Classical and proprietary Ayurvedic formulations — churna, tablets, syrups, oils and more — made under AYUSH licence with consistent, GMP-compliant processes and batch-wise NABL testing.
Churna, vati/gutika, syrups (asava/arishta), oils and taila-based products made to pharmacopoeial specification.
Custom-developed products with your own marker compounds and finished-goods specification.
Herbal extract capsules and tablets manufactured to consistent potency batch after batch.
Share your product and use-case — we suggest the right test panel.
Clear pricing with turnaround time and sample requirements.
Pan-India sample collection with proper chain-of-custody.
Compliant, audit-ready PDFs with expert interpretation.
Low MOQs for market testing and new launches, scaling quickly based on traction.
Consistent quality batch after batch, from herbal syrups to capsules to drops.
From pilot batch to commercial volumes, with reliable delivery timelines.
"We were a small herbal brand just starting out, and Amar Pharma supported us with flexible batch sizes and complete guidance on compliance. Their team really felt like an extension of ours."
"Working with Amar Pharma has given us confidence in our product line. From herbal syrups to capsules, their consistency and GMP-compliant processes have helped us scale without compromising on quality."
"We began with a pilot batch and quickly grew to commercial volumes. Amar Pharma handled the transition smoothly with strong technical know-how and reliable delivery timelines."
Yes. We start lean for market testing and scale quickly based on traction.
Yes — our formulation team works with you on ingredient selection, taste masking and stability from the earliest development stage.
Certificate of Analysis from our NABL-accredited lab, along with manufacturing and batch records as required for your compliance file.
We support labeling and packaging execution to your specification and applicable regulatory requirements.
Yes — our testing and documentation are built to support export and international regulatory submissions.
Lead time depends on formulation complexity and batch size — share your requirement and we'll confirm a timeline.
Share your requirement and our team will confirm feasibility, MOQ and timeline.
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