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up and up ranitidine - 11673-047-02 - (Ranitidine)

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Drug Information of up and up ranitidine

Product NDC: 11673-047
Proprietary Name: up and up ranitidine
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 up and up ranitidine

Product NDC: 11673-047
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078653
Marketing Category: ANDA
Start Marketing Date: 20120503

Package Information of up and up ranitidine

Package NDC: 11673-047-02
Package Description: 1 BOTTLE in 1 CARTON (11673-047-02) > 24 TABLET in 1 BOTTLE

NDC Information of up and up ranitidine

NDC Code 11673-047-02
Proprietary Name up and up ranitidine
Package Description 1 BOTTLE in 1 CARTON (11673-047-02) > 24 TABLET in 1 BOTTLE
Product NDC 11673-047
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ranitidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120503
Marketing Category Name ANDA
Labeler Name Target Corporation
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of up and up ranitidine


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