"65219-008-51" National Drug Code (NDC)

NDC Code	65219-008-51
Package Description	60 BAG in 1 CARTON (65219-008-51) / 50 mL in 1 BAG (65219-008-50)
Product NDC	65219-008
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Potassium Chloride
Non-Proprietary Name	Potassium Chloride
Dosage Form	INJECTION
Usage	INTRAVENOUS
Start Marketing Date	20210625
Marketing Category Name	ANDA
Application Number	ANDA211087
Manufacturer	Fresenius Kabi USA, LLC
Substance Name	POTASSIUM CHLORIDE
Strength	20
Strength Unit	meq/50mL
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]