RANITIDINE - 54868-4350-1 - (RANITIDINE)

Alphabetical Index


Drug Information of RANITIDINE

Product NDC: 54868-4350
Proprietary Name: RANITIDINE
Non Proprietary Name: RANITIDINE
Active Ingredient(s): 300    mg/1 & nbsp;   RANITIDINE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of RANITIDINE

Product NDC: 54868-4350
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075208
Marketing Category: ANDA
Start Marketing Date: 20030919

Package Information of RANITIDINE

Package NDC: 54868-4350-1
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (54868-4350-1)

NDC Information of RANITIDINE

NDC Code 54868-4350-1
Proprietary Name RANITIDINE
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (54868-4350-1)
Product NDC 54868-4350
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name RANITIDINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030919
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of RANITIDINE


General Information