Vitamin K2 (Mk-7) Capsule Suppliers & Bulk Manufacturers
Available Forms: capsule.
Available Strengths: 90 mcg, 200 mcg, or 1000 mcg
Reference Brands: Jarrow Formulas, NOW Foods, Thorne(US)
Category:
Nutraceuticals
Vitamin K2 (MK-7) capsules activate proteins that regulate calcium in the body, supporting bone mineralization and cardiovascular health. It helps prevent arterial calcification, enhances bone density, reduces fracture risk, and maintains healthy blood vessel elasticity. Benefits include improved bone strength, reduced cardiovascular disease risk, and overall circulatory health worldwide.
Vitamin K2 (MK-7) Capsule is available in capsule.
and strengths such as 90 mcg, 200 mcg, or 1000 mcg.
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, Vitamin K2 (MK-7) Capsule 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) |
Vitamin K2 (MK-7) Capsule 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:
Vitamin K2 (MK-7) capsules, marketed as MenaQ7, are regulated as dietary supplements in the US by the FDA and in the EU via EMA for supporting bone and cardiovascular health. Approval requires dossiers including safety assessments, ingredient sourcing, manufacturing standards, and efficacy data. In the US, the FDA reviews safety and labeling, while the EMA ensures compliance with regional safety and quality standards.
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