Ranitidine - 63739-266-10 - (Ranitidine)

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Drug Information of Ranitidine

Product NDC: 63739-266
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: 63739-266
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075180
Marketing Category: ANDA
Start Marketing Date: 20040701

Package Information of Ranitidine

Package NDC: 63739-266-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-266-10) > 10 TABLET in 1 BLISTER PACK

NDC Information of Ranitidine

NDC Code 63739-266-10
Proprietary Name Ranitidine
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-266-10) > 10 TABLET in 1 BLISTER PACK
Product NDC 63739-266
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040701
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
Substance Name RANITIDINE
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