Ranitidine - 0615-4513-31 - (Ranitidine)

Alphabetical Index


Drug Information of Ranitidine

Product NDC: 0615-4513
Proprietary Name: Ranitidine
Non Proprietary Name: Ranitidine
Active Ingredient(s): 150    mg/1 & nbsp;   Ranitidine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine

Product NDC: 0615-4513
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075165
Marketing Category: ANDA
Start Marketing Date: 20091106

Package Information of Ranitidine

Package NDC: 0615-4513-31
Package Description: 31 TABLET, FILM COATED in 1 BLISTER PACK (0615-4513-31)

NDC Information of Ranitidine

NDC Code 0615-4513-31
Proprietary Name Ranitidine
Package Description 31 TABLET, FILM COATED in 1 BLISTER PACK (0615-4513-31)
Product NDC 0615-4513
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20091106
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name RANITIDINE HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]

Complete Information of Ranitidine


General Information