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Smart Sense Complete - 49738-321-63 - (famotidine, calcium carbonate and magnesium hydroxide)

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Drug Information of Smart Sense Complete

Product NDC: 49738-321
Proprietary Name: Smart Sense 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 Smart Sense Complete

Product NDC: 49738-321
Labeler Name: Kmart Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077355
Marketing Category: ANDA
Start Marketing Date: 20110621

Package Information of Smart Sense Complete

Package NDC: 49738-321-63
Package Description: 25 TABLET, CHEWABLE in 1 BOTTLE (49738-321-63)

NDC Information of Smart Sense Complete

NDC Code 49738-321-63
Proprietary Name Smart Sense Complete
Package Description 25 TABLET, CHEWABLE in 1 BOTTLE (49738-321-63)
Product NDC 49738-321
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 20110621
Marketing Category Name ANDA
Labeler Name Kmart Corporation
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 Smart Sense Complete


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