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equaline complete - 41163-321-63 - (famotidine, calcium carbonate and magnesium hydroxide)

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Drug Information of equaline complete

Product NDC: 41163-321
Proprietary Name: equaline 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 equaline complete

Product NDC: 41163-321
Labeler Name: Supervalu Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077355
Marketing Category: ANDA
Start Marketing Date: 20080902

Package Information of equaline complete

Package NDC: 41163-321-63
Package Description: 25 TABLET, CHEWABLE in 1 BOTTLE (41163-321-63)

NDC Information of equaline complete

NDC Code 41163-321-63
Proprietary Name equaline complete
Package Description 25 TABLET, CHEWABLE in 1 BOTTLE (41163-321-63)
Product NDC 41163-321
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 20080902
Marketing Category Name ANDA
Labeler Name Supervalu 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 equaline complete


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