"66689-047-50" National Drug Code (NDC)

NDC Code	66689-047-50
Package Description	5 TRAY in 1 CASE (66689-047-50) / 10 CUP in 1 TRAY / 15 mL in 1 CUP (66689-047-01)
Product NDC	66689-047
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Potassium Chloride
Non-Proprietary Name	Potassium Chloride
Dosage Form	SOLUTION
Usage	ORAL
Start Marketing Date	20150215
End Marketing Date	20250531
Marketing Category Name	NDA
Application Number	NDA206814
Manufacturer	VistaPharm, LLC
Substance Name	POTASSIUM CHLORIDE
Strength	20
Strength Unit	meq/15mL
Pharmacy Classes	Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]