"63629-2217-1" National Drug Code (NDC)

NDC Code	63629-2217-1
Package Description	100 TABLET in 1 BOTTLE (63629-2217-1)
Product NDC	63629-2217
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Magnesium Oxide
Non-Proprietary Name	Magnesium Oxide
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20201110
Marketing Category Name	OTC MONOGRAPH FINAL
Application Number	part331
Manufacturer	Bryant Ranch Prepack
Substance Name	MAGNESIUM OXIDE
Strength	253
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]