UP AND UP DUAL ACTION ACID REDUCER ANTACID

Product NDC

82442-321

11-digit product format

824420321

Labeler code

82442

Product ID

82442-321_1d1f2bed-e173-402f-875a-af1a73c87d96

Type

HUMAN OTC DRUG

Nonproprietary name

famotidine, calcium carbonate and magnesium hydroxide

Dosage form

TABLET, CHEWABLE

Route

ORAL

Labeler

Target Corporation

Application

ANDA077355

Marketing category

ANDA

Marketing start

2025-01-08

Substance

CALCIUM CARBONATE; FAMOTIDINE; MAGNESIUM HYDROXIDE

Active strength

800; 10; 165 mg/1; mg/1; mg/1

Pharmacologic 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]

NDC exclude flag

No

Listing certified through

2026-12-31

Current FDA listing

Yes