Vitamin C (Ascorbic Acid) Tablets/Capsules Suppliers & Bulk Manufacturers
Available Forms: Tablet/Capsules
Available Strengths: 500 mg, 1000 mg, and 2000 mg in tablets, capsules
Reference Brands: NOW Foods, Nature’s Way, Solgar(US)
Category: Nutraceuticals
Vitamin C (Ascorbic Acid) is an antioxidant that supports immune function, collagen synthesis, and tissue repair. It enhances wound healing, skin health, and antioxidant protection. Benefits include increased immunity, reduced inflammation, improved skin elasticity, and protection against oxidative stress, promoting overall health and wellness worldwide. Vitamin C (Ascorbic Acid) tablets/capsules is available in Tablet/Capsules and strengths such as 500 mg, 1000 mg, and 2000 mg in tablets, capsules. 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 C (Ascorbic Acid) tablets/capsules 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 C (Ascorbic Acid) tablets/capsules 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 C (Ascorbic Acid) tablets and capsules are widely available as dietary supplements in both the US and EU. In the US, the FDA classifies them as food supplements, requiring minimal dossiers, primarily related to labeling and manufacturing. In the EU, compliance involves adherence to food safety standards and labeling regulations under regional authorities. Dossiers should include ingredient sourcing, safety data, manufacturing practices, and quality controls. For guidance on dossier preparation, regulatory pathways, and market access, visit PharmaTradz. Proper compliance supports timely approval, safe consumption, and global availability, helping consumers worldwide maintain immune health, antioxidant support, and overall wellness effectively across regions.
The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
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