"43386-050-19" National Drug Code (NDC)

NDC Code	43386-050-19
Package Description	438.4 g in 1 BOTTLE (43386-050-19)
Product NDC	43386-050
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Gavilyte-n
Non-Proprietary Name	Polyethylene Glycol-3350, Sodium Chloride, Potassium Chloride And Sodium Bicarbonate
Dosage Form	POWDER, FOR SOLUTION
Usage	ORAL
Start Marketing Date	20090528
Marketing Category Name	ANDA
Application Number	ANDA090019
Manufacturer	Lupin Pharmaceuticals,Inc.
Substance Name	POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE
Strength	420; 1.48; 5.72; 11.2
Strength Unit	g/438.4g; g/438.4g; g/438.4g; g/438.4g
Pharmacy Classes	Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], 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]