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acid reducer plus antacid - 55312-321-63 - (famotidine, calcium carbonate and magnesium hydroxide)

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Drug Information of acid reducer plus antacid

Product NDC: 55312-321
Proprietary Name: acid reducer plus antacid
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 acid reducer plus antacid

Product NDC: 55312-321
Labeler Name: Western Family Foods Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077355
Marketing Category: ANDA
Start Marketing Date: 20080827

Package Information of acid reducer plus antacid

Package NDC: 55312-321-63
Package Description: 25 TABLET, CHEWABLE in 1 BOTTLE (55312-321-63)

NDC Information of acid reducer plus antacid

NDC Code 55312-321-63
Proprietary Name acid reducer plus antacid
Package Description 25 TABLET, CHEWABLE in 1 BOTTLE (55312-321-63)
Product NDC 55312-321
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 20080827
Marketing Category Name ANDA
Labeler Name Western Family Foods 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 acid reducer plus antacid


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