Label:
PLASMA-LYTE A- sodium chloride, sodium gluconate, sodium acetate, potassium chloride and magnesium chloride injection, s...
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  • NDC Code(s): 0338-9591-01, 0338-9591-12
  • Packager: Baxter Healthcare Company
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Unapproved drug for use in drug shortage

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated October 14, 2024

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  • Health Care Provider Letter
    DHCP Letter 1 of 17 ...
  • PACKAGE/LABEL PRINCIPAL DISPLAY PANEL
    Container Label - JB2544 1000 mL DIN 02339358 - PLASMA-LYTE A - INJECTION - PLASMA-LYTE A, Injectable - Norme Baxter Std - APPROX mmol/L Na – 140 K – 5 Mg – 1.5 Cl – 98 - ACETATE – 27 ...
  • INGREDIENTS AND APPEARANCE
    Product Information