"51316-588-63" National Drug Code (NDC)

NDC Code	51316-588-63
Package Description	25 TABLET, CHEWABLE in 1 BOTTLE (51316-588-63)
Product NDC	51316-588
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Complete Acid Reducer
Non-Proprietary Name	Famotidine, Calcium Carbonate, Magnesium Hydroxide
Dosage Form	TABLET, CHEWABLE
Usage	ORAL
Start Marketing Date	20260406
Marketing Category Name	ANDA
Application Number	ANDA077355
Manufacturer	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED
Substance Name	CALCIUM CARBONATE; FAMOTIDINE; MAGNESIUM HYDROXIDE
Strength	800; 10; 165
Strength Unit	mg/1; mg/1; mg/1
Pharmacy Classes	Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC], Increased Coagulation Factor Activity [PE], 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], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]