like Famotidine, Nifedipine, Zaltoprofen and key intermediates.

Regulatory & GMP Compliance

Compliant with cGMP standards and inspected by CDSCO & PMDA (Japan).

Suleshvari Pharma Ltd
About Us

Manufacturing Excellence in Pharmaceuticals

Suleshvari Pharma Pvt. Ltd., a part of the Parnasha Group, is engaged in the manufacturing of Active Pharmaceutical Ingredients (APIs) and drug intermediates on a large scale in India.

Since its establishment in 2004, the company has focused on development, manufacturing, and marketing of high-quality pharmaceutical intermediates and APIs for domestic and global markets.

Values That Guide Us

Excellence

Pursuing the highest standards

Responsibility

Safety in every
operation

Trust

Built through
integrity

Consistency

Dependable manufacturing partner

Sustainability

Committed to a greener tomorrow

Manufacturing & Infrastructure

The infrastructure is equipped with stainless steel and glass-lined reactors, supported by controlled agitation systems, temperature monitoring, and safety mechanisms. This enables efficient and consistent production of pharmaceutical intermediates and APIs while maintaining process reliability and operational safety.

Designed to support scalable manufacturing, the facility operates with a focus on quality, compliance, and environmentally responsible practices.

Suleshvari Pharma Ltd

What Defines Us

20+

Years of
Experience

Modern Facility

Equipped with advanced
reactors & systems

Multiple APIs

Including regulated
market products

FDA Standard

Global compliance
& inspections

Sustainability

Green chemistry practices, safety protocols, MSDS compliance, and environmentally responsible operations

Quality Commitment

Strict adherence to cGMP with robust QA systems including CAPA, change control, and batch release processes.