"63323-139-40" National Drug Code (NDC)

NDC Code	63323-139-40
Package Description	25 VIAL, SINGLE-DOSE in 1 TRAY (63323-139-40) / 40 mL in 1 VIAL, SINGLE-DOSE
Product NDC	63323-139
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Sodium Chloride
Non-Proprietary Name	Sodium Chloride
Dosage Form	INJECTION, SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	20000906
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	Fresenius Kabi USA, LLC
Substance Name	SODIUM CHLORIDE
Strength	146
Strength Unit	mg/mL
Pharmacy Classes	Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]