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Ranitidine - Acid Reducer - 51660-351-50 - (Ranitidine)

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Drug Information of Ranitidine - Acid Reducer

Product NDC: 51660-351
Proprietary Name: Ranitidine - 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 Ranitidine - Acid Reducer

Product NDC: 51660-351
Labeler Name: Ohm Laboratories Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA200536
Marketing Category: ANDA
Start Marketing Date: 20120330

Package Information of Ranitidine - Acid Reducer

Package NDC: 51660-351-50
Package Description: 50 TABLET in 1 BOTTLE (51660-351-50)

NDC Information of Ranitidine - Acid Reducer

NDC Code 51660-351-50
Proprietary Name Ranitidine - Acid Reducer
Package Description 50 TABLET in 1 BOTTLE (51660-351-50)
Product NDC 51660-351
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ranitidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120330
Marketing Category Name ANDA
Labeler Name Ohm Laboratories Inc.
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ranitidine - Acid Reducer


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