
Hyaluronic Acid Injectable Suppliers & Bulk Manufacturers
Available Forms: Injectable Solutions
Available Strengths: 1 mL syringes
Reference Brands: Juvederm, Restylane, Belotero(US)
Category: Nutraceuticals
Hyaluronic Acid injectable is available in Injectable Solutions and strengths such as 1 mL syringes. 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, Hyaluronic Acid injectable 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) |
Hyaluronic Acid injectable 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.
The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
Product Description: Hyaluronic acid injectable dermal fillers, marketed as Restylane, Juvederm, and others, are approved in the US by the FDA and in the EU via EMA for facial volume restoration, wrinkle reduction, and contouring. Regulatory approval requires dossiers including clinical efficacy, safety data, manufacturing standards, and pharmacovigilance plans. The FDA reviews clinical trial and quality data for timely approval, while the EMA ensures regional compliance with safety and manufacturing standards. For dossier preparation, regulatory pathways, and market access, visit PharmaTradz. Proper regional adherence supports swift approval, safe administration, and global availability, helping improve aesthetic and reconstructive outcomes worldwide.
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