What strengths and dosage forms of SODIUM HYALURONATE are listed?

Sodium Hyaluronate 8mg/ml Suppliers & Bulk Manufacturers

Available Forms: Injection

Available Strengths: 8mg/ml

Reference Brands:

Injection contains Sodium hyaluronate 8mg. It is used to relieve knee pain due to osteoarthritis. Osteoarthritis is a joint disorder which involves wearing down of the protective layer (cartilage) covering the ends of the bones caused due to loss of quality of the cushioning (synovial) fluid in the joint.

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Product Description: Injection should not be used if you have infections or skin disorders around the knee. Avoid activities such as jogging, heavy lifting, tennis, and standing for a long time immediately after you have the injection and for the next two days. Talk to your doctor if you are allergic to eggs, poultry, and feathers, before taking this medicine.

Sodium Hyaluronate — third party manufacturing & bulk supply

Sodium Hyaluronate 8mg/ml is available through PharmaTradz for wholesale and bulk supply as well as on a third party (contract) manufacturing basis. Buyers sourcing this product generally take one of three routes:

Wholesale / bulk supply Stock or scheduled supply from an existing manufacturer. The fastest route where the product is already registered in your market.

Third party manufacturing Manufactured to your specification and packed under your own brand and label — suits distributors and brand owners building a portfolio in their market.

Dossier licensing Where a CTD, EU-CTD or ACTD dossier exists it can often be licensed for filing in your name, compressing market entry from years to months.

Indicative minimum order quantity

Sodium Hyaluronate is supplied as Injection — an injectable dosage form, so the indicative MOQ is 50,000 units. Actual MOQ is confirmed by the allocated manufacturer against your pack presentation and destination market. See full supply terms for dossier formats, market availability and shelf life.

Manufacturers of Sodium Hyaluronate listed on PharmaTradz hold site-level approvals across WHO-GMP, EU-GMP, USFDA, ANVISA and TGA, verified at onboarding.

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