Basic information
Drug category type
12.5 g/bottle (25%, 50 mL)
Specification
12.5g（25%，50mL）
Standard dose
Clinical Decision · Fluid Resuscitation for Shock
Approval number
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Execution standard
<p>Imported Drug Registration Standard: JS20180028</p>
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 25% human albumin (w/v) for single-dose intravenous administration. 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 acetyltryptophanate as stabilizers. This product is iso-osmotic to five 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 during the shelf life of this product. This product does not contain 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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<p>Imported Drug Registration Standard: JS20180028</p>
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