ZANTAC - 0173-0344-14 - (ranitidine hydrochloride)

Alphabetical Index


Drug Information of ZANTAC

Product NDC: 0173-0344
Proprietary Name: ZANTAC
Non Proprietary Name: ranitidine hydrochloride
Active Ingredient(s): 150    mg/1 & nbsp;   ranitidine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ZANTAC

Product NDC: 0173-0344
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018703
Marketing Category: NDA
Start Marketing Date: 19891001

Package Information of ZANTAC

Package NDC: 0173-0344-14
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (0173-0344-14)

NDC Information of ZANTAC

NDC Code 0173-0344-14
Proprietary Name ZANTAC
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (0173-0344-14)
Product NDC 0173-0344
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ranitidine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19891001
Marketing Category Name NDA
Labeler Name GlaxoSmithKline 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 ZANTAC


General Information