"51662-1373-1" National Drug Code (NDC)

NDC Code	51662-1373-1
Package Description	50 mL in 1 BAG (51662-1373-1)
Product NDC	51662-1373
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Magnesium Sulfate
Non-Proprietary Name	Magnesium Sulfate
Dosage Form	INJECTION, SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	20191209
Marketing Category Name	ANDA
Application Number	ANDA206485
Manufacturer	HF Acquisition Co LLC, DBA HealthFirst
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]