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dual action - 56062-321-63 - (famotidine, calcium carbonate and magnesium hydroxide)

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Drug Information of dual action

Product NDC: 56062-321
Proprietary Name: dual action
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 dual action

Product NDC: 56062-321
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077355
Marketing Category: ANDA
Start Marketing Date: 20081205

Package Information of dual action

Package NDC: 56062-321-63
Package Description: 25 TABLET, CHEWABLE in 1 BOTTLE (56062-321-63)

NDC Information of dual action

NDC Code 56062-321-63
Proprietary Name dual action
Package Description 25 TABLET, CHEWABLE in 1 BOTTLE (56062-321-63)
Product NDC 56062-321
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 20081205
Marketing Category Name ANDA
Labeler Name Publix Super Markets 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 dual action


General Information