"83335-001-12" National Drug Code (NDC)

NDC Code	83335-001-12
Package Description	120 mg in 1 BOTTLE, PLASTIC (83335-001-12)
Product NDC	83335-001
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Magnesium Oxide
Non-Proprietary Name	Magnesium Oxide
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20230316
Marketing Category Name	OTC MONOGRAPH DRUG
Application Number	M001
Manufacturer	Wittman Pharma, Inc.
Substance Name	MAGNESIUM OXIDE
Strength	241.3
Strength Unit	mg/1000mg
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]