"37808-503-63" National Drug Code (NDC)

NDC Code	37808-503-63
Package Description	25 TABLET, CHEWABLE in 1 BOTTLE (37808-503-63)
Product NDC	37808-503
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Dual Action Complete
Non-Proprietary Name	Famotidine, Calcium Carbonate And Magnesium Hydroxide
Dosage Form	TABLET, CHEWABLE
Usage	ORAL
Start Marketing Date	20160407
Marketing Category Name	ANDA
Application Number	ANDA077355
Manufacturer	H E B
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]