Ranitidine - 76237-231-30 - (Ranitidine)

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Drug Information of Ranitidine

Product NDC: 76237-231
Proprietary Name: Ranitidine
Non Proprietary Name: Ranitidine
Active Ingredient(s): 150    mg/1 & nbsp;   Ranitidine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ranitidine

Product NDC: 76237-231
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075165
Marketing Category: ANDA
Start Marketing Date: 20111026

Package Information of Ranitidine

Package NDC: 76237-231-30
Package Description: 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-231-30) > 5 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Ranitidine

NDC Code 76237-231-30
Proprietary Name Ranitidine
Package Description 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-231-30) > 5 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 76237-231
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ranitidine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111026
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
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