"70121-1720-3" National Drug Code (NDC)

NDC Code	70121-1720-3
Package Description	12 POUCH in 1 CARTON (70121-1720-3) / 1 BAG in 1 POUCH / 100 mL in 1 BAG
Product NDC	70121-1720
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Magnesium Sulfate
Non-Proprietary Name	Magnesium Sulfate In Water For
Dosage Form	INJECTION
Usage	INTRAVENOUS
Start Marketing Date	20230220
Marketing Category Name	ANDA
Application Number	ANDA216597
Manufacturer	Amneal Pharmaceuticals LLC
Substance Name	MAGNESIUM SULFATE HEPTAHYDRATE
Strength	40
Strength Unit	mg/mL
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]