"0338-0221-03" National Drug Code (NDC)

NDC Code	0338-0221-03
Package Description	500 mL in 1 BAG (0338-0221-03)
Product NDC	0338-0221
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	19790202
Marketing Category Name	NDA
Application Number	NDA017378
Manufacturer	Baxter Healthcare Corporation
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; mg/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]