Ranitidine - 63941-351-50 - (Ranitidine Hydrochloride)

Alphabetical Index


Drug Information of Ranitidine

Product NDC: 63941-351
Proprietary Name: Ranitidine
Non Proprietary Name: Ranitidine Hydrochloride
Active Ingredient(s): 150    mg/1 & nbsp;   Ranitidine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine

Product NDC: 63941-351
Labeler Name: Valu Merchandisers Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA200536
Marketing Category: ANDA
Start Marketing Date: 20120330

Package Information of Ranitidine

Package NDC: 63941-351-50
Package Description: 50 TABLET in 1 BOTTLE (63941-351-50)

NDC Information of Ranitidine

NDC Code 63941-351-50
Proprietary Name Ranitidine
Package Description 50 TABLET in 1 BOTTLE (63941-351-50)
Product NDC 63941-351
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ranitidine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120330
Marketing Category Name ANDA
Labeler Name Valu Merchandisers Company
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ranitidine


General Information