"0338-1719-40" National Drug Code (NDC)

NDC Code	0338-1719-40
Package Description	40 BAG in 1 CARTON (0338-1719-40) / 50 mL in 1 BAG
Product NDC	0338-1719
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Magnesium Sulfate
Non-Proprietary Name	Magnesium Sulfate Heptahydrate
Dosage Form	INJECTION, SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	20200601
Marketing Category Name	ANDA
Application Number	ANDA211966
Manufacturer	Baxter Healthcare Corporation
Substance Name	MAGNESIUM SULFATE HEPTAHYDRATE
Strength	4
Strength Unit	g/50mL
Pharmacy Classes	Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]