"0990-7116-09" National Drug Code (NDC)

NDC Code	0990-7116-09
Package Description	12 POUCH in 1 CASE (0990-7116-09) / 1 BAG in 1 POUCH / 1000 mL in 1 BAG
Product NDC	0990-7116
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	20191201
Marketing Category Name	NDA
Application Number	NDA019686
Manufacturer	ICU Medical Inc.
Substance Name	POTASSIUM CHLORIDE; SODIUM CHLORIDE
Strength	2.98; 9
Strength Unit	g/1000mL; g/1000mL
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]