Last verified: April 2026
Manufacturers -- Quality and Licensing Guide
Classical Ayurvedic texts document that the preparation method determines the therapeutic outcome -- a principle that applies equally to modern manufacturing. This page documents the major licensed Ayurvedic manufacturers in India, quality standards to look for, and how to verify manufacturer credentials.
Eight major licensed manufacturers
Quality standards to look for
Schedule T GMP compliance
All legally sold Ayurvedic medicines in India must be manufactured under Schedule T GMP conditions. This covers: facility hygiene, equipment standards, raw material testing, in-process quality control, finished product testing, and batch record keeping. Schedule T GMP is the minimum standard -- not the gold standard.
API compliance with testing documentation
API (Ayurvedic Pharmacopoeia of India) monographs specify: botanical identity markers, moisture content, ash values, extractive values, heavy metal limits, and specific active compound content where applicable. Manufacturers who test against API standards and provide Certificates of Analysis (CoA) offer a higher quality assurance level than Schedule T alone.
WHO-GMP and third-party testing
WHO-GMP certification (issued by the CDSCO -- Central Drugs Standard Control Organisation) meets international pharmaceutical manufacturing standards. Required for export to regulated markets (EU, US, Canada, Australia). Third-party testing by accredited labs (NABL-accredited laboratories) for heavy metals (particularly for Bhasma preparations), pesticide residues, and active compound content is the highest available standard for Indian Ayurvedic products.