Green Tea Extract Capsule Or Tablet. Suppliers & Bulk Manufacturers
Available Forms: Capsule or tablet.
Available Strengths: 250 mg, 500 mg, and 750 mg
Reference Brands: NOW Foods, Nature’s Way, Solgar(US)
Category:
Nutraceuticals
Green tea extract capsules and tablets contain catechins, especially EGCG, which act as antioxidants, reducing oxidative stress. They support metabolism, weight management, cardiovascular health, and improved brain function. Benefits include increased fat burning, enhanced energy, reduced inflammation, and overall antioxidant protection worldwide.
Green tea extract capsule or tablet. is available in Capsule or tablet.
and strengths such as 250 mg, 500 mg, and 750 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, Green tea 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) |
Green tea 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:
Green tea extract capsules and tablets, marketed as dietary supplements, are regulated in the US by the FDA and in the EU via EMA as food supplements. Regulatory dossiers should include safety assessments, ingredient sourcing, manufacturing standards, and efficacy evidence. The FDA reviews safety and labeling, while the EMA ensures compliance with regional safety and quality standards.
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