Ranitidine - 63941-352-60 - (Ranitidine Hydrochloride)

Alphabetical Index


Drug Information of Ranitidine

Product NDC: 63941-352
Proprietary Name: Ranitidine
Non Proprietary Name: Ranitidine Hydrochloride
Active Ingredient(s): 75    mg/1 & nbsp;   Ranitidine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine

Product NDC: 63941-352
Labeler Name: Valu Merchandisers Company
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA201745
Marketing Category: ANDA
Start Marketing Date: 20120710

Package Information of Ranitidine

Package NDC: 63941-352-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (63941-352-60)

NDC Information of Ranitidine

NDC Code 63941-352-60
Proprietary Name Ranitidine
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (63941-352-60)
Product NDC 63941-352
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ranitidine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120710
Marketing Category Name ANDA
Labeler Name Valu Merchandisers Company
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ranitidine


General Information