Home > National Drug Code (NDC) > DG Health Dual Action Complete

DG Health Dual Action Complete - 55910-321-52 - (famotidine, calcium carbonate and magnesium hydroxide)

Alphabetical Index


Drug Information of DG Health Dual Action Complete

Product NDC: 55910-321
Proprietary Name: DG Health Dual Action Complete
Non Proprietary Name: famotidine, calcium carbonate and magnesium hydroxide
Active Ingredient(s): 800; 10; 165    mg/1; mg/1; mg/1 & nbsp;   famotidine, calcium carbonate and magnesium hydroxide
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of DG Health Dual Action Complete

Product NDC: 55910-321
Labeler Name: Dolgencorp Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077355
Marketing Category: ANDA
Start Marketing Date: 20090716

Package Information of DG Health Dual Action Complete

Package NDC: 55910-321-52
Package Description: 10 TABLET, CHEWABLE in 1 BOTTLE (55910-321-52)

NDC Information of DG Health Dual Action Complete

NDC Code 55910-321-52
Proprietary Name DG Health Dual Action Complete
Package Description 10 TABLET, CHEWABLE in 1 BOTTLE (55910-321-52)
Product NDC 55910-321
Product Type Name HUMAN OTC DRUG
Non Proprietary Name famotidine, calcium carbonate and magnesium hydroxide
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20090716
Marketing Category Name ANDA
Labeler Name Dolgencorp Inc
Substance Name CALCIUM CARBONATE; FAMOTIDINE; MAGNESIUM HYDROXIDE
Strength Number 800; 10; 165
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of DG Health Dual Action Complete


General Information