Ranitidine - 55289-319-20 - (Ranitidine)

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Drug Information of Ranitidine

Product NDC: 55289-319
Proprietary Name: Ranitidine
Non Proprietary Name: Ranitidine
Active Ingredient(s): 150    mg/1 & nbsp;   Ranitidine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine

Product NDC: 55289-319
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077824
Marketing Category: ANDA
Start Marketing Date: 20091216

Package Information of Ranitidine

Package NDC: 55289-319-20
Package Description: 20 TABLET in 1 BOTTLE, PLASTIC (55289-319-20)

NDC Information of Ranitidine

NDC Code 55289-319-20
Proprietary Name Ranitidine
Package Description 20 TABLET in 1 BOTTLE, PLASTIC (55289-319-20)
Product NDC 55289-319
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091216
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
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