"63323-686-10" National Drug Code (NDC)

NDC Code	63323-686-10
Package Description	10 BAG in 1 CARTON (63323-686-10) / 1000 mL in 1 BAG (63323-686-01)
Product NDC	63323-686
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Potassium Chloride In Sodium Chloride
Non-Proprietary Name	Sodium Chloride And Potassium Chloride
Dosage Form	INJECTION, SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	20210602
Marketing Category Name	ANDA
Application Number	ANDA212347
Manufacturer	Fresenius Kabi USA, LLC
Substance Name	POTASSIUM CHLORIDE; SODIUM CHLORIDE
Strength	150; 900
Strength Unit	mg/100mL; mg/100mL
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 Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]