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UP AND UP ACID REDUCER - 11673-271-39 - (Ranitidine)

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Drug Information of UP AND UP ACID REDUCER

Product NDC: 11673-271
Proprietary Name: UP AND UP ACID REDUCER
Non Proprietary Name: Ranitidine
Active Ingredient(s): 75    mg/1 & nbsp;   Ranitidine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of UP AND UP ACID REDUCER

Product NDC: 11673-271
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA076760
Marketing Category: ANDA
Start Marketing Date: 20090731

Package Information of UP AND UP ACID REDUCER

Package NDC: 11673-271-39
Package Description: 1 BOTTLE in 1 CARTON (11673-271-39) > 30 TABLET in 1 BOTTLE

NDC Information of UP AND UP ACID REDUCER

NDC Code 11673-271-39
Proprietary Name UP AND UP ACID REDUCER
Package Description 1 BOTTLE in 1 CARTON (11673-271-39) > 30 TABLET in 1 BOTTLE
Product NDC 11673-271
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ranitidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090731
Marketing Category Name ANDA
Labeler Name Target Corporation
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of UP AND UP ACID REDUCER


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