"51525-6831-4" National Drug Code (NDC)

NDC Code	51525-6831-4
Package Description	4 L in 1 BOTTLE (51525-6831-4)
Product NDC	51525-6831
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Trilyte
Proprietary Name Suffix	With Flavor Packs
Non-Proprietary Name	Polyethylene Glyocol 3350, Sodium Chloride, Sodium Bicarbonate And Potassium Chloride
Dosage Form	POWDER, FOR SOLUTION
Usage	NASOGASTRIC; ORAL
Start Marketing Date	20161001
End Marketing Date	20210930
Marketing Category Name	ANDA
Application Number	ANDA076491
Manufacturer	Wallace Pharmaceuticals Inc.
Substance Name	POLYETHYLENE GLYCOL 3350; SODIUM CHLORIDE; SODIUM BICARBONATE; POTASSIUM CHLORIDE
Strength	420; 11.2; 5.72; 1.48
Strength Unit	g/4L; g/4L; g/4L; g/4L
Pharmacy Classes	Osmotic Activity [MoA],Osmotic Laxative [EPC],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]