Ayush Chemopharma Pvt. Ltd. is a pharmaceutical API manufacturing company based at G.I.D.C. Panoli, Ankleshwar, Gujarat, India. Established in 2014, the company has grown into a dependable manufacturing partner for pharmaceutical companies that require consistent, quality-assured active pharmaceutical ingredients for their formulation needs.
Our facility is built around controlled manufacturing processes, in-process quality checks, and validated batch documentation, allowing us to serve pharmaceutical manufacturers, distributors, contract manufacturing organizations, and export partners with the same level of reliability, order after order.
Over the years, we have built our reputation on three principles: consistent product quality, transparent documentation, and dependable delivery timelines. These principles guide every batch that leaves our facility.
To become a trusted pharmaceutical intermediate manufacturer, recognized for consistent quality, innovation, and responsible manufacturing practices worldwide.
To manufacture high-quality pharmaceutical intermediates through reliable processes, advanced technology, and continuous improvement while meeting evolving customer requirements.
We value quality, integrity, safety, innovation, and customer commitment, building long-term relationships through responsible practices and consistent product excellence.
Choosing an API manufacturer means trusting them with your production timelines and your finished product’s quality. At Ayush Chemopharma Pvt. Ltd., we’ve built our process around consistency, transparency, and reliability the things pharmaceutical buyers actually value.
Every batch is tested against defined specifications before release, so what you receive today matches what performed well last time. No surprises, no rework.
Certificates of Analysis, MSDS, and other required documents are ready with every shipment. Your regulatory and vendor-qualification process stays smooth.
From sample quantities to full bulk orders, our production planning adapts to your requirement. You’re never locked into ordering more than you need.
We plan our production schedules around realistic timelines and communicate proactively. Your manufacturing line doesn’t wait on us.
When pharmaceutical companies evaluate a new API manufacturer, certain questions come up again and again — around quality, documentation, order handling, and reliability. Below, we’ve answered the questions we hear most often from formulation companies, distributors, and export buyers considering Ayush Chemopharma Pvt. Ltd. as their API partner.
We manufacture a range of active pharmaceutical ingredients, including Diclofenac Sodium, Diclofenac Potassium, Fluconazole, Aceclofenac, Pregabalin, Oxcarbazepine, and other pharmaceutical API products. Our product range is manufactured for use by pharmaceutical companies in tablet, capsule, and other dosage form manufacturing. If you’re looking for a specific molecule not listed on our website, feel free to reach out to our team directly, as we continue to expand our product range.
Yes, our manufacturing practices are aligned with WHO-GMP principles. We follow documented standard operating procedures, maintain batch manufacturing records, and carry out quality control testing at each stage of production. Compliance-related documentation is available to buyers on request, particularly for vendor qualification and audit purposes.
Yes, we understand that pharmaceutical buyers need to evaluate a product before committing to a larger purchase. We provide sample quantities for most of our API products, along with relevant technical documentation, so your team can run internal testing before finalizing an order.
Minimum order quantities vary by product and depend on current production planning. We’re able to accommodate smaller trial orders as well as large bulk requirements. Share your expected quantity with our sales team, and we’ll confirm feasibility and pricing accordingly.
Batch-to-batch consistency comes from following the same validated process parameters and testing protocols for every production run. Our quality control team reviews each batch against defined specifications before approval, so buyers placing repeat orders can expect the same product performance each time.
Yes, we supply our API products to international buyers, including importers, distributors, and pharmaceutical manufacturers across various regions. Our export shipments are supported with the documentation typically required for customs clearance, and we work with logistics partners experienced in handling pharmaceutical cargo.
In many cases, yes. If your formulation process requires a specific particle size, purity threshold, or additional testing parameters, share these details with our technical team. We’ll review the request and confirm whether it can be accommodated for your order.
Our standard packing includes HDPE drums with polybag lining, available in various quantities to suit different order sizes. For bulk or export orders, we also offer custom packaging configurations designed to protect product integrity during transportation.
Our technical team remains available for any questions related to the product after delivery, whether it’s about the Certificate of Analysis, storage conditions, or handling recommendations. We aim to be a long-term technical resource, not just a one-time supplier.
