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Up and Up dual action acid controller complete - 11673-321-71 - (famotidine, calcium carbonate and magnesium hydroxide)

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Drug Information of Up and Up dual action acid controller complete

Product NDC: 11673-321
Proprietary Name: Up and Up dual action acid controller 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 Up and Up dual action acid controller complete

Product NDC: 11673-321
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077355
Marketing Category: ANDA
Start Marketing Date: 20090626

Package Information of Up and Up dual action acid controller complete

Package NDC: 11673-321-71
Package Description: 50 TABLET, CHEWABLE in 1 BOTTLE (11673-321-71)

NDC Information of Up and Up dual action acid controller complete

NDC Code 11673-321-71
Proprietary Name Up and Up dual action acid controller complete
Package Description 50 TABLET, CHEWABLE in 1 BOTTLE (11673-321-71)
Product NDC 11673-321
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 20090626
Marketing Category Name ANDA
Labeler Name Target 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 Up and Up dual action acid controller complete


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