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Dual Action Complete - 30142-321-71 - (famotidine, calcium carbonate and magnesium hydroxide)

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Drug Information of Dual Action Complete

Product NDC: 30142-321
Proprietary Name: 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 Dual Action Complete

Product NDC: 30142-321
Labeler Name: Kroger Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077355
Marketing Category: ANDA
Start Marketing Date: 20080909

Package Information of Dual Action Complete

Package NDC: 30142-321-71
Package Description: 50 TABLET, CHEWABLE in 1 BOTTLE (30142-321-71)

NDC Information of Dual Action Complete

NDC Code 30142-321-71
Proprietary Name Dual Action Complete
Package Description 50 TABLET, CHEWABLE in 1 BOTTLE (30142-321-71)
Product NDC 30142-321
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 20080909
Marketing Category Name ANDA
Labeler Name Kroger Company
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 Complete


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