Ginkgo Biloba Extract Capsule Or Tablet. Suppliers & Bulk Manufacturers
Available Forms: Capsule or tablet.
Available Strengths: 120 mg, 240 mg, or 600 mg
Reference Brands: Nature’s Way, NOW Foods, Gaia Herbs(US)
Category:
Nutraceuticals
Ginkgo biloba extract capsules and tablets enhance blood flow and neuroprotection by dilating blood vessels and reducing oxidative stress. They support cognitive function, memory, mental clarity, and reduce dizziness or vertigo. Benefits include improved circulation, enhanced brain health, and antioxidant protection, promoting overall wellness.
Ginkgo Biloba Extract capsule or tablet. is available in Capsule or tablet.
and strengths such as 120 mg, 240 mg, or 600 mg.
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, Ginkgo Biloba Extract capsule or 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) |
Ginkgo Biloba Extract capsule or 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:
Ginkgo biloba extract capsules and tablets, marketed as dietary supplements, are regulated in the US by the FDA and in the EU via EMA as herbal supplements. Regulatory dossiers should include safety assessments, ingredient sourcing, manufacturing standards, and efficacy data. The FDA reviews safety and labeling, while the EMA ensures compliance with regional safety and quality regulations.
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