"0409-2168-02" National Drug Code (NDC)

NDC Code	0409-2168-02
Package Description	25 VIAL, SINGLE-USE in 1 TRAY (0409-2168-02) > 20 mL in 1 VIAL, SINGLE-USE (0409-2168-16)
Product NDC	0409-2168
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	20050331
Marketing Category Name	ANDA
Application Number	ANDA202411
Manufacturer	Hospira, 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]