Basic information
Drug category type
10 g/bottle (20%, 50 mL).
Specification
20%
Standard dose
Clinical Decision · Fluid Resuscitation for Shock
Approval number
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Execution standard
<p>Imported Drug Registration Standard: JS20170024</p>
Shelf life
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Product information
This product should be a slightly viscous, clear yellow or green to brown liquid, and should not be turbid. This product is a sterile aqueous solution for intravenous infusion, containing albumin components from human blood. This product is prepared from the plasma of US donors. It is produced by ethanol fractionation and heated at 60°C for 10 hours to inactivate infectious pathogens. Results from viral validation studies demonstrate that the manufacturing process of this product, particularly ethanol fractionation, removes both enveloped and non-enveloped viruses. Additionally, heat treatment at 60°C for 10 hours effectively inactivates viruses. This product uses sodium N-acetyltryptophanate and sodium caprylate as stabilizers and contains no preservatives.
Store below 25°C and protect from light. Do not freeze.
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<p>Imported Drug Registration Standard: JS20170024</p>
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