Ranitidine - 68788-9874-0 - (Ranitidine)

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Drug Information of Ranitidine

Product NDC: 68788-9874
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: 68788-9874
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077824
Marketing Category: ANDA
Start Marketing Date: 20120227

Package Information of Ranitidine

Package NDC: 68788-9874-0
Package Description: 100 TABLET in 1 BOTTLE (68788-9874-0)

NDC Information of Ranitidine

NDC Code 68788-9874-0
Proprietary Name Ranitidine
Package Description 100 TABLET in 1 BOTTLE (68788-9874-0)
Product NDC 68788-9874
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120227
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
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