MEDIOCON INC supplies Vitis viniferae Leaves Dry Extract as a botanical raw material for nutraceutical, dietary supplement, herbal and functional-food applications.
Vitis vinifera is commonly known as the grapevine. Grape leaves contain naturally occurring polyphenols, flavonoids and other plant constituents. Dry extracts are produced by processing the leaves and concentrating the desired botanical constituents.
The exact phytochemical profile and marker content depend on the botanical source, plant part, extraction process and standardization. Therefore, specific marker values should be confirmed from the applicable product specification and batch COA rather than assumed.
MEDIOCON INC can supply Vitis viniferae Leaves Dry Extract according to the required grade, standardization, packaging and quality documentation.
The material is derived from the leaves of Vitis vinifera, the grapevine.
Grape leaves naturally contain various polyphenolic and flavonoid compounds, with the exact profile depending on cultivar, growing conditions and processing.
The product is supplied as a dry extract powder, suitable for incorporation into appropriate formulations.
Botanical identity, extraction ratio, moisture, microbial quality, heavy metals, pesticide residues and applicable marker compounds should be evaluated according to the approved specification and batch COA.
Vitis viniferae Leaves Dry Extract can be used in:
| Parameter | Specification |
|---|---|
| Appearance | Greenish-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 Vitis viniferae Leaves Dry 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 Vitis viniferae Leaves Dry 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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