Podophyllum Resin

Podophyllum Resin and Podophyllotoxin Manufacturer

We are a cGMP-certified manufacturer and bulk supplier of Podophyllum Resin and Podophyllotoxin for pharmaceutical applications. Both products are manufactured under controlled cGMP conditions and supplied with complete COAs and MSDS for regulated international markets.

Podophyllum Resin

Podophyllum Resin is a resinous extract obtained from Podophyllum species using cGMP-compliant extraction and concentration processes. As a Podophyllum Resin manufacturer, we standardize key quality parameters to ensure consistent resin composition and batch-to-batch reliability.

Podophyllum Resin is commonly used in pharmaceutical and topical formulations where defined resin content and controlled quality are required. The product is supplied in bulk, export-ready packaging with full regulatory documentation.

Podophyllotoxin

Podophyllotoxin is a high-purity lignan compound manufactured from Podophyllum Resin through controlled purification processes under cGMP systems. As a Podophyllotoxin manufacturer, we ensure defined assay, impurity control and consistent performance for regulated pharmaceutical use.

Podophyllotoxin is widely used as a pharmaceutical intermediate in the manufacture of specialized therapeutic formulations. Podophyllotoxin supplied by us is available in bulk packaging with complete COA and MSDS for global supply.

Quality and Supply

All Podophyllum Resin and Podophyllotoxin products are produced under cGMP systems with validated quality control, batch traceability and export compliance, making them suitable for regulated pharmaceutical markets worldwide.

Podophyllum Resin & Podophyllotoxin – FAQ

Podophyllum Resin is a crude extract, while Podophyllotoxin is a purified active compound derived from the resin.

Podophyllotoxin is commonly used as an intermediate for pharmaceutical applications.

Yes, both are manufactured under cGMP-controlled processes.

Both products are supplied in bulk with full quality documentation.

An open part of the Drug Master File (DMF) is available upon request and can be shared after signing a confidentiality agreement (CDA) with the customer.

Please fill out the form and a dedicated associate will be in touch with you within 24 hours.

At INGA, we ensure quality at economical prices. With over 60 years experience, we hold long-standing relationships with all our clients.

Get In Touch Enquire Now