"47335-992-02" National Drug Code (NDC)

NDC Code	47335-992-02
Package Description	1 BAG in 1 POUCH (47335-992-02) > 100 mL in 1 BAG
Product NDC	47335-992
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Magnesium Sulfate
Non-Proprietary Name	Magnesium Sulfate Heptahydrate
Dosage Form	INJECTION, SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	20210801
Marketing Category Name	ANDA
Application Number	ANDA213917
Manufacturer	Sun Pharmaceutical Industries, Inc.
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]