Ranitidine - 67046-651-60 - (Ranitidine)

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Drug Information of Ranitidine

Product NDC: 67046-651
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: 67046-651
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077824
Marketing Category: ANDA
Start Marketing Date: 20100630

Package Information of Ranitidine

Package NDC: 67046-651-60
Package Description: 60 TABLET in 1 BLISTER PACK (67046-651-60)

NDC Information of Ranitidine

NDC Code 67046-651-60
Proprietary Name Ranitidine
Package Description 60 TABLET in 1 BLISTER PACK (67046-651-60)
Product NDC 67046-651
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100630
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
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