"0409-7115-09" National Drug Code (NDC)

NDC Code	0409-7115-09
Package Description	12 POUCH in 1 CASE (0409-7115-09) > 1 BAG in 1 POUCH > 1000 mL in 1 BAG
Product NDC	0409-7115
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	19881017
End Marketing Date	20200901
Marketing Category Name	NDA
Application Number	NDA019686
Manufacturer	Hospira, Inc.
Substance Name	SODIUM CHLORIDE; POTASSIUM CHLORIDE
Strength	9; 1.49
Strength Unit	g/1000mL; g/1000mL
Pharmacy Classes	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]