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Acid Reducer - 21130-047-71 - (Ranitidine)

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Drug Information of Acid Reducer

Product NDC: 21130-047
Proprietary Name: Acid Reducer
Non Proprietary Name: Ranitidine
Active Ingredient(s): 150    mg/1 & nbsp;   Ranitidine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Acid Reducer

Product NDC: 21130-047
Labeler Name: Safeway
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078653
Marketing Category: ANDA
Start Marketing Date: 20080220

Package Information of Acid Reducer

Package NDC: 21130-047-71
Package Description: 1 BOTTLE in 1 CARTON (21130-047-71) > 50 TABLET in 1 BOTTLE

NDC Information of Acid Reducer

NDC Code 21130-047-71
Proprietary Name Acid Reducer
Package Description 1 BOTTLE in 1 CARTON (21130-047-71) > 50 TABLET in 1 BOTTLE
Product NDC 21130-047
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ranitidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080220
Marketing Category Name ANDA
Labeler Name Safeway
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Acid Reducer


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