"51316-407-63" National Drug Code (NDC)

NDC Code	51316-407-63
Package Description	25 TABLET, CHEWABLE in 1 BOTTLE (51316-407-63)
Product NDC	51316-407
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Complete Acid Reducer
Non-Proprietary Name	Famotidine, Calcium Carbonate And Magnesium Hydroxide
Dosage Form	TABLET, CHEWABLE
Usage	ORAL
Start Marketing Date	20260713
Marketing Category Name	ANDA
Application Number	ANDA077355
Manufacturer	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Substance Name	FAMOTIDINE; CALCIUM CARBONATE; MAGNESIUM HYDROXIDE
Strength	10; 800; 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]