"37808-673-38" National Drug Code (NDC)

NDC Code	37808-673-38
Package Description	296 mL in 1 BOTTLE, PLASTIC (37808-673-38)
Product NDC	37808-673
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Magnesium Citrate
Non-Proprietary Name	Magnesium Citrate
Dosage Form	SOLUTION
Usage	ORAL
Start Marketing Date	20210817
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M007
Manufacturer	H E BUTT
Substance Name	MAGNESIUM CITRATE
Strength	.059
Strength Unit	g/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]