Visitor Monitoring Drug Details: ZANTAC 25
 
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Drug Details

Drug Name: ZANTAC 25
FDA Application No: (NDA) 020251
Active Ingredient(s): RANITIDINE HYDROCHLORIDE
Company: GLAXOSMITHKLINE
Original Approval or Tentative Approval Date: March 31, 1994
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
ZANTAC 150 RANITIDINE HYDROCHLORIDEEQ 150MG BASETABLET, EFFERVESCENT; ORAL Prescription Yes None
ZANTAC 150 RANITIDINE HYDROCHLORIDEEQ 150MG BASE/PACKETGRANULE, EFFERVESCENT; ORAL Prescription Yes None
ZANTAC 25 RANITIDINE HYDROCHLORIDEEQ 25MG BASETABLET, EFFERVESCENT; ORAL Prescription No None


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