"0338-0162-01" National Drug Code (NDC)

NDC Code	0338-0162-01
Package Description	30 BAG in 1 CARTON (0338-0162-01) / 100 mL in 1 BAG
Product NDC	0338-0162
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Sodium Chloride
Non-Proprietary Name	Sodium Chloride
Dosage Form	INJECTION
Usage	INTRAVENOUS
Start Marketing Date	19921207
Marketing Category Name	NDA
Application Number	NDA020178
Manufacturer	Baxter Healthcare Corporation
Substance Name	SODIUM CHLORIDE
Strength	900
Strength Unit	mg/100mL
Pharmacy Classes	Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]