"52268-302-01" National Drug Code (NDC)

NDC Code	52268-302-01
Package Description	4 L in 1 PACKAGE (52268-302-01)
Product NDC	52268-302
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nulytely
Non-Proprietary Name	Polyethylene Glycol 3350, Sodium Chloride, Sodium Bicarbonate And Potassium Chloride
Dosage Form	POWDER, FOR SOLUTION
Usage	ORAL
Start Marketing Date	19910422
End Marketing Date	20240831
Marketing Category Name	NDA
Application Number	NDA019797
Manufacturer	Braintree Laboratories, Inc.
Substance Name	POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE
Strength	420; 1.48; 5.72; 11.2
Strength Unit	g/4L; g/4L; g/4L; g/4L
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]