You can pay by credit card or by invoice after credit review.

After your order has been processed, you will receive an email with a link that will take you to a secure site to enter your payment information.

No, our sodium hyaluronate products are non-taxable.

Sodium hyaluronate products are shipped using HS code 3913.90.2090

To generate an automatic quote for research-grade or hydrogel products, please visit our quotation page. For GMP injectable-grade (for clinical or commercial products) or for custom modifications, please complete our online inquiry.

For products that are in-stock, lead time is usually one week. We endeavor to maintain a stock of all standard products at all times, but incoming orders affect stocking levels. If lead time is critical, please complete our online inquiry. and identify your product interest and desired shipment date.

Exact costs are not known until time of shipment. Estimated cost for U.S. orders are $40-80 USD, and $120-190 USD for non-U.S. destinations.

We typically see a polydispersity of 1.1 – 1.3 using the MALLS (multi-angle light laser scattering) Technique. Since research-grade products are derived from GMP lots, there is no difference in results from research to clinical use.

The recommended temperature for storing sodium hyaluronate is -20C +/-5C.

Lifecore’s sodium hyaluronate has low bioburden. You can sterilize solutions by sterile filtration. Lifecore also offers sterile sodium hyaluronate and can custom prepare sterile sodium hyaluronate solutions with viscosities higher than a typical lab can process. Please complete our online inquiry if you are interested in purchasing sterile sodium hyaluronate.

We measure the IV (intrinsic viscosity) of each lot, and then use the Mark- Houwink equation to convert it to MW.

Research-use only sodium hyaluronate is derived from GMP lots and can be used in animal studies.

Our sodium hyaluronate is produced via a bacterial fermentation process. Our products are non-animal sourced and produced in the United States.

Sodium hyaluronate is used in finished medical products as:

• A raw material in medical device products
• An excipient in drug products
• An active pharmaceutical ingredient in drug products

Lifecore has simplified your finished product regulatory approval process by maintaining the following regulatory files applicable to sodium hyaluronate that can be incorporated by reference into your submissions. Each file has been referenced many times for both drug products and medical device products.

• United States Drug Master File (DMF)
• European Certificate of Suitability

The US DMF is reviewed along with each finished product submission that refers to it. As such, the DMF is not approved by FDA.

The European Certificate of Suitability is reviewed and approved at the time Lifecore applies for the certificate by the European Directorate for the Quality of Medicines (EDQM). As such, minimal review is required by the competent authority reviewing your finished product marketing authorization application (MAA). The certificate of suitability is accepted in many countries outside of Europe as well.

We have standard options from 5 kDa – 1.8 MDa.

Please feel free to reach out using our contact page here.