RANITIDINE - 55648-907-09 - (RANITIDINE)

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Drug Information of RANITIDINE

Product NDC: 55648-907
Proprietary Name: RANITIDINE
Non Proprietary Name: RANITIDINE
Active Ingredient(s): 300    mg/1 & nbsp;   RANITIDINE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of RANITIDINE

Product NDC: 55648-907
Labeler Name: WOCKHARDT LIMITED
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075208
Marketing Category: ANDA
Start Marketing Date: 19981217

Package Information of RANITIDINE

Package NDC: 55648-907-09
Package Description: 3750 TABLET in 1 DRUM (55648-907-09)

NDC Information of RANITIDINE

NDC Code 55648-907-09
Proprietary Name RANITIDINE
Package Description 3750 TABLET in 1 DRUM (55648-907-09)
Product NDC 55648-907
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name RANITIDINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19981217
Marketing Category Name ANDA
Labeler Name WOCKHARDT LIMITED
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