MEDIOCON INC supplies Feverfew Extract as a botanical raw material for nutraceutical, dietary supplement, herbal and functional-food applications.
Feverfew is a botanical derived from Tanacetum parthenium, a flowering plant traditionally used in herbal preparations. Feverfew extracts may contain naturally occurring sesquiterpene lactones, with parthenolide commonly used as a characteristic marker for standardized extracts.
The exact composition of Feverfew Extract depends on the plant material, extraction process, extract ratio and standardization. Therefore, the parthenolide content, extraction ratio and other analytical specifications should be confirmed from the applicable product specification and batch COA rather than assumed.
MEDIOCON INC can supply Feverfew Extract according to the required grade, standardization, packaging and quality specifications.
Feverfew Extract is obtained from Tanacetum parthenium.
Parthenolide is a commonly monitored characteristic constituent of Feverfew extracts. The actual concentration should always be confirmed from the supplier's specification.
For raw-material applications, Feverfew Extract is generally supplied as a dry extract powder, rather than as capsules or tablets.
Because Feverfew Extract contains multiple naturally occurring constituents, it should be treated as a complex botanical extract rather than a single chemical compound.
Feverfew Extract can be used in:
| Parameter | Specification |
|---|---|
| Appearance | Yellowish-brown to brown powder |
Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Feverfew Extract Manufacturer & Supplier in India | MEDIOCON INC and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our Feverfew Extract Manufacturer & Supplier in India | MEDIOCON INC is manufactured under strict quality management protocols compliant with WHO-GMP, ISO 9001:2015, and major pharmacopoeial standards (IP, BP, USP, EP). Every batch undergoes full analytical testing before release with a Certificate of Analysis.
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