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Rx Act Heartburn Relief - 37808-047-09 - (Ranitidine)

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Drug Information of Rx Act Heartburn Relief

Product NDC: 37808-047
Proprietary Name: Rx Act Heartburn Relief
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 Rx Act Heartburn Relief

Product NDC: 37808-047
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078653
Marketing Category: ANDA
Start Marketing Date: 20080220

Package Information of Rx Act Heartburn Relief

Package NDC: 37808-047-09
Package Description: 1 BOTTLE in 1 CARTON (37808-047-09) > 65 TABLET in 1 BOTTLE

NDC Information of Rx Act Heartburn Relief

NDC Code 37808-047-09
Proprietary Name Rx Act Heartburn Relief
Package Description 1 BOTTLE in 1 CARTON (37808-047-09) > 65 TABLET in 1 BOTTLE
Product NDC 37808-047
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 H E B
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Rx Act Heartburn Relief


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