Ranitidine - 60505-0025-6 - (ranitidine hydrochloride)

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Drug Information of Ranitidine

Product NDC: 60505-0025
Proprietary Name: Ranitidine
Non Proprietary Name: ranitidine hydrochloride
Active Ingredient(s): 150    mg/1 & nbsp;   ranitidine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine

Product NDC: 60505-0025
Labeler Name: Apotex Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074680
Marketing Category: ANDA
Start Marketing Date: 19970913

Package Information of Ranitidine

Package NDC: 60505-0025-6
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (60505-0025-6)

NDC Information of Ranitidine

NDC Code 60505-0025-6
Proprietary Name Ranitidine
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (60505-0025-6)
Product NDC 60505-0025
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ranitidine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19970913
Marketing Category Name ANDA
Labeler Name Apotex Corp
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