"50090-7432-0" National Drug Code (NDC)

NDC Code	50090-7432-0
Package Description	120 TABLET in 1 BOTTLE (50090-7432-0)
Product NDC	50090-7432
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Magnesium Oxide
Non-Proprietary Name	Magnesium Oxide
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20201015
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M001
Manufacturer	A-S Medication Solutions
Substance Name	MAGNESIUM OXIDE
Strength	400
Strength Unit	mg/1
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]