"67414-700-01" National Drug Code (NDC)

NDC Code	67414-700-01
Package Description	1 POUCH in 1 CARTON (67414-700-01) / 50 TABLET in 1 POUCH
Product NDC	67414-700
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Pepcid Complete Dual Action Berry Flavor
Non-Proprietary Name	Famotidine, Calcium Carbonate, Magnesium Hydroxide
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20260730
Marketing Category Name	NDA
Application Number	NDA020958
Manufacturer	Jones Healthcare Group - Packaging Services, Inc
Substance Name	FAMOTIDINE; CALCIUM CARBONATE; MAGNESIUM HYDROXIDE
Strength	10; 800; 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]