"63868-935-10" National Drug Code (NDC)

NDC Code	63868-935-10
Package Description	296 mL in 1 BOTTLE, GLASS (63868-935-10)
Product NDC	63868-935
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Magnesium Citrate
Non-Proprietary Name	Magnesium Citrate
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20140630
End Marketing Date	20250228
Marketing Category Name	OTC MONOGRAPH NOT FINAL
Application Number	part334
Manufacturer	QUALITY CHOICE (Chain Drug Marketing Association)
Substance Name	MAGNESIUM CITRATE
Strength	1.745
Strength Unit	g/29.6mL
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]