Ranitidine - 55289-505-30 - (Ranitidine)

Alphabetical Index


Drug Information of Ranitidine

Product NDC: 55289-505
Proprietary Name: Ranitidine
Non Proprietary Name: Ranitidine
Active Ingredient(s): 300    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: 55289-505
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075165
Marketing Category: ANDA
Start Marketing Date: 20091106

Package Information of Ranitidine

Package NDC: 55289-505-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-505-30)

NDC Information of Ranitidine

NDC Code 55289-505-30
Proprietary Name Ranitidine
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-505-30)
Product NDC 55289-505
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 PD-Rx Pharmaceuticals, 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