"82442-321-71" National Drug Code (NDC)

NDC Code	82442-321-71
Package Description	50 TABLET, CHEWABLE in 1 BOTTLE (82442-321-71)
Product NDC	82442-321
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Up And Up Dual Action Acid Reducer Antacid
Non-Proprietary Name	Famotidine, Calcium Carbonate And Magnesium Hydroxide
Dosage Form	TABLET, CHEWABLE
Usage	ORAL
Start Marketing Date	20250108
Marketing Category Name	ANDA
Application Number	ANDA077355
Manufacturer	Target Corporation
Substance Name	CALCIUM CARBONATE; FAMOTIDINE; MAGNESIUM HYDROXIDE
Strength	800; 10; 165
Strength Unit	mg/1; mg/1; mg/1
Pharmacy Classes	Calculi Dissolution Agent [EPC], Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [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]