"0338-9591-12" National Drug Code (NDC)

NDC Code	0338-9591-12
Package Description	12 BAG in 1 CARTON (0338-9591-12) / 1000 mL in 1 BAG (0338-9591-01)
Product NDC	0338-9591
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Plasma-lyte A
Non-Proprietary Name	Sodium Chloride, Sodium Gluconate, Sodium Acetate, Potassium Chloride And Magnesium Chloride
Dosage Form	INJECTION, SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	20241106
Marketing Category Name	UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE
Manufacturer	Baxter Healthcare Company
Substance Name	MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE
Strength	30; 37; 368; 526; 502
Strength Unit	mg/100mL; mg/100mL; mg/100mL; mg/100mL; ug/100mL
Pharmacy Classes	Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]