Ranitidine - 49884-544-10 - (ranitidine)

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Drug Information of Ranitidine

Product NDC: 49884-544
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: 49884-544
Labeler Name: Par Pharmaceutical Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075180
Marketing Category: ANDA
Start Marketing Date: 19990128

Package Information of Ranitidine

Package NDC: 49884-544-10
Package Description: 1000 TABLET in 1 BOTTLE (49884-544-10)

NDC Information of Ranitidine

NDC Code 49884-544-10
Proprietary Name Ranitidine
Package Description 1000 TABLET in 1 BOTTLE (49884-544-10)
Product NDC 49884-544
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ranitidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19990128
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical 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