Visitor Monitoring Drug Details: ZANTAC IN PLASTIC CONTAINER
 
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Drug Details

Drug Name: ZANTAC IN PLASTIC CONTAINER
FDA Application No: (NDA) 019593
Active Ingredient(s): RANITIDINE HYDROCHLORIDE
Company: GLAXOSMITHKLINE
Original Approval or Tentative Approval Date: December 17, 1986
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
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
ZANTAC IN PLASTIC CONTAINER RANITIDINE HYDROCHLORIDEEQ 50MG BASE/100MLINJECTABLE; INJECTION Discontinued No None
ZANTAC IN PLASTIC CONTAINER RANITIDINE HYDROCHLORIDEEQ 1MG BASE/MLINJECTABLE; INJECTION Prescription Yes None


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