"0338-0691-04" National Drug Code (NDC)

NDC Code	0338-0691-04
Package Description	14 BAG in 1 CARTON (0338-0691-04) / 1000 mL in 1 BAG
Product NDC	0338-0691
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Potassium Chloride In Sodium Chloride
Non-Proprietary Name	Potassium Chloride And Sodium Chloride
Dosage Form	INJECTION, SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	19790202
Marketing Category Name	NDA
Application Number	NDA017648
Manufacturer	Baxter Healthcare Corporation
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]