High-Quality Active Pharmaceutical Ingredient for Orthopedic and Viscosupplementation Formulations
Sodium Hyaluronate API (CAS 9067-32-7) is an active pharmaceutical ingredient in the Orthopedic / Viscosupplementation API category, manufactured by Swapnroop Drugs and Pharmaceuticals, a WHO-GMP certified facility in Chhatrapati Sambhaji Nagar (Aurangabad), Maharashtra, India. It is supplied in IP/BP/EP/USP pharmacopeial grades, with MOQ starting at 1 kg for sampling and 25 kg for commercial bulk orders, full CoA/MSDS documentation, and export support to USA, UK, Germany, UAE, Saudi Arabia, Brazil, South Africa, Nigeria, Kenya, Australia, and Southeast Asian markets.
| Parameter | Specification |
|---|---|
| Appearance | White to off-white fibrous/powder |
| Identification | IR & HPLC compliant |
| Assay (HPLC) | 98.0% – 102.0% |
| Loss on Drying | NMT 1.0% |
| Residue on Ignition | NMT 0.2% |
| Heavy Metals | NMT 10 ppm |
| pH (1% Solution) | 2.0 – 4.0 |
| Individual Impurity | ≤ 0.5% |
| Total Impurities | ≤ 1.5% |
Get Bulk Quote for Sodium Hyaluronate API
WHO-GMP certified · CoA + MSDS included · Ships to 40+ countries
Sodium Hyaluronate API is positioned for companies seeking a dependable active pharmaceutical ingredient source backed by organized quality systems and scalable supply support.
Our manufacturing and supply approach for Sodium Hyaluronate emphasizes dependable commercial support, efficient order management, and pharma-focused service for long-term buyers.
Sodium Hyaluronate is commonly assessed on quality consistency, handling profile, packaging suitability, and documentation readiness before it is approved for downstream formulation use.
Sodium Hyaluronate API is manufactured under WHO-GMP certified processes with in-house quality control covering identification, assay, related substances, and heavy-metal testing for every batch. Each shipment is released against a Certificate of Analysis (CoA) and Material Safety Data Sheet (MSDS), with DMF-grade dossier support (stability data and Genotoxic Impurity Report) available for USFDA, EMA, and CDSCO regulatory submissions.
Swapnroop exports Sodium Hyaluronate API to pharmaceutical buyers across USA, UK, Germany, UAE, Saudi Arabia, Brazil, South Africa, Nigeria, Kenya, Australia, and Southeast Asian markets, with export documentation, phytosanitary/regulatory paperwork, and logistics coordination handled for both sea and air freight consignments.
We offer Sodium Hyaluronate in pharma-oriented packaging formats including sealed inner protection and moisture-barrier layers, helping maintain handling quality during storage, shipping, and routine supply movement.
Get Bulk QuoteShare your required quantity and pharmacopeial grade via WhatsApp or email.
We share CoA, MSDS, and applicable DMF-grade documents for evaluation.
Confirm a 1 kg sample or place a commercial bulk order (25 kg+).
Standard lead time is 2–4 weeks with full export documentation handled.
“Reliable supplier of Sodium Hyaluronate API. Consistent quality with full CoA documentation and on-time delivery.”
— Formulation Development Lead
“WHO-GMP certified quality with excellent technical support. Sodium Hyaluronate API meets all pharmacopoeial specifications.”
— Formulation Development Lead
Other APIs available from Swapnroop Pharma
The CAS number for Sodium Hyaluronate API is 9067-32-7. It is an Active Pharmaceutical Ingredient manufactured by Swapnroop Drugs and Pharmaceuticals in Maharashtra, India.
Sodium Hyaluronate API is available in IP, BP, EP, and USP pharmacopeial grades with HPLC-verified purity. All batches include full CoA, MSDS, and pharmacopeial identification testing.
Minimum order is 1 kg for sampling and 25 kg for commercial bulk supply of Sodium Hyaluronate API. Standard lead time is 2–4 weeks from our Aurangabad, Maharashtra facility.
Yes, Swapnroop provides full DMF-grade documentation for Sodium Hyaluronate API including CoA, MSDS, Genotoxic Impurity Report, Stability Data, and regulatory dossier support for USFDA, EMA, and CDSCO.
Molecular weight range and viscosity grade of Sodium Hyaluronate can be discussed based on the buyer's injectable formulation requirement. Please share your target specification when requesting a quote.
For companies evaluating Sodium Hyaluronate API manufacturer options in India, this page offers a clear overview of the product profile, quality approach, and supply readiness.
Our team works with buyers who need Sodium Hyaluronate API backed by practical documentation support, organized batch handling, and efficient supply communication for ongoing business.