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acid reducer - 42507-141-72 - (Famotidine)

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Drug Information of acid reducer

Product NDC: 42507-141
Proprietary Name: acid reducer
Non Proprietary Name: Famotidine
Active Ingredient(s): 10    mg/1 & nbsp;   Famotidine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of acid reducer

Product NDC: 42507-141
Labeler Name: HyVee Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA075400
Marketing Category: ANDA
Start Marketing Date: 20091019

Package Information of acid reducer

Package NDC: 42507-141-72
Package Description: 1 BOTTLE in 1 CARTON (42507-141-72) > 60 TABLET in 1 BOTTLE

NDC Information of acid reducer

NDC Code 42507-141-72
Proprietary Name acid reducer
Package Description 1 BOTTLE in 1 CARTON (42507-141-72) > 60 TABLET in 1 BOTTLE
Product NDC 42507-141
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Famotidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091019
Marketing Category Name ANDA
Labeler Name HyVee Inc
Substance Name FAMOTIDINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of acid reducer


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