"11673-010-71" National Drug Code (NDC)

NDC Code	11673-010-71
Package Description	50 TABLET, CHEWABLE in 1 BOTTLE (11673-010-71)
Product NDC	11673-010
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Up And Up Famotidine Complete
Non-Proprietary Name	Famotidine, Calcium Carbonate, Magnesium Hydroxide
Dosage Form	TABLET, CHEWABLE
Usage	ORAL
Start Marketing Date	20150506
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]