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><span style = "color: rgb(0,0,0);">Registration Standard for Imported Drugs: JS20180016</span></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 plasma separated from US donors. It is produced by ethanol fractionation and heated at 60 ℃ for 10 hours to inactivate infectious pathogens. Results from viral validation studies show that the manufacturing process of this product, especially ethanol fractionation, removes enveloped and non-enveloped viruses. In addition, heat treatment at 60 ℃ for 10 hours effectively inactivates viruses. This product uses N-acetyltryptophan sodium and sodium caprylate as stabilizers and contains no preservatives.
Store below 30°C, protected from light. Do not freeze.
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<p><span style = "color: rgb(0,0,0);">Registration Standard for Imported Drugs: JS20180016</span></p>
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See how SinoMDB organizes medicine information from public regulatory records, clinical medication references, and drug interaction materials.