"0517-2020-25" National Drug Code (NDC)

NDC Code	0517-2020-25
Package Description	25 VIAL, SINGLE-DOSE in 1 TRAY (0517-2020-25) > 20 mL in 1 VIAL, SINGLE-DOSE
Product NDC	0517-2020
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nutrilyte Ii
Non-Proprietary Name	Multi-electrolyte
Dosage Form	INJECTION, SOLUTION, CONCENTRATE
Usage	INTRAVENOUS
Start Marketing Date	19901001
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	American Regent, Inc.
Substance Name	POTASSIUM ACETATE; SODIUM CHLORIDE; SODIUM ACETATE; MAGNESIUM CHLORIDE; CALCIUM CHLORIDE
Strength	98; 74.5; 64.6; 25.5; 16.55
Strength Unit	mg/mL; mg/mL; mg/mL; mg/mL; mg/mL
Pharmacy Classes	Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient]