"10135-721-01" National Drug Code (NDC)

NDC Code	10135-721-01
Package Description	100 TABLET in 1 BOTTLE (10135-721-01)
Product NDC	10135-721
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Magnesium Oxide
Non-Proprietary Name	Magnesium Oxide
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20231101
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M001
Manufacturer	Marlex Pharmaceuticals Inc.
Substance Name	MAGNESIUM OXIDE
Strength	420
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]