"51662-1372-1" National Drug Code (NDC)

NDC Code	51662-1372-1
Package Description	20 mL in 1 VIAL, SINGLE-DOSE (51662-1372-1)
Product NDC	51662-1372
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Magnesium Sulfate
Non-Proprietary Name	Magnesium Sulfate
Dosage Form	INJECTION, SOLUTION
Usage	INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date	20191014
Marketing Category Name	NDA
Application Number	NDA019316
Manufacturer	HF Acquisition Co LLC, DBA HealthFirst
Substance Name	MAGNESIUM SULFATE HEPTAHYDRATE
Strength	500
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]