Ranitidine - 63739-489-10 - (Ranitidine)

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Drug Information of Ranitidine

Product NDC: 63739-489
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: 63739-489
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077824
Marketing Category: ANDA
Start Marketing Date: 20121106

Package Information of Ranitidine

Package NDC: 63739-489-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-489-10) > 10 TABLET in 1 BLISTER PACK

NDC Information of Ranitidine

NDC Code 63739-489-10
Proprietary Name Ranitidine
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-489-10) > 10 TABLET in 1 BLISTER PACK
Product NDC 63739-489
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121106
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
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