"40032-060-19" National Drug Code (NDC)

NDC Code	40032-060-19
Package Description	278.26 g in 1 BOTTLE (40032-060-19)
Product NDC	40032-060
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Polyethylene Glycol-3350 And Electrolytes With Flavor Pack
Non-Proprietary Name	Polyethylene Glycol-3350 And Electrolytes With Flavor Pack
Dosage Form	POWDER, FOR SOLUTION
Usage	ORAL
Start Marketing Date	20090601
Marketing Category Name	ANDA
Application Number	ANDA090186
Manufacturer	Novel Laboratories, Inc.
Substance Name	POLYETHYLENE GLYCOL 3350; SODIUM CHLORIDE; SODIUM BICARBONATE; POTASSIUM CHLORIDE; SODIUM SULFATE ANHYDROUS
Strength	240; 5.84; 6.72; 2.98; 22.72
Strength Unit	g/278.26g; g/278.26g; g/278.26g; g/278.26g; g/278.26g
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],Potassium Compounds [CS],Potassium Salt [EPC],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]