Ginseng/ Asian Ginseng Extract Capsule/Tablet Suppliers & Bulk Manufacturers
Available Forms: Capsule/tablet.
Available Strengths: 100 mg to 8000mg
Reference Brands: Nature’s Way, Gaia Herbs, Solgar(US)
Category:
Nutraceuticals
Ginseng extract caplets and tablets contain active compounds like ginsenosides, which boost energy, mental alertness, and immune function. They support stress reduction, enhance physical endurance, and improve cognitive performance. Benefits include increased vitality, reduced fatigue, better focus, and overall wellness in supporting mental and physical health worldwide.
Ginseng/ Asian Ginseng Extract Capsule/tablet is available in Capsule/tablet.
and strengths such as 100 mg to 8000mg.
Sourced from GMP-certified and ISO-compliant manufacturers, this API meets
global pharmacopeia standards (USP/EP/JP as applicable). Ideal for pharmaceutical
formulation and commercial manufacturing, Ginseng/ Asian Ginseng Extract Capsule/tablet is supplied in
bulk quantities with complete regulatory support including DMF, COA, and MSDS.
|
Technical Specifications & Supply Details
|
| Lead Time |
7 to 60 days (depending on batch size & schedule) |
| MOQ |
As per manufacturer’s batch size |
| COA |
Available with every batch |
| Regulatory Dossier / DMF |
Available upon request |
| Export Documentation |
FSC, COA, Manufacturing License, Product Permission |
| Standards |
IP, BP, USP |
| Certifications |
WHO-GMP, EU-GMP, USFDA (as applicable) |
Ginseng/ Asian Ginseng Extract Capsule/tablet can be exported to over 30 countries across Asia, Africa, Europe,
and Latin America. Flexible packaging, competitive pricing, and a verified supplier
network make Pharmatradz a trusted sourcing partner for pharmaceutical companies
and contract manufacturers worldwide.
Product Description:
Ginseng extract caplets and tablets, marketed as dietary supplements, are regulated in the US by the FDA and in the EU via EMA as food supplements. Approval requires dossiers including safety data, ingredient sourcing, manufacturing standards, and efficacy evidence. In the US, the FDA reviews safety and labeling, while the EMA ensures compliance with regional safety and quality standards.
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