Basic information
Drug category type
10 g/bottle (20%, 50 mL)
Specification
10g
Standard dose
Clinical Decision · Fluid Resuscitation for Shock
Approval number
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Execution standard
Imported Drug Registration Standard: JS20180029
Shelf life
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Product information
This product is a slightly viscous, nearly colorless, yellow, amber, or green clear liquid, and should not appear turbid. This product is a sterile aqueous solution containing 20% human albumin (w/v) for single-dose intravenous injection. It is prepared from pooled human plasma obtained from venous blood using the cold ethanol fractionation method. Each gram of albumin in this product contains 0.08 mmol sodium caprylate and 0.08 mmol sodium acetyltryptophan as stabilizers. This product is iso-osmotic to four times its volume of normal human plasma. Each liter of this product contains 130-160 mEq of sodium ions. The aluminum content in the solution does not exceed 200 μg/L throughout the shelf life of the product. This product contains no preservatives. The plasma used to manufacture this product is sourced from FDA-approved plasma centers in the United States. This product undergoes heat treatment at 60 °C for 10 hours to prevent virus transmission.
Store below 30°C, protected from light. Do not freeze.
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Imported Drug Registration Standard: JS20180029
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