Ranitidine - 50436-6930-3 - (Ranitidine)

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Drug Information of Ranitidine

Product NDC: 50436-6930
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: 50436-6930
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078542
Marketing Category: ANDA
Start Marketing Date: 20081119

Package Information of Ranitidine

Package NDC: 50436-6930-3
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (50436-6930-3)

NDC Information of Ranitidine

NDC Code 50436-6930-3
Proprietary Name Ranitidine
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (50436-6930-3)
Product NDC 50436-6930
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20081119
Marketing Category Name ANDA
Labeler Name Unit Dose Services
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