"70518-1607-0" National Drug Code (NDC)

NDC Code	70518-1607-0
Package Description	25 VIAL, SINGLE-DOSE in 1 TRAY (70518-1607-0) > 10 mL in 1 VIAL, SINGLE-DOSE
Product NDC	70518-1607
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Magnesium Sulfate
Non-Proprietary Name	Magnesium Sulfate Heptahydrate
Dosage Form	INJECTION, SOLUTION
Usage	INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date	20181029
Marketing Category Name	ANDA
Application Number	ANDA206039
Manufacturer	REMEDYREPACK INC.
Substance Name	MAGNESIUM SULFATE HEPTAHYDRATE
Strength	500
Strength Unit	mg/mL
Pharmacy Classes	Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]