Ranitidine - 35356-670-18 - (Ranitidine)

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Drug Information of Ranitidine

Product NDC: 35356-670
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: 35356-670
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077824
Marketing Category: ANDA
Start Marketing Date: 20091216

Package Information of Ranitidine

Package NDC: 35356-670-18
Package Description: 180 TABLET in 1 BOTTLE (35356-670-18)

NDC Information of Ranitidine

NDC Code 35356-670-18
Proprietary Name Ranitidine
Package Description 180 TABLET in 1 BOTTLE (35356-670-18)
Product NDC 35356-670
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091216
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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